Targets of immunomodulation in bacterial endophthalmitis.
Endophthalmitis toll-like receptor cytokine chemokine intravitreal injection immunomodulation
Journal
Progress in retinal and eye research
ISSN: 1873-1635
Titre abrégé: Prog Retin Eye Res
Pays: England
ID NLM: 9431859
Informations de publication
Date de publication:
11 2019
11 2019
Historique:
received:
12
03
2019
revised:
20
05
2019
accepted:
23
05
2019
pubmed:
1
6
2019
medline:
25
4
2020
entrez:
1
6
2019
Statut:
ppublish
Résumé
Bacterial infection of the posterior segment of the eye (endophthalmitis) leads to a robust host response that often results in irreversible damage to the layers of the retina, significant vision loss, and in some patients, enucleation of the globe. While a great deal of effort has gone into understanding the role of bacterial virulence factors in disease initiation and propagation, it is becoming increasingly clear that the host response to infection plays a major role in causing the damage associated with endophthalmitis. Researchers have identified the host receptors which detect infecting organisms and initiate the cascade of events that result in inflammation. This inflammation may damage nonregenerative tissues of the eye while attempting to clear the infection. Both Gram-positive and Gram-negative bacteria can cause endophthalmitis. These organisms initiate an immune response by activating toll-like receptor (TLR) pathways. Once an inflammatory response is initiated, the expression of immunomodulators, such as proinflammatory chemokines and cytokines, affect the recruitment of PMNs and other inflammatory cells into the eye. We and others have reported that knockout mice that do not express specific inflammatory pathways and molecules have an attenuated response to infection and retain significant retinal function. These findings suggest that host immune mediators are important components of the response to infections in the posterior segment of the eye, and the timing and level of their production may be related to the severity of the damage and the ultimate visual outcome. If that is the case, a better understanding of the complex and often redundant role of these pathways and inflammatory mediators may identify host molecules as potential anti-inflammatory therapeutic targets. This review highlights potential anti-inflammatory targets during acute inflammation in endophthalmitis, compares and contrasts those with findings in other models of ocular inflammation, and translates current immunomodulatory strategies for other types of infection and inflammation to this blinding disease. Given the poor visual outcomes seen in patients treated with antibiotics alone or in combination with corticosteroids, immunomodulation in addition to antibiotic therapy might be more effective in preserving vision than current regimens.
Identifiants
pubmed: 31150824
pii: S1350-9462(19)30027-8
doi: 10.1016/j.preteyeres.2019.05.004
pmc: PMC6881541
mid: NIHMS1531168
pii:
doi:
Substances chimiques
Cytokines
0
Toll-Like Receptor 2
0
Toll-Like Receptor 4
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
100763Subventions
Organisme : NEI NIH HHS
ID : R21 EY028066
Pays : United States
Organisme : NEI NIH HHS
ID : P30 EY021725
Pays : United States
Organisme : NEI NIH HHS
ID : R01 EY025947
Pays : United States
Organisme : NEI NIH HHS
ID : R01 EY024140
Pays : United States
Organisme : NEI NIH HHS
ID : R21 EY022466
Pays : United States
Organisme : NEI NIH HHS
ID : R01 EY012985
Pays : United States
Organisme : NEI NIH HHS
ID : R01 EY028810
Pays : United States
Informations de copyright
Copyright © 2019 Elsevier Ltd. All rights reserved.
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