Xie Chun, Sharma Ruchi, Wang Hongwei, Zhou Xin J, Mohan Chandra
Simmons Arthritis Research Center, Division of Rheumatology, Center for Immunology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
J Immunol. 2004 Apr 15;172(8):5047-55. doi: 10.4049/jimmunol.172.8.5047.
The genetic basis of immune-mediated nephritis is poorly understood. Recent studies have demonstrated that the NZW mouse strain is more prone to immune-mediated nephritis compared with C57BL/6 and BALB/c strains. The present study extends these findings by challenging 12 additional inbred strains of mice with rabbit anti-mouse glomerular basement membrane (GBM) reactive sera. Compared with control sera-injected mice and anti-GBM-injected A/J, AKR/J, C3H/HeJ, DBA/2J, MRL/MpJ, NOD/LtJ, P/J, SJL/J, and SWR/J mice, the anti-GBM-injected BUB/BnJ, DBA/1J, and 129/svJ mice developed severe proteinuria and azotemia. Their kidneys exhibited pronounced glomerulonephritis, with crescent formation, as well as tubulointerstitial disease, with these phenotypes being particularly profound in 129/svJ mice. However, these strains did not appear to differ in the nature of their xenogeneic immune response to the administered rabbit sera, either quantitatively or qualitatively. Collectively, these findings allude to the presence of genetic elements in the BUB/BnJ, DBA/1J, and 129/svJ genomes that may potentially confer susceptibility to immune-mediated nephritis. Detailed studies to dissect out the immunological and genetic basis of renal disease in these three strains are clearly warranted.
免疫介导性肾炎的遗传基础尚不清楚。最近的研究表明,与C57BL/6和BALB/c品系相比,NZW小鼠品系更容易患免疫介导性肾炎。本研究通过用兔抗小鼠肾小球基底膜(GBM)反应性血清攻击另外12个近交系小鼠,扩展了这些发现。与注射对照血清的小鼠以及注射抗GBM的A/J、AKR/J、C3H/HeJ、DBA/2J、MRL/MpJ、NOD/LtJ、P/J、SJL/J和SWR/J小鼠相比,注射抗GBM的BUB/BnJ、DBA/1J和129/svJ小鼠出现了严重的蛋白尿和氮质血症。它们的肾脏表现出明显的肾小球肾炎,伴有新月体形成,以及肾小管间质疾病,这些表型在129/svJ小鼠中尤为明显。然而,这些品系在对所给予的兔血清的异种免疫反应的性质上,在数量或质量上似乎没有差异。总体而言,这些发现暗示BUB/BnJ、DBA/1J和129/svJ基因组中存在可能潜在导致免疫介导性肾炎易感性的遗传因素。显然有必要对这三个品系的肾脏疾病的免疫学和遗传基础进行详细研究。