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Multiplex Screening Assay for Identifying Cytotoxic CD8+ T Cell Epitopes

Identifieur interne : 000138 ( Main/Exploration ); précédent : 000137; suivant : 000139

Multiplex Screening Assay for Identifying Cytotoxic CD8+ T Cell Epitopes

Auteurs : Chek Meng Poh [République populaire de Chine] ; Jian Zheng [États-Unis] ; Rudragouda Channappanavar [États-Unis] ; Zi Wei Chang [Singapour] ; Thi H. O. Nguyen [Australie] ; Laurent Rénia [Singapour] ; Katherine Kedzierska [Australie] ; Stanley Perlman [États-Unis] ; Leo L. M. Poon [République populaire de Chine]

Source :

RBID : PMC:7078160

Abstract

The cytotoxicity of epitope-specific CD8+ T cells is usually measured indirectly through IFNγ production. Existing assays that directly measure this activity are limited mainly to measurements of up to two specificities in a single reaction. Here, we develop a multiplex cytotoxicity assay that allows direct, simultaneous measurement of up to 23 different specificities of CD8+ T cells in a single reaction. This can greatly reduce the amount of starting clinical materials for a systematic screening of CD8+ T cell epitopes. In addition, this greatly enhanced capacity enables the incorporation of irrelevant epitopes for determining the non-specific killing activity of CD8+ T cells, thereby allowing to measure the actual epitope-specific cytotoxicity activities. This technique is shown to be useful to study both human and mouse CD8+ T cells. Besides, our results from human PBMCs and three independent infectious animal models (MERS, influenza and malaria) further reveal that IFNγ expression by epitope-specific CD8+ T cells does not always correlate with their cell-killing potential, highlighting the need for using cytotoxicity assays in specific contexts (e.g., evaluating vaccine candidates). Overall, our approach opens up new possibilities for comprehensive analyses of CD8+ T cell cytotoxicity in a practical manner.


Url:
DOI: 10.3389/fimmu.2020.00400
PubMed: 32218786
PubMed Central: 7078160


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<p>The cytotoxicity of epitope-specific CD8
<sup>+</sup>
T cells is usually measured indirectly through IFNγ production. Existing assays that directly measure this activity are limited mainly to measurements of up to two specificities in a single reaction. Here, we develop a multiplex cytotoxicity assay that allows direct, simultaneous measurement of up to 23 different specificities of CD8
<sup>+</sup>
T cells in a single reaction. This can greatly reduce the amount of starting clinical materials for a systematic screening of CD8
<sup>+</sup>
T cell epitopes. In addition, this greatly enhanced capacity enables the incorporation of irrelevant epitopes for determining the non-specific killing activity of CD8
<sup>+</sup>
T cells, thereby allowing to measure the actual epitope-specific cytotoxicity activities. This technique is shown to be useful to study both human and mouse CD8
<sup>+</sup>
T cells. Besides, our results from human PBMCs and three independent infectious animal models (MERS, influenza and malaria) further reveal that IFNγ expression by epitope-specific CD8
<sup>+</sup>
T cells does not always correlate with their cell-killing potential, highlighting the need for using cytotoxicity assays in specific contexts (e.g., evaluating vaccine candidates). Overall, our approach opens up new possibilities for comprehensive analyses of CD8
<sup>+</sup>
T cell cytotoxicity in a practical manner.</p>
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