Cruz-Adalia Aranzazu, Veiga Esteban
Department of Molecular and Cellular Biology, Centro Nacional de Biotecnología, Consejo Superior de Investigaciones, Científicas (CNB-CSIC) , Madrid , Spain.
Front Immunol. 2016 Oct 7;7:405. doi: 10.3389/fimmu.2016.00405. eCollection 2016.
During infections, the first reaction of the host against microbial pathogens is carried out by innate immune cells, which recognize conserved structures on pathogens, called pathogen-associated molecular patterns. Afterward, some of these innate cells can phagocytose and destroy the pathogens, secreting cytokines that would modulate the immune response to the challenge. This rapid response is normally followed by the adaptive immunity, more specific and essential for a complete pathogen clearance in many cases. Some innate immune cells, usually named antigen-presenting cells, such as macrophages or dendritic cells, are able to process internalized invaders and present their antigens to lymphocytes, triggering the adaptive immune response. Nevertheless, the traditional boundary of separated roles between innate and adaptive immunity has been blurred by several studies, showing that very specialized populations of lymphocytes (cells of the adaptive immunity) behave similarly to cells of the innate immunity. These "innate-like" lymphocytes include γδ T cells, invariant NKT cells, B-1 cells, mucosal-associated invariant T cells, marginal zone B cells, and innate response activator cells, and together with the newly described innate lymphoid cells are able to rapidly respond to bacterial infections. Strikingly, our recent data suggest that conventional CD4 T cells, the paradigm of cells of the adaptive immunity, also present innate-like behavior, capturing bacteria in a process called transinfection. Transinfected CD4 T cells digest internalized bacteria like professional phagocytes and secrete large amounts of proinflammatory cytokines, protecting for further bacterial challenges. In the present review, we will focus on the data showing such innate-like behavior of lymphocytes following bacteria encounter.
在感染期间,宿主针对微生物病原体的第一反应由先天免疫细胞执行,这些细胞识别病原体上保守的结构,即病原体相关分子模式。之后,其中一些先天免疫细胞可以吞噬并破坏病原体,分泌细胞因子来调节对这种挑战的免疫反应。这种快速反应通常会继之以适应性免疫,在许多情况下,适应性免疫更具特异性且对完全清除病原体至关重要。一些先天免疫细胞,通常称为抗原呈递细胞,如巨噬细胞或树突状细胞,能够处理内化的入侵者并将其抗原呈递给淋巴细胞,从而触发适应性免疫反应。然而,先天免疫和适应性免疫之间传统的分离作用界限已被多项研究模糊,这些研究表明非常特殊的淋巴细胞群体(适应性免疫细胞)的行为与先天免疫细胞相似。这些“类先天”淋巴细胞包括γδT细胞、不变自然杀伤T细胞、B-1细胞、黏膜相关不变T细胞、边缘区B细胞和先天反应激活细胞,它们与新描述的先天淋巴细胞一起能够对细菌感染迅速做出反应。引人注目的是,我们最近的数据表明,传统的CD4 T细胞,即适应性免疫细胞的典范,也表现出类先天行为,在一个称为转染的过程中捕获细菌。被转染的CD4 T细胞像专业吞噬细胞一样消化内化的细菌,并分泌大量促炎细胞因子,以抵御进一步的细菌挑战。在本综述中,我们将重点关注显示淋巴细胞在遇到细菌后出现这种类先天行为的数据。