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The role of CD4(+) T cells in tumor and chronic viral immune responses
Immunotherapies are mainly aimed to promote a CD8(+) T cell response rather than a CD4(+) T cell response as cytotoxic T lymphocytes (CTLs) can directly kill target cells. Recently, CD4(+) T cells have received more attention due to their diverse roles in tumors and chronic viral infections. In anti...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10565399/ https://www.ncbi.nlm.nih.gov/pubmed/37829505 http://dx.doi.org/10.1002/mco2.390 |
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author | Xie, Luoyingzi Fang, Jingyi Yu, Juncheng Zhang, Weinan He, Zhiqiang Ye, Lilin Wang, Huaizhi |
author_facet | Xie, Luoyingzi Fang, Jingyi Yu, Juncheng Zhang, Weinan He, Zhiqiang Ye, Lilin Wang, Huaizhi |
author_sort | Xie, Luoyingzi |
collection | PubMed |
description | Immunotherapies are mainly aimed to promote a CD8(+) T cell response rather than a CD4(+) T cell response as cytotoxic T lymphocytes (CTLs) can directly kill target cells. Recently, CD4(+) T cells have received more attention due to their diverse roles in tumors and chronic viral infections. In antitumor and antichronic viral responses, CD4(+) T cells relay help signals through dendritic cells to indirectly regulate CD8(+) T cell response, interact with B cells or macrophages to indirectly modulate humoral immunity or macrophage polarization, and inhibit tumor blood vessel formation. Additionally, CD4(+) T cells can also exhibit direct cytotoxicity toward target cells. However, regulatory T cells exhibit immunosuppression and CD4(+) T cells become exhausted, which promote tumor progression and chronic viral persistence. Finally, we also outline immunotherapies based on CD4(+) T cells, including adoptive cell transfer, vaccines, and immune checkpoint blockade. Overall, this review summarizes diverse roles of CD4(+) T cells in the antitumor or protumor and chronic viral responses, and also highlights the immunotherapies based on CD4(+) T cells, giving a better understanding of their roles in tumors and chronic viral infections. |
format | Online Article Text |
id | pubmed-10565399 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105653992023-10-12 The role of CD4(+) T cells in tumor and chronic viral immune responses Xie, Luoyingzi Fang, Jingyi Yu, Juncheng Zhang, Weinan He, Zhiqiang Ye, Lilin Wang, Huaizhi MedComm (2020) Reviews Immunotherapies are mainly aimed to promote a CD8(+) T cell response rather than a CD4(+) T cell response as cytotoxic T lymphocytes (CTLs) can directly kill target cells. Recently, CD4(+) T cells have received more attention due to their diverse roles in tumors and chronic viral infections. In antitumor and antichronic viral responses, CD4(+) T cells relay help signals through dendritic cells to indirectly regulate CD8(+) T cell response, interact with B cells or macrophages to indirectly modulate humoral immunity or macrophage polarization, and inhibit tumor blood vessel formation. Additionally, CD4(+) T cells can also exhibit direct cytotoxicity toward target cells. However, regulatory T cells exhibit immunosuppression and CD4(+) T cells become exhausted, which promote tumor progression and chronic viral persistence. Finally, we also outline immunotherapies based on CD4(+) T cells, including adoptive cell transfer, vaccines, and immune checkpoint blockade. Overall, this review summarizes diverse roles of CD4(+) T cells in the antitumor or protumor and chronic viral responses, and also highlights the immunotherapies based on CD4(+) T cells, giving a better understanding of their roles in tumors and chronic viral infections. John Wiley and Sons Inc. 2023-10-10 /pmc/articles/PMC10565399/ /pubmed/37829505 http://dx.doi.org/10.1002/mco2.390 Text en © 2023 The Authors. MedComm published by Sichuan International Medical Exchange & Promotion Association (SCIMEA) and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Reviews Xie, Luoyingzi Fang, Jingyi Yu, Juncheng Zhang, Weinan He, Zhiqiang Ye, Lilin Wang, Huaizhi The role of CD4(+) T cells in tumor and chronic viral immune responses |
title | The role of CD4(+) T cells in tumor and chronic viral immune responses |
title_full | The role of CD4(+) T cells in tumor and chronic viral immune responses |
title_fullStr | The role of CD4(+) T cells in tumor and chronic viral immune responses |
title_full_unstemmed | The role of CD4(+) T cells in tumor and chronic viral immune responses |
title_short | The role of CD4(+) T cells in tumor and chronic viral immune responses |
title_sort | role of cd4(+) t cells in tumor and chronic viral immune responses |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10565399/ https://www.ncbi.nlm.nih.gov/pubmed/37829505 http://dx.doi.org/10.1002/mco2.390 |
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