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造血干细胞移植中的风险评估:次要组织相容性抗原

Risk assessment in haematopoietic stem cell transplantation: minor histocompatibility antigens.

作者信息

Hambach Lothar, Spierings Eric, Goulmy Els

机构信息

Department of Immunohaematology and Blood Transfusion, Leiden University Medical Centre, Post Box 9600, 2300 RC Leiden, The Netherlands.

出版信息

Best Pract Res Clin Haematol. 2007 Jun;20(2):171-87. doi: 10.1016/j.beha.2006.09.002.

Abstract

Minor histocompatibility (H) antigens are key molecules in graft-versus-host disease (GvHD) and the graft-versus-tumour effect after allogeneic stem-cell transplantation (SCT). Today, molecular typing methods allow an easy assessment of differences in minor H antigens between patient and donors, so that the GvHD risk in individual patients can be estimated. However, the large number of minor H antigens prevents matching for them to avoid GvHD. Interestingly, mismatching for minor H antigens might improve the outcome of allogeneic SCT. Some minor H antigens are expressed mainly by malignant cells and can therefore serve as excellent targets for cancer immunotherapy. Thus, mismatching for tumour-expressed minor H antigens allows boosting of the curative effect of allogeneic SCT. Current research is elucidating the impact of e.g. donor immunization, immunodominance, or functional expression of minor H antigens on the extent of the GvH response.

摘要

次要组织相容性(H)抗原是异基因干细胞移植(SCT)后移植物抗宿主病(GvHD)和移植物抗肿瘤效应的关键分子。如今,分子分型方法可轻松评估患者与供体之间次要H抗原的差异,从而能够估计个体患者发生GvHD的风险。然而,大量的次要H抗原使得难以通过匹配来避免GvHD。有趣的是,次要H抗原不匹配可能会改善异基因SCT的疗效。一些次要H抗原主要由恶性细胞表达,因此可作为癌症免疫治疗的理想靶点。因此,肿瘤表达的次要H抗原不匹配可增强异基因SCT的治疗效果。目前的研究正在阐明例如供体免疫、免疫优势或次要H抗原的功能表达对移植物抗宿主反应程度的影响。

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