Different antiganglioside antibody pattern between relapsing-remitting and progressive multiple sclerosis
Multiple sclerosis (MS) is an autoimmune disorder, but an unique antigen has not been found. Antiganglioside antibodies (AGA) have been reported in MS, nevertheless, a clinical significance of AGA in MS has not been established. The aims of this study were to study AGA in sera of MS patients and to...
Saved in:
Published in | Acta neurologica Scandinavica Vol. 93; no. 2-3; p. 99 |
---|---|
Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Denmark
01.02.1996
|
Subjects | |
Online Access | Get more information |
Cover
Loading…
Abstract | Multiple sclerosis (MS) is an autoimmune disorder, but an unique antigen has not been found. Antiganglioside antibodies (AGA) have been reported in MS, nevertheless, a clinical significance of AGA in MS has not been established. The aims of this study were to study AGA in sera of MS patients and to investigate relationships between AGA and clinical course of MS.
42 patients with MS who fulfilled the criteria of clinically definite disease (59% RRMS, 21% SPMS, 20% PPMS), 89 patients with systemic lupus erythematosus and 36 healthy controls were studied. A modification of previously described ELISA techniques was used to estimate serum IgG and IgM anti-GM1, asialoGM1 and anti-GD1a antibodies.
47.6% of the patients showed AGA reactivity. Anti-GM1 was found in 38% of MS patients, anti-asialoGM1 in 23.8% and anti-GD1a in 33.3%. IgG was the isotype more commonly found. A correlation between presence of AGA and progressive disease and between anti-GD1a and PPMS was found.
The presence of AGA in MS patients is elevated. In contrast with the results of others authors, a strong correlation between AGA and progressive disease is showed in our study. |
---|---|
AbstractList | Multiple sclerosis (MS) is an autoimmune disorder, but an unique antigen has not been found. Antiganglioside antibodies (AGA) have been reported in MS, nevertheless, a clinical significance of AGA in MS has not been established. The aims of this study were to study AGA in sera of MS patients and to investigate relationships between AGA and clinical course of MS.
42 patients with MS who fulfilled the criteria of clinically definite disease (59% RRMS, 21% SPMS, 20% PPMS), 89 patients with systemic lupus erythematosus and 36 healthy controls were studied. A modification of previously described ELISA techniques was used to estimate serum IgG and IgM anti-GM1, asialoGM1 and anti-GD1a antibodies.
47.6% of the patients showed AGA reactivity. Anti-GM1 was found in 38% of MS patients, anti-asialoGM1 in 23.8% and anti-GD1a in 33.3%. IgG was the isotype more commonly found. A correlation between presence of AGA and progressive disease and between anti-GD1a and PPMS was found.
The presence of AGA in MS patients is elevated. In contrast with the results of others authors, a strong correlation between AGA and progressive disease is showed in our study. |
Author | Acarín, N Durán, I Galán, I Tintoré, M Fernández, A L Montalban, X Río, J |
