SIGNALS DELIVERED VIA THE QA-2 MOLECULE CAN SYNERGIZE WITH LIMITING ANTI-CD3-INDUCED SIGNALS TO CAUSE LYMPHOCYTE-T ACTIVATION

被引:8
作者
HAHN, AB
TIAN, H
WIEGAND, G
SOLOSKI, MJ
机构
[1] Department of Medicine, Division of Molecular and Clinical Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD
关键词
D O I
10.3109/08820139209072259
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Qa-2 is a glycolipid anchored, MHC encoded class I molecule expressed at high levels on all murine peripheral T lymphocytes. Anti-Qa-2 antibodies have previously been found to stimulate T cells to proliferate in the presence of crosslinking antibody and PMA. We have examined the effect of anti-Qa-2 antibodies on T cells stimulated with a suboptimal concentration of immobilized anti-CD3. When anti-Qa-2 antibodies were co-immobilized with limiting anti-CD3, in the absence of PMA, a clear augmentation of T cell proliferation was seen. Interestingly, the co-stimulatory anti-Qa-2 antibodies could be directed against epitopes mapped to either the alpha-3 or the alpha-1/alpha-2 Qa-2 domains. As was the case with activation induced by soluble/crosslinked anti-Qa-2 antibodies plus PMA, CD8+ T cells were less able to be costimulated with anti-Qa-2 antibodies than CD4+ cells. Surprisingly, Ca2+ mobilization was only seen when two anti-Qa-2 antibodies reactive to separate structural domains were co-crosslinked on the surface of Indo-1 loaded T cells with a suboptimal concentration of anti-CD3. Collectively these results raise questions regarding the mechanism of Qa-2 mediated signaling and its potential role in T cell activation.
引用
收藏
页码:203 / 217
页数:15
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