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Host Immune Response and Associated Clinical Features in a Primary Cytomegalovirus Eye Infection Model Using Anterior Chamber Inoculation

PURPOSE: To investigate the pathogenesis of cytomegalovirus (CMV)-associated anterior segment infection in immunocompetent hosts and evaluate the effects of ganciclovir and glucocorticoid treatment in management of the disease. METHODS: We used an inoculation model to reproduce CMV anterior segment...

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Autores principales: Su, Chien-Chia, Gao, Chia-Mao, Peng, Fu-Ti, Jou, Tzuu-Shuh, Wang, I-Jong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9123510/
https://www.ncbi.nlm.nih.gov/pubmed/35579904
http://dx.doi.org/10.1167/iovs.63.5.18
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author Su, Chien-Chia
Gao, Chia-Mao
Peng, Fu-Ti
Jou, Tzuu-Shuh
Wang, I-Jong
author_facet Su, Chien-Chia
Gao, Chia-Mao
Peng, Fu-Ti
Jou, Tzuu-Shuh
Wang, I-Jong
author_sort Su, Chien-Chia
collection PubMed
description PURPOSE: To investigate the pathogenesis of cytomegalovirus (CMV)-associated anterior segment infection in immunocompetent hosts and evaluate the effects of ganciclovir and glucocorticoid treatment in management of the disease. METHODS: We used an inoculation model to reproduce CMV anterior segment infection in immunocompetent rats. Flow cytometry, cytokine analysis, histopathological sections, and quantitative polymerase chain reaction were performed to investigate the immune response after CMV infection. The effects of ganciclovir and glucocorticoid treatment were also assessed. RESULTS: Anterior chamber inoculation of CMV in rats provoked characteristic pathological features of human CMV anterior segment infection. The innate and adaptive immunity sequentially developed in an anterior segment after inoculation, and the elevation of intraocular pressure (IOP) was highly associated with ocular infiltration and inflammation. Early ocular immune response reduced virus DNA in the anterior segment and alleviated viral lymphadenopathy. Early intervention with ganciclovir enhanced the release of cytokines associated with T response and facilitated recruitment of NKT and T cells in drainage lymph nodes. Glucocorticoid treatment, alone or combined with ganciclovir, decreased elevation of IOP but also impeded DNA clearance. CONCLUSIONS: The inoculation model reproduced characteristic pathological features of human CMV anterior segment infection. The use of glucocorticoid in current practice may hinder viral clearance, and ganciclovir therapy can assist cytokine expression to combat the virus.
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spelling pubmed-91235102022-05-22 Host Immune Response and Associated Clinical Features in a Primary Cytomegalovirus Eye Infection Model Using Anterior Chamber Inoculation Su, Chien-Chia Gao, Chia-Mao Peng, Fu-Ti Jou, Tzuu-Shuh Wang, I-Jong Invest Ophthalmol Vis Sci Immunology and Microbiology PURPOSE: To investigate the pathogenesis of cytomegalovirus (CMV)-associated anterior segment infection in immunocompetent hosts and evaluate the effects of ganciclovir and glucocorticoid treatment in management of the disease. METHODS: We used an inoculation model to reproduce CMV anterior segment infection in immunocompetent rats. Flow cytometry, cytokine analysis, histopathological sections, and quantitative polymerase chain reaction were performed to investigate the immune response after CMV infection. The effects of ganciclovir and glucocorticoid treatment were also assessed. RESULTS: Anterior chamber inoculation of CMV in rats provoked characteristic pathological features of human CMV anterior segment infection. The innate and adaptive immunity sequentially developed in an anterior segment after inoculation, and the elevation of intraocular pressure (IOP) was highly associated with ocular infiltration and inflammation. Early ocular immune response reduced virus DNA in the anterior segment and alleviated viral lymphadenopathy. Early intervention with ganciclovir enhanced the release of cytokines associated with T response and facilitated recruitment of NKT and T cells in drainage lymph nodes. Glucocorticoid treatment, alone or combined with ganciclovir, decreased elevation of IOP but also impeded DNA clearance. CONCLUSIONS: The inoculation model reproduced characteristic pathological features of human CMV anterior segment infection. The use of glucocorticoid in current practice may hinder viral clearance, and ganciclovir therapy can assist cytokine expression to combat the virus. The Association for Research in Vision and Ophthalmology 2022-05-17 /pmc/articles/PMC9123510/ /pubmed/35579904 http://dx.doi.org/10.1167/iovs.63.5.18 Text en Copyright 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Immunology and Microbiology
Su, Chien-Chia
Gao, Chia-Mao
Peng, Fu-Ti
Jou, Tzuu-Shuh
Wang, I-Jong
Host Immune Response and Associated Clinical Features in a Primary Cytomegalovirus Eye Infection Model Using Anterior Chamber Inoculation
title Host Immune Response and Associated Clinical Features in a Primary Cytomegalovirus Eye Infection Model Using Anterior Chamber Inoculation
title_full Host Immune Response and Associated Clinical Features in a Primary Cytomegalovirus Eye Infection Model Using Anterior Chamber Inoculation
title_fullStr Host Immune Response and Associated Clinical Features in a Primary Cytomegalovirus Eye Infection Model Using Anterior Chamber Inoculation
title_full_unstemmed Host Immune Response and Associated Clinical Features in a Primary Cytomegalovirus Eye Infection Model Using Anterior Chamber Inoculation
title_short Host Immune Response and Associated Clinical Features in a Primary Cytomegalovirus Eye Infection Model Using Anterior Chamber Inoculation
title_sort host immune response and associated clinical features in a primary cytomegalovirus eye infection model using anterior chamber inoculation
topic Immunology and Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9123510/
https://www.ncbi.nlm.nih.gov/pubmed/35579904
http://dx.doi.org/10.1167/iovs.63.5.18
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