In the eye of the storm: SARS-CoV-2 infection and replication at the ocular surface?

被引:32
作者
Armstrong, Lyle [1 ]
Collin, Joseph [1 ]
Mostafa, Islam [1 ]
Queen, Rachel [1 ]
Figueiredo, Francisco C. [1 ,2 ,3 ]
Lako, Majlinda [1 ]
机构
[1] Newcastle Univ, Biosci Inst, Fac Med Sci, Newcastle Upon Tyne, Tyne & Wear, England
[2] Royal Victoria Infirm, Dept Ophthalmol, Newcastle Upon Tyne, Tyne & Wear, England
[3] Newcastle Univ, Newcastle Upon Tyne, Tyne & Wear, England
基金
英国生物技术与生命科学研究理事会;
关键词
ACE2; conjunctiva; cornea; coronavirus; COVID-19; limbus; ocular surface; organ and animal models; SARS-CoV-2; scRNA-Seq; tears; therapy; TMPRSS2; RESPIRATORY SYNDROME CORONAVIRUS; HUMAN LACRIMAL GLAND; COVID-19; CELLS; ANATOMY; TROPISM; MUCINS; MODEL; ENTRY; ACE2;
D O I
10.1002/sctm.20-0543
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) first emerged in December 2019 and spread quickly causing the coronavirus disease 2019 (COVID-19) pandemic. Recent single cell RNA-Seq analyses have shown the presence of SARS-CoV-2 entry factors in the human corneal, limbal, and conjunctival superficial epithelium, leading to suggestions that the human ocular surface may serve as an additional entry gateway and infection hub for SARS-CoV-2. In this article, we review the ocular clinical presentations of COVID-19 and the features of the ocular surface that may underline the overall low ocular SARS-CoV-2 infection. We critically evaluate the studies performed in nonhuman primates, ex vivo organ culture ocular models, stem cell derived eye organoids and the differences in infection efficiency observed in different parts of human ocular surface epithelium. Finally, we highlight the additional work that needs to be carried out to understand the immune response of the ocular surface to SARS-CoV-2 infection, which can be translated into prophylactic treatments that may be applied to other organ systems.
引用
收藏
页码:976 / 986
页数:11
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