Haploidentical γδ T Cells Induce Complete Remission in Chemorefractory B-cell Non-Hodgkin Lymphoma.

IF 3.2 4区 医学 Q3 IMMUNOLOGY Journal of Immunotherapy Pub Date : 2023-02-01 DOI:10.1097/CJI.0000000000000450
Anna Bold, Johannes Gaertner, Alexander Bott, Volker Mordstein, Kerstin Schaefer-Eckart, Martin Wilhelm
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引用次数: 2

Abstract

The transformation of chronic lymphocytic leukemia to an aggressive lymphoma, called Richter transformation, is often accompanied by resistance to chemotherapy and high mortality. Thus, novel therapeutic strategies are required for the successful treatment of these patients. One possibility is cellular immunotherapy with chimeric antigen receptor T cells. However, the time delay until cells are available and the limited number of effector cells due to the impaired immune system of these patients potentially compromises the efficacy of this approach. Another promising attempt might be the therapy with γδ T cells. Once activated, they exhibit various antitumor effects against several types of malignancies. Furthermore, they can be safely used in an allogeneic setting and can be multiplied in vivo as already demonstrated in clinical studies. In vitro data, in addition, show that the cytotoxicity of γδ T cells can be significantly enhanced by monoclonal antibodies. Here we present a patient, who suffered from Richter transformation and did not respond to several lines of immunochemotherapy. Due to the lack of further therapy options, we conducted an individual therapy with adoptive transfer of haploidentical γδ T cells combined with the application of the monoclonal antibody obinutuzumab. A histologically confirmed complete remission was achieved through this therapy approach, whereby relevant side effects were not seen. This case highlights the potential of γδ T cells and the feasibility of this therapeutic approach for further clinical trials.

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单倍体γδ T细胞诱导化疗难治性b细胞非霍奇金淋巴瘤完全缓解
慢性淋巴细胞白血病向侵袭性淋巴瘤的转化,称为Richter转化,通常伴随着对化疗的抵抗和高死亡率。因此,需要新的治疗策略来成功治疗这些患者。一种可能性是使用嵌合抗原受体T细胞进行细胞免疫治疗。然而,细胞可用的时间延迟和由于这些患者免疫系统受损而导致的效应细胞数量有限,可能会损害这种方法的有效性。另一个有希望的尝试可能是用γδ T细胞治疗。一旦激活,它们对几种类型的恶性肿瘤表现出不同的抗肿瘤作用。此外,它们可以安全地用于异体环境,并且可以在体内繁殖,这已经在临床研究中得到证实。此外,体外实验数据表明,单克隆抗体可显著增强γδ T细胞的细胞毒性。在这里,我们提出了一个病人,谁遭受了里希特转化和没有响应的几线免疫化疗。由于缺乏进一步的治疗选择,我们采用了单克隆抗体obinutuzumab结合单克隆抗体的单克隆转移单倍体γδ T细胞的个体化治疗。组织学证实,通过这种治疗方法完全缓解,因此没有看到相关的副作用。这个病例强调了γδ T细胞的潜力和这种治疗方法在进一步临床试验中的可行性。
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来源期刊
Journal of Immunotherapy
Journal of Immunotherapy 医学-免疫学
CiteScore
6.90
自引率
0.00%
发文量
79
审稿时长
6-12 weeks
期刊介绍: Journal of Immunotherapy features rapid publication of articles on immunomodulators, lymphokines, antibodies, cells, and cell products in cancer biology and therapy. Laboratory and preclinical studies, as well as investigative clinical reports, are presented. The journal emphasizes basic mechanisms and methods for the rapid transfer of technology from the laboratory to the clinic. JIT contains full-length articles, review articles, and short communications.
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