Circulating interleukin-10 and interleukin-12 in Parkinson's disease

Background –  Interleukin (IL)‐12 is a heterodimeric cytokine produced by activated blood monocytes, macrophages and glial cells. It enhances differentiation and proliferation of T cells and increases production of proinflammatory cytokines. IL‐10 is a pleiotropic cytokine produced by both lymphocyt...

Full description

Saved in:
Bibliographic Details
Published inActa neurologica Scandinavica Vol. 119; no. 5; pp. 332 - 337
Main Authors Rentzos, M., Nikolaou, C., Andreadou, E., Paraskevas, G. P., Rombos, A., Zoga, M., Tsoutsou, A., Boufidou, F., Kapaki, E., Vassilopoulos, D.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.05.2009
Blackwell
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Background –  Interleukin (IL)‐12 is a heterodimeric cytokine produced by activated blood monocytes, macrophages and glial cells. It enhances differentiation and proliferation of T cells and increases production of proinflammatory cytokines. IL‐10 is a pleiotropic cytokine produced by both lymphocytes and mononuclear phagocytes including microglia. Recent studies demonstrated the neuroprotective effect of IL‐10. There is little information about the involvement of IL‐12 or IL‐10 in the pathophysiology of Parkinson’s disease (PD). Objectives –  The objective of our study was to assess the role of IL‐12 as a potential marker of immune reactions in patients with PD and to investigate whether IL‐10, an immunosuppressive cytokine, may have a neuroprotective effect in the pathogenesis of PD. Patients and methods –  We measured using immunoassay serum IL‐12 and IL‐10 levels in 41 patients with PD in comparison with serum levels in 19 healthy subjects (controls) age and sex matched. IL‐12 and IL‐10 levels were tested for correlation with sex, age, disease duration, Hoehn and Yahr stage and the UPDRS III score. Results –  The PD group presented with significantly increased IL‐10 levels when compared with the control group (P = 0.02). The increase observed was not affected by the treatment status. A strong and significant correlation between IL‐10 and IL‐12 levels was observed in patients with PD (RS = 0.7, P < 0.000001). Conclusions –  Our findings suggest that IL‐10 may be involved in the pathogenetic mechanisms of PD. The elevation of IL‐10 and the significant correlation between IL‐10 and IL‐12, a proinflammatory cytokine, may suggest that immunological disturbances and neuroprotective mechanisms are involved in patients with PD.
AbstractList Interleukin (IL)-12 is a heterodimeric cytokine produced by activated blood monocytes, macrophages and glial cells. It enhances differentiation and proliferation of T cells and increases production of proinflammatory cytokines. IL-10 is a pleiotropic cytokine produced by both lymphocytes and mononuclear phagocytes including microglia. Recent studies demonstrated the neuroprotective effect of IL-10. There is little information about the involvement of IL-12 or IL-10 in the pathophysiology of Parkinson's disease (PD).BACKGROUNDInterleukin (IL)-12 is a heterodimeric cytokine produced by activated blood monocytes, macrophages and glial cells. It enhances differentiation and proliferation of T cells and increases production of proinflammatory cytokines. IL-10 is a pleiotropic cytokine produced by both lymphocytes and mononuclear phagocytes including microglia. Recent studies demonstrated the neuroprotective effect of IL-10. There is little information about the involvement of IL-12 or IL-10 in the pathophysiology of Parkinson's disease (PD).The objective of our study was to assess the role of IL-12 as a potential marker of immune reactions in patients with PD and to investigate whether IL-10, an immunosuppressive cytokine, may have a neuroprotective effect in the pathogenesis of PD.OBJECTIVESThe objective of our study was to assess the role of IL-12 as a potential marker of immune reactions in patients with PD and to investigate whether IL-10, an immunosuppressive cytokine, may have a neuroprotective effect in the pathogenesis of PD.We measured using immunoassay serum IL-12 and IL-10 levels in 41 patients with PD in comparison with serum levels in 19 healthy subjects (controls) age and sex matched. IL-12 and IL-10 levels were tested for correlation with sex, age, disease duration, Hoehn and Yahr stage and the UPDRS III score.PATIENTS AND METHODSWe measured using immunoassay serum IL-12 and IL-10 levels in 41 patients with PD in comparison with serum levels in 19 healthy subjects (controls) age and sex matched. IL-12 and IL-10 levels were tested for correlation with sex, age, disease duration, Hoehn and Yahr stage and the UPDRS III score.The PD group presented with significantly increased IL-10 levels when compared with the control group (P = 0.02). The increase observed was not affected by the treatment status. A strong and significant correlation between IL-10 and IL-12 levels was observed in patients with PD (R(S) = 0.7, P < 0.000001).RESULTSThe PD group presented with significantly increased IL-10 levels when compared with the control group (P = 0.02). The increase observed was not affected by the treatment status. A strong and significant correlation between IL-10 and IL-12 levels was observed in patients with PD (R(S) = 0.7, P < 0.000001).Our findings suggest that IL-10 may be involved in the pathogenetic mechanisms of PD. The elevation of IL-10 and the significant correlation between IL-10 and IL-12, a proinflammatory cytokine, may suggest that immunological disturbances and neuroprotective mechanisms are involved in patients with PD.CONCLUSIONSOur findings suggest that IL-10 may be involved in the pathogenetic mechanisms of PD. The elevation of IL-10 and the significant correlation between IL-10 and IL-12, a proinflammatory cytokine, may suggest that immunological disturbances and neuroprotective mechanisms are involved in patients with PD.
Rentzos M, Nikolaou C, Andreadou E, Paraskevas GP, Rombos A, Zoga M, Tsoutsou A, Boufidou F, Kapaki E, Vassilopoulos D. Circulating interleukin-10 and interleukin-12 in Parkinson's disease.Acta Neurol Scand: DOI: 2009: 119: 332-337[copy ] 2008 The Authors Journal compilation [copy ] 2008 Blackwell Munksgaard.Background - Interleukin (IL)-12 is a heterodimeric cytokine produced by activated blood monocytes, macrophages and glial cells. It enhances differentiation and proliferation of T cells and increases production of proinflammatory cytokines. IL-10 is a pleiotropic cytokine produced by both lymphocytes and mononuclear phagocytes including microglia. Recent studies demonstrated the neuroprotective effect of IL-10. There is little information about the involvement of IL-12 or IL-10 in the pathophysiology of Parkinson's disease (PD).Objectives - The objective of our study was to assess the role of IL-12 as a potential marker of immune reactions in patients with PD and to investigate whether IL-10, an immunosuppressive cytokine, may have a neuroprotective effect in the pathogenesis of PD.Patients and methods - We measured using immunoassay serum IL-12 and IL-10 levels in 41 patients with PD in comparison with serum levels in 19 healthy subjects (controls) age and sex matched. IL-12 and IL-10 levels were tested for correlation with sex, age, disease duration, Hoehn and Yahr stage and the UPDRS III score.Results - The PD group presented with significantly increased IL-10 levels when compared with the control group (P = 0.02). The increase observed was not affected by the treatment status. A strong and significant correlation between IL-10 and IL-12 levels was observed in patients with PD (RS = 0.7, P < 0.000001).Conclusions - Our findings suggest that IL-10 may be involved in the pathogenetic mechanisms of PD. The elevation of IL-10 and the significant correlation between IL-10 and IL-12, a proinflammatory cytokine, may suggest that immunological disturbances and neuroprotective mechanisms are involved in patients with PD.
Background –  Interleukin (IL)‐12 is a heterodimeric cytokine produced by activated blood monocytes, macrophages and glial cells. It enhances differentiation and proliferation of T cells and increases production of proinflammatory cytokines. IL‐10 is a pleiotropic cytokine produced by both lymphocytes and mononuclear phagocytes including microglia. Recent studies demonstrated the neuroprotective effect of IL‐10. There is little information about the involvement of IL‐12 or IL‐10 in the pathophysiology of Parkinson’s disease (PD). Objectives –  The objective of our study was to assess the role of IL‐12 as a potential marker of immune reactions in patients with PD and to investigate whether IL‐10, an immunosuppressive cytokine, may have a neuroprotective effect in the pathogenesis of PD. Patients and methods –  We measured using immunoassay serum IL‐12 and IL‐10 levels in 41 patients with PD in comparison with serum levels in 19 healthy subjects (controls) age and sex matched. IL‐12 and IL‐10 levels were tested for correlation with sex, age, disease duration, Hoehn and Yahr stage and the UPDRS III score. Results –  The PD group presented with significantly increased IL‐10 levels when compared with the control group (P = 0.02). The increase observed was not affected by the treatment status. A strong and significant correlation between IL‐10 and IL‐12 levels was observed in patients with PD (RS = 0.7, P < 0.000001). Conclusions –  Our findings suggest that IL‐10 may be involved in the pathogenetic mechanisms of PD. The elevation of IL‐10 and the significant correlation between IL‐10 and IL‐12, a proinflammatory cytokine, may suggest that immunological disturbances and neuroprotective mechanisms are involved in patients with PD.
Interleukin (IL)-12 is a heterodimeric cytokine produced by activated blood monocytes, macrophages and glial cells. It enhances differentiation and proliferation of T cells and increases production of proinflammatory cytokines. IL-10 is a pleiotropic cytokine produced by both lymphocytes and mononuclear phagocytes including microglia. Recent studies demonstrated the neuroprotective effect of IL-10. There is little information about the involvement of IL-12 or IL-10 in the pathophysiology of Parkinson's disease (PD). The objective of our study was to assess the role of IL-12 as a potential marker of immune reactions in patients with PD and to investigate whether IL-10, an immunosuppressive cytokine, may have a neuroprotective effect in the pathogenesis of PD. We measured using immunoassay serum IL-12 and IL-10 levels in 41 patients with PD in comparison with serum levels in 19 healthy subjects (controls) age and sex matched. IL-12 and IL-10 levels were tested for correlation with sex, age, disease duration, Hoehn and Yahr stage and the UPDRS III score. The PD group presented with significantly increased IL-10 levels when compared with the control group (P = 0.02). The increase observed was not affected by the treatment status. A strong and significant correlation between IL-10 and IL-12 levels was observed in patients with PD (R(S) = 0.7, P < 0.000001). Our findings suggest that IL-10 may be involved in the pathogenetic mechanisms of PD. The elevation of IL-10 and the significant correlation between IL-10 and IL-12, a proinflammatory cytokine, may suggest that immunological disturbances and neuroprotective mechanisms are involved in patients with PD.