Author_xml | – sequence: 1 givenname: N surname: Acarín fullname: Acarín, N organization: Department of Neurology, Hospital General Universitari Vall d'Hebrón, Barcelona, Spain – sequence: 2 givenname: J surname: Río fullname: Río, J – sequence: 3 givenname: A L surname: Fernández fullname: Fernández, A L – sequence: 4 givenname: M surname: Tintoré fullname: Tintoré, M – sequence: 5 givenname: I surname: Durán fullname: Durán, I – sequence: 6 givenname: I surname: Galán fullname: Galán, I – sequence: 7 givenname: X surname: Montalban fullname: Montalban, X |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/8741126$$D View this record in MEDLINE/PubMed |
BookMark | eNotj8FLwzAYxXOYzG36JwjBe2u-NG3To0ydwsDL7iNtvpSMNi1Jpu6_N-je5b0fPB68NVm4ySEhj8BySHo65VAxljHBRA5NU-WxZQwkz38WZMVSzKoCxC1Zh3BKxGshlmQpawHAqxWxL9YY9OgiVS7aXrl-sFOwGv-4nfSFzipG9I62GL8RHfU4qDlY12ceRxtjSqms6eyn3mMI9gvpeB6inQekoRvQp8FwR26MGgLeX31DDm-vh-17tv_cfWyf91lXlkWT1abTpSxYaQQCkwUmVZ0E0OmX0WB4wxQvdAvACglNVwLTXJVSgxJtxTfk4X92Prcj6uPs7aj85Xh9zH8BGJJdtw |
CitedBy_id | crossref_primary_10_1016_j_jns_2014_12_035 crossref_primary_10_1016_j_jneuroim_2006_06_028 crossref_primary_10_1016_j_jocn_2003_12_013 crossref_primary_10_1016_S0022_510X_98_00054_9 crossref_primary_10_1097_01_wco_0000169742_37159_e9 crossref_primary_10_1177_1352458509106708 crossref_primary_10_3389_fimmu_2020_01891 crossref_primary_10_1177_1352458508096685 crossref_primary_10_1002_1531_8249_200005_47_5_685__AID_ANA28_3_0_CO_2_K crossref_primary_10_1016_j_jneuroim_2005_03_025 crossref_primary_10_1016_S0022_510X_02_00053_9 crossref_primary_10_1134_S1819712414040035 crossref_primary_10_1177_17562864231189919 crossref_primary_10_1371_journal_pone_0063326 crossref_primary_10_1111_cen3_12653 crossref_primary_10_1111_j_1468_1331_2004_00797_x crossref_primary_10_1111_j_1750_3639_2000_tb00272_x crossref_primary_10_1016_j_jaut_2004_03_004 crossref_primary_10_2217_clp_11_8 crossref_primary_10_1016_S0165_5728_01_00251_X crossref_primary_10_1016_S0140_6736_05_60642_3 crossref_primary_10_1177_135245859900500i603 crossref_primary_10_3390_ijms22147319 crossref_primary_10_1177_1352458507087468 crossref_primary_10_1016_j_jns_2006_05_070 crossref_primary_10_1093_brain_122_10_1941 crossref_primary_10_1111_j_1600_0404_2011_01554_x crossref_primary_10_1016_j_autrev_2014_07_002 crossref_primary_10_1177_135245850100700303 crossref_primary_10_1016_j_jneuroim_2018_04_002 crossref_primary_10_1002_ana_410440621 crossref_primary_10_1002__SICI_1521_4141_199905_29_05_1667__AID_IMMU1667_3_0_CO_2_U crossref_primary_10_1523_JNEUROSCI_4017_06_2007 crossref_primary_10_1016_S0165_5728_97_00213_0 crossref_primary_10_1093_brain_122_12_2297 crossref_primary_10_1111_jnc_14032 crossref_primary_10_1191_135248506ms1279oa crossref_primary_10_1097_00019052_200106000_00005 crossref_primary_10_1016_j_bbadis_2010_07_020 crossref_primary_10_1016_S0165_5728_00_00409_4 crossref_primary_10_3390_ijms23105330 crossref_primary_10_1002_jnr_10424 crossref_primary_10_1034_j_1600_0404_2002_01161_x crossref_primary_10_1016_S0967_5868_02_00270_9 |
ContentType | Journal Article |
DBID | CGR CUY CVF ECM EIF NPM |
DOI | 10.1111/j.1600-0404.1996.tb00182.x |
DatabaseName | Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed |
DatabaseTitle | MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) |
DatabaseTitleList | 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 | no_fulltext_linktorsrc |
Discipline | Medicine |
ExternalDocumentID | 8741126 |
