Hakroush Samy, Tampe Désirée, Baier Eva, Kluge Ingmar Alexander, Ströbel Philipp, Tampe Björn
Institute of Pathology, University Medical Center Göttingen, Germany; SYNLAB Pathology Hannover, SYNLAB Holding Germany, Augsburg, Germany.
Department of Nephrology and Rheumatology, University Medical Center Göttingen, Germany.
J Autoimmun. 2022 Dec;133:102924. doi: 10.1016/j.jaut.2022.102924. Epub 2022 Oct 6.
Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a small vessel vasculitis affecting multiple organ systems, including the kidney. The activation of the complement system contributes essentially to its pathogenesis by autoantibody-antigen recognition directed against host cells in ANCA-associated renal vasculitis. We herein provide evidence for intrarenal synthesis of complement C3 localized to distinct vascular compartments in ANCA-associated renal vasculitis that associated with distinct inflammatory signaling pathways. Therefore, a total number of 43 kidney biopsies with ANCA-associated renal vasculitis were retrospectively included and evaluated for presence/absence of C3 deposits localized to distinct vascular compartments in association with clinicopathological biopsy findings. In addition, intrarenal C3 mRNA expression levels specifically from microdissected tubulointerstitial and glomerular compartments were extracted from transcriptome datasets. C3 deposits were present in the glomerular tuft, interlobular arteries, peritubular capillaries, and venules in ANCA-associated renal vasculitis. Most C3 deposits are localized to the glomerular tuft overlapping with peritubular capillaries. The presence of C3 deposits in the glomerular tuft correlated with impaired kidney function and overall short-term survival. Intrarenal complement C3 deposits were not associated with consumption of respective serum levels, supporting the concept of intrarenal C3 synthesis. Finally, intrarenal synthesis of complement C3 was linked to distinct inflammatory signaling pathways in the kidney that is especially relevant in ANCA-associated renal vasculitis. Considering recent advances in AAV therapy with the emergence of new therapeutics that inhibit complement activation, we here provide novel insights into intrarenal complement synthesis and associated inflammatory signaling pathways in ANCA-associated renal vasculitis.
抗中性粒细胞胞浆抗体(ANCA)相关血管炎(AAV)是一种累及包括肾脏在内的多个器官系统的小血管血管炎。补体系统的激活通过针对ANCA相关肾血管炎中宿主细胞的自身抗体 - 抗原识别,在其发病机制中起关键作用。我们在此提供证据表明,在ANCA相关肾血管炎中,补体C3在肾脏内合成并定位于不同的血管腔室,且与不同的炎症信号通路相关。因此,我们回顾性纳入了43例ANCA相关肾血管炎的肾活检病例,并结合临床病理活检结果评估了定位于不同血管腔室的C3沉积物的有无。此外,从转录组数据集中提取了经显微切割的肾小管间质和肾小球腔室中特异性的肾内C3 mRNA表达水平。在ANCA相关肾血管炎中,C3沉积物存在于肾小球、小叶间动脉、肾小管周围毛细血管和小静脉中。大多数C3沉积物定位于与肾小管周围毛细血管重叠的肾小球。肾小球中C3沉积物的存在与肾功能受损和总体短期生存率相关。肾内补体C3沉积物与相应血清水平的消耗无关,支持肾内C3合成的概念。最后,补体C3的肾内合成与肾脏中不同的炎症信号通路相关,这在ANCA相关肾血管炎中尤为重要。考虑到随着抑制补体激活的新疗法的出现,AAV治疗的最新进展,我们在此提供了关于ANCA相关肾血管炎中肾内补体合成及相关炎症信号通路的新见解。