Author Paraskevas, G. P.
Tsoutsou, A.
Andreadou, E.
Vassilopoulos, D.
Kapaki, E.
Zoga, M.
Rentzos, M.
Nikolaou, C.
Rombos, A.
Boufidou, F.
Author_xml – sequence: 1
  givenname: M.
  surname: Rentzos
  fullname: Rentzos, M.
  organization: Department of Neurology
– sequence: 2
  givenname: C.
  surname: Nikolaou
  fullname: Nikolaou, C.
  organization: Microbiology Lab, Aeginition Hospital, School of Medicine, Athens National University, Athens, Greece
– sequence: 3
  givenname: E.
  surname: Andreadou
  fullname: Andreadou, E.
  organization: Department of Neurology
– sequence: 4
  givenname: G. P.
  surname: Paraskevas
  fullname: Paraskevas, G. P.
  organization: Department of Neurology
– sequence: 5
  givenname: A.
  surname: Rombos
  fullname: Rombos, A.
  organization: Department of Neurology
– sequence: 6
  givenname: M.
  surname: Zoga
  fullname: Zoga, M.
  organization: Microbiology Lab, Aeginition Hospital, School of Medicine, Athens National University, Athens, Greece
– sequence: 7
  givenname: A.
  surname: Tsoutsou
  fullname: Tsoutsou, A.
  organization: Microbiology Lab, Aeginition Hospital, School of Medicine, Athens National University, Athens, Greece
– sequence: 8
  givenname: F.
  surname: Boufidou
  fullname: Boufidou, F.
  organization: Department of Neurology
– sequence: 9
  givenname: E.
  surname: Kapaki
  fullname: Kapaki, E.
  organization: Department of Neurology
– sequence: 10
  givenname: D.
  surname: Vassilopoulos
  fullname: Vassilopoulos, D.
  organization: Department of Neurology
BackLink http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21325884$$DView record in Pascal Francis
https://www.ncbi.nlm.nih.gov/pubmed/18976327$$D View this record in MEDLINE/PubMed
BookMark eNqNkUtv1DAUhS3Uik4LfwFlA6wSrh-xnQVI1fSFNG1ZgFhaHsdGHjJOaydi-u9xmOlIdNNasnyP_Z0r655jdBD6YBEqMFQ4r0-rCnOAEhiwigDICjAGWm1eodn-4QDNAACXnGJ2hI5TWmVFBGOv0RGWjeCUiBk6m_toxk4PPvwqfBhs7Oz424cSQ6FD-_8VybL4pmMWqQ8fU9H6ZHWyb9Ch012yb3fnCfpxcf59flUubi-_zk8XpWGc01Lj2tVOLB2RhgAnFiwjbaONJMxpKhsqqF2CzJs5yxsJtOUGHKN1CwY4PUEftn3vYn8_2jSotU_Gdp0Oth-T4gKzmmDxLEigFgQanMF3O3Bcrm2r7qJf6_igHgeUgfc7QCejOxd1MD7tOYIpqaVkmfuy5UzsU4rWKeOHPNU-DFH7TmFQU3JqpaaA1BSQmpJT_5JTm9xAPmmw_8vz1s9b6x_f2YcX-9TpzflUZX-59fs02M3en3POE6WiVj9vLtUZNAtyfXGtgP4FGAK7zw
CODEN ANRSAS
CitedBy_id crossref_primary_10_1186_s13024_017_0158_z
crossref_primary_10_1016_j_cyto_2012_07_030
crossref_primary_10_1080_13554794_2011_654227
crossref_primary_10_1186_s12974_016_0588_5
crossref_primary_10_1016_j_ajpath_2021_09_006
crossref_primary_10_1007_BF03256398
crossref_primary_10_1007_s11481_013_9435_y
crossref_primary_10_3389_fnmol_2016_00089
crossref_primary_10_1016_j_neuroscience_2021_08_007
crossref_primary_10_3390_cells10030656
crossref_primary_10_1016_j_mehy_2019_109505
crossref_primary_10_1111_j_1471_4159_2009_06475_x
crossref_primary_10_3390_ijms25147741
crossref_primary_10_1016_j_parkreldis_2019_05_040
crossref_primary_10_1007_s00109_013_1026_0
crossref_primary_10_1007_s11055_020_01014_w
crossref_primary_10_1016_j_trsl_2015_12_003
crossref_primary_10_4161_hv_28578
crossref_primary_10_3390_ijms17020206
crossref_primary_10_1002_jnr_24185
crossref_primary_10_1007_s00115_017_0299_x
crossref_primary_10_1038_s41531_023_00457_5
crossref_primary_10_1042_NS20220063
crossref_primary_10_1159_000517798
crossref_primary_10_17116_jnevro2020120021110
crossref_primary_10_1111_jpi_12923
crossref_primary_10_1155_2018_5908359
crossref_primary_10_1097_WAD_0000000000000211
crossref_primary_10_1186_s12974_016_0763_8
crossref_primary_10_1371_journal_pone_0016038
crossref_primary_10_3389_fcell_2021_740758
crossref_primary_10_1002_syn_21941
crossref_primary_10_3923_jpt_2011_647_663
crossref_primary_10_1016_j_pneurobio_2016_04_006
crossref_primary_10_1038_s41598_018_28986_7
crossref_primary_10_1586_14737175_2016_1135056
crossref_primary_10_1016_j_jaad_2019_07_012
crossref_primary_10_3389_fneur_2018_01123
crossref_primary_10_3389_fnagi_2021_782082
crossref_primary_10_1155_2014_208408
crossref_primary_10_1093_ijnp_pyu103
crossref_primary_10_2174_0929867325666181009161048
crossref_primary_10_1111_bpa_12137
crossref_primary_10_1016_j_neuroscience_2014_10_028
crossref_primary_10_1038_s12276_021_00660_5
crossref_primary_10_1586_ern_11_163
crossref_primary_10_3389_fphar_2021_770762
crossref_primary_10_1007_s00702_017_1792_x
crossref_primary_10_1016_j_molimm_2025_02_003
crossref_primary_10_1007_s13311_013_0218_1
crossref_primary_10_1007_s12031_022_01984_1
crossref_primary_10_1016_j_neuropharm_2014_10_020
crossref_primary_10_1159_000356531
crossref_primary_10_1002_mds_25065
crossref_primary_10_1111_j_1365_2052_2010_02071_x
crossref_primary_10_3892_mmr_2014_2563
crossref_primary_10_1007_s12035_016_0147_1
crossref_primary_10_5936_csbj_201304004
crossref_primary_10_1016_j_nbd_2014_08_011
crossref_primary_10_1155_2015_628192
crossref_primary_10_3390_ijms23084148
crossref_primary_10_1111_j_1600_0404_2010_01441_x
crossref_primary_10_1089_jir_2012_0088
crossref_primary_10_1016_j_pnpbp_2017_06_036
crossref_primary_10_1186_1742_2094_9_238
crossref_primary_10_2174_0929867327666200320162436
crossref_primary_10_1016_j_freeradbiomed_2017_10_379
crossref_primary_10_1371_journal_pone_0074846
crossref_primary_10_1186_s12916_015_0310_y
crossref_primary_10_3390_biom10071017
Cites_doi 10.1016/0304-3940(94)90684-X
10.1016/S0065-2776(01)79002-5
10.3233/JAD-2003-5205
10.1016/S0165-5728(00)00404-5
10.1146/annurev.iy.11.040193.001121
10.1002/1098-1136(200102)33:2<97::AID-GLIA1009>3.0.CO;2-N
10.1080/09629350310001599701
10.4049/jimmunol.149.8.2736
10.1016/0022-510X(93)90285-7
10.1016/0304-3940(94)90508-8
10.1016/S0165-3806(02)00636-3
10.1523/JNEUROSCI.20-16-06309.2000
10.1111/j.1600-0404.1994.tb01674.x
10.1128/JVI.77.8.4502-4515.2003
10.1097/00001756-199701200-00011
10.1523/JNEUROSCI.21-09-03104.2001
10.2174/1381612053381620
10.1016/S0022-510X(03)00203-X
10.1159/000111278
10.1046/j.1460-9568.2000.00090.x
10.1212/WNL.44.8.1523
10.1016/S0753-3322(99)80079-1
10.1006/exnr.1999.7115
10.1212/WNL.38.8.1285
10.1016/S0165-5728(00)00355-6
10.1002/glia.440070113
10.1007/s00702-008-0028-5
10.1002/glia.20045
10.1046/j.1471-4159.1995.65062690.x
10.1016/0006-8993(95)00490-H
10.1016/0197-0186(95)00138-7
10.1002/jlb.65.6.815
10.1007/978-3-211-45295-0_56
10.1128/CDLI.8.6.1097-1103.2001
10.4049/jimmunol.150.7.2659
10.1128/CDLI.2.5.604-608.1995
10.1016/j.neurobiolaging.2006.04.011
10.1016/j.jneuroim.2005.01.010
10.1159/000112102
10.1016/0306-4522(90)90229-W
10.4049/jimmunol.165.3.1641
10.1111/j.1600-0404.2007.00894.x
10.1038/scientificamerican0197-52
10.1016/0304-3940(94)90746-3
10.1016/S0006-8993(02)02700-2
ContentType Journal Article
