The immunological link between neonatal lung and eye disease
Abstract Bronchopulmonary dysplasia (BPD) and retinopathy of prematurity (ROP) are two neonatal diseases of major clinical importance, arising in large part as a consequence of supplemental oxygen therapy used to promote the survival of preterm infants. The presence of coincident inflammation in the...
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doaj-331417e2b13847c2858f16ca0c0795c12021-08-26T06:40:28ZengWileyClinical & Translational Immunology2050-00682021-01-01108n/an/a10.1002/cti2.1322The immunological link between neonatal lung and eye diseaseLakshanie C Wickramasinghe0Peter vanWijngaarden1Evelyn Tsantikos2Margaret L Hibbs3Leukocyte Signalling Laboratory Department of Immunology and Pathology Central Clinical School Monash University Melbourne VIC AustraliaOphthalmology Department of Surgery University of Melbourne Melbourne VIC AustraliaLeukocyte Signalling Laboratory Department of Immunology and Pathology Central Clinical School Monash University Melbourne VIC AustraliaLeukocyte Signalling Laboratory Department of Immunology and Pathology Central Clinical School Monash University Melbourne VIC AustraliaAbstract Bronchopulmonary dysplasia (BPD) and retinopathy of prematurity (ROP) are two neonatal diseases of major clinical importance, arising in large part as a consequence of supplemental oxygen therapy used to promote the survival of preterm infants. The presence of coincident inflammation in the lungs and eyes of neonates receiving oxygen therapy indicates that a dysregulated immune response serves as a potential common pathogenic factor for both diseases. This review examines the current state of knowledge of immunological dysregulation in BPD and ROP, identifying similarities in the cellular subsets and inflammatory cytokines that are found in the alveoli and retina during the active phase of these diseases, indicating possible mechanistic overlap. In addition, we highlight gaps in the understanding of whether these responses emerge independently in the lung and retina as a consequence of oxygen exposure or arise because of inflammatory spill‐over from the lung. As BPD and ROP are anatomically distinct, they are often considered discreet disease entities and are therefore treated separately. We propose that an improved understanding of the relationship between BPD and ROP is key to the identification of novel therapeutic targets to treat or prevent both conditions simultaneously.https://doi.org/10.1002/cti2.1322bronchopulmonary dysplasiadisease associationinflammationneonatal immune systemretinopathy of prematuritysupplemental oxygen |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Lakshanie C Wickramasinghe Peter vanWijngaarden Evelyn Tsantikos Margaret L Hibbs |
spellingShingle |
Lakshanie C Wickramasinghe Peter vanWijngaarden Evelyn Tsantikos Margaret L Hibbs The immunological link between neonatal lung and eye disease Clinical & Translational Immunology bronchopulmonary dysplasia disease association inflammation neonatal immune system retinopathy of prematurity supplemental oxygen |
author_facet |
Lakshanie C Wickramasinghe Peter vanWijngaarden Evelyn Tsantikos Margaret L Hibbs |
author_sort |
Lakshanie C Wickramasinghe |
title |
The immunological link between neonatal lung and eye disease |
title_short |
The immunological link between neonatal lung and eye disease |
title_full |
The immunological link between neonatal lung and eye disease |
title_fullStr |
The immunological link between neonatal lung and eye disease |
title_full_unstemmed |
The immunological link between neonatal lung and eye disease |
title_sort |
immunological link between neonatal lung and eye disease |
publisher |
Wiley |
series |
Clinical & Translational Immunology |
issn |
2050-0068 |
publishDate |
2021-01-01 |
description |
Abstract Bronchopulmonary dysplasia (BPD) and retinopathy of prematurity (ROP) are two neonatal diseases of major clinical importance, arising in large part as a consequence of supplemental oxygen therapy used to promote the survival of preterm infants. The presence of coincident inflammation in the lungs and eyes of neonates receiving oxygen therapy indicates that a dysregulated immune response serves as a potential common pathogenic factor for both diseases. This review examines the current state of knowledge of immunological dysregulation in BPD and ROP, identifying similarities in the cellular subsets and inflammatory cytokines that are found in the alveoli and retina during the active phase of these diseases, indicating possible mechanistic overlap. In addition, we highlight gaps in the understanding of whether these responses emerge independently in the lung and retina as a consequence of oxygen exposure or arise because of inflammatory spill‐over from the lung. As BPD and ROP are anatomically distinct, they are often considered discreet disease entities and are therefore treated separately. We propose that an improved understanding of the relationship between BPD and ROP is key to the identification of novel therapeutic targets to treat or prevent both conditions simultaneously. |
topic |
bronchopulmonary dysplasia disease association inflammation neonatal immune system retinopathy of prematurity supplemental oxygen |
url |
https://doi.org/10.1002/cti2.1322 |
work_keys_str_mv |
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