Kono D H, Burlingame R W, Owens D G, Kuramochi A, Balderas R S, Balomenos D, Theofilopoulos A N
Department of Immunology, Scripps Research Institute, La Jolla, CA 92037.
Proc Natl Acad Sci U S A. 1994 Oct 11;91(21):10168-72. doi: 10.1073/pnas.91.21.10168.
Susceptibility to systemic lupus erythematosus has been unequivocally established to be an inherited trait, but the exact genes and how they confer susceptibility remain largely unknown. In this study of (NZB x NZW)F2 intercross mice, we used linkage analysis of markers covering > 90% of the autosomal genome and identified eight susceptibility loci (Lbw1 to -8, chromosomes 17, 4-7, 18, 1, 11, respectively) associated with antichromatin autoantibody production, glomerulonephritis, and/or mortality. Only one locus, the major histocompatibility complex, was linked to all three traits. Two other loci were associated with both glomerulonephritis and mortality, whereas the remaining loci were linked to one of the above traits. Two additional loci (Sbw1 and -2) that contributed to splenomegaly were also identified. The Sbw2 locus mapped to the identical region as Lbw2, a locus on chromosome 4 linked to glomerulonephritis and mortality, suggesting a single locus with pleiotropic effects. The results indicate that the immunopathologic features of lupus are affected by distinct, but additive, genetic contributions. Studies to determine the nature of the genes associated with these loci should help define the genetic mechanisms involved in this systemic autoimmune disease.
系统性红斑狼疮的易感性已被明确确认为一种遗传性状,但确切的基因以及它们如何赋予易感性在很大程度上仍不清楚。在这项对(NZB×NZW)F2杂交小鼠的研究中,我们对覆盖常染色体基因组90%以上的标记进行连锁分析,鉴定出八个与抗染色质自身抗体产生、肾小球肾炎和/或死亡率相关的易感位点(分别为Lbw1至-8,位于染色体17、4 - 7、18、1、11)。只有一个位点,即主要组织相容性复合体,与所有这三个性状相关。另外两个位点与肾小球肾炎和死亡率均相关,而其余位点则与上述性状之一相关。还鉴定出另外两个导致脾肿大的位点(Sbw1和-2)。Sbw2位点定位于与Lbw2相同的区域,Lbw2是位于4号染色体上与肾小球肾炎和死亡率相关的一个位点,提示存在一个具有多效性的单一位点。结果表明,狼疮的免疫病理特征受到不同但具有累加作用的遗传因素影响。确定与这些位点相关基因性质的研究应有助于明确这种系统性自身免疫疾病所涉及的遗传机制。