Copyright Copyright © 2008 The Authors. Journal compilation © 2008 Blackwell Munksgaard
2009 INIST-CNRS
Copyright_xml – notice: Copyright © 2008 The Authors. Journal compilation © 2008 Blackwell Munksgaard
– notice: 2009 INIST-CNRS
DBID BSCLL
AAYXX
CITATION
IQODW
CGR
CUY
CVF
ECM
EIF
NPM
7T5
7TK
H94
7X8
DOI 10.1111/j.1600-0404.2008.01103.x
DatabaseName Istex
CrossRef
Pascal-Francis
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
Immunology Abstracts
Neurosciences Abstracts
AIDS and Cancer Research Abstracts
MEDLINE - Academic
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
AIDS and Cancer Research Abstracts
Neurosciences Abstracts
Immunology Abstracts
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic
AIDS and Cancer Research Abstracts

MEDLINE
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1600-0404
EndPage 337
ExternalDocumentID 18976327
21325884
10_1111_j_1600_0404_2008_01103_x
ANE1103
ark_67375_WNG_D09L2MFM_0
Genre article
Journal Article
GroupedDBID ---
-~X
.3N
.55
.GA
.GJ
.Y3
05W
0R~
10A
1OB
1OC
23M
24P
31~
33P
36B
3O-
3SF
4.4
50Y
50Z
51W
51X
52M
52N
52O
52P
52R
52S
52T
52U
52V
52W
52X
53G
5GY
5HH
5LA
5VS
66C
702
7PT
7X7
8-0
8-1
8-3
8-4
8-5
8FI
8FJ
8UM
930
A01
A03
AAESR
AAEVG
AAHHS
AAJEY
AAKAS
AAONW
AASGY
AAXRX
AAZKR
ABCQN
ABCUV
ABDBF
ABEML
ABIVO
ABJNI
ABLJU
ABPVW
ABUWG
ABXGK
ACAHQ
ACBWZ
ACCFJ
ACCZN
ACGFS
ACMXC
ACPOU
ACPRK
ACSCC
ACXBN
ACXQS
ADBBV
ADEOM
ADIZJ
ADKYN
ADMGS
ADOZA
ADXAS
ADZCM
ADZMN
ADZOD
AEEZP
AEIMD
AENEX
AEQDE
AEUQT
AFBPY
AFEBI
AFFNX
AFGKR
AFKRA
AFPWT
AFZJQ
AHEFC
AHMBA
AIACR
AIURR
AIWBW
AJBDE
ALAGY
ALIPV
ALMA_UNASSIGNED_HOLDINGS
ALUQN
AMBMR
AMYDB
ASPBG
ATUGU
AVWKF
AZBYB
AZFZN
AZVAB
BAFTC
BDRZF
BENPR
BFHJK
BHBCM
BMXJE
BROTX
BRXPI
BSCLL
BY8
C45
CAG
CCPQU
COF
CS3
D-6
D-7
D-E
D-F
DCZOG
DPXWK
DR2
DRFUL
DRMAN
DRSTM
EAD
EAP
EAS
EBC
EBD
EBS
EJD
EMB
EMK
EMOBN
EPS
ESX
EX3
F00
F01
F04
F5P
FEDTE
FUBAC
FYBCS
FYUFA
FZ0
G-S
G.N
GODZA
H.X
H13
HF~
HMCUK
HVGLF
HZI
HZ~
IHE
IX1
J0M
K48
KBYEO
L7B
LATKE
LC2
LC3
LEEKS
LH4
LITHE
LOXES
LP6
LP7
LUTES
LW6
LYRES
MK4
MRFUL
MRMAN
MRSTM
MSFUL
MSMAN
MSSTM
MXFUL
MXMAN
MXSTM
N04
N05
N9A
NF~
O66
O9-
OIG
OVD
P2P
P2W
P2X
P2Z
P4B
P4D
PALCI
PIMPY
PQQKQ
Q.N
Q11
QB0
R.K
RHX
RIWAO
RJQFR
ROL
RX1
SAMSI
SUPJJ
SV3
TEORI
TUS
UB1
UKHRP
W8V
W99
WBKPD
WHWMO
WIH
WIJ
WIK
WOHZO
WOW
WQJ
WRC
WUP
WVDHM
WXI
WXSBR
X7M
XG1
YFH
ZGI
ZXP
ZZTAW
~IA
~WT
AANHP
ACCMX
ACRPL
ACUHS
ACYXJ
ADNMO
AAYXX
AGQPQ
CITATION
PHGZM
PHGZT
AAMMB
AEFGJ
AGXDD
AIDQK
AIDYY
IQODW
CGR
CUY
CVF
ECM
EIF
NPM
7T5
7TK
H94
7X8
ID FETCH-LOGICAL-c4663-a15f5f7bf28c2062e0e42d9ac824fa389373eb08eb04fe69803d6c0f435d0c063
IEDL.DBID DR2
ISSN 0001-6314
1600-0404
IngestDate Fri Jul 11 11:19:31 EDT 2025
Thu Jul 10 23:21:11 EDT 2025
Thu Apr 03 06:59:21 EDT 2025
Mon Jul 21 09:16:41 EDT 2025
Thu Apr 24 22:53:54 EDT 2025
Tue Jul 01 00:38:53 EDT 2025
Wed Jan 22 16:54:02 EST 2025
Wed Oct 30 09:50:14 EDT 2024
IsPeerReviewed true
IsScholarly true
Issue 5
Keywords Nervous system diseases
Parkinson's disease
Cytokine
Parkinson disease
Interleukin 12
IL-12
L-dopa treatment
IL-10
Cerebral disorder
immunological disturbances
Treatment
Central nervous system disease
Interleukin 10
Serum
Degenerative disease
Dopa
ELISA assay
Extrapyramidal syndrome
ELISA
Language English
License http://doi.wiley.com/10.1002/tdm_license_1.1
CC BY 4.0
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c4663-a15f5f7bf28c2062e0e42d9ac824fa389373eb08eb04fe69803d6c0f435d0c063
Notes ark:/67375/WNG-D09L2MFM-0
istex:6C01F78B971B51A6B72EC2625F4A90C7B26CDF2A
ArticleID:ANE1103
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
PMID 18976327
PQID 20572091
PQPubID 23462
PageCount 6
ParticipantIDs proquest_miscellaneous_67145217
proquest_miscellaneous_20572091
pubmed_primary_18976327
pascalfrancis_primary_21325884
crossref_citationtrail_10_1111_j_1600_0404_2008_01103_x
crossref_primary_10_1111_j_1600_0404_2008_01103_x
wiley_primary_10_1111_j_1600_0404_2008_01103_x_ANE1103
istex_primary_ark_67375_WNG_D09L2MFM_0
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate May 2009
PublicationDateYYYYMMDD 2009-05-01
PublicationDate_xml – month: 05
  year: 2009
  text: May 2009
PublicationDecade 2000
PublicationPlace Oxford, UK
PublicationPlace_xml – name: Oxford, UK
– name: Oxford
– name: Denmark
PublicationTitle Acta neurologica Scandinavica
PublicationTitleAlternate Acta Neurol Scand
PublicationYear 2009
Publisher Blackwell Publishing Ltd
Blackwell
Publisher_xml – name: Blackwell Publishing Ltd
– name: Blackwell
References Rieckmann P, Albrecht M, Kitze B et al. Cytokine mRNA levels in mononuclear blood cells from patients with multiple sclerosis. Neurology 1994;44:1523-6.
McGeer PL, Itagaki S, Boyes BE, McGeer EG. Reactive microglia are positive for HLA-DR in the substantia nigra of Parkinson's and Alzheimer's disease brains. Neurology 1988;38:1285-91.
Mogi M, Harada M, Kondo T et al. Interleukin-1 beta, interleukin-6, epidermal growth factor and transforming growth factor-alpha are elevated in the brain from Parkinsonian patients. Neurosci Lett 1994;180:147-50.
Chao CC, Hu S, Molitor TW et al. Activated microglia mediate neuronal cell injury via a nitric oxide mechanism. J Immunol 1992;149:2736-41.
Lees GF. The possible contribution of microglia and macrophages to delayed neuronal death after ischemia. J Neurol Sci 1993;114:119-22.
Minghetti L, Levi G. Induction of prostanoid biosynthesis by bacterial lipopolysaccharide and isoproterenol in rat microglial cultures. J Neurochem 1995;6:2690-8.
Szczepanic AM, Funes S, Petko W, Ringheim GE. IL-4, IL-10 and IL-13 modulate Abeta(1-42)-induced cytokine and chemokine production in primary murine microglia and a human monocyte cell line. J Neuroimmunol 2001;113:49-62.
Boka G, Anglade P, Wallach D et al. Immunocytochemical analysis of tumor necrosis factor and its receptors in Parkinson's disease. Neurosci Lett 1994;172:151-4.
Molina-Holgado F, Grencis R, Rothwell NJ. Actions of exogenous and endogenous IL-10 on glial responses to bacterial LPS/cytokines. Glia 2001;33:97-106.
Dickson DW, Lee SC, Mattiace LA et al. Microglia and cytokines in neurological disease, with special reference to AIDS and Alzheimer's disease. Glia 1993;9:75-83.
Mogi M, Harada M, Riederer P et al. Tumor necrosis factor-alpha (TNF-alpha) increases both in the brain and in the cerebrospinal fluid from Parkinsonian patients. Neurosci Lett 1994;165:208-10.
Waubant E, Gee L, Bacchetti P et al. Relationship between serum levels of IL-10, MRI activity and interferon beta-1a therapy in patients with relapsing remitting MS. J Neuroimmunol 2001;112:139-45.
Jifen L, Bruno G, Guang-Xian Zhang et al. Differential expression and regulation of IL-23 and IL-12 subunits and receptors in adult mouse microglia. J Neurol Sci 2003; 215:95-103.
