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首页> 外文期刊>Transfusion medicine reviews >Adoptive Immunotherapies After Allogeneic Hematopoietic Stem Cell Transplantation in Patients With Hematologic Malignancies
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Adoptive Immunotherapies After Allogeneic Hematopoietic Stem Cell Transplantation in Patients With Hematologic Malignancies

机译:异基因造血干细胞移植后血液系统恶性肿瘤患者的过继免疫治疗。

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Hematopoietic stem cell transplantation (HSCT) is the only curative therapy for patients with chemotherapy-resistant hematologic malignancies that are usually fatal in absence of treatment. Hematopoietic stem cell transplantation is associated with significant early and late morbidity and mortality. Graft-versus-host disease, infections, and relapse are the most important causes of mortality after HSCT. Until now, these complications have been managed mainly with pharmacological drugs, but in some situations, this approach clearly shows its limit. As such, there is a significant need for novel therapies for the treatment of complications after allogeneic HSCT. In this review, the currently available adoptive immunotherapies offering an alternative in case of treatment failure of HSCT complications will be described. The results of the main clinical trials based on immune cell infusion will be discussed and the strategies aiming at maximizing cytotoxic T-lymphocyte, regulatory T-cell, natural killer cell, cytokine-induced killer cell, and gamma delta T-cell efficacies in the context of immunotherapy approaches after allogeneic HSCT in patients with hematologic malignancies will be gathered. (C) 2015 Elsevier Inc. All rights reserved.
机译:造血干细胞移植(HSCT)是化疗耐药的血液系统恶性肿瘤患者的唯一治疗方法,这种恶性肿瘤通常在没有治疗的情况下会致命。造血干细胞移植与明显的早期和晚期发病率和死亡率有关。移植物抗宿主病,感染和复发是HSCT术后死亡的最重要原因。到目前为止,这些并发症主要是通过药理学来控制的,但是在某些情况下,这种方法清楚地表明了其局限性。因此,非常需要用于异基因HSCT后并发症治疗的新疗法。在这篇综述中,将描述当前可用的过继免疫疗法,该疗法可在HSCT并发症治疗失败的情况下提供另一种选择。将讨论基于免疫细胞输注的主要临床试验结果,以及旨在最大程度地提高细胞毒性T淋巴细胞,调节性T细胞,自然杀伤细胞,细胞因子诱导的杀伤细胞和伽马三角洲T细胞功效的策略。将收集血液系统恶性肿瘤患者同种异体造血干细胞移植后的免疫治疗方法。 (C)2015 Elsevier Inc.保留所有权利。

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