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Allogeneic Vγ9Vδ2 T-Cell Therapy Promotes Pulmonary Lesion Repair: An Open-Label, Single-Arm Pilot Study in Patients With Multidrug-Resistant Tuberculosis

The WHO’s “Global tuberculosis report 2020” lists tuberculosis (TB) as one of the leading causes of death globally. Existing anti-TB therapy strategies are far from adequate to meet the End TB Strategy goals set for 2035. Therefore, novel anti-TB therapy protocols are urgently needed. Here, we propo...

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Autores principales: Liang, Juan, Fu, Liang, Li, Man, Chen, Yuyuan, Wang, Yi, Lin, Yi, Zhang, Hailin, Xu, Yan, Qin, Linxiu, Liu, Juncai, Wang, Weiyu, Hao, Jianlei, Liu, Shuyan, Zhang, Peize, Lin, Li, Alnaggar, Mohammed, Zhou, Jie, Zhou, Lin, Guo, Huixin, Wang, Zhaoqin, Liu, Lei, Deng, Guofang, Zhang, Guoliang, Wu, Yangzhe, Yin, Zhinan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8715986/
https://www.ncbi.nlm.nih.gov/pubmed/34975844
http://dx.doi.org/10.3389/fimmu.2021.756495
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author Liang, Juan
Fu, Liang
Li, Man
Chen, Yuyuan
Wang, Yi
Lin, Yi
Zhang, Hailin
Xu, Yan
Qin, Linxiu
Liu, Juncai
Wang, Weiyu
Hao, Jianlei
Liu, Shuyan
Zhang, Peize
Lin, Li
Alnaggar, Mohammed
Zhou, Jie
Zhou, Lin
Guo, Huixin
Wang, Zhaoqin
Liu, Lei
Deng, Guofang
Zhang, Guoliang
Wu, Yangzhe
Yin, Zhinan
author_facet Liang, Juan
Fu, Liang
Li, Man
Chen, Yuyuan
Wang, Yi
Lin, Yi
Zhang, Hailin
Xu, Yan
Qin, Linxiu
Liu, Juncai
Wang, Weiyu
Hao, Jianlei
Liu, Shuyan
Zhang, Peize
Lin, Li
Alnaggar, Mohammed
Zhou, Jie
Zhou, Lin
Guo, Huixin
Wang, Zhaoqin
Liu, Lei
Deng, Guofang
Zhang, Guoliang
Wu, Yangzhe
Yin, Zhinan
author_sort Liang, Juan
collection PubMed
description The WHO’s “Global tuberculosis report 2020” lists tuberculosis (TB) as one of the leading causes of death globally. Existing anti-TB therapy strategies are far from adequate to meet the End TB Strategy goals set for 2035. Therefore, novel anti-TB therapy protocols are urgently needed. Here, we proposed an allogeneic Vγ9Vδ2 T-cell-based immunotherapy strategy and clinically evaluated its safety and efficacy in patients with multidrug-resistant TB (MDR-TB). Eight patients with MDR-TB were recruited in this open-label, single-arm pilot clinical study. Seven of these patients received allogeneic Vγ9Vδ2 T-cell therapy adjunct with anti-TB drugs in all therapy courses. Cells (1 × 10(8)) were infused per treatment every 2 weeks, with 12 courses of cell therapy conducted for each patient, who were then followed up for 6 months to evaluate the safety and efficacy of cell therapy. The eighth patient initially received four courses of cell infusions, followed by eight courses of cell therapy plus anti-MDR-TB drugs. Clinical examinations, including clinical response, routine blood tests and biochemical indicators, chest CT imaging, immune cell surface markers, body weight, and sputum Mycobacterium tuberculosis testing, were conducted. Our study revealed that allogeneic Vγ9Vδ2 T cells are clinically safe for TB therapy. These cells exhibited clinical efficacy in multiple aspects, including promoting the repair of pulmonary lesions, partially improving host immunity, and alleviating M. tuberculosis load in vivo, regardless of their application in the presence or absence of anti-TB drugs. This pilot study opens a new avenue for anti-TB treatment and exhibits allogeneic Vγ9Vδ2 T cells as promising candidates for developing a novel cell drug for TB immunotherapy. CLINICAL TRIAL REGISTRATION: (https://clinicaltrials.gov/ct2/results?cond=&term=NCT03575299&cntry=&state=&city=&dist=) ( NCT03575299).
