Universitäts-Augenklinik Tübingen, Elfriede-Aulhorn-Str. 7, 72076, Tübingen, Germany.
Ophthalmologe. 2021 Jan;118(Suppl 1):81-84. doi: 10.1007/s00347-020-01281-5.
Is the new coronavirus SARS-CoV‑2 able to infect ocular tissue and thus poses a risk of infection through the tissue in addition to the risk of contact? This is the question that has occupied ophthalmologists since the beginning of the outbreak. In order to infect a certain type of tissue specific receptors for each virus and sometimes also coreceptors or other proteins must be present. The aim of this review was to summarize and reflect the current state of research with the help of the currently available literature as of 28 May 2020. At the time of the research, angiotensin-converting enzyme 2 (ACE2) was clearly identified as the receptor and transmembrane serine protease 2 (TMPRSS2) as the necessary protease to enable the infection of human cells with SARS-CoV‑2. In the eye both ACE2 and TMPRSS2 are expressed, although sometimes very weakly and with varying degrees in different tissues. It is noteworthy that very different results were obtained with different methods. Several reasons can account for this effect: Firstly, the method of detection or preservation of the tissue, secondly, the possibly different expression of the tested tissue samples and thirdly, a possibly rapid loss of receptor expression post-mortem. Therefore, an infection of the eye seems possible, which has already been reported in various publications. The amount of virus or receptor expression necessary to cause an infection is not known. According to current state of knowledge the eye is not considered to be a high-risk tissue due to the low ACE2 and TMPRSS2 expression. Nevertheless, appropriate protective measures are necessary for both medical personnel and patients. In cases of corneal transplantation an infection of the donor tissue with SARS-CoV‑2 must be excluded.
新型冠状病毒(SARS-CoV-2)是否能够感染眼部组织,从而除了通过接触感染之外,还存在通过组织感染的风险?自疫情爆发以来,这一直是眼科医生关注的问题。为了感染特定类型的组织,每种病毒都必须存在针对该组织的特定受体,有时还需要核心受体或其他蛋白。本综述的目的是在截至 2020 年 5 月 28 日的现有文献的帮助下,总结和反映当前的研究状况。在研究过程中,血管紧张素转换酶 2(ACE2)被明确鉴定为受体,跨膜丝氨酸蛋白酶 2(TMPRSS2)为允许 SARS-CoV-2 感染人类细胞所必需的蛋白酶。在眼部,ACE2 和 TMPRSS2 均有表达,尽管在不同组织中的表达有时非常微弱且程度不同。值得注意的是,不同的方法得到了非常不同的结果。这种效应可能有几个原因:首先是检测或保存组织的方法,其次是测试组织样本的表达可能不同,第三是受体表达可能在死后迅速丧失。因此,眼部感染似乎是可能的,这已经在各种出版物中有所报道。引起感染所需的病毒或受体表达量尚不清楚。根据目前的知识状况,由于 ACE2 和 TMPRSS2 的表达水平较低,眼睛不被认为是高风险组织。然而,对于医务人员和患者来说,都需要采取适当的保护措施。在角膜移植的情况下,必须排除供体组织感染 SARS-CoV-2。