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原发性免疫缺陷病患者的过继性T细胞免疫疗法

Adoptive T Cell Immunotherapy for Patients with Primary Immunodeficiency Disorders.

作者信息

McLaughlin Lauren P, Bollard Catherine M, Keller Michael

机构信息

Center for Cancer and Immunology Research, Children's National Health System, Washington, DC, USA.

Division of Blood and Marrow Transplantation, Children's National Health System, Washington, DC, USA.

出版信息

Curr Allergy Asthma Rep. 2017 Jan;17(1):3. doi: 10.1007/s11882-017-0669-2.

Abstract

Primary immunodeficiency disorders (PID) are a group of inborn errors of immunity with a broad range of clinical severity but often associated with recurrent and serious infections. While hematopoietic stem cell transplantation (HSCT) can be curative for some forms of PID, chronic and/or refractory viral infections remain a cause of morbidity and mortality both before and after HSCT. Although antiviral pharmacologic agents exist for many viral pathogens, these are associated with significant costs and toxicities and may not be effective for increasingly drug-resistant pathogens. Thus, the emergence of adoptive immunotherapy with virus-specific T lymphocytes (VSTs) is an attractive option for addressing the underlying impaired T cell immunity in many PID patients. VSTs have been utilized for PID patients following HSCT in many prior phase I trials, and may potentially be beneficial before HSCT in patients with chronic viral infections. We review the various methods of generating VSTs, clinical experience using VSTs for PID patients, and current limitations as well as potential ways to broaden the clinical applicability of adoptive immunotherapy for PID patients.

摘要

原发性免疫缺陷病(PID)是一组先天性免疫缺陷疾病,临床严重程度范围广泛,但常与反复严重感染相关。虽然造血干细胞移植(HSCT)对某些形式的PID具有治愈作用,但慢性和/或难治性病毒感染在HSCT前后仍然是发病和死亡的原因。尽管针对许多病毒病原体都有抗病毒药物,但这些药物成本高昂且具有毒性,对于耐药性日益增强的病原体可能无效。因此,采用病毒特异性T淋巴细胞(VST)进行过继性免疫治疗的出现,是解决许多PID患者潜在的T细胞免疫受损问题的一个有吸引力的选择。在许多先前的I期试验中,VST已被用于HSCT后的PID患者,并且在患有慢性病毒感染的患者中,HSCT前使用VST可能也有益处。我们综述了生成VST的各种方法、将VST用于PID患者的临床经验、当前的局限性以及扩大过继性免疫治疗对PID患者临床适用性的潜在方法。

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