Endogenous interleukin-10 regulates Th1 responses that induce crescentic glomerulonephritis

Background Interleukin (TL)-10 plays a pivotal role in regulating the Th1/T h2 predominance of immune responses. Exogenously administered IL-10 suppres ses nephritogenic Th1 responses, inhibits macrophage function, and attenuat es crescentic glomerulonephritis (GN). To determine the role of endogenous IL-10, the development of the nephritogenic immune response and crescentic GN was compared in IL-10-deficient (IL-10-/-) and normal (IL10+/+) C57BL/6 mice. Methods. GN was initiated in sensitized mice by the intravenous administrat ion of sheep antimouse glomerular basement membrane globulin. Renal injury was evaluated 21 days later. Results. Following the administration of anti-glomerular basement membrane globulin, normal (IL-10+/+) C57BL/6 mice developed proliferative GN with oc casional crescents, glomerular CD4+ T-cell and macrophage accumulation, and fibrin deposition. Using an identical induction protocol, IL-10-/- mice de veloped more severe GN. Crescent formation (IL-10-/-,23 +/- 2% of glomeruli ; IL-10+/+,5 +/- 2%), glomerular CD4+ T cells [IL-10-/-, 1.0 +/- 0.2 cells per glomerular cross-section (c/gcs); IL-10 +/+, 0.3 +/- 0.05 c/gcs], glome rular macrophages (IL-10-/-, 4.8 +/- 0.3 c/gcs: IL-10 +/+, 1.7 +/- 0.2 c/gc s), fibrin deposition [fibrin score (range 0 to 3+); IL-10-/-, 1.10 +/- 0.0 4; IL-10+/+,0.6 +/- 0.07], and serum creatinine (IL-10-/-, 30 +/- 2 mu mol/ L; IL-10 +/+,23 +/- 1 mu mol/L) were all significantly increased in IL-10-/ - mice (P < 0.05). Circulating antibody (IL-10-/-, 1.05 +/- 0.16 OD units; IL-10+/+ ,0.63 +/- 0.08 OD units) and cutaneous delayed-type hypersensitivi ty (skin swelling; IL-10-/-,0,22 +/- 0.03 mm; IL-10+/+, 0.12 +/- 0.02 mm) t o the nephritogenic antigen (sheep globulin) were also increased (both P < 0.05). Interferon-gamma production by cultured splenocytes was increased (I L-10-/- 7.9 +/- 2.5 ng/4 x 10(6) cells, IL-10+/+ 0.28 +/- 0.09 ng/4 x 10(6) cells, P < 0.05), but IL-4 production was unchanged. Conclusions. Endogenous IL-10 counter-regulates nephritogenic Th1 responses and attenuates crescentic GN.