CXCR1- or CXCR2-modified CAR T cells co-opt IL-8 for maximal antitumor efficacy in solid tumors
CAR T-cell therapy efficacy in solid tumors is limited by inadequate T-cell migration and/or persistence in tumour microenvironment. Here, the authors show that the activity of tumour-antigen specific CAR T cells, in multiple preclinical mouse models, can be enhanced by co-expression of two IL-8 rec...
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Nature Portfolio
2019
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oai:doaj.org-article:de9a908e5e6e46b0b45bc79a9225470e2021-12-02T14:38:47ZCXCR1- or CXCR2-modified CAR T cells co-opt IL-8 for maximal antitumor efficacy in solid tumors10.1038/s41467-019-11869-42041-1723https://doaj.org/article/de9a908e5e6e46b0b45bc79a9225470e2019-09-01T00:00:00Zhttps://doi.org/10.1038/s41467-019-11869-4https://doaj.org/toc/2041-1723CAR T-cell therapy efficacy in solid tumors is limited by inadequate T-cell migration and/or persistence in tumour microenvironment. Here, the authors show that the activity of tumour-antigen specific CAR T cells, in multiple preclinical mouse models, can be enhanced by co-expression of two IL-8 receptors that mediate their migration into the tumor microenvironment when IL-8 production in tumor is naturally expressed or enhanced by radiation.Linchun JinHaipeng TaoAida KarachiYu LongAlicia Y. HouMeng NaKyle A. DysonAdam J. GrippinLoic P. DeleyrolleWang ZhangDidier A. RajonQiong J. WangJames C. YangJesse L. KresakElias J. SayourMaryam RahmanFrank J. BovaZhiguo LinDuane A. MitchellJianping HuangNature PortfolioarticleScienceQENNature Communications, Vol 10, Iss 1, Pp 1-13 (2019) |
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Science Q Linchun Jin Haipeng Tao Aida Karachi Yu Long Alicia Y. Hou Meng Na Kyle A. Dyson Adam J. Grippin Loic P. Deleyrolle Wang Zhang Didier A. Rajon Qiong J. Wang James C. Yang Jesse L. Kresak Elias J. Sayour Maryam Rahman Frank J. Bova Zhiguo Lin Duane A. Mitchell Jianping Huang CXCR1- or CXCR2-modified CAR T cells co-opt IL-8 for maximal antitumor efficacy in solid tumors |
description |
CAR T-cell therapy efficacy in solid tumors is limited by inadequate T-cell migration and/or persistence in tumour microenvironment. Here, the authors show that the activity of tumour-antigen specific CAR T cells, in multiple preclinical mouse models, can be enhanced by co-expression of two IL-8 receptors that mediate their migration into the tumor microenvironment when IL-8 production in tumor is naturally expressed or enhanced by radiation. |
format |
article |
author |
Linchun Jin Haipeng Tao Aida Karachi Yu Long Alicia Y. Hou Meng Na Kyle A. Dyson Adam J. Grippin Loic P. Deleyrolle Wang Zhang Didier A. Rajon Qiong J. Wang James C. Yang Jesse L. Kresak Elias J. Sayour Maryam Rahman Frank J. Bova Zhiguo Lin Duane A. Mitchell Jianping Huang |
author_facet |
Linchun Jin Haipeng Tao Aida Karachi Yu Long Alicia Y. Hou Meng Na Kyle A. Dyson Adam J. Grippin Loic P. Deleyrolle Wang Zhang Didier A. Rajon Qiong J. Wang James C. Yang Jesse L. Kresak Elias J. Sayour Maryam Rahman Frank J. Bova Zhiguo Lin Duane A. Mitchell Jianping Huang |
author_sort |
Linchun Jin |
title |
CXCR1- or CXCR2-modified CAR T cells co-opt IL-8 for maximal antitumor efficacy in solid tumors |
title_short |
CXCR1- or CXCR2-modified CAR T cells co-opt IL-8 for maximal antitumor efficacy in solid tumors |
title_full |
CXCR1- or CXCR2-modified CAR T cells co-opt IL-8 for maximal antitumor efficacy in solid tumors |
title_fullStr |
CXCR1- or CXCR2-modified CAR T cells co-opt IL-8 for maximal antitumor efficacy in solid tumors |
title_full_unstemmed |
CXCR1- or CXCR2-modified CAR T cells co-opt IL-8 for maximal antitumor efficacy in solid tumors |
title_sort |
cxcr1- or cxcr2-modified car t cells co-opt il-8 for maximal antitumor efficacy in solid tumors |
publisher |
Nature Portfolio |
publishDate |
2019 |
url |
https://doaj.org/article/de9a908e5e6e46b0b45bc79a9225470e |
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