MRC Centre for Transplantation, King's College London School of Medicine, London, England.
Am J Pathol. 2011 Dec;179(6):2683-90. doi: 10.1016/j.ajpath.2011.08.017. Epub 2011 Oct 8.
To explore the role of antigen-specific CD4(+) T cells in glomerulonephritis, we administered ovalbumin 323-339 peptide conjugated to glomerular-binding polyclonal antibody and induced disease in RAG1(-/-) mice with CD4(+) T cells from OT2 × RAG1(-/-) mice. These OT2 × RAG1(-/-) mice have a transgenic T-cell receptor specific for this peptide. When CD4(+) T cells were primed in vivo, crescentic glomerulonephritis developed after 21 days in mice given peptide-conjugated glomerular-binding antibody but not unconjugated antibody control. We then investigated the relative roles of T(H)1 and T(H)17 cells, using Fab(2) fragments of glomerular-binding antibody to exclude a role for antibody in this model. T cells from OT2 × RAG1(-/-) mice were polarized in vitro, and T(H)1 or T(H)17 cell lines were injected into mice that were also given peptide-conjugated Fab(2) or unconjugated Fab(2) control, giving four experimental groups. After 21 days crescentic glomerulonephritis was seen in mice receiving T(H)17 cells and peptide-conjugated Fab(2) but in none of the other three groups. These results suggest that T(H)17 but not T(H)1 cells can induce crescentic glomerulonephritis.
为了探索抗原特异性 CD4(+)T 细胞在肾小球肾炎中的作用,我们用与肾小球结合的多克隆抗体偶联的卵清蛋白 323-339 肽处理 RAG1(-/-)小鼠,并向其输注 OT2×RAG1(-/-)小鼠的 CD4(+)T 细胞以诱导疾病。这些 OT2×RAG1(-/-)小鼠具有针对该肽的转基因 T 细胞受体。当 CD4(+)T 细胞在体内被激活时,给予肽偶联的肾小球结合抗体而非未偶联抗体对照的小鼠在 21 天后会发展为新月体性肾小球肾炎。然后,我们使用肾小球结合抗体的 Fab(2)片段来研究 T(H)1 和 T(H)17 细胞的相对作用,以排除该模型中抗体的作用。从 OT2×RAG1(-/-)小鼠中体外极化 T 细胞,并将 T(H)1 或 T(H)17 细胞系注入也给予肽偶联 Fab(2)或未偶联 Fab(2)对照的小鼠中,共分为四个实验组。21 天后,接受 T(H)17 细胞和肽偶联 Fab(2)的小鼠出现新月体性肾小球肾炎,但在其他三组中均未出现。这些结果表明,T(H)17 而非 T(H)1 细胞可诱导新月体性肾小球肾炎。