Immunology Program, Garvan Institute of Medical Research, Darlinghurst, NSW 2010, Australia.
J Exp Med. 2012 Jul 2;209(7):1241-53. doi: 10.1084/jem.20120994.
The generation of high-affinity antibodies (Abs) plays a critical role in the neutralization and clearance of pathogens and subsequent host survival after natural infection with a variety of microorganisms. Most currently available vaccines rely on the induction of long-lived protective humoral immune responses by memory B cells and plasma cells, underscoring the importance of Abs in host protection. Ab responses against most antigens (Ags) require interactions between B cells and CD4(+) T helper cells, and it is now well recognized that T follicular helper cells (Tfh) specialize in providing cognate help to B cells and are fundamentally required for the generation of T cell-dependent B cell responses. Perturbations in the development and/or function of Tfh cells can manifest as immunopathologies, such as immunodeficiency, autoimmunity, and malignancy. Unraveling the cellular and molecular requirements underlying Tfh cell formation and maintenance will help to identify molecules that could be targeted for the treatment of immunological diseases that are characterized by insufficient or excessive Ab responses.
高亲和力抗体(Abs)的产生在中和和清除病原体以及随后的自然感染各种微生物后宿主的存活中起着关键作用。大多数现有的疫苗依赖于记忆 B 细胞和浆细胞诱导长寿保护性体液免疫应答,突出了 Abs 在宿主保护中的重要性。针对大多数抗原(Ags)的 Ab 反应需要 B 细胞和 CD4(+)T 辅助细胞之间的相互作用,现在人们已经认识到滤泡辅助 T 细胞(Tfh)专门为 B 细胞提供同源帮助,并且是产生 T 细胞依赖性 B 细胞应答的根本需要。Tfh 细胞的发育和/或功能紊乱可能表现为免疫病理学,如免疫缺陷、自身免疫和恶性肿瘤。阐明 Tfh 细胞形成和维持的细胞和分子要求将有助于确定可用于治疗以 Ab 反应不足或过度为特征的免疫性疾病的分子。