Dardalhon Valerie, Schubart Anna S, Reddy Jayagopala, Meyers Jennifer Hartt, Monney Laurent, Sabatos Catherine A, Ahuja Rakesh, Nguyen Khuong, Freeman Gordon J, Greenfield Edward A, Sobel Raymond A, Kuchroo Vijay K
Department of Neurology, Center for Neurologic Diseases, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.
J Immunol. 2005 Aug 1;175(3):1558-65. doi: 10.4049/jimmunol.175.3.1558.
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 in significant 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 autoimmune 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.
在Th1细胞和Th2细胞上差异表达的表面分子可能有助于在体内调节特异性免疫反应。利用一组单克隆抗体,我们已确定小鼠CD226在分化的Th1细胞表面特异性表达,而在Th2或Th0细胞表面不表达。虽然CD226在CD8细胞上组成性表达,但在激活后在CD4细胞上上调。Th1分化导致CD226表达增强,而在Th2极化时表达下调。我们证明CD226参与T细胞激活的调节;用抗CD226进行体内治疗可导致Th1细胞扩增显著减少,并诱导抑制T细胞激活的抗原呈递细胞(APC)。此外,抗CD226治疗可延迟Th1介导的自身免疫性疾病实验性自身免疫性脑脊髓炎的发病并减轻其严重程度。我们的数据表明,CD226是一种共刺激分子,在Th1细胞的激活和效应功能中起重要作用。