Nagatsu T, Sawada M. Inflammatory process in Parkinson's disease: role for cytokines. Curr Pharm Des 2005; 11:999-1016.
Jason J, Archibald LK, Nwanyanwu OC et al. Comparison of serum and cell-specific cytokines in humans. Clin Diagn Lab Immunol 2001;8:1097-103.
Grilli M, Barbieri I, Basudev H et al. Interleukin-10 modulates neuronal threshold of vulnerability to ischaemic damage. Eur J Neurosci 2000;12:2265-72.
Kim WG, Mohney RP, Wilson B et al. Regional difference in susceptibility to lipopolysaccharide-induced neurotoxicity in the rat brain: role of microglia. J Neurosci 2000;20:6309-16.
ΑRimoto T, Choi DY, Lu X et al. Interleukin-10 protects against inflammation-mediated degeneration of dopaminergic neurons in substantia nigra. Neurobiol Aging 2006;28:894-906.
Kremlev SG, Palmer C. Interleukin-10 inhibits endotoxin-induced pro-inflammatory cytokines in microglial cell cultures. J Neuroimmunol 2005;162:71-80.
Sheng WS, Hu S, Kravitz FH et al. Tumor necrosis factor alpha upregulates human microglial cell production of interleukin-10 in vitro. Clin Diagn Lab Immunol 1995; 2:604-8.
Combarros O, Sanchez-Juan P, Riancho JA et al. Aromatase and interleukin-10 genetic variants modulate Alzheimer's disease risk. J Neural Transm 2008;115:863-7.
Youdim MB, Riederer P. Understanding Parkinson's disease. Sci Am 1997;276:52-9.
Lee SC, Liu W, Dickson DW et al. Cytokine production by human fetal microglia and astrocytes. Differential induction by lipopolysaccharide and IL-1 beta. J Immunol 1993; 150:2659-67.
Froen JF, Munkeby BH, Stray-Pedersen B, Saugstad OD. Interleukin-10 reverses acute detrimental effects of endotoxin-induced inflammation on perinatal cerebral hypoxia-ischemia. Brain Res 2002;942:87-94.
Rentzos M, Nikolaou C, Andreadou E et al. Circulating interleukin-15 and RANTES chemokine in Parkinson's disease. Acta Neurol Scand 2007;116:374-9.
Matsuo M, Hamasaki Y, Fujiyama F, Miyazaki S. Eicosanoids are produced by microglia, not by astrocytes, in rat glial cell cultures. Brain Res 1995;685:201-4.
Szczepanic AM, Ringheim GE. IL-10 and glucocorticoids inhibit Abeta(1-42)-and lipopolysaccharide-induced proinflammatory cytokine and chemokine induction in the central nervous system. J Alzheimers Dis 2003;5:105-17.
Marques CP, Hu S, Sheng W et al. Interleukin-10 attenuates production of HSV-induced inflammatory mediators by human microglia. Glia 2004;47:358-66.
Chao CC, Hu S, Sheng WS, Peterson PK. Tumor necrosis factor-alpha production by human fetal microglial cells: regulation by other cytokines. Dev Neurosci 1995;17: 97-105.
Lawson LJ, Perry VH, Dri P, Gordon S. Heterogeneity in the distribution and morphology of microglia in the normal adult mouse brain. Neuroscience 1990;39:151-70.
Pelfrey CM, Rudick RA, Cotleur AC et al. Quantification of self-recognition in multiple sclerosis by single-cell analysis of cytokine production. J Immunol 2000;165:1641-51.
Espey MG, Chernyshev ON, Reinhard JF et al. Activated human microglia produce the excitotoxin quinolinic acid. Neuroreport 1997;8:431-4.
Larsen JP, Dupont E, Tandberg E. Clinical diagnosis of Parkinson's disease. Proposal of diagnostic subgroups classified at different levels of confidence. Acta Neurol Scand 1994;89:242-51.
Gangemi S, Basile G, Merendino AR et al. Effect of levodopa on interleukin-15 and RANTES circulating levels in patients affected by Parkinson's disease. Mediators Inflamm 2003;12:251-3.
Bessler H, Djaldetti R, Salman H et al. IL-1β, IL-2, IL-6 and TNF-a production by peripheral blood mononuclear cells from patients with Parkinson's disease. Biomed Pharmacother 1999;53:141-5.
Brosnan CF, Battistini L, Raine CS et al. Reactive nitrogen intermediates in human neuropathology: an overview. Dev Neurosci 1994;16:152-61.
Cheeran MC, Hu S, Sheng WS et al. CXCL10 production from cytomegalovirus-stimulated microglia is regulated by both human and viral interleukin-10. J Virol 2003;77:4502-15.
Williams K, Dooley N, Ulvestad E et al. IL-10 production by adult human derived microglial cells. Neurochem Int 1996;96:55-64.
Bachis A, Colangelo AM, Vicini S et al. Interleukin-10 prevents glutamate-mediated cerebellar granule cell death by blocking caspase-3-like activity. J Neurosci 2001;21:3104-12.
Hu S, Chao CC, Ehrlich LC et al. Inhibition of microglial cell RANTES production by IL-10 and TGF-beta. J Leukoc Biol 1999;65:815-21.
Ma X, Trinchieri G. Regulation of interleukin-12 production in antigen-presenting cells. Adv Immunol 2001; 79: 55-92.
Moore KW, O'Garra A, De Waal Malefyt R et al. Interleukin-10. Annu Rev Immunol 1993;11: 165-90.
Dietrich WD, Busto R, Bethea JR. Postischemic hypothermia and IL-10 treatment provide long-lasting neuroprotection of CA1 hippocampus following transient global ischemia in rats. Exp Neurol 1999;158:444-50.
Qian L, Hong JS, Flood PM. Role of microglia in inflammation-mediated degeneration of dopaminergic neurons: neuroprotective effect of interleukin-10. J Neural Transm Suppl 2006;70:367-71.
Mesples B, Plaisant F, Gressens P. Effects of interleukin-10 on neonatal excitotoxic brain lesions in mice. Brain Res Dev Brain Res 2003;141:25-32.
2006; 70
1993; 9
2003; 215
1995; 17
1990; 39
2004; 47
1994; 172
1988; 38
1997; 276
2000; 20
1992; 149
1994; 89
1994; 44
1996; 96
1999; 65
1995; 2
1995; 6
2003; 77
1997; 8
2001; 21
2003; 12
1994; 165
2001; 113
2001; 112
2005; 162
2007; 116
2000; 12
1994; 180
1993; 11
2006; 28
2001; 8
1993; 150
2002; 942
2003; 5
1994; 16
1999; 53
1995; 685
1999; 158
2008; 115
2000; 165
1993; 114
2001; 33
2001; 79
2005; 11
2003; 141
Boka (10.1111/j.1600-0404.2008.01103.x-BIB1) 1994; 172
Bachis (10.1111/j.1600-0404.2008.01103.x-BIB21) 2001; 21
Larsen (10.1111/j.1600-0404.2008.01103.x-BIB26) 1994; 89
Szczepanic (10.1111/j.1600-0404.2008.01103.x-BIB36) 2001; 113
Bessler (10.1111/j.1600-0404.2008.01103.x-BIB43) 1999; 53
Qian (10.1111/j.1600-0404.2008.01103.x-BIB28) 2006; 70
Αrimoto (10.1111/j.1600-0404.2008.01103.x-BIB29) 2006; 28
Mogi (10.1111/j.1600-0404.2008.01103.x-BIB2) 1994; 180
Lee (10.1111/j.1600-0404.2008.01103.x-BIB12) 1993; 150
Dickson (10.1111/j.1600-0404.2008.01103.x-BIB10) 1993; 9
Grilli (10.1111/j.1600-0404.2008.01103.x-BIB23) 2000; 12
Ma (10.1111/j.1600-0404.2008.01103.x-BIB16) 2001; 79
Sheng (10.1111/j.1600-0404.2008.01103.x-BIB19) 1995; 2
Molina-Holgado (10.1111/j.1600-0404.2008.01103.x-BIB24) 2001; 33
Chao (10.1111/j.1600-0404.2008.01103.x-BIB25) 1995; 17
Szczepanic (10.1111/j.1600-0404.2008.01103.x-BIB37) 2003; 5
Brosnan (10.1111/j.1600-0404.2008.01103.x-BIB8) 1994; 16
Mogi (10.1111/j.1600-0404.2008.01103.x-BIB3) 1994; 165
Kim (10.1111/j.1600-0404.2008.01103.x-BIB4) 2000; 20
Lees (10.1111/j.1600-0404.2008.01103.x-BIB13) 1993; 114
Youdim (10.1111/j.1600-0404.2008.01103.x-BIB7) 1997; 276
Gangemi (10.1111/j.1600-0404.2008.01103.x-BIB42) 2003; 12
Combarros (10.1111/j.1600-0404.2008.01103.x-BIB38) 2008; 115
Marques (10.1111/j.1600-0404.2008.01103.x-BIB31) 2004; 47
Cheeran (10.1111/j.1600-0404.2008.01103.x-BIB30) 2003; 77
Minghetti (10.1111/j.1600-0404.2008.01103.x-BIB15) 1995; 6
Espey (10.1111/j.1600-0404.2008.01103.x-BIB11) 1997; 8
Mesples (10.1111/j.1600-0404.2008.01103.x-BIB34) 2003; 141
Rieckmann (10.1111/j.1600-0404.2008.01103.x-BIB39) 1994; 44
Waubant (10.1111/j.1600-0404.2008.01103.x-BIB41) 2001; 112
Jifen (10.1111/j.1600-0404.2008.01103.x-BIB17) 2003; 215
Moore (10.1111/j.1600-0404.2008.01103.x-BIB18) 1993; 11
Pelfrey (10.1111/j.1600-0404.2008.01103.x-BIB40) 2000; 165
Nagatsu (10.1111/j.1600-0404.2008.01103.x-BIB27) 2005; 11
Williams (10.1111/j.1600-0404.2008.01103.x-BIB20) 1996; 96
Hu (10.1111/j.1600-0404.2008.01103.x-BIB33) 1999; 65
Dietrich (10.1111/j.1600-0404.2008.01103.x-BIB22) 1999; 158
Rentzos (10.1111/j.1600-0404.2008.01103.x-BIB44) 2007; 116
Chao (10.1111/j.1600-0404.2008.01103.x-BIB9) 1992; 149
Froen (10.1111/j.1600-0404.2008.01103.x-BIB32) 2002; 942
Jason (10.1111/j.1600-0404.2008.01103.x-BIB45) 2001; 8
Kremlev (10.1111/j.1600-0404.2008.01103.x-BIB35) 2005; 162
Lawson (10.1111/j.1600-0404.2008.01103.x-BIB5) 1990; 39
Matsuo (10.1111/j.1600-0404.2008.01103.x-BIB14) 1995; 685
McGeer (10.1111/j.1600-0404.2008.01103.x-BIB6) 1988; 38
References_xml – reference: Bachis A, Colangelo AM, Vicini S et al. Interleukin-10 prevents glutamate-mediated cerebellar granule cell death by blocking caspase-3-like activity. J Neurosci 2001;21:3104-12.
