The immunoglobulin superfamily member CD200R identifies cells involved in type 2 immune responses

Background The pathology of allergic diseases involves type 2 immune cells, such as Th2, ILC2, and basophils exerting their effect by production of IL‐4, IL‐5, and IL‐13. However, surface receptors that are specifically expressed on type 2 immune cells are less well documented. The aim of this inves...

Full description

Saved in:
Bibliographic Details
Published inAllergy (Copenhagen) Vol. 72; no. 7; pp. 1081 - 1090
Main Authors Blom, L. H., Martel, B. C., Larsen, L. F., Hansen, C. V., Christensen, M. P., Juel‐Berg, N., Litman, T., Poulsen, L. K.
Format Journal Article
LanguageEnglish
Published Denmark Blackwell Publishing Ltd 01.07.2017
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Background The pathology of allergic diseases involves type 2 immune cells, such as Th2, ILC2, and basophils exerting their effect by production of IL‐4, IL‐5, and IL‐13. However, surface receptors that are specifically expressed on type 2 immune cells are less well documented. The aim of this investigation was to identify surface markers associated with type 2 inflammation. Methods Naïve human CD4+ T cells were short‐term activated in the presence or absence of IL‐4 and analyzed for expression of >300 cell‐surface proteins. Ex vivo‐isolated peripheral blood mononuclear cells (PBMCs) from peanut‐allergic (PA) and nonallergic subjects were stimulated (14–16 h) with peanut extract to detect peanut‐specific CD4+CD154+ T cells. Biopsies were obtained for transcriptomic analysis from healthy controls and patients with extrinsic or intrinsic atopic dermatitis (AD) and psoriasis. Results Expression analysis of >300 surface proteins enabled identification of IL‐4‐upregulated surface proteins, such as CD90, CD108, CD109, and CD200R (CD200R1). Additional analysis of in vitro‐differentiated Th0, Th1, and Th2 cultures identified CD200R as upregulated on Th2 cells. From ex vivo‐isolated PBMCs, we found high expression of CD200R on Th2 and ILC2 cells and basophils. In PA subjects, the peanut‐specific Th2 (CD154+CRTh2+) cells expressed more CD200R than the non‐allergen‐specific Th2 (CD154−CRTh2+) cells. Moreover, costaining of CD161 and CD200R identified peanut‐specific highly differentiated IL‐4+IL‐5+ Th2 cells. Finally, transcriptomic analysis revealed upregulation of CD200R in lesional skin from subjects with an extrinsic AD phenotype compared to healthy skin. Conclusion These results indicate that CD200R expression strongly correlates with Th2 pathology; though, the mechanism is as yet elusive.
AbstractList Background The pathology of allergic diseases involves type 2 immune cells, such as Th2, ILC2, and basophils exerting their effect by production of IL‐4, IL‐5, and IL‐13. However, surface receptors that are specifically expressed on type 2 immune cells are less well documented. The aim of this investigation was to identify surface markers associated with type 2 inflammation. Methods Naïve human CD4+ T cells were short‐term activated in the presence or absence of IL‐4 and analyzed for expression of >300 cell‐surface proteins. Ex vivo‐isolated peripheral blood mononuclear cells (PBMCs) from peanut‐allergic (PA) and nonallergic subjects were stimulated (14–16 h) with peanut extract to detect peanut‐specific CD4+CD154+ T cells. Biopsies were obtained for transcriptomic analysis from healthy controls and patients with extrinsic or intrinsic atopic dermatitis (AD) and psoriasis. Results Expression analysis of >300 surface proteins enabled identification of IL‐4‐upregulated surface proteins, such as CD90, CD108, CD109, and CD200R (CD200R1). Additional analysis of in vitro‐differentiated Th0, Th1, and Th2 cultures identified CD200R as upregulated on Th2 cells. From ex vivo‐isolated PBMCs, we found high expression of CD200R on Th2 and ILC2 cells and basophils. In PA subjects, the peanut‐specific Th2 (CD154+CRTh2+) cells expressed more CD200R than the non‐allergen‐specific Th2 (CD154−CRTh2+) cells. Moreover, costaining of CD161 and CD200R identified peanut‐specific highly differentiated IL‐4+IL‐5+ Th2 cells. Finally, transcriptomic analysis revealed upregulation of CD200R in lesional skin from subjects with an extrinsic AD phenotype compared to healthy skin. Conclusion These results indicate that CD200R expression strongly correlates with Th2 pathology; though, the mechanism is as yet elusive.
