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Intranasal Immunization and Milk Collection in Studies of Maternal Immunization in New Zealand White Rabbits Oryctolagus cuniculus
Published on: July 31, 2021
Compromised SARS-CoV-2-specific placental antibody transfer.
Caroline Atyeo1, Krista M Pullen2, Evan A Bordt3
1Ragon Institute of MGH, MIT, and Harvard, Cambridge, MA 02139, USA; PhD Program in Virology, Division of Medical Sciences, Harvard University, Boston, MA 02115, USA.
Maternal SARS-CoV-2 infection, especially in the third trimester, reduces antibody transfer to infants. This study reveals altered antibody glycosylation and compensatory mechanisms, offering insights for maternal vaccine development.
Area of Science:
- Immunology
- Maternal-fetal medicine
- Virology
Background:
- Pregnant women experience more severe SARS-CoV-2 disease.
- The impact of maternal SARS-CoV-2 infection on infant immunity transfer is unclear.
- Maternal infections can compromise placental antibody transfer, but mechanisms are unknown.
Purpose of the Study:
- To investigate SARS-CoV-2-specific antibody transfer across the placenta.
- To characterize the Fc profile of transferred antibodies.
- To understand mechanisms affecting antibody transfer during pregnancy.
Main Methods:
- Systems serology was employed to analyze antibody profiles.
- Antibodies specific to influenza, pertussis, and SARS-CoV-2 were studied.
- Placental transfer and functional activity of antibodies were assessed.
Main Results:
- Influenza- and pertussis-specific antibodies transferred efficiently.
- SARS-CoV-2-specific antibody transfer was significantly reduced, especially in third-trimester infections.
- Reduced transfer was linked to altered antibody glycosylation and partially compensated by increased IgG and placental FCGR3A expression.
Conclusions:
- Maternal SARS-CoV-2 infection impairs antibody transfer to neonates.
- Altered antibody glycosylation and placental factors influence transfer efficiency.
- Findings suggest compensatory mechanisms and inform maternal vaccine strategies.
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