Klos Andreas, Tenner Andrea J, Johswich Kay-Ole, Ager Rahasson R, Reis Edimara S, Köhl Jörg
Institute of Medical Microbiology and Hospital Epidemiology, Medical School Hannover, MHH, Germany.
Mol Immunol. 2009 Sep;46(14):2753-66. doi: 10.1016/j.molimm.2009.04.027. Epub 2009 May 28.
The anaphylatoxin (AT) C3a, C5a and C5a-desArg are generally considered pro-inflammatory polypeptides generated after proteolytic cleavage of C3 and C5 in response to complement activation. Their well-appreciated effector functions include chemotaxis and activation of granulocytes, mast cells and macrophages. Recent evidence suggests that ATs are also generated locally within tissues by pathogen-, cell-, or contact system-derived proteases. This local generation of ATs is important for their pleiotropic biologic effects beyond inflammation. The ATs exert most of the biologic activities through ligation of three cognate receptors, i.e. the C3a receptor, the C5a receptor and the C5a receptor-like, C5L2. Here, we will discuss recent findings suggesting that ATs regulate cell apoptosis, lipid metabolism as well as innate and adaptive immune responses through their impact on antigen-presenting cells and T cells. As we will outline, such regulatory functions of ATs and their receptors play important roles in the pathogenesis of allergy, autoimmunity, neurodegenerative diseases, cancer and infections with intracellular pathogens.
过敏毒素(AT)C3a、C5a和C5a-去精氨酸通常被认为是在补体激活后C3和C5经蛋白水解裂解产生的促炎多肽。它们广为人知的效应功能包括趋化作用以及粒细胞、肥大细胞和巨噬细胞的激活。最近的证据表明,AT也可由病原体、细胞或接触系统衍生的蛋白酶在组织内局部产生。AT的这种局部产生对于其除炎症之外的多效生物学效应很重要。AT通过与三种同源受体(即C3a受体、C5a受体和C5a受体样分子C5L2)结合发挥其大部分生物学活性。在此,我们将讨论最近的研究发现,这些发现表明AT通过影响抗原呈递细胞和T细胞来调节细胞凋亡、脂质代谢以及固有免疫和适应性免疫反应。正如我们将概述的那样,AT及其受体的这种调节功能在过敏、自身免疫、神经退行性疾病、癌症以及细胞内病原体感染的发病机制中发挥重要作用。