Massengill S F, Goodenow M M, Sleasman J W
Department of Pediatrics, University of Florida, Gainesville, USA.
Am J Kidney Dis. 1998 Mar;31(3):418-26. doi: 10.1053/ajkd.1998.v31.pm9506678.
Autoimmune systemic lupus erythematosus (SLE) nephritis is characterized by the influx of mononuclear inflammatory cell infiltrates within the glomeruli and renal interstitium. To evaluate the possibility that intrarenal T cells result from the expansion of lymphocytes using limited T-cell receptor (TCR) genes, we analyzed the TCR Vbeta gene expression among infiltrating lymphocytes in renal tissue compared with simultaneous peripheral blood lymphocytes of four children with new-onset SLE nephritis. The TCR Vbeta gene expression in peripheral blood T cells from patients with SLE nephritis, when compared with normal controls, showed no preferential expansion or deletion of select Vbeta gene families. In contrast, when paired peripheral blood and renal tissue were analyzed, intrarenal lymphocytes in SLE nephritis demonstrated evidence of expansion of select Vbeta gene families. Sequence analysis of the V(D)J joining regions of the TCRbeta with the expanded families demonstrated a striking oligoclonality. These observations suggest that infiltrating T cells within renal tissue may use TCR Vbeta genes targeted toward nephritogenic antigens.
自身免疫性系统性红斑狼疮(SLE)肾炎的特征是肾小球和肾间质内有单核炎性细胞浸润。为了评估肾内T细胞是否由使用有限T细胞受体(TCR)基因的淋巴细胞扩增产生,我们分析了4例新发SLE肾炎患儿肾组织中浸润淋巴细胞与同期外周血淋巴细胞的TCR Vβ基因表达。与正常对照相比,SLE肾炎患者外周血T细胞的TCR Vβ基因表达未显示特定Vβ基因家族的优先扩增或缺失。相反,当分析配对的外周血和肾组织时,SLE肾炎中的肾内淋巴细胞显示出特定Vβ基因家族扩增的证据。对扩增家族的TCRβ的V(D)J连接区进行序列分析显示出明显的寡克隆性。这些观察结果表明,肾组织内浸润的T细胞可能使用针对致肾炎抗原的TCR Vβ基因。