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spelling pubmed-87159862021-12-30 Allogeneic Vγ9Vδ2 T-Cell Therapy Promotes Pulmonary Lesion Repair: An Open-Label, Single-Arm Pilot Study in Patients With Multidrug-Resistant Tuberculosis Liang, Juan Fu, Liang Li, Man Chen, Yuyuan Wang, Yi Lin, Yi Zhang, Hailin Xu, Yan Qin, Linxiu Liu, Juncai Wang, Weiyu Hao, Jianlei Liu, Shuyan Zhang, Peize Lin, Li Alnaggar, Mohammed Zhou, Jie Zhou, Lin Guo, Huixin Wang, Zhaoqin Liu, Lei Deng, Guofang Zhang, Guoliang Wu, Yangzhe Yin, Zhinan Front Immunol Immunology The WHO’s “Global tuberculosis report 2020” lists tuberculosis (TB) as one of the leading causes of death globally. Existing anti-TB therapy strategies are far from adequate to meet the End TB Strategy goals set for 2035. Therefore, novel anti-TB therapy protocols are urgently needed. Here, we proposed an allogeneic Vγ9Vδ2 T-cell-based immunotherapy strategy and clinically evaluated its safety and efficacy in patients with multidrug-resistant TB (MDR-TB). Eight patients with MDR-TB were recruited in this open-label, single-arm pilot clinical study. Seven of these patients received allogeneic Vγ9Vδ2 T-cell therapy adjunct with anti-TB drugs in all therapy courses. Cells (1 × 10(8)) were infused per treatment every 2 weeks, with 12 courses of cell therapy conducted for each patient, who were then followed up for 6 months to evaluate the safety and efficacy of cell therapy. The eighth patient initially received four courses of cell infusions, followed by eight courses of cell therapy plus anti-MDR-TB drugs. Clinical examinations, including clinical response, routine blood tests and biochemical indicators, chest CT imaging, immune cell surface markers, body weight, and sputum Mycobacterium tuberculosis testing, were conducted. Our study revealed that allogeneic Vγ9Vδ2 T cells are clinically safe for TB therapy. These cells exhibited clinical efficacy in multiple aspects, including promoting the repair of pulmonary lesions, partially improving host immunity, and alleviating M. tuberculosis load in vivo, regardless of their application in the presence or absence of anti-TB drugs. This pilot study opens a new avenue for anti-TB treatment and exhibits allogeneic Vγ9Vδ2 T cells as promising candidates for developing a novel cell drug for TB immunotherapy. CLINICAL TRIAL REGISTRATION: (https://clinicaltrials.gov/ct2/results?cond=&term=NCT03575299&cntry=&state=&city=&dist=) ( NCT03575299). Frontiers Media S.A. 2021-12-15 /pmc/articles/PMC8715986/ /pubmed/34975844 http://dx.doi.org/10.3389/fimmu.2021.756495 Text en Copyright © 2021 Liang, Fu, Li, Chen, Wang, Lin, Zhang, Xu, Qin, Liu, Wang, Hao, Liu, Zhang, Lin, Alnaggar, Zhou, Zhou, Guo, Wang, Liu, Deng, Zhang, Wu and Yin 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
Liang, Juan
Fu, Liang
Li, Man
Chen, Yuyuan
Wang, Yi
Lin, Yi
Zhang, Hailin
Xu, Yan
Qin, Linxiu
Liu, Juncai
Wang, Weiyu
Hao, Jianlei
Liu, Shuyan
Zhang, Peize
Lin, Li
Alnaggar, Mohammed
Zhou, Jie
Zhou, Lin
Guo, Huixin
Wang, Zhaoqin
Liu, Lei
Deng, Guofang
Zhang, Guoliang
Wu, Yangzhe
Yin, Zhinan
Allogeneic Vγ9Vδ2 T-Cell Therapy Promotes Pulmonary Lesion Repair: An Open-Label, Single-Arm Pilot Study in Patients With Multidrug-Resistant Tuberculosis
title Allogeneic Vγ9Vδ2 T-Cell Therapy Promotes Pulmonary Lesion Repair: An Open-Label, Single-Arm Pilot Study in Patients With Multidrug-Resistant Tuberculosis
title_full Allogeneic Vγ9Vδ2 T-Cell Therapy Promotes Pulmonary Lesion Repair: An Open-Label, Single-Arm Pilot Study in Patients With Multidrug-Resistant Tuberculosis
title_fullStr Allogeneic Vγ9Vδ2 T-Cell Therapy Promotes Pulmonary Lesion Repair: An Open-Label, Single-Arm Pilot Study in Patients With Multidrug-Resistant Tuberculosis
title_full_unstemmed Allogeneic Vγ9Vδ2 T-Cell Therapy Promotes Pulmonary Lesion Repair: An Open-Label, Single-Arm Pilot Study in Patients With Multidrug-Resistant Tuberculosis
title_short Allogeneic Vγ9Vδ2 T-Cell Therapy Promotes Pulmonary Lesion Repair: An Open-Label, Single-Arm Pilot Study in Patients With Multidrug-Resistant Tuberculosis
title_sort allogeneic vγ9vδ2 t-cell therapy promotes pulmonary lesion repair: an open-label, single-arm pilot study in patients with multidrug-resistant tuberculosis
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8715986/
https://www.ncbi.nlm.nih.gov/pubmed/34975844
http://dx.doi.org/10.3389/fimmu.2021.756495
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