BACKGROUNDThe pathology of allergic diseases involves type 2 immune cells, such as Th2, ILC2, and basophils exerting their effect by production of IL-4, IL-5, and IL-13. However, surface receptors that are specifically expressed on type 2 immune cells are less well documented. The aim of this investigation was to identify surface markers associated with type 2 inflammation.METHODSNaïve human CD4+ T cells were short-term activated in the presence or absence of IL-4 and analyzed for expression of >300 cell-surface proteins. Ex vivo-isolated peripheral blood mononuclear cells (PBMCs) from peanut-allergic (PA) and nonallergic subjects were stimulated (14-16 h) with peanut extract to detect peanut-specific CD4+ CD154+ T cells. Biopsies were obtained for transcriptomic analysis from healthy controls and patients with extrinsic or intrinsic atopic dermatitis (AD) and psoriasis.RESULTSExpression analysis of >300 surface proteins enabled identification of IL-4-upregulated surface proteins, such as CD90, CD108, CD109, and CD200R (CD200R1). Additional analysis of in vitro-differentiated Th0, Th1, and Th2 cultures identified CD200R as upregulated on Th2 cells. From ex vivo-isolated PBMCs, we found high expression of CD200R on Th2 and ILC2 cells and basophils. In PA subjects, the peanut-specific Th2 (CD154+ CRTh2+ ) cells expressed more CD200R than the non-allergen-specific Th2 (CD154- CRTh2+ ) cells. Moreover, costaining of CD161 and CD200R identified peanut-specific highly differentiated IL-4+ IL-5+ Th2 cells. Finally, transcriptomic analysis revealed upregulation of CD200R in lesional skin from subjects with an extrinsic AD phenotype compared to healthy skin.CONCLUSIONThese results indicate that CD200R expression strongly correlates with Th2 pathology; though, the mechanism is as yet elusive.
The pathology of allergic diseases involves type 2 immune cells, such as Th2, ILC2, and basophils exerting their effect by production of IL-4, IL-5, and IL-13. However, surface receptors that are specifically expressed on type 2 immune cells are less well documented. The aim of this investigation was to identify surface markers associated with type 2 inflammation. Naïve human CD4 T cells were short-term activated in the presence or absence of IL-4 and analyzed for expression of >300 cell-surface proteins. Ex vivo-isolated peripheral blood mononuclear cells (PBMCs) from peanut-allergic (PA) and nonallergic subjects were stimulated (14-16 h) with peanut extract to detect peanut-specific CD4 CD154 T cells. Biopsies were obtained for transcriptomic analysis from healthy controls and patients with extrinsic or intrinsic atopic dermatitis (AD) and psoriasis. Expression analysis of >300 surface proteins enabled identification of IL-4-upregulated surface proteins, such as CD90, CD108, CD109, and CD200R (CD200R1). Additional analysis of in vitro-differentiated Th0, Th1, and Th2 cultures identified CD200R as upregulated on Th2 cells. From ex vivo-isolated PBMCs, we found high expression of CD200R on Th2 and ILC2 cells and basophils. In PA subjects, the peanut-specific Th2 (CD154 CRTh2 ) cells expressed more CD200R than the non-allergen-specific Th2 (CD154 CRTh2 ) cells. Moreover, costaining of CD161 and CD200R identified peanut-specific highly differentiated IL-4 IL-5 Th2 cells. Finally, transcriptomic analysis revealed upregulation of CD200R in lesional skin from subjects with an extrinsic AD phenotype compared to healthy skin. These results indicate that CD200R expression strongly correlates with Th2 pathology; though, the mechanism is as yet elusive.
