Current status of antigen-specific T-cell immunotherapy for advanced renal-cell carcinoma

In renal-cell carcinoma (RCC), tumor-reactive T-cell responses can occur spontaneously or in response to systemic immunotherapy with cytokines and immune checkpoint inhibitors. Cancer vaccines and engineered T-cell therapies are designed to selectively augment tumor antigen-specific CD8 + T-cell res...

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Published inHuman vaccines & immunotherapeutics Vol. 17; no. 7; pp. 1882 - 1896
Main Authors Xu, Yuexin, Miller, Chris P., Warren, Edus H., Tykodi, Scott S.
Format Journal Article
LanguageEnglish
Published United States Taylor & Francis 03.07.2021
Taylor & Francis Group
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ISSN2164-5515
2164-554X
2164-554X
DOI10.1080/21645515.2020.1870846

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Summary:In renal-cell carcinoma (RCC), tumor-reactive T-cell responses can occur spontaneously or in response to systemic immunotherapy with cytokines and immune checkpoint inhibitors. Cancer vaccines and engineered T-cell therapies are designed to selectively augment tumor antigen-specific CD8 + T-cell responses with the goal to elicit tumor regression and avoid toxicities associated with nonspecific immunotherapies. In this review, we provide an overview of the central role of T-cell immunity in the treatment of advanced RCC. Clinical outcomes for antigen-targeted vaccines or other T-cell-engaging therapies for RCC are summarized and evaluated, and emerging new strategies to enhance the effectiveness of antigen-specific therapy for RCC are discussed.
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These authors contributed equally to this work.
ISSN:2164-5515
2164-554X
2164-554X
DOI:10.1080/21645515.2020.1870846