Published online Nov 14, 2018. doi: 10.3748/wjg.v24.i42.4787
Peer-review started: July 23, 2018
First decision: August 25, 2018
Revised: August 29, 2018
Accepted: October 5, 2018
Article in press: October 5, 2018
Published online: November 14, 2018
Processing time: 115 Days and 13.5 Hours
The delivery mode may impact newborn’s immune system with possible short-term and long-term consequences. Several studies suggest that caesarian section (C-section) may come at a price for the newborn. C-section delivery prevents the exposure of newborn to the mother’s microbiome in the birth canal. Whereas vaginal delivery and exposure to maternal microbiota via breastfeeding are evolutionary important to the newborn’s development and health. However, the impacts of mode of delivery in twins is not fully understood.
Disrupting the mother-to-child transmission of microbiota by C-sections may result in increased risk of asthma, celiac disease, obesity and autoimmune diseases. Thus, investigating the impact of delivery mode on newborns immune system development is crucial for protecting this highly fragile population.
We investigated whether delivery mode by C-section compared to vaginal delivery in twins can influence the immunological components of their cord blood and placenta. In addition, our aim was to determine if C-section delivery impacts the frequency of CD71+ erythroid cells in cord blood and placenta tissues.
We performed immune cells isolation from fresh cord blood and placenta tissues. Then, immunophenotyping was performed for different immune cell subsets in cord blood and placenta of twins. Finally, CD71+ erythroid cells were isolated for RNA isolation and quantitative polymerase chain reaction PCR (qPCR) analysis.
Our results indicated lower frequency of immune cells in cord blood of C-section delivered newborn compared to the vaginally delivered newborn. In contrast, we observed higher percentages of monocytes and neutrophils in placenta tissues of C-section delivered newborns and higher expression of inhibitory receptors on T cells. More importantly, we found lower frequency of CD71+ erythroid cells in both cord blood and placenta of C-section delivered newborn compared to the vaginally delivered newborn. Interestingly, CD71+ erythroid cells from C-section delivered newborn had a different gene profile compared to the vaginally delivered one.
Our study provides another piece of evidence that delivery mode can influence the newborn’s immune system. In particular, we have investigated this in a case of twins one delivered by C-section while the other by vaginal route. We have shown for the very first time that mode of delivery impacts the frequency and functionality of CD71+ erythroid cells in cord blood and placenta tissues. Our findings suggest mode of delivery may result in immunological changes with possible long-term effects on the offspring.
C-section delivery may negatively impact neonatal immune system. Our study is a clear example indicating immunological differences in cord blood and placenta tissues of twins. Further longitudinal studies are required to investigate potential short-term and long-term impacts of C-section vs vaginally delivery in twins.