– reference: Qian L, Hong JS, Flood PM. Role of microglia in inflammation-mediated degeneration of dopaminergic neurons: neuroprotective effect of interleukin-10. J Neural Transm Suppl 2006;70:367-71.
– reference: Rieckmann P, Albrecht M, Kitze B et al. Cytokine mRNA levels in mononuclear blood cells from patients with multiple sclerosis. Neurology 1994;44:1523-6.
– reference: Williams K, Dooley N, Ulvestad E et al. IL-10 production by adult human derived microglial cells. Neurochem Int 1996;96:55-64.
– reference: Rentzos M, Nikolaou C, Andreadou E et al. Circulating interleukin-15 and RANTES chemokine in Parkinson's disease. Acta Neurol Scand 2007;116:374-9.
– reference: ΑRimoto T, Choi DY, Lu X et al. Interleukin-10 protects against inflammation-mediated degeneration of dopaminergic neurons in substantia nigra. Neurobiol Aging 2006;28:894-906.
– reference: Jason J, Archibald LK, Nwanyanwu OC et al. Comparison of serum and cell-specific cytokines in humans. Clin Diagn Lab Immunol 2001;8:1097-103.
– reference: Marques CP, Hu S, Sheng W et al. Interleukin-10 attenuates production of HSV-induced inflammatory mediators by human microglia. Glia 2004;47:358-66.
– reference: Mesples B, Plaisant F, Gressens P. Effects of interleukin-10 on neonatal excitotoxic brain lesions in mice. Brain Res Dev Brain Res 2003;141:25-32.
– reference: Mogi M, Harada M, Kondo T et al. Interleukin-1 beta, interleukin-6, epidermal growth factor and transforming growth factor-alpha are elevated in the brain from Parkinsonian patients. Neurosci Lett 1994;180:147-50.
– reference: Boka G, Anglade P, Wallach D et al. Immunocytochemical analysis of tumor necrosis factor and its receptors in Parkinson's disease. Neurosci Lett 1994;172:151-4.
– reference: Dietrich WD, Busto R, Bethea JR. Postischemic hypothermia and IL-10 treatment provide long-lasting neuroprotection of CA1 hippocampus following transient global ischemia in rats. Exp Neurol 1999;158:444-50.
– reference: Chao CC, Hu S, Sheng WS, Peterson PK. Tumor necrosis factor-alpha production by human fetal microglial cells: regulation by other cytokines. Dev Neurosci 1995;17: 97-105.
– reference: Lees GF. The possible contribution of microglia and macrophages to delayed neuronal death after ischemia. J Neurol Sci 1993;114:119-22.
– reference: Matsuo M, Hamasaki Y, Fujiyama F, Miyazaki S. Eicosanoids are produced by microglia, not by astrocytes, in rat glial cell cultures. Brain Res 1995;685:201-4.
– reference: Espey MG, Chernyshev ON, Reinhard JF et al. Activated human microglia produce the excitotoxin quinolinic acid. Neuroreport 1997;8:431-4.
– reference: Youdim MB, Riederer P. Understanding Parkinson's disease. Sci Am 1997;276:52-9.
– reference: Minghetti L, Levi G. Induction of prostanoid biosynthesis by bacterial lipopolysaccharide and isoproterenol in rat microglial cultures. J Neurochem 1995;6:2690-8.
– reference: McGeer PL, Itagaki S, Boyes BE, McGeer EG. Reactive microglia are positive for HLA-DR in the substantia nigra of Parkinson's and Alzheimer's disease brains. Neurology 1988;38:1285-91.
– reference: Waubant E, Gee L, Bacchetti P et al. Relationship between serum levels of IL-10, MRI activity and interferon beta-1a therapy in patients with relapsing remitting MS. J Neuroimmunol 2001;112:139-45.
– reference: Nagatsu T, Sawada M. Inflammatory process in Parkinson's disease: role for cytokines. Curr Pharm Des 2005; 11:999-1016.
– reference: Cheeran MC, Hu S, Sheng WS et al. CXCL10 production from cytomegalovirus-stimulated microglia is regulated by both human and viral interleukin-10. J Virol 2003;77:4502-15.
– reference: Brosnan CF, Battistini L, Raine CS et al. Reactive nitrogen intermediates in human neuropathology: an overview. Dev Neurosci 1994;16:152-61.
– reference: Jifen L, Bruno G, Guang-Xian Zhang et al. Differential expression and regulation of IL-23 and IL-12 subunits and receptors in adult mouse microglia. J Neurol Sci 2003; 215:95-103.
– reference: Szczepanic AM, Ringheim GE. IL-10 and glucocorticoids inhibit Abeta(1-42)-and lipopolysaccharide-induced proinflammatory cytokine and chemokine induction in the central nervous system. J Alzheimers Dis 2003;5:105-17.
– reference: Sheng WS, Hu S, Kravitz FH et al. Tumor necrosis factor alpha upregulates human microglial cell production of interleukin-10 in vitro. Clin Diagn Lab Immunol 1995; 2:604-8.
– reference: Larsen JP, Dupont E, Tandberg E. Clinical diagnosis of Parkinson's disease. Proposal of diagnostic subgroups classified at different levels of confidence. Acta Neurol Scand 1994;89:242-51.
– reference: Szczepanic AM, Funes S, Petko W, Ringheim GE. IL-4, IL-10 and IL-13 modulate Abeta(1-42)-induced cytokine and chemokine production in primary murine microglia and a human monocyte cell line. J Neuroimmunol 2001;113:49-62.
– reference: Combarros O, Sanchez-Juan P, Riancho JA et al. Aromatase and interleukin-10 genetic variants modulate Alzheimer's disease risk. J Neural Transm 2008;115:863-7.
– reference: Hu S, Chao CC, Ehrlich LC et al. Inhibition of microglial cell RANTES production by IL-10 and TGF-beta. J Leukoc Biol 1999;65:815-21.
– reference: Pelfrey CM, Rudick RA, Cotleur AC et al. Quantification of self-recognition in multiple sclerosis by single-cell analysis of cytokine production. J Immunol 2000;165:1641-51.
– reference: Gangemi S, Basile G, Merendino AR et al. Effect of levodopa on interleukin-15 and RANTES circulating levels in patients affected by Parkinson's disease. Mediators Inflamm 2003;12:251-3.
– reference: Bessler H, Djaldetti R, Salman H et al. IL-1β, IL-2, IL-6 and TNF-a production by peripheral blood mononuclear cells from patients with Parkinson's disease. Biomed Pharmacother 1999;53:141-5.
– reference: Kremlev SG, Palmer C. Interleukin-10 inhibits endotoxin-induced pro-inflammatory cytokines in microglial cell cultures. J Neuroimmunol 2005;162:71-80.
– reference: Dickson DW, Lee SC, Mattiace LA et al. Microglia and cytokines in neurological disease, with special reference to AIDS and Alzheimer's disease. Glia 1993;9:75-83.
– reference: Ma X, Trinchieri G. Regulation of interleukin-12 production in antigen-presenting cells. Adv Immunol 2001; 79: 55-92.
– reference: Froen JF, Munkeby BH, Stray-Pedersen B, Saugstad OD. Interleukin-10 reverses acute detrimental effects of endotoxin-induced inflammation on perinatal cerebral hypoxia-ischemia. Brain Res 2002;942:87-94.
– reference: Kim WG, Mohney RP, Wilson B et al. Regional difference in susceptibility to lipopolysaccharide-induced neurotoxicity in the rat brain: role of microglia. J Neurosci 2000;20:6309-16.
– reference: Lee SC, Liu W, Dickson DW et al. Cytokine production by human fetal microglia and astrocytes. Differential induction by lipopolysaccharide and IL-1 beta. J Immunol 1993; 150:2659-67.
– reference: Molina-Holgado F, Grencis R, Rothwell NJ. Actions of exogenous and endogenous IL-10 on glial responses to bacterial LPS/cytokines. Glia 2001;33:97-106.
– reference: Moore KW, O'Garra A, De Waal Malefyt R et al. Interleukin-10. Annu Rev Immunol 1993;11: 165-90.
– reference: Lawson LJ, Perry VH, Dri P, Gordon S. Heterogeneity in the distribution and morphology of microglia in the normal adult mouse brain. Neuroscience 1990;39:151-70.
– reference: Grilli M, Barbieri I, Basudev H et al. Interleukin-10 modulates neuronal threshold of vulnerability to ischaemic damage. Eur J Neurosci 2000;12:2265-72.
– reference: Mogi M, Harada M, Riederer P et al. Tumor necrosis factor-alpha (TNF-alpha) increases both in the brain and in the cerebrospinal fluid from Parkinsonian patients. Neurosci Lett 1994;165:208-10.
