Hematopoietic cell transplantation for leukocyte adhesion deficiency: prevention of graft-versus-host-disease.

IF 2.1 4区 医学 Q2 HEMATOLOGY
Motoi Yamashita, Takahiro Kamiya, Hirokazu Kanegane
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引用次数: 0

Abstract

Introduction: Leukocyte adhesion deficiency (LAD) is a rare genetic disorder that impairs leukocyte migration, leading to severe immune dysfunction and recurrent infections. Although allogeneic hematopoietic cell transplantation (HCT) remains the primary curative treatment for severe LAD, it is complicated by a high incidence of graft-versus-host-disease (GVHD).

Areas covered: This narrative review outlines the key factors influencing GVHD development in patients with LAD-I, the most common LAD subtype, undergoing HCT. It explores established and emerging strategies for preventing GVHD, focusing on their effectiveness and outcomes. The literature search was conducted using PubMed to identify studies reporting HCT for LAD published 1989-2025.

Expert opinion: Conventional GVHD prophylaxis regimens, primarily involving calcineurin inhibitors, have proven insufficient in preventing GVHD in high-risk populations. Among patients undergoing haploidentical HCT, post-transplantation cyclophosphamide has shown efficacy in preventing GVHD, although these results were based on limited cases. Graft manipulation techniques such as CD34+ selection have also been explored. However, these approaches are often associated with high graft failure rate and poor survival. Alemtuzumab, which is used in conditioning regimens, has shown promise in lowering GVHD incidence. Further studies are essential to optimize GVHD prophylaxis and improve survival outcomes in patients with LAD undergoing HCT.

造血细胞移植治疗白细胞粘附不足:预防移植物抗宿主病。
白细胞粘附缺乏症(LAD)是一种罕见的遗传性疾病,它损害白细胞的迁移,导致严重的免疫功能障碍和复发性感染。尽管同种异体造血细胞移植(HCT)仍然是严重LAD的主要治疗方法,但移植物抗宿主病(GVHD)的高发使其复杂化。涵盖领域:本文概述了影响LAD- 1(最常见的LAD亚型)患者进行HCT的GVHD发展的关键因素。它探讨了预防GVHD的既定和新兴战略,重点是其有效性和结果。使用PubMed进行文献检索,以确定1989-2025年发表的关于LAD HCT的研究。专家意见:传统的GVHD预防方案,主要涉及钙调磷酸酶抑制剂,已被证明不足以预防高危人群的GVHD。在接受单倍体HCT的患者中,移植后环磷酰胺已显示出预防GVHD的有效性,尽管这些结果是基于有限的病例。移植操作技术,如CD34+选择也进行了探索。然而,这些入路往往伴随着高移植失败率和较差的生存率。用于调理方案的阿仑单抗已显示出降低GVHD发病率的希望。进一步的研究对于优化GVHD预防和改善行HCT的LAD患者的生存结果是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.70
自引率
3.60%
发文量
98
审稿时长
6-12 weeks
期刊介绍: Advanced molecular research techniques have transformed hematology in recent years. With improved understanding of hematologic diseases, we now have the opportunity to research and evaluate new biological therapies, new drugs and drug combinations, new treatment schedules and novel approaches including stem cell transplantation. We can also expect proteomics, molecular genetics and biomarker research to facilitate new diagnostic approaches and the identification of appropriate therapies. Further advances in our knowledge regarding the formation and function of blood cells and blood-forming tissues should ensue, and it will be a major challenge for hematologists to adopt these new paradigms and develop integrated strategies to define the best possible patient care. Expert Review of Hematology (1747-4086) puts these advances in context and explores how they will translate directly into clinical practice.
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