Virus-Specific T Cells: Promising Adoptive T Cell Therapy Against Infectious Diseases Following Hematopoietic Stem Cell Transplantation.

IF 3.1 Q2 PHARMACOLOGY & PHARMACY
Arsalan Jalili, Abbas Hajifathali, Mozhdeh Mohammadian, Ghazaleh Sankanian, Maryam Sayahinouri, Mahmoud Dehghani Ghorbi, Elham Roshandel, Nasser Aghdami
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Abstract

Hematopoietic stem cell transplantation (HSCT) is a life-saving therapy for various hematologic disorders. Due to the bone marrow suppression and its long recovery period, secondary infections, like cytomegalovirus (CMV), Epstein-Bar virus (EBV), and adenovirus (AdV), are the leading causes of morbidity and mortality in HSCT cases. Drug resistance to the antiviral pharmacotherapies makes researchers develop adoptive T cell therapies like virus-specific T cell therapy. These studies have faced major challenges such as finding the most effective T cell expansion methods, isolating the expected subtype, defining the functionality of the end-cell population, product quality control, and clinical complications after the injection. This review discusses the viral infections after HSCT, T cells characteristics during chronic viral infection, application of virus-specific T cells (VSTs) for refractory infections, standard methods for producing VSTs and their limitation, clinical experiences on VSTs, focusing on outcomes and side effects that can be helpful in decision-making for patients and further researches.

Abstract Image

Abstract Image

病毒特异性T细胞:造血干细胞移植后感染性疾病的有希望的过继T细胞疗法。
造血干细胞移植(HSCT)是一种挽救生命的治疗各种血液疾病。由于骨髓抑制和恢复期长,继发性感染,如巨细胞病毒(CMV)、eb病毒(EBV)和腺病毒(AdV),是HSCT病例发病和死亡的主要原因。对抗病毒药物疗法的耐药性促使研究人员开发出过继性T细胞疗法,如病毒特异性T细胞疗法。这些研究面临着重大挑战,如寻找最有效的T细胞扩增方法、分离预期亚型、确定终细胞群的功能、产品质量控制和注射后的临床并发症。本文综述了HSCT术后的病毒感染、慢性病毒感染过程中T细胞的特点、病毒特异性T细胞(VSTs)在难治性感染中的应用、产生VSTs的标准方法及其局限性、VSTs的临床应用经验,重点介绍了VSTs的结局和副作用,为患者的治疗决策和进一步的研究提供参考。
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来源期刊
Advanced pharmaceutical bulletin
Advanced pharmaceutical bulletin PHARMACOLOGY & PHARMACY-
CiteScore
6.80
自引率
2.80%
发文量
51
审稿时长
12 weeks
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