Background The pathology of allergic diseases involves type 2 immune cells, such as Th2, ILC2, and basophils exerting their effect by production of IL-4, IL-5, and IL-13. However, surface receptors that are specifically expressed on type 2 immune cells are less well documented. The aim of this investigation was to identify surface markers associated with type 2 inflammation. Methods Naïve human CD4+ T cells were short-term activated in the presence or absence of IL-4 and analyzed for expression of >300 cell-surface proteins. Ex vivo-isolated peripheral blood mononuclear cells (PBMCs) from peanut-allergic (PA) and nonallergic subjects were stimulated (14-16 h) with peanut extract to detect peanut-specific CD4+CD154+ T cells. Biopsies were obtained for transcriptomic analysis from healthy controls and patients with extrinsic or intrinsic atopic dermatitis (AD) and psoriasis. Results Expression analysis of >300 surface proteins enabled identification of IL-4-upregulated surface proteins, such as CD90, CD108, CD109, and CD200R (CD200R1). Additional analysis of in vitro-differentiated Th0, Th1, and Th2 cultures identified CD200R as upregulated on Th2 cells. From ex vivo-isolated PBMCs, we found high expression of CD200R on Th2 and ILC2 cells and basophils. In PA subjects, the peanut-specific Th2 (CD154+CRTh2+) cells expressed more CD200R than the non-allergen-specific Th2 (CD154-CRTh2+) cells. Moreover, costaining of CD161 and CD200R identified peanut-specific highly differentiated IL-4+IL-5+ Th2 cells. Finally, transcriptomic analysis revealed upregulation of CD200R in lesional skin from subjects with an extrinsic AD phenotype compared to healthy skin. Conclusion These results indicate that CD200R expression strongly correlates with Th2 pathology; though, the mechanism is as yet elusive.
Author Hansen, C. V.
Juel‐Berg, N.
Martel, B. C.
Litman, T.
Blom, L. H.
Poulsen, L. K.
Larsen, L. F.
Christensen, M. P.
Author_xml – sequence: 1
  givenname: L. H.
  orcidid: 0000-0003-2027-727X
  surname: Blom
  fullname: Blom, L. H.
  email: lars.blom@regionh.dk
  organization: Copenhagen University Hospital Herlev‐Gentofte
– sequence: 2
  givenname: B. C.
  surname: Martel
  fullname: Martel, B. C.
  organization: LEO Pharma A/S
– sequence: 3
  givenname: L. F.
  orcidid: 0000-0001-6433-3961
  surname: Larsen
  fullname: Larsen, L. F.
  organization: Copenhagen University Hospital Herlev‐Gentofte
– sequence: 4
  givenname: C. V.
  surname: Hansen
  fullname: Hansen, C. V.
  organization: Copenhagen University Hospital Herlev‐Gentofte
– sequence: 5
  givenname: M. P.
  surname: Christensen
  fullname: Christensen, M. P.
  organization: Copenhagen University Hospital Herlev‐Gentofte
– sequence: 6
  givenname: N.
  surname: Juel‐Berg
  fullname: Juel‐Berg, N.
  organization: Copenhagen University Hospital Herlev‐Gentofte
– sequence: 7
  givenname: T.
  surname: Litman
  fullname: Litman, T.
  organization: LEO Pharma A/S
– sequence: 8
  givenname: L. K.
  surname: Poulsen
  fullname: Poulsen, L. K.
  organization: Copenhagen University Hospital Herlev‐Gentofte
BackLink https://www.ncbi.nlm.nih.gov/pubmed/28106273$$D View this record in MEDLINE/PubMed
BookMark eNpdkU1LxDAQhoMouqse_AMS8OKlbj6aJjku6ycsCKLnkNqpZknT2mxX9t-b_dCDc5kX5pmXYd4xOgxtAIQuKLmhqSbW-xvKKdMHaES5VpnWWhyiEaFEZLng6gSNY1wQQiTT5BidMEVJwSQfIfv6Cdg1zRDaD9-Wg3cBx6GDvraN82vcQFNCj2e3jJAX7CoIS1c7iPgdvI_YhVXrV1AlgZfrDjDbmQHuIXZtiBDP0FFtfYTzfT9Fb_d3r7PHbP788DSbzrMFz4XOpLVSW2mJ1lSC4DkvZWU5K4kohGRKc6FKqIUUTPCagmQg87QI8K7zqtD8FF3vfLu-_RogLk3j4uZKG6AdoqGqoEJxWpCEXv1DF-3Qh3SdoTo9huaKqkRd7qmhbKAyXe8a26_N7_MSMNkB387D-m9OidmkYlIqZpuKmc7nW8F_AD_bftw
ContentType Journal Article
Copyright 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
Copyright © 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
Copyright_xml – notice: 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
– notice: 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
– notice: Copyright © 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
DBID CGR
CUY
CVF
ECM
EIF
NPM
7T5
H94
K9.
