Lang Mark L
Department of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.
Expert Rev Vaccines. 2009 Aug;8(8):1109-21. doi: 10.1586/erv.09.56.
CD1d-restricted natural killer (NKT) cells are important contributors to antigen-specific antibody responses. There is, therefore, considerable interest in the design and implementation of strategies to appropriately activate NKT cells and boost vaccine-induced protective antibody responses. In order to achieve these goals, investigators are examining the mechanisms by which NKT cells enhance antibody responses. Although information is limited, it is now appreciated that both cognate and noncognate interactions between CD1d-expressing B cells and NKT cells drive enhanced antibody responses. NKT cells may provide B-cell help in the form of direct receptor-mediated interactions as well as by secretion of soluble effectors, including cytokines. In this article, we review the evidence in support of these mechanisms and discuss how they likely take place in the context of interactions of NKT cells with other cell types, such as dendritic cells and helper T cells. We also discuss the evidence that NKT cells affect discrete differentiation events in the multistep process by which a naive B cell experiences antigen and develops into a memory B cell or an antibody-secreting plasma cell. Since most information on NKT cells and humoral immunity has been derived from murine studies, we discuss what is known about human NKT cells and humoral immunity. We offer thoughts on whether the findings in murine systems will translate to humans.
CD1d限制性自然杀伤(NKT)细胞是抗原特异性抗体反应的重要贡献者。因此,人们对设计和实施适当激活NKT细胞并增强疫苗诱导的保护性抗体反应的策略有着浓厚兴趣。为了实现这些目标,研究人员正在研究NKT细胞增强抗体反应的机制。尽管相关信息有限,但目前人们认识到,表达CD1d的B细胞与NKT细胞之间的同源和非同源相互作用都会驱动抗体反应增强。NKT细胞可能以直接受体介导的相互作用以及通过分泌可溶性效应分子(包括细胞因子)的形式为B细胞提供帮助。在本文中,我们回顾了支持这些机制的证据,并讨论了它们可能在NKT细胞与其他细胞类型(如树突状细胞和辅助性T细胞)相互作用的背景下如何发生。我们还讨论了NKT细胞影响幼稚B细胞经历抗原并发育成记忆B细胞或分泌抗体的浆细胞的多步骤过程中离散分化事件的证据。由于关于NKT细胞和体液免疫的大多数信息都来自小鼠研究,我们讨论了关于人类NKT细胞和体液免疫已知的情况。我们思考了小鼠系统中的发现是否会适用于人类。