Genre | Research Support, Non-U.S. Gov't 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 BY8 C45 CAG CCPQU CGR COF CS3 CUY CVF D-6 D-7 D-E D-F DCZOG DPXWK DR2 DRFUL DRMAN DRSTM EAD EAP EAS EBC EBD EBS ECM EIF 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~ NPM 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 |
ID | FETCH-LOGICAL-c5539-7fcd58305f4e1083eeee6c811db00fd1f290a23db1103819c510d2a58d1a4b62 |
ISSN | 0001-6314 |
IngestDate | Sat Sep 28 08:41:03 EDT 2024 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 2-3 |
Language | English |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c5539-7fcd58305f4e1083eeee6c811db00fd1f290a23db1103819c510d2a58d1a4b62 |
OpenAccessLink | https://doi.org/10.1111/j.1600-0404.1996.tb00182.x |
PMID | 8741126 |
ParticipantIDs | pubmed_primary_8741126 |
PublicationCentury | 1900 |
PublicationDate | February 1996 |
PublicationDateYYYYMMDD | 1996-02-01 |
PublicationDate_xml | – month: 02 year: 1996 text: February 1996 |
PublicationDecade | 1990 |
PublicationPlace | Denmark |
PublicationPlace_xml | – name: Denmark |
PublicationTitle | Acta neurologica Scandinavica |
PublicationTitleAlternate | Acta Neurol Scand |
PublicationYear | 1996 |
SSID | ssj0012744 |
Score | 1.7181319 |
Snippet | Multiple sclerosis (MS) is an autoimmune disorder, but an unique antigen has not been found. Antiganglioside antibodies (AGA) have been reported in MS,... |
SourceID | pubmed |
SourceType | Index Database |
StartPage | 99 |
SubjectTerms | Adult Autoantibodies - blood Autoimmune Diseases - diagnosis Autoimmune Diseases - immunology Female Gangliosides - immunology Humans Immunoglobulin G - blood Immunoglobulin M - blood Male Middle Aged Multiple Sclerosis - diagnosis Multiple Sclerosis - immunology Reference Values |
Title | Different antiganglioside antibody pattern between relapsing-remitting and progressive multiple sclerosis |
URI | https://www.ncbi.nlm.nih.gov/pubmed/8741126 |
Volume | 93 |
hasFullText | |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LSwMxEA5VUbyIT3yTgzeJNLvZdHssPhBBD1LBm2TzgB7cLbYK-l_8r84k6boWK2oPS5t0t92dL5N5DyFHWdq1ysFCEjY3TJgsZUoKznJtZSGcy4TvWnJ9Iy_vxNV9dt9qvTeilp7HxYl--zav5D9UhTGgK2bJ_oGy9UVhAN4DfeEIFIbjr2h8FrubYJQ41srAlNwK-2_6z0VlXrFuKpr86ngszF0Zon2APdnHQQh6DrUCKq95YyBRHWQ4gt-DXXQwaoqwPT1Wx74MZmCbwB58aox6aYT99LQKPviz8ou_5zYMVl8cUmjL9uN8YtDuHdc26f6gRLeC9-d_Wm9NTNyrQ5sbvJczmYaU0QnvDd0RI8YSljZYaeibNJvDS0yJF22B-ZbSG7hBVQqxnw3SDx897XMQnHhIzf9xcqr2dpyZI3OdHJnoDZqCoosKSysG3SrcVqxoG8PEZvy7ZbIYrzmlxnhxpr9KVqIeQnsBVGukZct1snQdIy02yKDGFp3CFp1gi0Zs0Ygt-g224MuGNrBFJ9iiNbY2Sf_ivH96yWJbDqYzWNqs47TJctgnnLAcJHgLL6lzzg3cpTPcJd22SlJTcCy-z7sa2L5JVJYbrkQhky0yX1al3SZUS6e1S3UirBJtDecrkD47eZEZZWAr3SFb4Rk9DEPplYf48HZnTeyR5U_s7ZMFByvdHoDYOC4OPfk-AMePa4k |
link.rule.ids | 783 |
linkProvider | National Library of Medicine |
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=Different+antiganglioside+antibody+pattern+between+relapsing-remitting+and+progressive+multiple+sclerosis&rft.jtitle=Acta+neurologica+Scandinavica&rft.au=Acar%C3%ADn%2C+N&rft.au=R%C3%ADo%2C+J&rft.au=Fern%C3%A1ndez%2C+A+L&rft.au=Tintor%C3%A9%2C+M&rft.date=1996-02-01&rft.issn=0001-6314&rft.volume=93&rft.issue=2-3&rft.spage=99&rft_id=info:doi/10.1111%2Fj.1600-0404.1996.tb00182.x&rft_id=info%3Apmid%2F8741126&rft_id=info%3Apmid%2F8741126&rft.externalDocID=8741126 |
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 |