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T 细胞疗法靶向 HLA-A02 限制的 HIV 抗原表位:一项使用 CD8+T 细胞的开放性细胞治疗试验。

T Cell Therapy Targeted on HLA-A02 Restricted HIV Antigen Epitopes: An Open Label Cellular Therapy Trial Using CD8+ T Cell.

机构信息

Biomarkers of Infection Related Diseases Beijing Key Laboratory, Beijing You'An Hospital, Capital Medical University, Beijing, China.

Center of Infectious Disease, Beijing You'An Hospital, Capital Medical University, Beijing, China.

出版信息

Front Immunol. 2019 Mar 18;10:437. doi: 10.3389/fimmu.2019.00437. eCollection 2019.

DOI:10.3389/fimmu.2019.00437
PMID:30941124
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6435000/
Abstract

To test the safety and efficacy of a T cell therapy targeting HLA-A02 restricted HIV antigen epitopes. This was a prospective open label clinical trial, which enrolled 28 HIV+ participants and 24 of them finished the trial. The study was publicly registered at Chinese Clinical Trial Registry, www.chictr.org.cn(ChiCTR-ICR-15005775). Autologous peripheral blood mononuclear cells were co-cultured with HLA-A02 restricted HIV antigen epitopes peptides to produce cell product for this therapy. The trial was divided into five time-points with the same interval period for infusion of the cell products or monitoring parameters. Symptoms, vital signs, and blood samples were collected to analyze the safety and efficacy of this therapy. Two cases of adverse effects happened during this trial in test group, which recovered without medical intervention. There was no severe adverse effect that occurred. Both symptoms and laboratory tests have no statistical significant difference between test and control group. Flowcytometry analysis showed the expression of the PD-1 and CD95 molecule on the cell surface were downregulated post-treatment in the test group. This autologous HIV-antigen specific effector CD8+ T cellular therapy was safe. It might have an impact on immune suppression that can provide useful reference to future cell therapy trials.

摘要

为了测试靶向 HLA-A02 限制的 HIV 抗原表位的 T 细胞疗法的安全性和有效性。这是一项前瞻性、开放性标签的临床试验,共纳入 28 名 HIV+参与者,其中 24 名完成了试验。该研究在中国临床试验注册中心(www.chictr.org.cn,注册号 ChiCTR-ICR-15005775)进行了公开注册。自体外周血单核细胞与 HLA-A02 限制的 HIV 抗原表位肽共培养,以产生细胞产品进行该治疗。试验分为五个时间点,每个时间点输注细胞产品或监测参数的间隔相同。收集症状、生命体征和血液样本,以分析该疗法的安全性和疗效。在试验组中发生了两例不良事件,但无需医疗干预即可恢复。未发生严重不良事件。症状和实验室检查在试验组和对照组之间无统计学显著差异。流式细胞术分析显示,治疗后试验组细胞表面 PD-1 和 CD95 分子的表达下调。这种自体 HIV 抗原特异性效应 CD8+T 细胞疗法是安全的。它可能对免疫抑制有影响,可以为未来的细胞治疗试验提供有用的参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5311/6435000/2ed2349788ce/fimmu-10-00437-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5311/6435000/413a86f3f9fb/fimmu-10-00437-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5311/6435000/6f50d4a40c5b/fimmu-10-00437-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5311/6435000/2ed2349788ce/fimmu-10-00437-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5311/6435000/413a86f3f9fb/fimmu-10-00437-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5311/6435000/6f50d4a40c5b/fimmu-10-00437-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5311/6435000/2ed2349788ce/fimmu-10-00437-g0003.jpg

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