Program in Immunology, Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109-981024, USA.
Immunol Cell Biol. 2011 Mar;89(3):396-407. doi: 10.1038/icb.2010.124. Epub 2011 Feb 8.
Minor histocompatibility (H) antigens are major targets of a graft-versus-leukemia (GVL) effect mediated by donor CD8(+) and CD4(+) T cells following allogeneic hematopoietic cell transplantation (HCT) between human leukocyte antigen identical individuals. In the 15 years since the first molecular characterization of human minor H antigens, significant strides in minor H antigen discovery have been made as a consequence of advances in cellular, genetic and molecular techniques. Much has been learned about the mechanisms of minor H antigen immunogenicity, their expression on normal and malignant cells, and their role in GVL responses. T cells specific for minor H antigens expressed on leukemic cells, including leukemic stem cells, can be isolated and expanded in vitro and infused into allogeneic HCT recipients to augment the GVL effect to prevent and treat relapse. The first report of the adoptive transfer of minor H antigen-specific T-cell clones to patients with leukemic relapse in 2010 illustrates the potential for the manipulation of alloreactivity for therapeutic benefit. This review describes the recent developments in T-cell recognition of human minor H antigens, and efforts to translate these discoveries to reduce leukemia relapse after allogeneic HCT.
次要组织相容性 (H) 抗原是同种异体造血细胞移植 (HCT) 后供体 CD8(+)和 CD4(+)T 细胞介导移植物抗白血病 (GVL) 效应的主要靶点。自首次对人类次要 H 抗原进行分子特征描述以来,由于细胞、遗传和分子技术的进步,在次要 H 抗原发现方面取得了重大进展。人们对次要 H 抗原免疫原性的机制、它们在正常和恶性细胞上的表达以及它们在 GVL 反应中的作用有了更多的了解。可以在体外分离和扩增针对白血病细胞(包括白血病干细胞)上表达的次要 H 抗原的 T 细胞,并输注到同种异体 HCT 受者中,以增强 GVL 效应,从而预防和治疗复发。2010 年首次报道了将次要 H 抗原特异性 T 细胞克隆过继转移到白血病复发患者中,这说明了为了治疗益处而操纵同种异体反应性的潜力。本文描述了 T 细胞识别人类次要 H 抗原的最新进展,以及为减少同种异体 HCT 后白血病复发而进行的这些发现转化的努力。