Department of Molecular Protozoology, Research Institute for Microbial Diseases, Osaka University, Suita, Japan.
Department of Immunochemistry, Research Institute for Microbial Diseases, Osaka University, Suita, Japan.
Front Immunol. 2022 Jun 15;13:901864. doi: 10.3389/fimmu.2022.901864. eCollection 2022.
infection causes the most severe form of malaria. It has been hypothesized that directly suppresses host immune responses because sufficient acquired immunity is often not induced even by repeated infections in malaria-endemic areas. It is known that many kinds of -derived proteins are expressed on the surface of -infected erythrocytes (IEs), and these proteins have long been thought to be a key to the elucidation of the host immune evasion mechanisms. Our recent studies have revealed that the -derived erythrocyte surface antigen, RIFIN, the largest multiple gene family protein in the genome, suppresses host immune cell activation through direct interaction with human inhibitory immune receptors. In this review, we will discuss the molecular mechanisms for host immune evasion by -infected erythrocyte surface antigens. In addition, we will discuss the recently identified host immune response to using specialized antibodies that target host--derived molecule interactions.
感染引起最严重的疟疾形式。据推测,疟原虫直接抑制宿主免疫反应,因为即使在疟疾流行地区反复感染,也常常不能诱导足够的获得性免疫。已知疟原虫感染的红细胞(IEs)表面表达多种 - 衍生蛋白,这些蛋白长期以来一直被认为是阐明宿主免疫逃避机制的关键。我们最近的研究表明,疟原虫衍生的红细胞表面抗原 RIFIN 是疟原虫基因组中最大的多基因家族蛋白,通过与人类抑制性免疫受体的直接相互作用抑制宿主免疫细胞的激活。在这篇综述中,我们将讨论疟原虫感染红细胞表面抗原逃避宿主免疫的分子机制。此外,我们还将讨论最近发现的针对宿主 - 衍生分子相互作用的靶向宿主免疫反应的特异性抗体。