Oxelius V A, Sjöstedt L, Willers S, Löw B
Department of Pediatrics, University Hospital, Lund, Sweden.
Int Arch Allergy Immunol. 1996 May;110(1):73-8. doi: 10.1159/000237314.
To find out whether IgG genes are involved in atopy we studied 26 of 101 laboratory technicians who had developed laboratory animal allergy (LAA). The genes for the constant region of the heavy chains of IgG subclasses were analyzed by serum Gm allotypes, representing products on allelic level of the IGHCG1, IGHCG2 and IGHCG3 on chromosome 14q32. There was a significantly increased frequency of the GM(f,f;n,n;b,b) genotype (57.7 instead of 22.3%, p < 0.001) representing IgG1, IgG2 and IgG3 molecules and in particular increased frequency of Gm genotypes with the homozygous expression of G2m (n,n) (69.2 instead of 27.4%, p < 0.001) and of the Gm(f,n,b) haplotype (75 instead of 44.8%, p < 0.001) compared to a normal Caucasian population. An increased HLA-DR4 content of the LAA group (61.5 instead of 33.7%, p < 0.01) was further investigated for Gm allotypes. Among 16 HLA-DR4 LAA individuals, the Gm(f,f;n,n;b,b) genotype (56.3 instead of 22.3%, p < 0.01) and the Gm genotypes with the homozygous expression G2m(n,n) (62.6 instead of 27.4%, p < 0.01) dominated. However, the HLA-DR4 frequency among Gm(f,f;n,n;b,b) of LAA patients did not deviate from the frequency of healthy individuals of the same Gm genotype. The increased frequency of HLA-DR4 antigen in LAA patients might be due to its association to the Gm(f,f;n,n;b,b) genotype. This study supports the following concept: the susceptibility of developing LAA is associated with Gm allotypes Glm(f) expressed from IGHCG1, G2m(n) from IGHCG2 and G3m(b) from IGHCG3 on both alleles situated close to IGHCE on chromosome 14q32. The association of LAA to Gm allotypes [Gm(f,f;n,n;b,b)] expressed from chromosome 14q32 and of HLA class II antigens (HLA-DR4) expressed from chromosome 6p21.3 further confirms the polygenic inheritance of the immune response in atopy.
为了探究免疫球蛋白G(IgG)基因是否与特应性有关,我们对101名已患实验动物过敏(LAA)的实验室技术人员中的26人进行了研究。通过血清Gm同种异型分析IgG亚类重链恒定区的基因,这些同种异型代表位于14号染色体q32区域的IGHCG1、IGHCG2和IGHCG3等位基因水平的产物。代表IgG1、IgG2和IgG3分子的GM(f,f;n,n;b,b)基因型频率显著增加(57.7%而非22.3%,p<0.001),特别是G2m(n,n)纯合表达的Gm基因型频率增加(69.2%而非27.4%,p<0.001),以及Gm(f,n,b)单倍型频率增加(75%而非44.8%,p<0.001),与正常白种人群相比。进一步研究了LAA组中增加的HLA - DR4含量(61.5%而非33.7%,p<0.01)与Gm同种异型的关系。在16名HLA - DR4阳性的LAA个体中,GM(f,f;n,n;b,b)基因型(56.3%而非22.3%,p<0.01)和G2m(n,n)纯合表达的Gm基因型(62.6%而非27.4%,p<0.01)占主导。然而,LAA患者中GM(f,f;n,n;b,b)基因型的HLA - DR4频率与相同Gm基因型健康个体的频率并无差异。LAA患者中HLA - DR4抗原频率增加可能是由于其与GM(f,f;n,n;b,b)基因型相关。本研究支持以下概念:患LAA的易感性与位于14号染色体q32上靠近IGHCE的两个等位基因上分别由IGHCG1表达的Gm同种异型Glm(f)、IGHCG2表达的G2m(n)和IGHCG3表达的G3m(b)有关。LAA与14号染色体q32表达的Gm同种异型[GM(f,f;n,n;b,b)]以及6号染色体p21.3表达的HLA II类抗原(HLA - DR4)之间的关联进一步证实了特应性免疫反应的多基因遗传。