7X8
DOI 10.1111/all.13129
DatabaseName Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
Immunology Abstracts
AIDS and Cancer Research Abstracts
ProQuest Health & Medical Complete (Alumni)
MEDLINE - Academic
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
AIDS and Cancer Research Abstracts
ProQuest Health & Medical Complete (Alumni)
Immunology Abstracts
MEDLINE - Academic
DatabaseTitleList
MEDLINE - Academic
MEDLINE
AIDS and Cancer Research Abstracts
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 1398-9995
EndPage 1090
ExternalDocumentID 28106273
ALL13129
Genre article
Journal Article
GrantInformation_xml – fundername: Else and Helene Alstrups Foundation
– fundername: Toyota Foundation
GroupedDBID .3N
.GA
.GJ
.Y3
05W
0R~
10A
1OB
1OC
23M
24P
2WC
31~
33P
36B
3SF
4.4
50Y
50Z
51W
51X
52M
52N
52O
52P
52R
52S
52T
52U
52V
52W
52X
53G
5GY
5HH
5LA
5RE
5VS
66C
702
7PT
8-0
8-1
8-3
8-4
8-5
8F7
8UM
930
A01
A03
AAESR
AAEVG
AAHHS
AAKAS
AANLZ
AAONW
AASGY
AAXRX
AAZKR
ABCQN
ABCUV
ABEML
ABJNI
ABLJU
ABOCM
ABPVW
ABQWH
ABXGK
ACAHQ
ACBWZ
ACCFJ
ACCZN
ACGFS
ACGOF
ACMXC
ACPOU
ACPRK
ACSCC
ACXBN
ACXQS
ADBBV
ADBTR
ADEOM
ADIZJ
ADKYN
ADMGS
ADOZA
ADXAS
ADZCM
ADZMN
AEEZP
AEIGN
AEIMD
AENEX
AEQDE
AEUQT
AEUYR
AFBPY
AFEBI
AFFNX
AFFPM
AFGKR
AFPWT
AFRAH
AFZJQ
AHBTC
AHEFC
AHMBA
AIACR
AITYG
AIURR
AIWBW
AJBDE
ALAGY
ALMA_UNASSIGNED_HOLDINGS
ALUQN
AMBMR
AMYDB
AOETA
ATUGU
AZBYB
AZFZN
AZVAB
BAFTC
BAWUL
BDRZF
BFHJK
BHBCM
BMXJE
BROTX
BRXPI
BY8
C45
CAG
COF
CS3
D-6
D-7
D-E
D-F
DC6
DCZOG
DIK
DPXWK
DR2
DRFUL
DRMAN
DRSTM
E3Z
EBS
EJD
EMOBN
ESX
EX3
F00
F01
F04
F5P
FEDTE
FUBAC
FZ0
G-S
G.N
GODZA
H.X
HF~
HGLYW
HVGLF
HZI
HZ~
IHE
IX1
J0M
K48
KBYEO
LATKE
LC2
LC3
LEEKS
LH4
LITHE
LOXES
LP6
LP7
LUTES
LW6
LYRES
MEWTI
MK4
MRFUL
MRMAN
MRSTM
MSFUL
MSMAN
MSSTM
MXFUL
MXMAN
MXSTM
N04
N05
N9A
NF~
O66
O9-
OIG
OK1
OVD
P2P
P2W
P2X
P2Z
P4B
P4D
P6G
PALCI
PQQKQ
Q.N
Q11
QB0
R.K
RIWAO
RJQFR
ROL
RX1
SAMSI
SUPJJ
TEORI
TR2
UB1
V9Y
W8V
W99
WBKPD
WHWMO
WIH
WIJ
WIK
WIN
WOHZO
WOW
WQJ
WRC
WUP
WVDHM
WXI
WXSBR
XG1
Y6R
ZGI
ZXP
ZZTAW
~IA
~KM
~WT
ACXME
CGR
CUY
CVF
ECM
EIF
NPM
7T5
H94
K9.
