Vaccine & Infectious Disease Organization/International Vaccine Center, University of Saskatchewan, 120 Veterinary Road, Saskatoon, Saskatchewan, Canada, S7N 5E3.
Cell Tissue Res. 2011 Jan;343(1):131-40. doi: 10.1007/s00441-010-1031-3. Epub 2010 Sep 8.
B lymphocytes are well known because of their key role in mediating humoral immune responses. Upon encounter with antigen and on cognate interaction with T cells, they differentiate into antibody-secreting plasma cells, which are critical for protection against a variety of pathogens. In addition to their antibody-production function, B cells are efficient antigen-presenting cells and express a variety of pathogen recognition receptors (PRRs). Engagement of these PRRs with their respective ligands results in cytokine and chemokine secretion and the upregulation of co-stimulatory molecules. These events constitute innate immune responses. Toll-like receptor (TLR) activation provides a third signal for B cell activation and is essential for optimal antigen-specific antibody responses. In some situations, TLR activation in B cells can result in autoimmunity. The purpose of this review is to provide some insights into the way that TLRs influence innate and adaptive B cell responses.
B 淋巴细胞因其在介导体液免疫应答中的关键作用而广为人知。在与抗原接触并与 T 细胞发生同源相互作用后,它们分化为产生抗体的浆细胞,这对于抵抗各种病原体至关重要。除了产生抗体的功能外,B 细胞还是有效的抗原呈递细胞,并表达多种病原体识别受体(PRRs)。这些 PRRs 与各自的配体结合,导致细胞因子和趋化因子的分泌以及共刺激分子的上调。这些事件构成了先天免疫反应。Toll 样受体(TLR)的激活为 B 细胞的激活提供了第三个信号,对于最佳的抗原特异性抗体反应是必不可少的。在某些情况下,B 细胞中 TLR 的激活可导致自身免疫。本文的目的是提供一些有关 TLR 如何影响先天和适应性 B 细胞反应的见解。