Atsumi T
Second Department of Medicine, Hokkaido University School of Medicine, Sapporo, Japan.
Hokkaido Igaku Zasshi. 1992 May;67(3):408-19.
Human TNF alpha locus locates between HLA-B and DR region on the short arm of chromosome 6. The 5.5 kb and 10.5 kb of TNF alpha restriction fragment length polymorphic (RFLP) bands were identified by Southern hybridization using a restriction enzyme, NcoI. The frequencies of those bands were not different among patients with systemic lupus erythematosus (SLE), those with rheumatoid arthritis and normal controls. In the lupus patients, proteinuria was more frequent in the patients with the 5.5 kb RFLP band (19/39: 48.7%) than those without 5.5 kb band (7/35: 20%) (p less than 0.05). Furthermore, this band was strongly associated with the haplotype HLA B44-DRw13-DQw1. In order to investigate the association between this gene polymorphism and the production of TNF alpha, peripheral blood mononuclear cells from patients with SLE and normal controls were cultured for 24 hours with lipopolysaccharide and concanavalin A and the amount of TNF alpha in the supernatant was measured by enzyme linked immunosorbent assay. The TNF alpha production of lupus patients was not statistically different from that of normal controls. The production of TNF alpha was not related to 5.5 kb RFLP band, but in the patients with SLE, the mean value of TNF alpha in patients with the 5.5 kb RFLP band tended to be higher than those without the band. Lupus patients were divided into two groups by the production of TNF alpha i.e. low TNF alpha inducibility group and high TNF alpha inducibility group. Patients with proteinuria were more frequent in patients of the high TNF alpha inducibility group than those of low TNF alpha inducibility group (p less than 0.05). There were four patients with HLA B44-DRw13-DQw1 who had the 5.5 kb RFLP band and three of them belonged to the high TNF alpha inducibility group with nephrosis. These data suggest that TNF alpha and HLA are possibly associated with the severity of lupus nephritis.
人类肿瘤坏死因子α(TNFα)基因座位于6号染色体短臂上的HLA - B和DR区域之间。使用限制性内切酶NcoI通过Southern杂交鉴定出5.5 kb和10.5 kb的TNFα限制性片段长度多态性(RFLP)条带。这些条带的频率在系统性红斑狼疮(SLE)患者、类风湿性关节炎患者和正常对照之间没有差异。在狼疮患者中,具有5.5 kb RFLP条带的患者蛋白尿更常见(19/39:48.7%),高于无5.5 kb条带的患者(7/35:20%)(p<0.05)。此外,该条带与单倍型HLA B44 - DRw13 - DQw1密切相关。为了研究这种基因多态性与TNFα产生之间的关联,将SLE患者和正常对照的外周血单个核细胞用脂多糖和伴刀豆球蛋白A培养24小时,并用酶联免疫吸附测定法测量上清液中TNFα的量。狼疮患者的TNFα产生与正常对照在统计学上没有差异。TNFα的产生与5.5 kb RFLP条带无关,但在SLE患者中,具有5.5 kb RFLP条带的患者TNFα平均值倾向于高于无该条带的患者。狼疮患者根据TNFα的产生分为两组,即低TNFα诱导性组和高TNFα诱导性组。高TNFα诱导性组患者蛋白尿比低TNFα诱导性组更常见(p<0.05)。有4名具有HLA B44 - DRw13 - DQw1且有5.5 kb RFLP条带的患者,其中3名属于伴有肾病的高TNFα诱导性组。这些数据表明TNFα和HLA可能与狼疮性肾炎的严重程度有关。