Platelet-mediated modulation of adaptive immunity: unique delivery of CD154 signal by platelet-derived membrane vesicles

被引:204
作者
Sprague, Daniel L. [2 ,3 ,4 ]
Elzey, Bennett D. [5 ]
Crist, Scott A. [5 ]
Waldschmidt, Thomas J. [6 ]
Jensen, Robert J. [2 ]
Ratliff, Timothy L. [1 ,2 ,3 ,4 ,7 ]
机构
[1] Purdue Univ, Purdue Canc Ctr, W Lafayette, IN 47907 USA
[2] Univ Iowa, Dept Urol, Iowa City, IA 52242 USA
[3] Univ Iowa, Med Scientist Training Program, Iowa City, IA 52242 USA
[4] Univ Iowa, Dept Microbiol, Iowa City, IA 52242 USA
[5] Purdue Univ, Dept Comparat Pathol, W Lafayette, IN 47907 USA
[6] Univ Iowa, Dept Pathol, Iowa City, IA 52242 USA
[7] Univ Iowa, Interdisciplinary Immunol Program, Iowa City, IA 52242 USA
关键词
D O I
10.1182/blood-2007-06-097410
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although mounting evidence indicates that platelets participate in the modulation of both innate and adaptive immunity, the mechanisms by which platelets exert these effects have not been clearly defined. The study reported herein uses a previously documented adoptive transfer model to investigate the ability of platelet-derived membrane vesicles to communicate activation signals to the B-cell compartment. The findings demonstrate for the first time that platelet-derived membrane vesicles are sufficient to deliver CD154 to stimulate antigen-specific IgG production and modulate germinal center formation through cooperation with responses elicited by CD4(+) T cells. The data are consistent with the hypothesis that platelets modulate inflammation and adaptive immunity at sites distant from the location of activation and that platelet-derived membrane vesicles are sufficient to mediate the effect.
引用
收藏
页码:5028 / 5036
页数:9
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