Manufacturing of Human T-lymphoid Progenitors from Two Different Hematopoietic Stem Cell Sources and Perspective for New Immunotherapies

P. Gaudeaux, R. D. Moirangthem, Pauline Rault, H. Sadek, F. Carbone, Marieke, Lavaert, A. Joshi, T. Taghon, I. André, O. Nègre, T. Soheili
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引用次数: 1

Abstract

Manufacturing of Human T-lymphoid Progenitors from Two Different Hematopoietic Stem Cell Sources and Perspective for New Immunotherapies. Abstract The adaptive immune system depends on the efficient response of lymphocytes, protecting the organism from infection or malignant diseases. T-cell immunodeficiency, innate or acquired, put the patient at risk for developing opportunistic infections and cancers. We previously described a novel approach to overcome the major limitations of T-cell immunotherapy and hematopoietic stem cell transplant (HSCT) by transplanting human T-lymphoid progenitors (HTLP), with the aim to achieve shortened immune reconstitution and fully functional naïve T-cell repertoire in immunodeficient or immunocompromised patients. By complementing our DL4-based cell culture with TNFα we developed and scaled-up clinical strategies involving hematopoietic stem and progenitor cells (HSPC) differentiated into T-lymphoid progenitors. We discuss here recent advances made in the characterization of different cell sources used as starting materials for T-lymphoid progenitors manufacturing, as well as gene modification of these cells, highlighting new perspectives for the development of therapeutical strategies.
两种不同造血干细胞来源制造人t淋巴细胞祖细胞及新免疫疗法的前景
从两种不同的造血干细胞来源制备人T淋巴细胞祖细胞和新免疫疗法的前景。摘要适应性免疫系统依赖于淋巴细胞的有效反应,保护机体免受感染或恶性疾病。先天性或后天性T细胞免疫缺陷使患者面临机会感染和癌症的风险。我们之前描述了一种新的方法,通过移植人类T淋巴细胞祖细胞(HTLP)来克服T细胞免疫疗法和造血干细胞移植(HSCT)的主要局限性,目的是在免疫缺陷或免疫功能低下的患者中实现缩短的免疫重建和全功能的幼稚T细胞库。通过用TNFα补充我们基于DL4的细胞培养,我们开发并扩大了涉及造血干细胞和祖细胞(HSPC)分化为T淋巴细胞祖细胞的临床策略。我们在这里讨论了用作T淋巴细胞祖细胞制造起始材料的不同细胞源的表征以及这些细胞的基因修饰方面的最新进展,强调了治疗策略发展的新前景。
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