7X8
ID FETCH-LOGICAL-j3459-7aa79a7a09917e5343b7da32b05657289358bef575253f1e72e74459eec94d693
IEDL.DBID DR2
ISSN 0105-4538
IngestDate Fri Aug 16 05:10:13 EDT 2024
Fri Sep 13 08:54:13 EDT 2024
Fri May 24 00:03:52 EDT 2024
Sat Aug 24 00:46:04 EDT 2024
IsPeerReviewed true
IsScholarly true
Issue 7
Keywords CD154
atopic dermatitis
CD200R
peanut-specific Th cells
Th2
Language English
License 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-j3459-7aa79a7a09917e5343b7da32b05657289358bef575253f1e72e74459eec94d693
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ORCID 0000-0003-2027-727X
0000-0001-6433-3961
PMID 28106273
PQID 1906214818
PQPubID 34098
PageCount 10
ParticipantIDs proquest_miscellaneous_1861583160
proquest_journals_1906214818
pubmed_primary_28106273
wiley_primary_10_1111_all_13129_ALL13129
PublicationCentury 2000
PublicationDate July 2017
PublicationDateYYYYMMDD 2017-07-01
PublicationDate_xml – month: 07
  year: 2017
  text: July 2017
PublicationDecade 2010
PublicationPlace Denmark
PublicationPlace_xml – name: Denmark
– name: Zurich
PublicationTitle Allergy (Copenhagen)
PublicationTitleAlternate Allergy
PublicationYear 2017
Publisher Blackwell Publishing Ltd
Publisher_xml – name: Blackwell Publishing Ltd
References 2004; 200
2010; 10
2004; 103
2015; 96
1997; 89
1999; 162
2003; 171
1999; 163
2011; 35
2011; 79
2011; 12
2012; 14
2014; 134
2004; 77
2015; 82
2013; 13
2005; 202
2004; 173
2004; 172
2004; 34
2016; 65
2013; 397
2009; 124
2009; 183
2016; 137
2006; 126
1998; 95
2012; 7
2012; 67
2016; 25
1990; 172
2011; 187
2005; 79
References_xml – volume: 79
  start-page: 167
  year: 2011
  end-page: 174
  article-title: SPICE: exploration and analysis of post‐cytometric complex multivariate datasets
  publication-title: Cytometry A
– volume: 172
  start-page: 7744
  year: 2004
  end-page: 7749
  article-title: CD200 is a ligand for all members of the CD200R family of immunoregulatory molecules
  publication-title: J Immunol
– volume: 137
  start-page: 907
  year: 2016
  end-page: 918
  article-title: Hematopoietic prostaglandin D synthase defines a proeosinophilic pathogenic effector human TH2 cell subpopulation with enhanced function
  publication-title: J Allergy Clin Immunol
– volume: 79
  start-page: 488
  year: 2005
  end-page: 491
  article-title: Augmented induction of CD4+CD25+ Treg using monoclonal antibodies to CD200R
  publication-title: Transplantation
– volume: 12
  start-page: 167
  year: 2011
  end-page: 177
  article-title: Mouse CCL8, a CCR8 agonist, promotes atopic dermatitis by recruiting IL‐5+ T(H)2 cells
  publication-title: Nat Immunol
– volume: 187
  start-page: 3111
  year: 2011
  end-page: 3120
  article-title: Hierarchical IL‐5 expression defines a subpopulation of highly differentiated human Th2 cells
  publication-title: J Immunol
– volume: 202
  start-page: 793
  year: 2005
  end-page: 804
  article-title: Independent roles for IL‐2 and GATA‐3 in stimulating naive CD4+ T cells to generate a Th2‐inducing cytokine environment
  publication-title: J Exp Med
– volume: 7
  start-page: e35466
  year: 2012
  article-title: Chronic infection drives expression of the inhibitory receptor CD200R, and its ligand CD200, by mouse and human CD4 T cells
  publication-title: PLoS One
– volume: 397
  start-page: 55
  year: 2013
  end-page: 60
  article-title: In vitro Th1 and Th2 cell polarization is severely influenced by the initial ratio of naive and memory CD4+ T cells
  publication-title: J Immunol Methods
– volume: 67
  start-page: 574
  year: 2012
  end-page: 581
  article-title: 1alpha,25‐dihydroxyvitamin D3 promotes CD200 expression by human peripheral and airway‐resident T cells
  publication-title: Thorax
– volume: 124
  start-page: 1326
  year: 2009
  end-page: 1332
  article-title: Eosinophilic gastrointestinal disease and peanut allergy are alternatively associated with IL‐5+ and IL‐5(−) T(H)2 responses
  publication-title: J Allergy Clin Immunol
– volume: 25
  start-page: 453
  year: 2016
  end-page: 459
  article-title: Distinct molecular signatures of mild extrinsic and intrinsic atopic dermatitis
  publication-title: Exp Dermatol
– volume: 200
  start-page: 507
  year: 2004
  end-page: 517
  article-title: Basophils produce IL‐4 and accumulate in tissues after infection with a Th2‐inducing parasite
  publication-title: J Exp Med
– volume: 126
  start-page: 1043
  year: 2006
  end-page: 1051
  article-title: IL‐13‐stimulated human keratinocytes preferentially attract CD4+CCR4+ T cells: possible role in atopic dermatitis
