Department of Anatomy and Cell Biology, George Washington University School of Medicine and Health Sciences, Washington, DC; Department of Ophthalmology, George Washington University School of Medicine and Health Sciences, Washington, DC.
Department of Pathology, Anatomy and Cell Biology, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania; Department of Ophthalmology, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania.
Transl Res. 2021 Oct;236:52-71. doi: 10.1016/j.trsl.2021.05.005. Epub 2021 May 27.
The eye is regarded as an immune privileged site. Since the presence of a vasculature would impair vision, the vasculature of the eye is located outside of the central light path. As a result, many regions of the eye evolved mechanisms to deliver immune cells to sites of dysgenesis, injury, or in response to the many age-related pathologies. While the purpose of these immune responses is reparative or protective, cytokines released by immune cells compromise visual acuity by inducing inflammation and fibrosis. The response to traumatic or pathological injury is distinct in different regions of the eye. Age-related diseases impact both the anterior and posterior segment and lead to reduced quality of life and blindness. Here we focus attention on the role that inflammation and fibrosis play in the progression of age-related pathologies of the cornea and the lens as well as in glaucoma, the formation of epiretinal membranes, and in proliferative vitreoretinopathy.
眼睛被视为免疫特惠部位。由于血管的存在会损害视力,因此眼睛的血管位于中央光路之外。因此,眼睛的许多区域都进化出了将免疫细胞输送到发育不良、损伤或对许多与年龄相关的病理反应部位的机制。虽然这些免疫反应的目的是修复或保护,但免疫细胞释放的细胞因子通过诱导炎症和纤维化来损害视力。眼睛不同区域对创伤或病理性损伤的反应是不同的。与年龄相关的疾病会影响前节和后节,导致生活质量下降和失明。在这里,我们关注炎症和纤维化在角膜和晶状体的年龄相关性病变以及青光眼、视网膜前膜形成和增生性玻璃体视网膜病变进展中的作用。