期刊
IMMUNITY
卷 19, 期 1, 页码 9-19出版社
CELL PRESS
DOI: 10.1016/S1074-7613(03)00177-8
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资金
- NCI NIH HHS [CA096691] Funding Source: Medline
- NHLBI NIH HHS [HL63017, HL63943] Funding Source: Medline
- NIDDK NIH HHS [DK54014] Funding Source: Medline
Platelets are highly reactive components of the circulatory system with well-documented hemostatic function. Recent studies extend platelet function to modulation of local inflammatory events through the release of chemokines, cytokines, and a number of immunomodulatory ligands, including CD154. We hypothesized that platelet-derived CD154 modulates adaptive immunity. The data reported herein demonstrate that platelets, via CD154, induce dendritic cell maturation, B cell isotype switching, and augment CD8(+) T cell responses both in vitro and in vivo. Platelet transfusion studies demonstrate that platelet-derived CD154 alone is sufficient to induce isotype switching and augment T lymphocyte function during viral infection, leading to enhanced protection against viral rechallenge. Additionally, depletion of platelets in normal mice results in decreased antigen-specific antibody production.
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