Cell-derived anaphylatoxins as key mediators of antibody-dependent type II autoimmunity in mice
Varsha Kumar, … , Reinhold E. Schmidt, J. Engelbert Gessner
Varsha Kumar, … , Reinhold E. Schmidt, J. Engelbert Gessner
Published February 1, 2006
Citation Information: J Clin Invest. 2006;116(2):512-520. https://doi.org/10.1172/JCI25536.
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Research Article Immunology

Cell-derived anaphylatoxins as key mediators of antibody-dependent type II autoimmunity in mice

Abstract

Complement C5a, a potent anaphylatoxin, is a candidate target molecule for the treatment of inflammatory diseases, such as myocardial ischemia/reperfusion injury, RA, and the antiphospholipid syndrome. In contrast, up until now, no specific contribution of C5a and its receptor, C5aR, was recognized in diseases of antibody-dependent type II autoimmunity. Here we identify C5a as a novel key mediator of autoimmune hemolytic anemia (AIHA) and show that mice lacking C5aR are partially resistant to this IgG autoantibody–induced disease model. Upon administration of anti-erythrocyte antibodies, upregulation of activating Fcγ receptors (FcγRs) on Kupffer cells, as observed in WT mice, was absent in C5aR-deficient mice, and FcγR-mediated in vivo erythrophagocytosis was impaired. Surprisingly, in mice deficient in FcγRI and FcγRIII, anti-erythrocyte antibody–induced C5 and C5a production was abolished, demonstrating the existence of a previously unidentified FcγR-mediated C5a-generating pathway. These results show that the development of a full-blown antibody-dependent autoimmune disease requires C5a — produced by and acting on FcγR — and may suggest therapeutic benefits of C5 and/or C5a/C5aR blockade in AIHA and other diseases closely related to type II autoimmune injury.

Authors

Varsha Kumar, Syed R. Ali, Stephanie Konrad, Jörg Zwirner, J. Sjef Verbeek, Reinhold E. Schmidt, J. Engelbert Gessner

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Reduced Kupffer cell–mediated rbc destruction in FcγRI/III–/– and C5aR–/...
Reduced Kupffer cell–mediated rbc destruction in FcγRI/III–/– and C5aR–/– mice during 34-3C mAb–induced AIHA. (A) WT C57BL/6 (open circles), FcγRI/III–/– (filled circles), and C5aR–/– (filled squares) mice injected with 300 μg of anti-rbc 34-3C mAb were analyzed for Kupffer cell–mediated in vivo phagocytosis at the indicated times. Results are shown as the percentage of Mac-1–selected Kupffer cells containing more than 2 ingested rbcs ± SD obtained from 4–9 mice in each group. (B) H&E-stained liver sections obtained from the indicated mice at days 0 and 2 after AIHA induction were analyzed for erythrophagocytosis by light microscopy. Shown is the mean cell count ± SEM of rbc-containing liver cells per microscopic field (original magnifications, ×40 and ×100) obtained from 3–5 mice in each group. (A and B) Significant differences were determined by Student’s t test (*P < 0.05; **P < 0.001).