Allen R D, Dobkins J A, Harper J M, Slayback D L
Department of Biology, Indiana University-Purdue University at Indianapolis, IN, USA.
Immunology. 1999 Feb;96(2):254-61. doi: 10.1046/j.1365-2567.1999.00626.x.
Graft-versus-host disease (GVHD) is the major complication occurring after bone marrow transplantation. The severity of GVHD varies widely, with this variation generally being attributed to variation in the degree of disparity between host and donor for minor histocompatibility antigens. However, it is also possible that other forms of polymorphism, such as polymorphisms in immune effector molecules, might play a significant role in determining GVHD severity. In order to investigate this hypothesis, we are studying the genetic factors that influence GVHD development in a murine model. We here report the first results of this analysis, which demonstrate that a locus on Chromosome 1 of the mouse, and possibly also a locus on Chromosome 4, exert considerable influence over the development of one aspect of acute GVHD - splenomegaly - in a parent-->F1 murine model. These results demonstrate that non-MHC genes can exert quite significant effects on the development of GVHD-associated pathology and that gene mapping can be used as a tool to identify these loci. Further analysis of such loci will allow identification of the mechanism whereby they influence GVHD and may lead in the future to improved selection of donors for human bone marrow transplantation.
移植物抗宿主病(GVHD)是骨髓移植后发生的主要并发症。GVHD的严重程度差异很大,这种差异通常归因于宿主与供体之间次要组织相容性抗原的差异程度。然而,其他形式的多态性,如免疫效应分子中的多态性,在决定GVHD严重程度方面也可能起重要作用。为了研究这一假设,我们正在小鼠模型中研究影响GVHD发生的遗传因素。我们在此报告该分析的首批结果,这些结果表明,在亲代→F1小鼠模型中,小鼠1号染色体上的一个位点以及可能还有4号染色体上的一个位点,对急性GVHD的一个方面——脾肿大的发展有相当大的影响。这些结果表明,非MHC基因可对GVHD相关病理的发展产生相当显著的影响,并且基因定位可作为识别这些位点的工具。对这些位点的进一步分析将有助于确定它们影响GVHD的机制,并可能在未来改善人类骨髓移植供体的选择。