Trowbridge H O
Department of Pathology, School of Dental Medicine, University of Pennsylvania, Philadelphia.
J Endod. 1990 Feb;16(2):54-61. doi: 10.1016/S0099-2399(06)81564-5.
Macrophages and lymphocytes play essential roles in cell-mediated mechanisms involved in chronic inflammation. During the development of specific immunity, macrophages are required to process and present antigen to immunocompetent T cells. They also serve as "accessory" cells to lymphocytes by releasing soluble factors involved in host defense. In order to carry out their role more effectively, macrophages have the property of being activated, a process that provides them with greater ability to phagocytose and kill ingested microorganisms. Activated T cells serve as key effector cells that are capable of producing lymphokines which modify the behavior of other cells. In this way, they are able to facilitate or suppress an immune response. Chronic inflammation is often associated with irreversible destruction of parenchymal tissue, and fibrous connective tissue fills the resultant defect. Proliferation of fibroblasts, collagen production, and neovascularization are enhanced by the secretion of cytokines by T cells and macrophages.
巨噬细胞和淋巴细胞在参与慢性炎症的细胞介导机制中发挥着重要作用。在特异性免疫的发展过程中,巨噬细胞需要处理并将抗原呈递给具有免疫活性的T细胞。它们还通过释放参与宿主防御的可溶性因子,充当淋巴细胞的“辅助”细胞。为了更有效地发挥其作用,巨噬细胞具有被激活的特性,这一过程赋予它们更强的吞噬和杀死摄入微生物的能力。活化的T细胞作为关键效应细胞,能够产生改变其他细胞行为的淋巴因子。通过这种方式,它们能够促进或抑制免疫反应。慢性炎症通常与实质组织的不可逆破坏相关,纤维结缔组织会填充由此产生的缺损。T细胞和巨噬细胞分泌的细胞因子会增强成纤维细胞的增殖、胶原蛋白的产生以及新血管形成。