2022
DOI: 10.1165/rcmb.2021-0535oc
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Unique Allergic Asthma Phenotypes in Offspring of House Dust Mite–exposed Mice

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Cited by 9 publications
(7 citation statements)
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“…Behavioural outcomes included locomotion [ 50 , 73 , 74 ], social activity [ 50 , 73 , 74 ], anxiety-like behaviours [ 50 , 73 , 74 ] and repetitive behaviours [ 73 , 74 ]. Nonlung organ outcomes include neuronal morphology [ 32 , 72 ] and adrenal medulla histology and protein expression [ 31 , 75 ]. Genetic and epigenetic outcomes included whole-genome DNA methylation changes [ 62 ], genotype profiling of splenic dendritic cells [ 62 ], gene expression in airways [ 76 ] and the microglial transcriptome [ 77 ].…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Behavioural outcomes included locomotion [ 50 , 73 , 74 ], social activity [ 50 , 73 , 74 ], anxiety-like behaviours [ 50 , 73 , 74 ] and repetitive behaviours [ 73 , 74 ]. Nonlung organ outcomes include neuronal morphology [ 32 , 72 ] and adrenal medulla histology and protein expression [ 31 , 75 ]. Genetic and epigenetic outcomes included whole-genome DNA methylation changes [ 62 ], genotype profiling of splenic dendritic cells [ 62 ], gene expression in airways [ 76 ] and the microglial transcriptome [ 77 ].…”
Section: Resultsmentioning
confidence: 99%
“…Fewer studies (15%) sensitised and challenged mothers with HDM, which is the most prevalent allergen in human asthma [ 80 ]. Allergic asthma can be further divided into a mild–moderate phenotype driven by T-helper type 2 cells (Th2), or a moderate–severe phenotype driven by T-helper type 1 or 17 cells (Th1/Th17) [ 72 , 81 ]. Importantly, the specific cells involved in the allergic immune response can alter progeny outcomes.…”
Section: Discussionmentioning
confidence: 99%
“…19 Further evidence of immune programming of T cells comes from another murine model of maternal asthma where asthmatic offspring exhibited a moderate to severe T H 1/T H 17 inflammatory signature in response to allergen challenge, compared with the milder T H 2 signature of their mothers. 20 In sheep, near-term fetuses from asthmatic mothers had lower lung surfactant expression, lower type II alveolar epithelial cell density, and higher proportions of CD44 positive lymphocytes in the thymus, 21,22 which could lead to poorer neonatal lung function and greater inflammatory response, respectively. This evidence from preclinical models suggests that the in utero environment of an asthmatic mother alters lung and immune development of progeny.…”
Section: Introductionmentioning
confidence: 99%
“…In this model, reduced maternal ovalbumin exposure pre-mating or blocking interleukin 4 (IL-4) by anti-mouse IL-4 antibody prevented adverse respiratory outcomes for the offspring of asthmatic mothers 19 . Further evidence of immune programming of T cells comes from another murine model of maternal asthma where asthmatic offspring exhibited a moderate to severe T H 1/T H 17 inflammatory signature in response to allergen challenge, compared with the milder T H 2 signature of their mothers 20 . In sheep, near-term fetuses from asthmatic mothers had lower lung surfactant expression, lower type II alveolar epithelial cell density, and higher proportions of CD44 positive lymphocytes in the thymus, 21,22 which could lead to poorer neonatal lung function and greater inflammatory response, respectively.…”
Section: Introductionmentioning
confidence: 99%
“…In this issue of the Journal , Lebold and colleagues (pp. 89–98 ) report on their investigations of allergic airway inflammation and airway hyperresponsiveness (AHR) in mouse pups born from allergen-challenged dams ( 7 ). In the model, female mice were chronically challenged with PBS or a common household allergen, house dust mite (HDM), before and during pregnancy.…”
mentioning
confidence: 99%