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Treatment of aggressive T-cell lymphoma/leukemia with anti-CD4 CAR T cells

T-cell lymphomas are aggressive lymphomas that often resist current therapy options or present with relapsed disease, making the development of more effective treatment regimens clinically important. Previously, we have shown that CD4 CAR can effectively target T-cell malignancies in preclinical stu...

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Autores principales: Feng, Jia, Xu, Haichan, Cinquina, Andrew, Wu, Zehua, Zhang, Wenli, Sun, Lihua, Chen, Qi, Tian, Lei, Song, Le, Pinz, Kevin G., Wada, Masayuki, Jiang, Xun, Hanes, William M., Ma, Yupo, Zhang, Hongyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9511023/
https://www.ncbi.nlm.nih.gov/pubmed/36172388
http://dx.doi.org/10.3389/fimmu.2022.997482
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author Feng, Jia
Xu, Haichan
Cinquina, Andrew
Wu, Zehua
Zhang, Wenli
Sun, Lihua
Chen, Qi
Tian, Lei
Song, Le
Pinz, Kevin G.
Wada, Masayuki
Jiang, Xun
Hanes, William M.
Ma, Yupo
Zhang, Hongyu
author_facet Feng, Jia
Xu, Haichan
Cinquina, Andrew
Wu, Zehua
Zhang, Wenli
Sun, Lihua
Chen, Qi
Tian, Lei
Song, Le
Pinz, Kevin G.
Wada, Masayuki
Jiang, Xun
Hanes, William M.
Ma, Yupo
Zhang, Hongyu
author_sort Feng, Jia
collection PubMed
description T-cell lymphomas are aggressive lymphomas that often resist current therapy options or present with relapsed disease, making the development of more effective treatment regimens clinically important. Previously, we have shown that CD4 CAR can effectively target T-cell malignancies in preclinical studies. As IL-15 has been shown to strengthen the anti-tumor response, we have modified CD4 CAR to secrete an IL-15/IL-15sushi complex. These CD4-IL15/IL15sushi CAR T cells and NK92 cells efficiently eliminated CD4+ leukemic cell lines in co-culture assays. Additionally, CD4-IL15/IL15sushi CAR out-performed CD4 CAR in in vivo models, demonstrating a benefit to IL-15/IL-15sushi inclusion. In a Phase I clinical trial, CD4-IL15/IL15sushi CAR T cells were tested for safety in three patients with different T-cell lymphomas. Infusion of CD4-IL15/IL15sushi CAR T cells was well-tolerated by the patients without significant adverse effects and led to the remission of their lymphomas. Additionally, infusion led to the depletion of CD4+ Treg cells and expansion of CD3+CD8+ T cells and NK cells. These results suggest that CD4-IL15/IL15sushi CAR T cells may be a safe and effective treatment for patients with relapsed or refractory T-cell lymphomas, where new treatment options are needed.
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spelling pubmed-95110232022-09-27 Treatment of aggressive T-cell lymphoma/leukemia with anti-CD4 CAR T cells Feng, Jia Xu, Haichan Cinquina, Andrew Wu, Zehua Zhang, Wenli Sun, Lihua Chen, Qi Tian, Lei Song, Le Pinz, Kevin G. Wada, Masayuki Jiang, Xun Hanes, William M. Ma, Yupo Zhang, Hongyu Front Immunol Immunology T-cell lymphomas are aggressive lymphomas that often resist current therapy options or present with relapsed disease, making the development of more effective treatment regimens clinically important. Previously, we have shown that CD4 CAR can effectively target T-cell malignancies in preclinical studies. As IL-15 has been shown to strengthen the anti-tumor response, we have modified CD4 CAR to secrete an IL-15/IL-15sushi complex. These CD4-IL15/IL15sushi CAR T cells and NK92 cells efficiently eliminated CD4+ leukemic cell lines in co-culture assays. Additionally, CD4-IL15/IL15sushi CAR out-performed CD4 CAR in in vivo models, demonstrating a benefit to IL-15/IL-15sushi inclusion. In a Phase I clinical trial, CD4-IL15/IL15sushi CAR T cells were tested for safety in three patients with different T-cell lymphomas. Infusion of CD4-IL15/IL15sushi CAR T cells was well-tolerated by the patients without significant adverse effects and led to the remission of their lymphomas. Additionally, infusion led to the depletion of CD4+ Treg cells and expansion of CD3+CD8+ T cells and NK cells. These results suggest that CD4-IL15/IL15sushi CAR T cells may be a safe and effective treatment for patients with relapsed or refractory T-cell lymphomas, where new treatment options are needed. Frontiers Media S.A. 2022-09-12 /pmc/articles/PMC9511023/ /pubmed/36172388 http://dx.doi.org/10.3389/fimmu.2022.997482 Text en Copyright © 2022 Feng, Xu, Cinquina, Wu, Zhang, Sun, Chen, Tian, Song, Pinz, Wada, Jiang, Hanes, Ma and Zhang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Feng, Jia
Xu, Haichan
Cinquina, Andrew
Wu, Zehua
Zhang, Wenli
Sun, Lihua
Chen, Qi
Tian, Lei
Song, Le
Pinz, Kevin G.
Wada, Masayuki
Jiang, Xun
Hanes, William M.
Ma, Yupo
Zhang, Hongyu
Treatment of aggressive T-cell lymphoma/leukemia with anti-CD4 CAR T cells
title Treatment of aggressive T-cell lymphoma/leukemia with anti-CD4 CAR T cells
title_full Treatment of aggressive T-cell lymphoma/leukemia with anti-CD4 CAR T cells
title_fullStr Treatment of aggressive T-cell lymphoma/leukemia with anti-CD4 CAR T cells
title_full_unstemmed Treatment of aggressive T-cell lymphoma/leukemia with anti-CD4 CAR T cells
title_short Treatment of aggressive T-cell lymphoma/leukemia with anti-CD4 CAR T cells
title_sort treatment of aggressive t-cell lymphoma/leukemia with anti-cd4 car t cells
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9511023/
https://www.ncbi.nlm.nih.gov/pubmed/36172388
http://dx.doi.org/10.3389/fimmu.2022.997482
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