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...

Full description

Bibliographic Details
Main Authors: Lakshanie C Wickramasinghe, Peter vanWijngaarden, Evelyn Tsantikos, Margaret L Hibbs
Format: Article
Language:English
Published: Wiley 2021-01-01
Series:Clinical & Translational Immunology
Subjects:
Online Access:https://doi.org/10.1002/cti2.1322
id doaj-331417e2b13847c2858f16ca0c0795c1
record_format Article
spelling 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 AT lakshaniecwickramasinghe theimmunologicallinkbetweenneonatallungandeyedisease
AT petervanwijngaarden theimmunologicallinkbetweenneonatallungandeyedisease
AT evelyntsantikos theimmunologicallinkbetweenneonatallungandeyedisease
AT margaretlhibbs theimmunologicallinkbetweenneonatallungandeyedisease
AT lakshaniecwickramasinghe immunologicallinkbetweenneonatallungandeyedisease
AT petervanwijngaarden immunologicallinkbetweenneonatallungandeyedisease
AT evelyntsantikos immunologicallinkbetweenneonatallungandeyedisease
AT margaretlhibbs immunologicallinkbetweenneonatallungandeyedisease
_version_ 1721195979458215936