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用于免疫缺陷病的T淋巴细胞去除移植

T-lymphocyte depleted transplants for inborn errors of immunity.

作者信息

Slatter M A, Maschan M A, Gennery A R

机构信息

Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.

Paediatric Stem Cell Transplant Unit, Great North Children's Hospital, Newcastle Upon Tyne, UK.

出版信息

Expert Rev Clin Immunol. 2023 Jul-Dec;19(11):1315-1324. doi: 10.1080/1744666X.2023.2245146. Epub 2023 Aug 9.

DOI:10.1080/1744666X.2023.2245146
PMID:37554030
Abstract

INTRODUCTION

Hematopoietic stem cell transplantation is a curative treatment for many inborn errors of immunity (IEI). Incremental improvements and advances in care have led to high rates of >85% survival and cure in many of these diseases. Improvements in HLA-classification and matching have led to increased survival using HLA-matched donors, but survival using T-lymphocyte-depleted mismatched grafts remained significantly worse until fairly recently. Advances in T-lymphocyte depletion methods and graft engineering, although not specific to IEI, have been widely adopted and instrumental in changing the landscape of donor selection, such that a donor should now be possible for every patient.

AREAS COVERED

A literature review focusing on T-lymphocyte depletion methodologies and treatment results was performed. The importance of early T-lymphocyte immunoreconstitution to protect against viral infection is reviewed. Two main platforms now dominate the field - immune-magnetic selection of specific cell types and post-transplant chemotherapeutic targeting of rapidly proliferating allo-reactive T-lymphocytes - the emerging literature on these reports, focusing on IEI, is explored, as well as the impact of serotherapy on early immunoreconstitution.

EXPERT OPINION

Pharmacokinetic monitoring of serotherapy agents, and use of co-stimulatory molecule blockade are likely to become more widespread. Post-transplant cyclophosphamide or TCR depletion strategies are likely to become the dominant methods of transplantation for nonmalignant diseases.

摘要

引言

造血干细胞移植是治疗多种先天性免疫缺陷(IEI)的一种治愈性疗法。护理方面的逐步改进和进展已使许多此类疾病的生存率和治愈率超过85%。HLA分型和匹配的改进提高了使用HLA匹配供体时的生存率,但直到最近,使用T淋巴细胞去除的不匹配移植物时的生存率仍显著较低。T淋巴细胞去除方法和移植物工程方面的进展虽并非专门针对IEI,但已被广泛采用并有助于改变供体选择的格局,以至于现在应为每位患者找到供体。

涵盖领域

进行了一项聚焦于T淋巴细胞去除方法和治疗结果的文献综述。回顾了早期T淋巴细胞免疫重建对预防病毒感染的重要性。目前该领域主要有两个平台——特定细胞类型的免疫磁选和移植后对快速增殖的同种异体反应性T淋巴细胞的化疗靶向——探讨了有关这些报告的新兴文献,重点是IEI,以及血清疗法对早期免疫重建的影响。

专家观点

血清疗法药物的药代动力学监测以及共刺激分子阻断的应用可能会更广泛。移植后环磷酰胺或TCR去除策略可能会成为非恶性疾病移植的主要方法。

相似文献

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T-lymphocyte depleted transplants for inborn errors of immunity.用于免疫缺陷病的T淋巴细胞去除移植
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Approaches to the removal of T-lymphocytes to minimize graft-versus-host disease in patients with primary immunodeficiencies who do not have a matched sibling donor.对于没有匹配同胞供体的原发性免疫缺陷患者,为尽量减少移植物抗宿主病而去除T淋巴细胞的方法。
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T-cell replete haploidentical donor transplantation using post-transplant CY: an emerging standard-of-care option for patients who lack an HLA-identical sibling donor.移植后使用环磷酰胺的T细胞充足的单倍体相合供体移植:为缺乏HLA相合同胞供体的患者提供的一种新兴的标准治疗选择。
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