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通过CD40L表面捕获分离有活力的抗原特异性CD4 T细胞。

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

作者信息

Cohen George B, Kaur Amitinder, Johnson R Paul

机构信息

Department of Biochemistry and Volen Center for Complex Systems, Brandeis University, 415 South Street, Waltham, MA 02454, USA.

出版信息

J Immunol Methods. 2005 Jul;302(1-2):103-15. doi: 10.1016/j.jim.2005.05.002.

Abstract

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 TNFalpha or IFNgamma 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.

摘要

最近已开发出多种用于鉴定抗原特异性细胞的技术,但这些技术鉴定所有记忆T细胞亚类的能力常常被忽视。在此,我们描述了一种使用CD40L和CD69表面染色分离活的抗原特异性CD4 T细胞的新方法,并证明了其在分离恒河猴抗原特异性CD4 T细胞中的实用性。该技术成功的关键在于在抗原刺激的同时对CD40L进行染色。基于CD40L/CD69表面标志物上调来分离CD4 T细胞,可鉴定出效应性和中枢记忆性CD4 T细胞。相比之下,大多数中枢记忆性CD4 T细胞不分泌TNFα或IFNγ,因此基于其分泌的技术无法鉴定出这些细胞。因此,本文所述方法补充了现有的分离活的抗原特异性CD4 T细胞的方法,为在非人类灵长类动物模型中研究人类疾病开辟了新途径,并且在诱导反应主要受T细胞中枢记忆限制的情况下可能证明是有益的。

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