  publication-title: J Invest Dermatol
– volume: 13
  start-page: 145
  year: 2013
  end-page: 149
  article-title: Innate lymphoid cells–a proposal for uniform nomenclature
  publication-title: Nat Rev Immunol
– volume: 163
  start-page: 1654
  year: 1999
  end-page: 1660
  article-title: An immunoadhesin incorporating the molecule OX‐2 is a potent immunosuppressant that prolongs allo‐ and xenograft survival
  publication-title: J Immunol
– volume: 10
  start-page: 264
  year: 2010
  article-title: The landscape of human genes involved in the immune response to parasitic worms
  publication-title: BMC Evol Biol
– volume: 82
  start-page: 125
  year: 2015
  end-page: 134
  article-title: Human atopic dermatitis skin‐derived T cells can induce a reaction in mouse keratinocytes in vivo
  publication-title: Scand J Immunol
– volume: 65
  start-page: 265
  year: 2016
  end-page: 272
  article-title: Different cytokine profiles of skin‐derived T cell cultures from patients with atopic dermatitis and psoriasis
  publication-title: Inflamm Res
– volume: 14
  start-page: R123
  year: 2012
  article-title: Aberrant CD200/CD200R1 expression and function in systemic lupus erythematosus contributes to abnormal T‐cell responsiveness and dendritic cell activity
  publication-title: Arthritis Res Ther
– volume: 173
  start-page: 6786
  year: 2004
  end-page: 6793
  article-title: Molecular mechanisms of CD200 inhibition of mast cell activation
  publication-title: J Immunol
– volume: 10
  start-page: 225
  year: 2010
  end-page: 235
  article-title: How are T(H)2‐type immune responses initiated and amplified?
  publication-title: Nat Rev Immunol
– volume: 134
  start-page: 1329
  year: 2014
  end-page: 1338
  article-title: IL‐9 is a key component of memory TH cell peanut‐specific responses from children with peanut allergy
  publication-title: J Allergy Clin Immunol
– volume: 183
  start-page: 4879
  year: 2009
  end-page: 4886
  article-title: Essential roles for Dok2 and RasGAP in CD200 receptor‐mediated regulation of human myeloid cells
  publication-title: J Immunol
– volume: 172
  start-page: 921
  year: 1990
  end-page: 929
  article-title: Generation of interleukin 4 (IL‐4)‐producing cells in vivo and in vitro: IL‐2 and IL‐4 are required for in vitro generation of IL‐4‐producing cells
  publication-title: J Exp Med
– volume: 89
  start-page: 587
  year: 1997
  end-page: 596
  article-title: The transcription factor GATA‐3 is necessary and sufficient for Th2 cytokine gene expression in CD4 T cells
  publication-title: Cell
– volume: 103
  start-page: 2691
  year: 2004
  end-page: 2698
  article-title: CD200 is a novel p53‐target gene involved in apoptosis‐associated immune tolerance
  publication-title: Blood
– volume: 95
  start-page: 6930
  year: 1998
  end-page: 6935
  article-title: T1/ST2 is preferentially expressed on murine Th2 cells, independent of interleukin 4, interleukin 5, and interleukin 10, and important for Th2 effector function
  publication-title: Proc Natl Acad Sci U S A
– volume: 162
  start-page: 1278
  year: 1999
  end-page: 1286
  article-title: Selective expression of a novel surface molecule by human Th2 cells in vivo
  publication-title: J Immunol
– volume: 35
  start-page: 733
  year: 2011
  end-page: 745
  article-title: Eomesodermin controls interleukin‐5 production in memory T helper 2 cells through inhibition of activity of the transcription factor GATA3
  publication-title: Immunity
– volume: 34
  start-page: 1688
  year: 2004
  end-page: 1694
  article-title: The CD200 and CD200 receptor cell surface proteins interact through their N‐terminal immunoglobulin‐like domains
  publication-title: Eur J Immunol
– volume: 77
  start-page: 1138
  year: 2004
  end-page: 1144
  article-title: Induction of tolerance‐inducing antigen‐presenting cells in bone marrow cultures in vitro using monoclonal antibodies to CD200R
  publication-title: Transplantation
– volume: 96
  start-page: 104
  year: 2015
  end-page: 120
  article-title: Genome‐wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms
  publication-title: Am J Hum Genet
– volume: 171
  start-page: 3034
  year: 2003
  end-page: 3046
  article-title: Characterization of the CD200 receptor family in mice and humans and their interactions with CD200
  publication-title: J Immunol
SSID ssj0007290
Score 2.3926883
Snippet Background The pathology of allergic diseases involves type 2 immune cells, such as Th2, ILC2, and basophils exerting their effect by production of IL‐4, IL‐5,...
