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用于检测恒河猴体内肽特异性γ干扰素分泌细胞的酶联免疫斑点试验。

ELISPOT assay for detection of peptide specific interferon-gamma secreting cells in rhesus macaques.

作者信息

Kumar A, Weiss W, Tine J A, Hoffman S L, Rogers W O

机构信息

Malaria Program, Naval Medical Research Center, Silver Spring, MD 20910, USA.

出版信息

J Immunol Methods. 2001 Jan 1;247(1-2):49-60. doi: 10.1016/s0022-1759(00)00310-0.

Abstract

A reliable procedure to measure antigen specific T cell responses in rhesus macaques is required to determine the efficacy of vaccines and immunotherapies. The currently available T cell assays are poorly quantifiable or technically difficult to perform. Classical 51Cr-release cytotoxic T cell (CTL) assays are cumbersome and difficult to quantitate reproducibly. Detection of specific T-cell using MHC-peptide tetrameric complexes is highly sensitive, but requires knowledge of MHC type and prior identification of T cell epitopes. We therefore developed a rhesus interferon-gamma (IFN-gamma) ELISPOT assay capable of detecting IFN-gamma secretion in response to stimulation with pooled 20-mer peptides. Peripheral blood mononuclear cells (PBMCs) from rhesus monkeys immunized with a DNA vaccine and recombinant canary pox encoding the Plasmodium knowlesi circumsporozoite protein (PkCSP) were incubated with pools of peptides from PkCSP. Positive responses to peptide pools and individual peptides ranging from 100 to 450 spot forming cells (SFC)/10(6) PBMC were detected in four of four immunized monkeys and in zero of two control monkeys. In two monkeys studied in detail, the IFN-gamma response was focussed on a single 20-mer peptide, QGDGANAGQPQAQGDGANAG, and was dependent on CD4(+), but not CD8(+), T cells. Background responses in control monkeys and preimmunization PBMCs ranged from 10 to 50 SFC/10(6) PBMC. The average within assay and between assay coefficients of variation (CV) for this peptide ELISPOT were 21.9 and 24.7%, respectively. This peptide IFN-gamma assay will be a useful tool for evaluation of T cell responses in rhesus macaques.

摘要

为了确定疫苗和免疫疗法的疗效,需要一种可靠的方法来测量恒河猴体内抗原特异性T细胞反应。目前可用的T细胞检测方法难以定量或在技术上难以操作。经典的51Cr释放细胞毒性T细胞(CTL)检测方法繁琐且难以进行可重复的定量。使用MHC-肽四聚体复合物检测特异性T细胞高度敏感,但需要了解MHC类型并事先鉴定T细胞表位。因此,我们开发了一种恒河猴干扰素-γ(IFN-γ)ELISPOT检测方法,该方法能够检测对20聚体肽池刺激的反应中IFN-γ的分泌。用编码诺氏疟原虫环子孢子蛋白(PkCSP)的DNA疫苗和重组金丝雀痘病毒免疫的恒河猴外周血单个核细胞(PBMC)与来自PkCSP的肽池一起孵育。在四只免疫的猴子中,四只均检测到对肽池和单个肽的阳性反应,范围为100至450个斑点形成细胞(SFC)/10(6) PBMC,而两只对照猴子均未检测到阳性反应。在详细研究的两只猴子中,IFN-γ反应集中在单个20聚体肽QGDGANAGQPQAQGDGANAG上,并且依赖于CD4(+) T细胞,而非CD8(+) T细胞。对照猴子和免疫前PBMC的背景反应范围为10至50 SFC/10(6) PBMC。该肽ELISPOT检测方法的平均批内和批间变异系数(CV)分别为21.9%和24.7%。这种肽IFN-γ检测方法将成为评估恒河猴T细胞反应的有用工具。

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