– reference: Chao CC, Hu S, Molitor TW et al. Activated microglia mediate neuronal cell injury via a nitric oxide mechanism. J Immunol 1992;149:2736-41.
– volume: 149
  start-page: 2736
  year: 1992
  end-page: 41
  article-title: Activated microglia mediate neuronal cell injury via a nitric oxide mechanism
  publication-title: J Immunol
– volume: 2
  start-page: 604
  year: 1995
  end-page: 8
  article-title: Tumor necrosis factor alpha upregulates human microglial cell production of interleukin‐10
  publication-title: Clin Diagn Lab Immunol
– volume: 116
  start-page: 374
  year: 2007
  end-page: 9
  article-title: Circulating interleukin‐15 and RANTES chemokine in Parkinson’s disease
  publication-title: Acta Neurol Scand
– volume: 20
  start-page: 6309
  year: 2000
  end-page: 16
  article-title: Regional difference in susceptibility to lipopolysaccharide‐induced neurotoxicity in the rat brain: role of microglia
  publication-title: J Neurosci
– volume: 70
  start-page: 367
  year: 2006
  end-page: 71
  article-title: Role of microglia in inflammation‐mediated degeneration of dopaminergic neurons: neuroprotective effect of interleukin‐10
  publication-title: J Neural Transm Suppl
– volume: 141
  start-page: 25
  year: 2003
  end-page: 32
  article-title: Effects of interleukin‐10 on neonatal excitotoxic brain lesions in mice
  publication-title: Brain Res Dev Brain Res
– volume: 150
  start-page: 2659
  year: 1993
  end-page: 67
  article-title: Cytokine production by human fetal microglia and astrocytes. Differential induction by lipopolysaccharide and IL‐1 beta
  publication-title: J Immunol
– volume: 685
  start-page: 201
  year: 1995
  end-page: 4
  article-title: Eicosanoids are produced by microglia, not by astrocytes, in rat glial cell cultures
  publication-title: Brain Res
– volume: 79
  start-page: 55
  year: 2001
  end-page: 92
  article-title: Regulation of interleukin‐12 production in antigen‐presenting cells
  publication-title: Adv Immunol
– volume: 65
  start-page: 815
  year: 1999
  end-page: 21
  article-title: Inhibition of microglial cell RANTES production by IL‐10 and TGF‐beta
  publication-title: J Leukoc Biol
– volume: 12
  start-page: 251
  year: 2003
  end-page: 3
  article-title: Effect of levodopa on interleukin‐15 and RANTES circulating levels in patients affected by Parkinson’s disease
  publication-title: Mediators Inflamm
– volume: 47
  start-page: 358
  year: 2004
  end-page: 66
  article-title: Interleukin‐10 attenuates production of HSV‐induced inflammatory mediators by human microglia
  publication-title: Glia
– volume: 942
  start-page: 87
  year: 2002
  end-page: 94
  article-title: Interleukin‐10 reverses acute detrimental effects of endotoxin‐induced inflammation on perinatal cerebral hypoxia–ischemia
  publication-title: Brain Res
– volume: 11
  start-page: 165
  year: 1993
  end-page: 90
  article-title: Interleukin‐10
  publication-title: Annu Rev Immunol
– volume: 44
  start-page: 1523
  year: 1994
  end-page: 6
  article-title: Cytokine mRNA levels in mononuclear blood cells from patients with multiple sclerosis
  publication-title: Neurology
– volume: 172
  start-page: 151
  year: 1994
  end-page: 4
  article-title: Immunocytochemical analysis of tumor necrosis factor and its receptors in Parkinson’s disease
  publication-title: Neurosci Lett
– volume: 180
  start-page: 147
  year: 1994
  end-page: 50
  article-title: Interleukin‐1 beta, interleukin‐6, epidermal growth factor and transforming growth factor‐alpha are elevated in the brain from Parkinsonian patients
  publication-title: Neurosci Lett
– volume: 215
  start-page: 95
  year: 2003
  end-page: 103
  article-title: Differential expression and regulation of IL‐23 and IL‐12 subunits and receptors in adult mouse microglia
  publication-title: J Neurol Sci
– volume: 21
  start-page: 3104
  year: 2001
  end-page: 12
  article-title: Interleukin‐10 prevents glutamate‐mediated cerebellar granule cell death by blocking caspase‐3‐like activity
  publication-title: J Neurosci
– volume: 16
  start-page: 152
  year: 1994
  end-page: 61
  article-title: Reactive nitrogen intermediates in human neuropathology: an overview
  publication-title: Dev Neurosci
– volume: 276
  start-page: 52
  year: 1997
  end-page: 9
  article-title: Understanding Parkinson’s disease
  publication-title: Sci Am
– volume: 6
  start-page: 2690
  year: 1995
  end-page: 8
  article-title: Induction of prostanoid biosynthesis by bacterial lipopolysaccharide and isoproterenol in rat microglial cultures
  publication-title: J Neurochem
– volume: 114
  start-page: 119
  year: 1993
  end-page: 22
  article-title: The possible contribution of microglia and macrophages to delayed neuronal death after ischemia
  publication-title: J Neurol Sci
– volume: 9
  start-page: 75
  year: 1993
  end-page: 83
  article-title: Microglia and cytokines in neurological disease, with special reference to AIDS and Alzheimer’s disease
  publication-title: Glia
– volume: 115
  start-page: 863
  year: 2008
  end-page: 7
  article-title: Aromatase and interleukin‐10 genetic variants modulate Alzheimer’s disease risk
  publication-title: J Neural Transm
– volume: 8
  start-page: 1097
  year: 2001
  end-page: 103
  article-title: Comparison of serum and cell‐specific cytokines in humans
  publication-title: Clin Diagn Lab Immunol
– volume: 5
  start-page: 105
  year: 2003
  end-page: 17
  article-title: IL‐10 and glucocorticoids inhibit Abeta(1‐42)‐and lipopolysaccharide‐induced proinflammatory cytokine and chemokine induction in the central nervous system
  publication-title: J Alzheimers Dis
– volume: 39
  start-page: 151
  year: 1990
  end-page: 70
  article-title: Heterogeneity in the distribution and morphology of microglia in the normal adult mouse brain
  publication-title: Neuroscience
– volume: 162
  start-page: 71
  year: 2005
  end-page: 80
  article-title: Interleukin‐10 inhibits endotoxin‐induced pro‐inflammatory cytokines in microglial cell cultures
  publication-title: J Neuroimmunol
– volume: 53
  start-page: 141
  year: 1999
  end-page: 5
  article-title: IL‐1β, IL‐2, IL‐6 and TNF‐a production by peripheral blood mononuclear cells from patients with Parkinson’s disease
  publication-title: Biomed Pharmacother
– volume: 11
  start-page: 999
  year: 2005
  end-page: 1016
  article-title: Inflammatory process in Parkinson’s disease: role for cytokines
  publication-title: Curr Pharm Des
– volume: 96
  start-page: 55
  year: 1996
  end-page: 64
  article-title: IL‐10 production by adult human derived microglial cells
  publication-title: Neurochem Int
– volume: 113
  start-page: 49
  year: 2001
  end-page: 62
  article-title: IL‐4, IL‐10 and IL‐13 modulate Abeta(1‐42)‐induced cytokine and chemokine production in primary murine microglia and a human monocyte cell line
  publication-title: J Neuroimmunol
– volume: 17
  start-page: 97
  year: 1995
  end-page: 105
  article-title: Tumor necrosis factor‐alpha production by human fetal microglial cells: regulation by other cytokines
  publication-title: Dev Neurosci
– volume: 89
  start-page: 242
  year: 1994
  end-page: 51
  article-title: Clinical diagnosis of Parkinson’s disease. Proposal of diagnostic subgroups classified at different levels of confidence
  publication-title: Acta Neurol Scand
– volume: 8
  start-page: 431
  year: 1997
  end-page: 4
  article-title: Activated human microglia produce the excitotoxin quinolinic acid
  publication-title: Neuroreport
– volume: 38
  start-page: 1285
  year: 1988
  end-page: 91
  article-title: Reactive microglia are positive for HLA‐DR in the substantia nigra of Parkinson’s and Alzheimer’s disease brains
  publication-title: Neurology
– volume: 77
  start-page: 4502
  year: 2003
  end-page: 15
  article-title: CXCL10 production from cytomegalovirus‐stimulated microglia is regulated by both human and viral interleukin‐10
  publication-title: J Virol
– volume: 165
  start-page: 1641
  year: 2000
  end-page: 51
  article-title: Quantification of self‐recognition in multiple sclerosis by single‐cell analysis of cytokine production
  publication-title: J Immunol
– volume: 165
  start-page: 208
  year: 1994
  end-page: 10
  article-title: Tumor necrosis factor‐alpha (TNF‐alpha) increases both in the brain and in the cerebrospinal fluid from Parkinsonian patients
  publication-title: Neurosci Lett
– volume: 158
  start-page: 444
  year: 1999
  end-page: 50
  article-title: Postischemic hypothermia and IL‐10 treatment provide long‐lasting neuroprotection of CA1 hippocampus following transient global ischemia in rats
  publication-title: Exp Neurol
– volume: 28
  start-page: 894
  year: 2006
  end-page: 906
  article-title: Interleukin‐10 protects against inflammation‐mediated degeneration of dopaminergic neurons in substantia nigra
  publication-title: Neurobiol Aging
– volume: 33
  start-page: 97
  year: 2001
  end-page: 106
  article-title: Actions of exogenous and endogenous IL‐10 on glial responses to bacterial LPS/cytokines
  publication-title: Glia
– volume: 12
  start-page: 2265
  year: 2000
  end-page: 72
  article-title: Interleukin‐10 modulates neuronal threshold of vulnerability to ischaemic damage
  publication-title: Eur J Neurosci
– volume: 112
  start-page: 139
  year: 2001
  end-page: 45
  article-title: Relationship between serum levels of IL‐10, MRI activity and interferon beta‐1a therapy in patients with relapsing remitting MS
  publication-title: J Neuroimmunol
– volume: 172
  start-page: 151
  year: 1994
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB1
  article-title: Immunocytochemical analysis of tumor necrosis factor and its receptors in Parkinson’s disease
  publication-title: Neurosci Lett
  doi: 10.1016/0304-3940(94)90684-X
– volume: 79
  start-page: 55
  year: 2001
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB16
  article-title: Regulation of interleukin-12 production in antigen-presenting cells
  publication-title: Adv Immunol
  doi: 10.1016/S0065-2776(01)79002-5
– volume: 5
  start-page: 105
  year: 2003
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB37
  article-title: IL-10 and glucocorticoids inhibit Abeta(1-42)-and lipopolysaccharide-induced proinflammatory cytokine and chemokine induction in the central nervous system
  publication-title: J Alzheimers Dis
  doi: 10.3233/JAD-2003-5205
– volume: 113
  start-page: 49
  year: 2001
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB36
  article-title: IL-4, IL-10 and IL-13 modulate Abeta(1-42)-induced cytokine and chemokine production in primary murine microglia and a human monocyte cell line
  publication-title: J Neuroimmunol
  doi: 10.1016/S0165-5728(00)00404-5
– volume: 11
  start-page: 165
  year: 1993
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB18
  article-title: Interleukin-10
  publication-title: Annu Rev Immunol
  doi: 10.1146/annurev.iy.11.040193.001121
– volume: 33
  start-page: 97
  year: 2001
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB24
  article-title: Actions of exogenous and endogenous IL-10 on glial responses to bacterial LPS/cytokines
  publication-title: Glia
  doi: 10.1002/1098-1136(200102)33:2<97::AID-GLIA1009>3.0.CO;2-N
– volume: 12
  start-page: 251
  year: 2003