The pathology of allergic diseases involves type 2 immune cells, such as Th2, ILC2, and basophils exerting their effect by production of IL-4, IL-5, and IL-13....
Background The pathology of allergic diseases involves type 2 immune cells, such as Th2, ILC2, and basophils exerting their effect by production of IL-4, IL-5,...
BACKGROUNDThe pathology of allergic diseases involves type 2 immune cells, such as Th2, ILC2, and basophils exerting their effect by production of IL-4, IL-5,...
SourceID proquest
pubmed
wiley
SourceType Aggregation Database
Index Database
Publisher
StartPage 1081
SubjectTerms Allergens
Allergens - immunology
Allergic diseases
Antigens, Surface - genetics
Antigens, Surface - metabolism
Atopic dermatitis
Basophils - immunology
Basophils - metabolism
CD154
CD200R
CD4 antigen
CD40L protein
CD90 antigen
Cell surface
Culture
Cytokines - metabolism
Dermatitis
Gene Expression
Helper cells
Humans
Hypersensitivity - genetics
Hypersensitivity - immunology
Hypersensitivity - metabolism
Immune response
Immunoglobulins
Immunology
Interleukin 13
Interleukin 4
Interleukin 5
Leukocytes (basophilic)
Leukocytes (mononuclear)
Lymphocytes
Lymphocytes T
Neurodegenerative diseases
Pathology
Peanut Hypersensitivity - genetics
Peanut Hypersensitivity - immunology
Peanut Hypersensitivity - metabolism
peanut‐specific Th cells
Peripheral blood mononuclear cells
Proteins
Psoriasis
Receptors, Cell Surface - genetics
Receptors, Cell Surface - metabolism
Skin diseases
Surface markers
T cell receptors
T-Lymphocyte Subsets - immunology
T-Lymphocyte Subsets - metabolism
Th2
Th2 Cells - immunology
Th2 Cells - metabolism
Thy-1 Antigens - metabolism
Title The immunoglobulin superfamily member CD200R identifies cells involved in type 2 immune responses
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fall.13129
https://www.ncbi.nlm.nih.gov/pubmed/28106273
https://www.proquest.com/docview/1906214818/abstract/
https://search.proquest.com/docview/1861583160
Volume 72
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LS8QwEB7Eg3jx_VhfRPDgpcs2SZsWT8uqiKgHUfAglKQ7C6trV7a7Hvz1zjTd9YEH8ZbSpDTMI99MJl8Ajlyu4x65xMAgRTo6zuPASmuDyEmlnUkjeuJqi5v44l5fPkQPc3AyPQvj-SFmCTe2jMpfs4FbV34xcjsYNENFyxX5XybSY0B0-0kdZer8CuGHQJNV16xCXMUzG_kbqvwOUqtV5nwZHqf_54tLnpuTsWvm7z-oG_85gRVYqtGnaHt1WYU5LNZg4breX18HS1oj-nxkZMhMIVylLsrJK458HkS8IN8fIjqnpPW3ot_1pUZYCs7_l6JfkLN7wy41BOd2hfQfQzHypbhYbsD9-dld5yKoL2EInpSO0sBYa1JrLCHJ0GCktHKma5V0Ld4wpXBNRYnDHqE-GaleiEai0TQQMU91N07VJswXwwK3QWiWA8GL1KlQExBxtqWNSySSF8lNnjZgbyqOrLakMguZSJlitjBpwOHsNdkAT8wWOJxQn4RwWaLCuNWALS_G7NWTdWQyCZmJWTXguBLG7MU0-iExZJUYsvbVVdXY-XvXXViUvM5X9bt7MD8eTXCfUMrYHVTq-AHt5-A3
