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单倍体相合干细胞移植中的自然杀伤(NK)细胞同种异体反应性

Natural Killer (NK) Cell Alloreactivity in Haploidentical Stem Cell Transplantation.

作者信息

Luis-Hidalgo Mar, Piñana José Luis, Solano Carlos, Planelles Dolores

机构信息

Centro de Transfusión de la Comunidad Valenciana, 46014 Valencia, Spain.

Hospital Clínico Universitario de Valencia, 46010 Valencia, Spain.

出版信息

Cells. 2025 Jul 16;14(14):1091. doi: 10.3390/cells14141091.

DOI:10.3390/cells14141091
PMID:40710344
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12293795/
Abstract

This paper conducts a literature review on the role of natural killer cells in haploidentical hematopoietic stem cell transplantation. Theoretical concepts related to genes are introduced regarding their structure, nomenclature, genetic organization, polymorphism, and inheritance pattern, types of KIR proteins and receptors, HLA ligands for KIR receptors, and the definition of different NK alloreactivity prediction models for the donor of haploidentical hematopoietic stem cell transplantation and the recipient. These models include the following and consider incompatibility: ligand-ligand, receptor-ligand, gene-gene, and KIR haplotype models or the donor group. These models consider the presence or absence of specific ligands or receptors and/or genes in the donor and recipient to predict alloreactivity. Determining the best model for predicting KIR alloreactivity and its significance in donor selection algorithms for haploidentical transplantation is still under investigation.

摘要

本文对自然杀伤细胞在单倍体造血干细胞移植中的作用进行了文献综述。介绍了与基因相关的理论概念,包括其结构、命名、遗传组织、多态性和遗传模式、KIR蛋白和受体的类型、KIR受体的HLA配体,以及单倍体造血干细胞移植供体和受体不同NK同种异体反应性预测模型的定义。这些模型包括以下几种,并考虑不相容性:配体-配体、受体-配体、基因-基因和KIR单倍型模型或供体组。这些模型考虑供体和受体中特定配体或受体和/或基因的存在与否来预测同种异体反应性。确定预测KIR同种异体反应性的最佳模型及其在单倍体移植供体选择算法中的意义仍在研究中。

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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4565/12293795/bbcdf935ac4c/cells-14-01091-g005.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4565/12293795/5b6afdfd93bf/cells-14-01091-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4565/12293795/017def77deb8/cells-14-01091-g003.jpg
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本文引用的文献

1
Role of Centromeric and Telomeric Haplotypes of Killer-Cell Immunoglobulin-Like Receptors (KIRs) in Disease Susceptibility: A Research Review.杀伤细胞免疫球蛋白样受体(KIRs)着丝粒和端粒单倍型在疾病易感性中的作用:一项研究综述。
Cureus. 2025 May 8;17(5):e83728. doi: 10.7759/cureus.83728. eCollection 2025 May.
2
Frequency and Distribution of KIR Genotypes of Donors-Recipient Pairs in the Haploidentical Haematopoietic Stem Cell Transplantation Setting: Collaborative Study by the Spanish Working Group in Histocompatibility and Transplant Immunology (GETHIT) and the Spanish Haematopoietic Transplantation and Cell Therapy Group (GETH-TC).
HLA. 2025 May;105(5):e70248. doi: 10.1111/tan.70248.
3
Memory T-cell enriched haploidentical transplantation with NK cell addback results in promising long-term outcomes: a phase II trial.记忆 T 细胞富集的半相合 NK 细胞回输移植具有良好的长期疗效:一项 II 期临床试验。
J Hematol Oncol. 2024 Jun 27;17(1):50. doi: 10.1186/s13045-024-01567-0.
4
A retrospective analysis to evaluate if KIR B haplotype donors associate with a reduced risk of relapse in patients with haematological malignancies following haploidentical transplantation at the Blood and Bone Marrow Transplant Unit at Hammersmith Hospital ICHNHST.回顾性分析评估 KIR B 单倍型供体是否与 Hammersmith 医院 ICHNHST 血液和骨髓移植科进行的血缘单倍体移植后血液恶性肿瘤患者的复发风险降低相关。
HLA. 2024 Jan;103(1):e15214. doi: 10.1111/tan.15214. Epub 2023 Sep 15.
5
Donor selection for KIR alloreactivity is associated with superior survival in haploidentical transplant with PTCy.供者 KIR 同种反应性选择与 PTCy 半相合移植中优越的生存相关。
Front Immunol. 2022 Oct 13;13:1033871. doi: 10.3389/fimmu.2022.1033871. eCollection 2022.
6
Immunogenomics of Killer Cell Immunoglobulin-Like Receptor (KIR) and HLA Class I: Coevolution and Consequences for Human Health.杀伤细胞免疫球蛋白样受体 (KIR) 和 HLA 类 I 的免疫基因组学:协同进化及其对人类健康的影响。
J Allergy Clin Immunol Pract. 2022 Jul;10(7):1763-1775. doi: 10.1016/j.jaip.2022.04.036. Epub 2022 May 10.
7
KIR in Allogeneic Hematopoietic Stem Cell Transplantation: Need for a Unified Paradigm for Donor Selection.KIR 在异基因造血干细胞移植中的作用:供者选择需要统一的模式。
Front Immunol. 2022 Feb 15;13:821533. doi: 10.3389/fimmu.2022.821533. eCollection 2022.
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Cells. 2021 Nov 10;10(11):3108. doi: 10.3390/cells10113108.
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Cells. 2021 Jul 14;10(7):1777. doi: 10.3390/cells10071777.