INRS-Institut Armand-Frappier and Center for Host-Parasite Interactions, 531 Boulevard des Prairies, Laval, H7V 1B7, Canada.
INRS-Institut Armand-Frappier and Center for Host-Parasite Interactions, 531 Boulevard des Prairies, Laval, H7V 1B7, Canada.
Trends Parasitol. 2018 Feb;34(2):155-171. doi: 10.1016/j.pt.2017.10.001. Epub 2017 Oct 28.
B cells are notorious actors for the host's protection against several infectious diseases. So much so that early vaccinology seated its principles upon their long-term protective antibody secretion capabilities. Indeed, there are many examples of acute infectious diseases that are combated by functional humoral responses. However, some chronic infectious diseases actively induce immune deregulations that often lead to defective, if not deleterious, humoral immune responses. In this review we summarize how Leishmania and Trypanosoma spp. directly manipulate B cell responses to induce polyclonal B cell activation, hypergammaglobulinemia, low-specificity antibodies, limited B cell survival, and regulatory B cells, contributing therefore to immunopathology and the establishment of persistent infections.
B 细胞是宿主抵御多种传染病的著名效应器。因此,早期疫苗学的原理是基于它们长期产生保护性抗体的能力。事实上,有许多急性传染病是通过功能性体液免疫反应来对抗的。然而,一些慢性传染病会主动诱导免疫失调,这往往导致体液免疫反应缺陷,如果不是有害的话。在这篇综述中,我们总结了利什曼原虫和锥虫属如何直接操纵 B 细胞反应,诱导多克隆 B 细胞活化、高丙种球蛋白血症、低特异性抗体、有限的 B 细胞存活和调节性 B 细胞,从而导致免疫病理和持续性感染的建立。