Nanoparticle ocular immunotherapy for herpesvirus surface eye infections evaluated in cat infection model.

Ocular herpes simplex type 1 (HSV-1) infections can trigger conjunctivitis, keratitis, uveitis, and occasionally retinitis, and is a major cause of blindness worldwide. The infections are lifelong and can often recrudesce during periods of stress or immune suppression. Currently HSV-1 infections of...

Full description

Bibliographic Details
Main Authors: Michael Lappin, Kathryn Wotman, Lyndah Chow, Maggie Williams, Jennifer Hawley, Steven Dow
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2023-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0279462
_version_ 1797866830076837888
author Michael Lappin
Kathryn Wotman
Lyndah Chow
Maggie Williams
Jennifer Hawley
Steven Dow
author_facet Michael Lappin
Kathryn Wotman
Lyndah Chow
Maggie Williams
Jennifer Hawley
Steven Dow
author_sort Michael Lappin
collection DOAJ
description Ocular herpes simplex type 1 (HSV-1) infections can trigger conjunctivitis, keratitis, uveitis, and occasionally retinitis, and is a major cause of blindness worldwide. The infections are lifelong and can often recrudesce during periods of stress or immune suppression. Currently HSV-1 infections of the eye are managed primarily with anti-viral eye drops, which require frequent administration, can cause irritation, and may take weeks for full resolution of symptoms. We therefore evaluated the effectiveness of an ocular immune activating nanoparticle eye drop as a novel approach to treating HSV-1 infection, using a cat feline herpesvirus -1 (FHV-1) ocular infection model. In vitro studies demonstrated significant induction of both type I and II interferon responses by the liposome-dual TLR 3/9 agonist nanoparticles, along with suppression of FHV-1 replication. In cats with naturally occurring eye infections either proven or suspected to involve FHV-1, ocular nanoparticle treated animals experienced resolution of signs within several days of treatment, including resolution of keratitis and corneal ulcers. In a cat model of recrudescent FHV-1 infection, cats treated twice daily with immune nanoparticle eye drops experienced significant lessening of ocular signs of infection and significantly fewer episodes of viral shedding compared to control cats. Treatment was well-tolerated by all cats, without signs of drug-induced ocular irritation. We concluded therefore that non-specific ocular immunotherapy offers significant promise as a novel approach to treatment of HSV-1 and FHV-1 ocular infections.
first_indexed 2024-04-09T23:30:33Z
format Article
id doaj.art-3df5aa1e868046c3a2bb3a6557fce59a
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-04-09T23:30:33Z
publishDate 2023-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-3df5aa1e868046c3a2bb3a6557fce59a2023-03-21T05:31:47ZengPublic Library of Science (PLoS)PLoS ONE1932-62032023-01-01181e027946210.1371/journal.pone.0279462Nanoparticle ocular immunotherapy for herpesvirus surface eye infections evaluated in cat infection model.Michael LappinKathryn WotmanLyndah ChowMaggie WilliamsJennifer HawleySteven DowOcular herpes simplex type 1 (HSV-1) infections can trigger conjunctivitis, keratitis, uveitis, and occasionally retinitis, and is a major cause of blindness worldwide. The infections are lifelong and can often recrudesce during periods of stress or immune suppression. Currently HSV-1 infections of the eye are managed primarily with anti-viral eye drops, which require frequent administration, can cause irritation, and may take weeks for full resolution of symptoms. We therefore evaluated the effectiveness of an ocular immune activating nanoparticle eye drop as a novel approach to treating HSV-1 infection, using a cat feline herpesvirus -1 (FHV-1) ocular infection model. In vitro studies demonstrated significant induction of both type I and II interferon responses by the liposome-dual TLR 3/9 agonist nanoparticles, along with suppression of FHV-1 replication. In cats with naturally occurring eye infections either proven or suspected to involve FHV-1, ocular nanoparticle treated animals experienced resolution of signs within several days of treatment, including resolution of keratitis and corneal ulcers. In a cat model of recrudescent FHV-1 infection, cats treated twice daily with immune nanoparticle eye drops experienced significant lessening of ocular signs of infection and significantly fewer episodes of viral shedding compared to control cats. Treatment was well-tolerated by all cats, without signs of drug-induced ocular irritation. We concluded therefore that non-specific ocular immunotherapy offers significant promise as a novel approach to treatment of HSV-1 and FHV-1 ocular infections.https://doi.org/10.1371/journal.pone.0279462
spellingShingle Michael Lappin
Kathryn Wotman
Lyndah Chow
Maggie Williams
Jennifer Hawley
Steven Dow
Nanoparticle ocular immunotherapy for herpesvirus surface eye infections evaluated in cat infection model.
PLoS ONE
title Nanoparticle ocular immunotherapy for herpesvirus surface eye infections evaluated in cat infection model.
title_full Nanoparticle ocular immunotherapy for herpesvirus surface eye infections evaluated in cat infection model.
title_fullStr Nanoparticle ocular immunotherapy for herpesvirus surface eye infections evaluated in cat infection model.
title_full_unstemmed Nanoparticle ocular immunotherapy for herpesvirus surface eye infections evaluated in cat infection model.
title_short Nanoparticle ocular immunotherapy for herpesvirus surface eye infections evaluated in cat infection model.
title_sort nanoparticle ocular immunotherapy for herpesvirus surface eye infections evaluated in cat infection model
url https://doi.org/10.1371/journal.pone.0279462
work_keys_str_mv AT michaellappin nanoparticleocularimmunotherapyforherpesvirussurfaceeyeinfectionsevaluatedincatinfectionmodel
AT kathrynwotman nanoparticleocularimmunotherapyforherpesvirussurfaceeyeinfectionsevaluatedincatinfectionmodel
AT lyndahchow nanoparticleocularimmunotherapyforherpesvirussurfaceeyeinfectionsevaluatedincatinfectionmodel
AT maggiewilliams nanoparticleocularimmunotherapyforherpesvirussurfaceeyeinfectionsevaluatedincatinfectionmodel
AT jenniferhawley nanoparticleocularimmunotherapyforherpesvirussurfaceeyeinfectionsevaluatedincatinfectionmodel
AT stevendow nanoparticleocularimmunotherapyforherpesvirussurfaceeyeinfectionsevaluatedincatinfectionmodel