CD226 is specifically expressed on the surface of Th1 cells and regulates their expansion and effector functions

被引:123
作者
Dardalhon, V
Schubart, AS
Reddy, J
Meyers, JH
Monney, L
Sabatos, CA
Ahuja, R
Nguyen, K
Freeman, GJ
Greenfield, EA
Sobel, RA
Kuchroo, VK
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Ctr Neurol Dis,Inst Med,Dept Neurol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA
[4] Univ Calif Berkeley, Dept Mol & Cellular Biol, Berkeley, CA 94720 USA
[5] Millennium Pharmaceut, Cambridge, MA 02139 USA
[6] Vet Adm Hlth Care Syst, Palo Alto, CA USA
[7] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA 95305 USA
关键词
D O I
10.4049/jimmunol.175.3.1558
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Surface molecules that are differentially expressed on Th1 and Th2 cells may be useful in regulating specific immune responses in vivo. Using a panel of mAbs, we have identified murine CD226 as specifically expressed on the surface of differentiated Th1 cells but not Th2 or Th0 cells. Although CD226 is constitutively expressed on CD8 cells, it is up-regulated on CD4 cells upon activation. Th1 differentiation results in enhanced CD226 expression, whereas expression is down-regulated upon Th2 polarization. We demonstrate that CD226 is involved in the regulation of T cell activation; in vivo treatment with anti-CD226 results insignificant reduction of Th1 cell expansion and in the induction of APCs that inhibit T cell activation. Furthermore, anti-CD226 treatment delays the onset and reduces the severity of a Th1-mediated autoinmume disease, experimental autoimmune encephalomyelitis. Our data suggest that CD226 is a costimulatory molecule that plays an important role in activation and effector functions of Th1 cells.
引用
收藏
页码:1558 / 1565
页数:8
相关论文
共 44 条
[1]   Functional diversity of helper T lymphocytes [J].
Abbas, AK ;
Murphy, KM ;
Sher, A .
NATURE, 1996, 383 (6603) :787-793
[2]  
Anumanthan A, 1998, J IMMUNOL, V161, P2780
[3]   Myelin oligodendrocyte glycoprotein-specific T cell receptor transgenic mice develop spontaneous autoimmune optic neuritis [J].
Bettelli, E ;
Pagany, M ;
Weiner, HL ;
Linington, C ;
Sobel, RA ;
Kuchroo, AK .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (09) :1073-1081
[4]   Differential expression of chemokine receptors and chemotactic responsiveness of type 1 T helper cells (Th1s) and Th2s [J].
Bonecchi, R ;
Bianchi, G ;
Bordignon, PP ;
D'Ambrosio, D ;
Lang, R ;
Borsatti, A ;
Sozzani, S ;
Allavena, P ;
Gray, PA ;
Mantovani, A ;
Sinigaglia, F .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (01) :129-134
[5]   Identification of PVR (CD155) and nectin-2 (CD112) as cell surface ligands for the human DNAM-1 (CD226) activating molecule [J].
Bottino, C ;
Castriconi, R ;
Pende, D ;
Rivera, P ;
Nanni, M ;
Carnemolla, B ;
Cantoni, C ;
Grassi, J ;
Marcenaro, S ;
Reymond, N ;
Vitale, M ;
Moretta, L ;
Lopez, M ;
Moretta, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 198 (04) :557-567
[6]   Autopathogenic T helper cell type 1 (Th1) and protective Th2 clones differ in their recognition of the autoantigenic peptide of myelin proteolipid protein [J].
Das, MP ;
Nicholson, LB ;
Greer, JM ;
Kuchroo, VK .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (06) :867-876
[7]  
Das MRP, 1996, J NEUROIMMUNOL, V71, P3
[8]   Migratory activity and functional changes of green fluorescent effector cells before and during experimental autoimmune encephalomyelitis [J].
Flügel, A ;
Berkowicz, T ;
Ritter, T ;
Labeur, M ;
Jenne, DE ;
Li, ZX ;
Ellwart, JW ;
Willem, M ;
Lassmann, H ;
Wekerle, H .
IMMUNITY, 2001, 14 (05) :547-560
[9]   c-maf promotes T helper cell type 2 (Th2) and attenuates Th1 differentiation by both interleukin 4-dependent and -independent mechanisms [J].
Ho, IC ;
Lo, D ;
Glimcher, LH .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (10) :1859-1866
[10]  
HO LC, 1996, CELL, V85, P973