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在缺乏功能性放射敏感的宿主造血衍生抗原呈递细胞的情况下,通过性别错配的 H-Y 抗原诱导急性移植物抗宿主病。

Induction of acute GVHD by sex-mismatched H-Y antigens in the absence of functional radiosensitive host hematopoietic-derived antigen-presenting cells.

机构信息

Department of Internal Medicine, University of Michigan Comprehensive Cancer Center, Ann Arbor, USA.

出版信息

Blood. 2012 Apr 19;119(16):3844-53. doi: 10.1182/blood-2011-10-384057. Epub 2011 Nov 18.

Abstract

It is currently thought that acute GVHD cannot be elicited in the absence of Ag presentation by radiosensitive host hematopoietic-derived APCs after allogeneic BM transplantation. Because clinical data suggest that sex-mismatched H-Y Ags may be important minor histocompatibility Ags for GVH responses, we directly tested their relevance and ability to initiate GVHD when presented by either the hematopoietic- (host or donor) or the nonhematopoietic-derived APCs. H-Y minor Ag incompatibility elicited both CD4(+) and CD8(+) T-cell driven GVHD lethality. Studies with various well-established BM chimera recipients, in contrast to the current views, have reported that in the absence of functional radiosensitive host hematopoietic-derived APCs, H-Y Ag presentation by either the donor hematopoietic-derived or the host nonhematopoietic-derived APCs is sufficient for inducing GVHD. Our data further suggest that infusion of sufficient numbers of alloreactive donor T cells will induce GVHD in the absence of radiosensitive host hematopoietic-derived APCs.

摘要

目前认为,在同种异体骨髓移植后,缺乏放射敏感的宿主造血衍生 APC 对 Ag 的呈递,急性移植物抗宿主病 (GVHD) 就不能被引发。因为临床数据表明,性别错配的 H-Y Ag 可能是 GVH 反应的重要次要组织相容性 Ag,所以我们直接检测了它们在由造血衍生(宿主或供体)或非造血衍生 APC 呈递时的相关性和引发 GVHD 的能力。H-Y 次要 Ag 不匹配引发了 CD4(+)和 CD8(+) T 细胞驱动的 GVHD 致死性。与目前的观点相反,与各种已建立的骨髓嵌合体受体的研究表明,在缺乏功能正常的放射敏感的宿主造血衍生 APC 的情况下,供体造血衍生或宿主非造血衍生 APC 对 H-Y Ag 的呈递足以诱导 GVHD。我们的数据进一步表明,输注足够数量的同种反应性供体 T 细胞将在缺乏放射敏感的宿主造血衍生 APC 的情况下诱导 GVHD。

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