T cell stimulation usually requires direct contact with viable antigen-presenting cells (APCs). However, we show here that small exosome-like membrane vesicles shed from APCs can be recognized by naive CD8(+) T cells in the absence of viable APCs; T cell antigen receptor-dependent binding of vesicles by CD8(+) cells is MHC class I/pepticle-specific and requires that the vesicles coexpress intercellular adhesion molecule 1 (ICAM-1, CD54), although not B7 (B7-1). In the absence of B7, T cell binding of vesicles is nonimmunogenic. By contrast, vesicles expressing both ICAM-1 and B7 are strongly immunogenic and cause purified APC-depleted CD8(+) cells to mount peptide-specific proliferative responses and differentiate into effector cells.
机构:
Univ Washington, Howard Hughes Med Inst, Dept Immunol, Seattle, WA 98195 USAUniv Washington, Howard Hughes Med Inst, Dept Immunol, Seattle, WA 98195 USA
den Haan, JMM
Bevan, MJ
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机构:
Univ Washington, Howard Hughes Med Inst, Dept Immunol, Seattle, WA 98195 USAUniv Washington, Howard Hughes Med Inst, Dept Immunol, Seattle, WA 98195 USA
机构:
Univ Washington, Howard Hughes Med Inst, Dept Immunol, Seattle, WA 98195 USAUniv Washington, Howard Hughes Med Inst, Dept Immunol, Seattle, WA 98195 USA
den Haan, JMM
Bevan, MJ
论文数: 0引用数: 0
h-index: 0
机构:
Univ Washington, Howard Hughes Med Inst, Dept Immunol, Seattle, WA 98195 USAUniv Washington, Howard Hughes Med Inst, Dept Immunol, Seattle, WA 98195 USA