Isolation of viable antigen-specific CD4 T cells by CD40L surface trapping

被引:21
作者
Cohen, GB
Kaur, A
Johnson, RP
机构
[1] Brandeis Univ, Dept Biochem, Waltham, MA 02454 USA
[2] Brandeis Univ, Volen Ctr Complex Syst, Waltham, MA 02454 USA
[3] Harvard Univ, Sch Med, New England Primate Res Ctr, Dept Immunol, Southborough, MA 01772 USA
[4] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Infect Dis Unit, Charlestown, MA 02129 USA
[5] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Partners AIDS Res Ctr, Charlestown, MA 02129 USA
关键词
CD4 T cell; CD154; CD40L; rhesus macaque;
D O I
10.1016/j.jim.2005.05.002
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A number of techniques have recently been developed for the identification of antigen-specific cells, yet the ability of these techniques to identify all subclasses of memory T cells has often been overlooked. Here we describe a novel approach for the isolation of live antigen-specific CD4 T cells using CD40L and CD69 surface staining and demonstrate its utility for isolating antigen-specific rhesus macaque CD4 T cells. Critical to the success of the technique was staining for CD40L concurrent with antigen stimulation. Isolation of CD4 T cells based on CD40L/CD69 surface marker upregulation identified both effector and central memory CD4 T cells. In contrast, the majority of central memory CD4 T cells did not secrete TNF alpha or IFN gamma and thus would not be identified by techniques based on their secretion. The methodology described here therefore complements existing approaches for isolating viable antigen-specific CD4 T cells, opens new avenues for investigating human diseases in nonhuman primate animal models and may prove beneficial in instances where the induced response is largely T cell central memory restricted. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:103 / 115
页数:13
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