4.8 Article

Direct stimulation of naive T cells by membrane vesicles from antigen-presenting cells: Distinct roles for CD54 and B7 molecules

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NATL ACAD SCIENCES
DOI: 10.1073/pnas.1131852100

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  1. NCI NIH HHS [CA38355, R37 CA038355] Funding Source: Medline
  2. NIAID NIH HHS [AI46710, AI21487, R01 AI046710] Funding Source: Medline
  3. NIA NIH HHS [P01 AG001743, AG01743] Funding Source: Medline

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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.

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