link.rule.ids 315,786,790,1382,27957,27958,46329,46753
linkProvider Wiley-Blackwell
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3NT9swFH9iTNq4wGADCowZaQcuqRrbiROJS1VAHSscEEhcUGSnr1K3kqKm5cBfz3txWj7EYdrNUewo1vvw7z0__wzw0-U6HpBLDAxSpKPjPA6stDaInFTamTSiJ662uIi71_rsJrpZgqP5WRjPD7FIuLFlVP6aDZwT0i-s3I5GzVDRevUBPpK5R1VAdflMHmXqDAshiECTXde8QlzHsxj6Hq58DVOrdeZ0DW7nf-jLS_42Z1PXzB_fkDf-7xS-wGoNQEXba8w6LGGxAZ_O6y32r2BJccSQT42MmSyEC9VFObvHiU-FiDvkK0RE55gU_1IM-77aCEvBWwClGBbk7x6wTw3B6V0h_cdQTHw1Lpbf4Pr05KrTDep7GII_SkdpYKw1qTWWwGRoMFJaOdO3SroW75lSxKaixOGAgJ-M1CBEI9FoGoiYp7ofp2oTlotxgdsgNAuCEEbqVKgJizjb0sYlEsmR5CZPG7A3l0dWG1OZhcylTGFbmDTgYPGazIAnZgscz6hPQtAsUWHcasCWl2N27_k6MpmETMasGnBYSWPxYh4AkRiySgxZu9erGjv_3vUHfO5enfey3q-L37uwInnZr8p592B5OpnhdwItU7df6eYTEW3kWQ
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3NT9swFH_iQ0JcNmAb64BhJA5cUjW2EyfihCgVGwUhNCQOSJGdvEoFllZNu8P--r0Xp4VNHNBujmJHsd6Hf-_5-WeAQ5freEAuMTBIkY6O8ziw0togclJpZ9KInrja4io-v9Xf76K7JTien4Xx_BCLhBtbRu2v2cDHxeCFkdunp3aoaLlahlUdK8kq3b155o4yTYKFAESgyawbWiEu41kMfQ1W_o1S62Wm9x7u5z_oq0se27Opa-e__-Fu_M8ZbMC7Bn6KE68vm7CE5RasXTYb7B_AktqIIZ8ZGTFVCJepi2o2xolPhIifyBeIiNMuqf2NGBa-1ggrwRsAlRiW5O1-YUENwcldIf3HUEx8LS5WH-G2d_bj9DxobmEIHpSO0sBYa1JrLEHJ0GCktHKmsEq6Du-YUrymosThgGCfjNQgRCPRaBqImKe6iFP1CVbKUYmfQWiWA-GL1KlQExJxtqONSySSG8lNnrZgdy6OrDGlKguZSZmCtjBpwcHiNRkBT8yWOJpRn4SAWaLCuNOCbS_GbOzZOjKZhEzFrFpwVAtj8WIe_pAYsloM2Um_Xze-vL3rPqxdd3tZ_9vVxQ6sS17z61reXViZTma4R4hl6r7WmvkHeTvjCA
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=The+immunoglobulin+superfamily+member+CD200R+identifies+cells+involved+in+type+2+immune+responses&rft.jtitle=Allergy+%28Copenhagen%29&rft.au=Blom%2C+L.+H.&rft.au=Martel%2C+B.+C.&rft.au=Larsen%2C+L.+F.&rft.au=Hansen%2C+C.+V.&rft.date=2017-07-01&rft.issn=0105-4538&rft.eissn=1398-9995&rft.volume=72&rft.issue=7&rft.spage=1081&rft.epage=1090&rft_id=info:doi/10.1111%2Fall.13129&rft.externalDBID=10.1111%252Fall.13129&rft.externalDocID=ALL13129
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0105-4538&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0105-4538&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0105-4538&client=summon