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB42
  article-title: Effect of levodopa on interleukin-15 and RANTES circulating levels in patients affected by Parkinson’s disease
  publication-title: Mediators Inflamm
  doi: 10.1080/09629350310001599701
– volume: 149
  start-page: 2736
  year: 1992
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB9
  article-title: Activated microglia mediate neuronal cell injury via a nitric oxide mechanism
  publication-title: J Immunol
  doi: 10.4049/jimmunol.149.8.2736
– volume: 114
  start-page: 119
  year: 1993
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB13
  article-title: The possible contribution of microglia and macrophages to delayed neuronal death after ischemia
  publication-title: J Neurol Sci
  doi: 10.1016/0022-510X(93)90285-7
– volume: 180
  start-page: 147
  year: 1994
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB2
  article-title: Interleukin-1 beta, interleukin-6, epidermal growth factor and transforming growth factor-alpha are elevated in the brain from Parkinsonian patients
  publication-title: Neurosci Lett
  doi: 10.1016/0304-3940(94)90508-8
– volume: 141
  start-page: 25
  year: 2003
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB34
  article-title: Effects of interleukin-10 on neonatal excitotoxic brain lesions in mice
  publication-title: Brain Res Dev Brain Res
  doi: 10.1016/S0165-3806(02)00636-3
– volume: 20
  start-page: 6309
  year: 2000
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB4
  article-title: Regional difference in susceptibility to lipopolysaccharide-induced neurotoxicity in the rat brain: role of microglia
  publication-title: J Neurosci
  doi: 10.1523/JNEUROSCI.20-16-06309.2000
– volume: 89
  start-page: 242
  year: 1994
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB26
  article-title: Clinical diagnosis of Parkinson’s disease. Proposal of diagnostic subgroups classified at different levels of confidence
  publication-title: Acta Neurol Scand
  doi: 10.1111/j.1600-0404.1994.tb01674.x
– volume: 77
  start-page: 4502
  year: 2003
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB30
  article-title: CXCL10 production from cytomegalovirus-stimulated microglia is regulated by both human and viral interleukin-10
  publication-title: J Virol
  doi: 10.1128/JVI.77.8.4502-4515.2003
– volume: 8
  start-page: 431
  year: 1997
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB11
  article-title: Activated human microglia produce the excitotoxin quinolinic acid
  publication-title: Neuroreport
  doi: 10.1097/00001756-199701200-00011
– volume: 21
  start-page: 3104
  year: 2001
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB21
  article-title: Interleukin-10 prevents glutamate-mediated cerebellar granule cell death by blocking caspase-3-like activity
  publication-title: J Neurosci
  doi: 10.1523/JNEUROSCI.21-09-03104.2001
– volume: 11
  start-page: 999
  year: 2005
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB27
  article-title: Inflammatory process in Parkinson’s disease: role for cytokines
  publication-title: Curr Pharm Des
  doi: 10.2174/1381612053381620
– volume: 215
  start-page: 95
  year: 2003
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB17
  article-title: Differential expression and regulation of IL-23 and IL-12 subunits and receptors in adult mouse microglia
  publication-title: J Neurol Sci
  doi: 10.1016/S0022-510X(03)00203-X
– volume: 17
  start-page: 97
  year: 1995
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB25
  article-title: Tumor necrosis factor-alpha production by human fetal microglial cells: regulation by other cytokines
  publication-title: Dev Neurosci
  doi: 10.1159/000111278
– volume: 12
  start-page: 2265
  year: 2000
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB23
  article-title: Interleukin-10 modulates neuronal threshold of vulnerability to ischaemic damage
  publication-title: Eur J Neurosci
  doi: 10.1046/j.1460-9568.2000.00090.x
– volume: 44
  start-page: 1523
  year: 1994
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB39
  article-title: Cytokine mRNA levels in mononuclear blood cells from patients with multiple sclerosis
  publication-title: Neurology
  doi: 10.1212/WNL.44.8.1523
– volume: 53
  start-page: 141
  year: 1999
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB43
  article-title: IL-1β, IL-2, IL-6 and TNF-a production by peripheral blood mononuclear cells from patients with Parkinson’s disease
  publication-title: Biomed Pharmacother
  doi: 10.1016/S0753-3322(99)80079-1
– volume: 158
  start-page: 444
  year: 1999
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB22
  article-title: Postischemic hypothermia and IL-10 treatment provide long-lasting neuroprotection of CA1 hippocampus following transient global ischemia in rats
  publication-title: Exp Neurol
  doi: 10.1006/exnr.1999.7115
– volume: 38
  start-page: 1285
  year: 1988
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB6
  article-title: Reactive microglia are positive for HLA-DR in the substantia nigra of Parkinson’s and Alzheimer’s disease brains
  publication-title: Neurology
  doi: 10.1212/WNL.38.8.1285
– volume: 112
  start-page: 139
  year: 2001
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB41
  article-title: Relationship between serum levels of IL-10, MRI activity and interferon beta-1a therapy in patients with relapsing remitting MS
  publication-title: J Neuroimmunol
  doi: 10.1016/S0165-5728(00)00355-6
– volume: 9
  start-page: 75
  year: 1993
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB10
  article-title: Microglia and cytokines in neurological disease, with special reference to AIDS and Alzheimer’s disease
  publication-title: Glia
  doi: 10.1002/glia.440070113
– volume: 115
  start-page: 863
  year: 2008
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB38
  article-title: Aromatase and interleukin-10 genetic variants modulate Alzheimer’s disease risk
  publication-title: J Neural Transm
  doi: 10.1007/s00702-008-0028-5
– volume: 47
  start-page: 358
  year: 2004
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB31
  article-title: Interleukin-10 attenuates production of HSV-induced inflammatory mediators by human microglia
  publication-title: Glia
  doi: 10.1002/glia.20045
– volume: 6
  start-page: 2690
  year: 1995
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB15
  article-title: Induction of prostanoid biosynthesis by bacterial lipopolysaccharide and isoproterenol in rat microglial cultures
  publication-title: J Neurochem
  doi: 10.1046/j.1471-4159.1995.65062690.x
– volume: 685
  start-page: 201
  year: 1995
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB14
  article-title: Eicosanoids are produced by microglia, not by astrocytes, in rat glial cell cultures
  publication-title: Brain Res
  doi: 10.1016/0006-8993(95)00490-H
– volume: 96
  start-page: 55
  year: 1996
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB20
  article-title: IL-10 production by adult human derived microglial cells
  publication-title: Neurochem Int
  doi: 10.1016/0197-0186(95)00138-7
– volume: 65
  start-page: 815
  year: 1999
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB33
  article-title: Inhibition of microglial cell RANTES production by IL-10 and TGF-beta
  publication-title: J Leukoc Biol
  doi: 10.1002/jlb.65.6.815
– volume: 70
  start-page: 367
  year: 2006
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB28
  article-title: Role of microglia in inflammation-mediated degeneration of dopaminergic neurons: neuroprotective effect of interleukin-10
  publication-title: J Neural Transm Suppl
  doi: 10.1007/978-3-211-45295-0_56
– volume: 8
  start-page: 1097
  year: 2001
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB45
  article-title: Comparison of serum and cell-specific cytokines in humans
  publication-title: Clin Diagn Lab Immunol
  doi: 10.1128/CDLI.8.6.1097-1103.2001
– volume: 150
  start-page: 2659
  year: 1993
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB12
  article-title: Cytokine production by human fetal microglia and astrocytes. Differential induction by lipopolysaccharide and IL-1 beta
  publication-title: J Immunol
  doi: 10.4049/jimmunol.150.7.2659
– volume: 2
  start-page: 604
  year: 1995
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB19
  article-title: Tumor necrosis factor alpha upregulates human microglial cell production of interleukin-10 in vitro
  publication-title: Clin Diagn Lab Immunol
  doi: 10.1128/CDLI.2.5.604-608.1995
– volume: 28
  start-page: 894
  year: 2006
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB29
  article-title: Interleukin-10 protects against inflammation-mediated degeneration of dopaminergic neurons in substantia nigra
  publication-title: Neurobiol Aging
  doi: 10.1016/j.neurobiolaging.2006.04.011
– volume: 162
  start-page: 71
  year: 2005
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB35
  article-title: Interleukin-10 inhibits endotoxin-induced pro-inflammatory cytokines in microglial cell cultures
  publication-title: J Neuroimmunol
  doi: 10.1016/j.jneuroim.2005.01.010
– volume: 16
  start-page: 152
  year: 1994
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB8
  article-title: Reactive nitrogen intermediates in human neuropathology: an overview
  publication-title: Dev Neurosci
  doi: 10.1159/000112102
– volume: 39
  start-page: 151
  year: 1990
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB5
  article-title: Heterogeneity in the distribution and morphology of microglia in the normal adult mouse brain
  publication-title: Neuroscience
  doi: 10.1016/0306-4522(90)90229-W
– volume: 165
  start-page: 1641
  year: 2000
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB40
  article-title: Quantification of self-recognition in multiple sclerosis by single-cell analysis of cytokine production
  publication-title: J Immunol
  doi: 10.4049/jimmunol.165.3.1641
– volume: 116
  start-page: 374
  year: 2007
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB44
  article-title: Circulating interleukin-15 and RANTES chemokine in Parkinson’s disease
  publication-title: Acta Neurol Scand
  doi: 10.1111/j.1600-0404.2007.00894.x
– volume: 276
  start-page: 52
  year: 1997
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB7
  article-title: Understanding Parkinson’s disease
  publication-title: Sci Am
  doi: 10.1038/scientificamerican0197-52
– volume: 165
  start-page: 208
  year: 1994
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB3
  article-title: Tumor necrosis factor-alpha (TNF-alpha) increases both in the brain and in the cerebrospinal fluid from Parkinsonian patients
  publication-title: Neurosci Lett
  doi: 10.1016/0304-3940(94)90746-3
– volume: 942
  start-page: 87
  year: 2002
  ident: 10.1111/j.1600-0404.2008.01103.x-BIB32
  article-title: Interleukin-10 reverses acute detrimental effects of endotoxin-induced inflammation on perinatal cerebral hypoxia-ischemia
  publication-title: Brain Res
  doi: 10.1016/S0006-8993(02)02700-2
SSID ssj0012744
Score 2.2115612
Snippet Background –  Interleukin (IL)‐12 is a heterodimeric cytokine produced by activated blood monocytes, macrophages and glial cells. It enhances differentiation...
