Hoffman R W, Sharp G C, Irvin W S, Anderson S K, Hewett J E, Pandey J P
Department of Veterans Affairs, Harry S. Truman Memorial Veterans Hospital, Columbia, MO 65201.
Arthritis Rheum. 1991 Apr;34(4):453-8. doi: 10.1002/art.1780340410.
The distribution of the immunoglobulin Km(1) and Gm phenotypes was examined in patients with connective tissue diseases, including systemic lupus erythematosus, mixed connective tissue disease, and scleroderma, whose sera were characterized for antibodies against nuclear antigens and polypeptides of U small nuclear ribonucleoproteins. We found a strong association between Km(1) phenotype and susceptibility to systemic lupus erythematosus (P less than 0.00001, relative risk = 17). We also found a positive association between the Km(1) phenotype and the presence of anti-double-stranded DNA antibodies. The presence of certain immunoglobulin genes or gene families may have a role in susceptibility to the development of autoantibodies and/or of connective tissue disease.
在患有结缔组织疾病(包括系统性红斑狼疮、混合性结缔组织病和硬皮病)的患者中,检测了免疫球蛋白Km(1)和Gm表型的分布情况,这些患者的血清以抗核抗原和U小核核糖核蛋白多肽的抗体为特征。我们发现Km(1)表型与系统性红斑狼疮易感性之间存在强烈关联(P小于0.00001,相对风险 = 17)。我们还发现Km(1)表型与抗双链DNA抗体的存在呈正相关。某些免疫球蛋白基因或基因家族的存在可能在自身抗体和/或结缔组织病发生的易感性中起作用。