Commercial human 3D corneal epithelial equivalents for modeling epithelial infection in herpes keratitis

被引:0
|
作者
Borodianskiy-Shteinberg, Tatiana [1 ]
Bisht, Punam [1 ,3 ]
Das, Biswajit [1 ,4 ]
Kinchington, Paul R. [2 ]
Goldstein, Ronald S. [1 ]
机构
[1] Bar Ilan Univ, Mina & Everard Goodman Fac Life Sci, IL-52900 Ramat Gan, Israel
[2] Univ Pittsburgh, Dept Ophthalmol & Mol Microbiol & Genet, Pittsburgh, PA 15213 USA
[3] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[4] Harvard Med Sch, Dept Biol Chem & Mol Pharmacol, Boston, MA USA
基金
以色列科学基金会;
关键词
Herpes keratitis; 3D culture; Herpesvirus; Drug testing; Herpes zoster ophthalmicus; VARICELLA-ZOSTER-VIRUS; EMBRYONIC STEM-CELLS; SIMPLEX-VIRUS; EXPRESSION; RESISTANCE; ACYCLOVIR; NEURONS; ENTRY; IL-6; VZV;
D O I
10.1016/j.virol.2024.110096
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Herpes stromal keratitis is the leading cause of infectious blindness in the western world. Infection by HSV1 is most common, but VZV and hCMV also infect the cornea. Multiple models of HSV1 corneal infection exist, but none for VZV and hCMV because of their host specificity. Here, we used commercially available 3D human corneal epithelial equivalents (HCEE) to study infection by these herpesviruses. HCEE was infected by HSV-1 and hCMV without requiring scarification and resulted in spreading infections. Spread of HSV-1 infection was rapid, while that of hCMV was slow. In contrast, infections with VZV required damage to the HCEE and did not spread. Acyclovir dramatically reduced replication of HSV-1 in this model. We conclude that highly quality-controlled, readily available HCEE is a useful model to study human-restricted herpesvirus infection of the human corneal epithelium and for screening of antiviral drugs for treating HSK in an 3D model system.
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页数:9
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