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Isolation of Group 2 Innate Lymphoid Cells from Mouse Nasal Mucosa to Detect the Expression of CD226
Published on: May 10, 2022
Cord blood group 2 innate lymphoid cells are associated with lung function at 6 weeks of age
Gabriela Martins Costa Gomes1, Patricia de Gouveia Belinelo1, Malcolm R Starkey1,2,3
1Priority Research Centre GrowUpWell® - Hunter Medical Research Institute The University of Newcastle Newcastle NSW Australia.
Insights
Infant lung function is linked to fetal immune cells. Higher levels of fetal group 2 innate lymphoid cells (ILC2) in cord blood correlate with poorer lung function in newborns born to mothers with asthma.
Area of Science:
- Immunology
- Neonatal Health
- Respiratory Medicine
Background:
- Maternal asthma during pregnancy is associated with reduced offspring lung function.
- Human fetal lungs exhibit a 10-fold higher accumulation of group 2 innate lymphoid cells (ILC2) compared to adult lungs.
- Limited data exists on fetal ILC2 levels and their impact on early-life respiratory health.
Purpose of the Study:
- To investigate cord blood immune cell populations in infants born to mothers with asthma.
- To explore the association between fetal ILC2 numbers and infant lung function.
Main Methods:
- Cord blood samples were collected from infants of asthmatic mothers.
- Immune cells were analyzed using traditional gating and computational methods (t-SNE, PhenoGraph).
- Infant lung function was assessed at 6 weeks using tPTEF/tE% and Lung Clearance Index (LCI).
Main Results:
- 91 out of 110 infants were immunophenotyped.
- Lung function measurements were obtained from 43 (tPTEF/tE%) and 34 (LCI) infants.
- Increased fetal ILC2 numbers, specifically with CRTh2 expression, were associated with poorer infant lung function at 6 weeks.
Conclusions:
- Fetal immune responses, particularly ILC2 levels, may influence or predict early-life lung function outcomes.
- This suggests a potential link between the fetal immune environment and respiratory health trajectory.
Objective:
Offspring born to mothers with asthma in pregnancy are known to have lower lung function which tracks with age. Human group 2 innate lymphoid cells (ILC2) accumulate in foetal lungs, at 10-fold higher levels compared to adult lungs. However, there are no data on foetal ILC2 numbers and the association with respiratory health outcomes such as lung function in early life. We aimed to investigate cord blood immune cell populations from babies born to mothers with asthma in pregnancy.
Methods:
Cord blood from babies born to asthmatic mothers was collected, and cells were stained in whole cord blood. Analyses were done using traditional gating approaches and computational methodologies (t-distributed stochastic neighbour embedding and PhenoGraph algorithms). At 6 weeks of age, the time to peak tidal expiratory flow as a percentage of total expiratory flow time (tPTEF/tE%) was determined as well as Lung Clearance Index (LCI), during quiet natural sleep.
Results:
Of 110 eligible infants (March 2017 to November 2019), 91 were successfully immunophenotyped (82.7%). Lung function was attempted in 61 infants (67.0%), and 43 of those infants (70.5% of attempted) had technically acceptable tPTEF/tE% measurements. Thirty-four infants (55.7% of attempted) had acceptable LCI measurements. Foetal ILC2 numbers with increased expression of chemoattractant receptor-homologous molecule (CRTh2), characterised by two distinct analysis methodologies, were associated with poorer infant lung function at 6 weeks of age."
Conclusion:
Foetal immune responses may be a surrogate variable for or directly influence lung function outcomes in early life.
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