Journal
FRONTIERS IN IMMUNOLOGY
Volume 13, Issue -, Pages -Publisher
FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2022.900556
Keywords
COVID-19; vaccination; pregnancy; gamma delta-T cells; V delta 1(+) T cells; V delta 2(+) T cells
Categories
Funding
- National Natural Science Foundation of China
- Natural Science Foundation of Guangdong Province, China
- Basic and Applied Basic Research Fund of Guangdong Province
- [32000616]
- [31570898]
- [2021A1515011441]
- [2020A1515111203]
- [2016A030313112]
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This study investigated the effects of COVID-19 vaccination on gamma delta-T cells in pregnant women. The results showed that the frequency of CD3(+)gamma delta-T+ cells was lower in vaccinated pregnant women compared to unvaccinated pregnant women. However, there was no significant difference in the frequency of CD3(+)gamma delta-T+ cells between non-pregnant vaccinated women and vaccinated pregnant women. Additionally, there were no significant differences in the frequencies of different subsets of gamma delta-T cells between pregnant women with or without COVID-19 vaccination.
Up to now, there has been insufficient clinical data to support the safety and effects of vaccination on pregnancy post COVID-19 vaccination. The gamma delta-T cells are considered an important component in the immune system to fight against viral infection and exhibit critical roles throughout the pregnancy period. However, the immunological roles of gamma delta-T cells in pregnant women with the COVID-19 vaccination remain unclear. Therefore, the objective of this study is to investigate the alteration of frequency and expression pattern of activation receptors and inhibitory receptors in gamma delta-T cell and its subsets in peripheral blood samples collected from non-pregnant vaccinated women, vaccinated pregnant women, and unvaccinated pregnant women. Our findings indicated that the frequency of CD3(+)gamma delta-T+ cells is lower in vaccinated pregnant women than in unvaccinated pregnant women. But no significant difference was found in the frequency of CD3(+)gamma delta-T+ cells between non-pregnant vaccinated women and vaccinated pregnant women. In addition, there were no significant differences in the frequencies of CD3(+)gamma delta-T+V delta 1(+)T cells, CD3(+)gamma delta-T+V delta 2(+)T cells, CD3(+)gamma delta-T+V delta 1(-)V delta 2(-)T cells, and V delta 1(+)T cell/V delta 2(+)T cell ratio between the pregnant women with or without COVID-19 vaccination. Similar results were found after comparing non-pregnant and pregnant women who received the COVID-19 vaccine. However, there was a significant difference in the fraction of V delta 1(-)V delta 2(-)T cells in CD3(+)gamma delta-T+ cells between non-pregnant vaccinated women and vaccinated pregnant women. The frequency of NKG2D(+) cells in V delta 2(+)T cells was not significantly different in the vaccinated pregnant women when compared to that in unvaccinated pregnant women or non-pregnant vaccinated women. But the percentage of NKG2D(+) cells in V delta 1(+)T cells was the lowest in pregnant women after COVID-19 vaccination. Furthermore, down-regulation of NKP46 and NKP30 were found in V delta 2(+)T and V delta 1(+)T cells in the vaccinated pregnant women, respectively. After the vaccination, up-regulation of PD-1 expression in V delta 1(+)T cells and V delta 2(+)T cells indicated gamma delta-T cells could respond to COVID-19 vaccination and display an exhausted phenotype following activation. In conclusion, COVID-19 vaccination influences subtypes of gamma delta-T cells during pregnancy, but the side effects might be limited. The phenotypical changes of V delta 1(+)T cells and V delta 2(+)T cells will be a promising predictor for evaluating the clinical outcome of the COVID-19 vaccine.
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