Interleukin (IL)-12 is a heterodimeric cytokine produced by activated blood monocytes, macrophages and glial cells. It enhances differentiation and...
Rentzos M, Nikolaou C, Andreadou E, Paraskevas GP, Rombos A, Zoga M, Tsoutsou A, Boufidou F, Kapaki E, Vassilopoulos D. Circulating interleukin-10 and...
SourceID proquest
pubmed
pascalfrancis
crossref
wiley
istex
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 332
SubjectTerms Aged
Aged, 80 and over
Biological and medical sciences
Biomarkers - analysis
Biomarkers - blood
Chemotaxis, Leukocyte - immunology
Cytoprotection - immunology
Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
ELISA
Encephalitis - blood
Encephalitis - immunology
Encephalitis - physiopathology
Female
Gliosis - blood
Gliosis - immunology
Gliosis - physiopathology
Humans
IL-10
IL-12
Immune Tolerance - immunology
immunological disturbances
Interleukin-10 - analysis
Interleukin-10 - blood
Interleukin-12 - analysis
Interleukin-12 - blood
l-dopa treatment
Male
Medical sciences
Middle Aged
Neurology
Parkinson Disease - blood
Parkinson Disease - immunology
Parkinson Disease - physiopathology
Parkinson's disease
Phagocytes - immunology
Predictive Value of Tests
Serum
Up-Regulation - immunology
Title Circulating interleukin-10 and interleukin-12 in Parkinson's disease
URI https://api.istex.fr/ark:/67375/WNG-D09L2MFM-0/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1600-0404.2008.01103.x
https://www.ncbi.nlm.nih.gov/pubmed/18976327
https://www.proquest.com/docview/20572091
https://www.proquest.com/docview/67145217
Volume 119
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1La9wwEBYlhdJL3w-nbepD6c2L3vIeQ5ptCN09lIbmJiRZLmGDU_YBoaf8hFz79_JLOiN73TqkEEoPBmN7bGs8I33jeRHyzhkPM573hdISDJSqdkXJmChUhW6p6I1P6WPTmT44kofH6riLf8JcmLY-RP_DDTUjzdeo4M4vh0quMStaUtmFRMJKJkaIJzF0C_HR576SFMNCeC0SZoUWTA6Dem680WCluotMP8fISbcE5tVt14ubYOkQ5aZlavKQzDcDbKNT5qP1yo_Cj2u1H_8PBx6RBx2azXdb8XtM7sTmCbk37fz1T8nh3skipAZhzbccK1MsTuN6ftJcXVwymrumun6Qw4EcM7FTUtrVxc9l3rmQnpGjyf6XvYOi695QBAkwpnBM1ao2vuZl4FTzSKPk1diFksvaJZwkoqclbLKOelxSUelAa8BvFQ2AnJ6TreasiS9J7pwAq9J7pasgjXGOC6END2Be80rJKiNm86Vs6EqbY4eNU_uHiQOsssiqrvEmssqeZ4T1lN_b8h63oHmfhKEnAKZgeJxR9uvso_1Ax5_4dDK1NCM7A2npCTgTHBOEM_J2Iz4WtBpdNa6JZ-slPE8ZDlDu71dowyRAL5ORF63c_X7_EiCm4HBGJ-m59cDs7mwf97b_lfAVud862zAe9DXZWi3W8Q1gtpXfSdr4C3HAMB0
linkProvider Wiley-Blackwell
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1La9wwEBYlgbaXvh_uI_Gh9OZFlmTJewxpttt0vYeS0NyEJMshZHHKPiDklJ-Qa_9efklnZK9bhxRC6cFgZI8f4xnpG8-LkA9GWZjxrE0yKcBAKSuT5GnKk6xEt5S3yob0sWIqx4di_yg7atsBYS5MUx-i--GGmhHma1Rw_CHd13KJadGCijYmEpYyPgBAuYkNvoN99a2rJZViKbwGC6eJ5Knoh_XceqXeWrWJbD_H2EmzAPZVTd-L24BpH-eGhWr0mMzWr9jEp5wOVks7cBc3qj_-Jx48IY9aQBvvNBL4lNzz9TNyv2hd9s_J_u7J3IUeYfVxjMUp5jO_Oj2pry-vUhqburw5yGAgxmTskJd2fflzEbdepBfkcLR3sDtO2gYOiROAZBKTZlVWKVux3DEqmadesHJoXM5EZQJU4t7SHDZReTnMKS-loxVAuJI6AE8vyUZ9VvvXJDaGg2FpbSZLJ5QyhnEuFXNgYbMyE2VE1PpTaddWN8cmGzP9h5UDrNLIqrb3JrJKn0ck7Sh_NBU-7kDzMUhDRwBMwQg5lenv08_6Ex1OWDEqNI3IVk9cOgKWcoY5whHZXsuPBsVGb42p_dlqAffLFAM09_czpEoFoC8VkVeN4P1-_hxQJmdwRAbxufOL6Z3pHu69-VfCbfJgfFBM9OTL9Otb8rDxvWF46DuysZyv_HuAcEu7FVTzF3K7NDg
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3JatxAEG2CDSaX7IvixNYh5KahN3VrjsbjieN4hhBi4lvTm4wZI5tZwOTkT_A1v-cvSZWkUTLGARNyEAhJJalLVd2vVBsh7612MOM5l-VKgoESSpsVjIksD-iWik67On1sNFb7R_LgOD9u458wF6apD9H9cEPNqOdrVPCLUK4qucKsaEllGxIJK5noAZ5cl4oWKOGDr10pKYaV8BoozDIlmFyN6rnzTitL1Tpy_RJDJ-0MuFc2bS_uwqWrMLdep4aPyWQ5wiY8ZdJbzF3P_7hV_PH_sOAJedTC2XSnkb-n5EGsnpGNUeuwf04Odk-nvu4QVp2kWJpiehYXk9Pq5uqa0dRW4fZBDgdSTMWus9Jurn7O0taH9IIcDfe-7e5nbfuGzEvAMZlleZmX2pW88JwqHmmUPPStL7gsbQ2URHS0gE2WUfULKoLytAQAF6gH6PSSrFXnVXxNUmsFmJXO5Sp4qbW1XAiluQf7modchoTo5Zcyvq1tji02zswfNg6wyiCr2s6byCpzmRDWUV409T3uQfOhFoaOAJiC8XE6N9_HH82A9g_5aDgyNCFbK9LSEXAmOGYIJ2R7KT4G1Bp9NbaK54sZPC_XHLDc369QmknAXjohrxq5-_3-BWBMweGMqqXn3gMzO-M93Hvzr4TbZOPLYGgOP40_b5KHjeMNY0PfkrX5dBHfAX6bu61aMX8Bt5Iy8A
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Circulating+interleukin-10+and+interleukin-12+in+Parkinson%27s+disease&rft.jtitle=Acta+neurologica+Scandinavica&rft.au=Rentzos%2C+M&rft.au=Nikolaou%2C+C&rft.au=Andreadou%2C+E&rft.au=Paraskevas%2C+G+P&rft.date=2009-05-01&rft.eissn=1600-0404&rft.volume=119&rft.issue=5&rft.spage=332&rft_id=info:doi/10.1111%2Fj.1600-0404.2008.01103.x&rft_id=info%3Apmid%2F18976327&rft.externalDocID=18976327
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0001-6314&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0001-6314&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0001-6314&client=summon