ICAM-1 enhances MHC-peptide activation of CD8+ T cells without an organized immunological synapse

被引:0
|
作者
Goldstein, JS
Chen, T
Gubina, E
Pastor, RW
Kozlowski, S
机构
[1] US FDA, Div Monoclonal Ab, Ctr Biol Evaluat & Res, Bethesda, MD 20892 USA
[2] US FDA, Div Bacterial & Allergen Prod & Parasitol, Ctr Biol Evaluat & Res, Bethesda, MD 20014 USA
关键词
T lymphocyte; adhesion molecule; MHC; cellular activation;
D O I
10.1002/1521-4141(200011)30:11<3266::AID-IMMU3266>3.0.CO;2-F
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In addition to the TCR-ligand interaction, other receptor-ligand pairs, such as LFA-1 and ICAM-1, play a major role in the activation of T cells. Recent studies of T cell activation suggest a coordinated movement of LFA-1 and ICAM-1 in forming a defined zone in the immunological synapse. It is unclear from these studies whether the organized molecular geometry of the immunological synapse is necessary for ICAM-1 enhancement of T cell activation. In this report, we demonstrate that ICAM-1 can enhance the activation of CD8(+) T cells by MHC-peptide in the absence of an organized immunologic synapse. Therefore, although the molecular organization of the immunologic synapse may amplify stimuli, it is not an absolute requirement for either CD8(+) T cell activation or the ICAIW-1 enhancement of TCR activation.
引用
收藏
页码:3266 / 3270
页数:5
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