Montufar-Solis Dina, Klein John R
The University of Texas Health Science Center at Houston, Department of Diagnostic Sciences, Dental Branch, Houston, TX 77030, USA.
Curr Immunol Rev. 2005 Jan;1(1):13-20. doi: 10.2174/1573395052952914.
T cells are present in large numbers in the epithelial lining of the small and large intestine of humans and mice. Those cells, referred to as intraepithelial lymphocytes (IELs), are critical for maintaining an effective mucosal immune response against the onslaught of enteric infectious agents and intestinal neoplasia. However, because intestinal immunity must by necessity occur rapidly and efficiently, it is concomitantly important that the local intestinal immune response be curtailed so as not to result in conditions that lead to a destructive inflammatory environment as occurs in inflammatory bowel disease (IBD). Although many aspects of the IEL activation process remain to be understood, emerging evidence indicates that costimulatory molecules on IELs are critical for activation and that they hold the key to regulating intestinal immunity across many levels. In this article, the involvement of three IEL costimulatory molecules (CD43, OX40, and Ly-6C) - working independently or in collaboration-will be discussed in the context of immunity and disease in the human and mouse intestine, and the involvement of those in sustaining the IELs in a uniquely precarious but effective state of activation readiness will be explored.
T细胞大量存在于人类和小鼠小肠及大肠的上皮组织中。这些细胞被称为上皮内淋巴细胞(IEL),对于维持针对肠道感染因子侵袭和肠道肿瘤形成的有效黏膜免疫反应至关重要。然而,由于肠道免疫必须迅速且高效地发生,因此同样重要的是,局部肠道免疫反应应受到抑制,以免导致如炎症性肠病(IBD)中出现的那种具有破坏性的炎症环境。尽管IEL激活过程的许多方面仍有待了解,但新出现的证据表明,IEL上的共刺激分子对于激活至关重要,并且它们是在多个层面调节肠道免疫的关键。在本文中,将在人类和小鼠肠道免疫及疾病的背景下讨论三种IEL共刺激分子(CD43、OX40和Ly-6C)独立或协同发挥作用的情况,并探讨它们在使IEL维持在一种独特的不稳定但有效的激活准备状态中的作用。