Neutralizing and binding antibody responses to SARS-CoV-2 with hybrid immunity in pregnancy.

Publication date: Aug 27, 2024

Hybrid immunity against SARS-CoV-2 has not been well studied in pregnancy. We conducted a comprehensive analysis of neutralizing antibodies (nAb) and binding antibodies in pregnant individuals who received mRNA vaccination, natural infection, or both. A third vaccine dose augmented nAb levels compared to the two-dose regimen or natural infection alone; this effect was more pronounced in hybrid immunity. There was reduced anti-Omicron nAb, but the maternal-fetal transfer efficiency remained comparable to that of other variants. Vaccine-induced nAbs were transferred more efficiently than infection-induced nAbs. Anti-spike receptor binding domain (RBD) IgG was associated with nAb against wild-type (Wuhan-Hu-1) following breakthrough infection. Both vaccination and infection-induced anti-RBD IgA, which was more durable than anti-nucleocapsid IgA. IgA response was attenuated in pregnancy compared to non-pregnant controls. These data provide additional evidence of augmentation of humoral immune responses in hybrid immunity in pregnancy.

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Concepts Keywords
Efficiency Anti
Mrna Antibodies
Nucleocapsid Binding
Pregnant Cov
Vaccine Hybrid
Iga
Immunity
Induced
Infection
Nab
Neutralizing
Pregnancy
Pregnant
Sars
Vaccination

Semantics

Type Source Name
disease VO vaccination
disease MESH infection
disease VO vaccine dose
disease VO dose
disease VO efficiency
disease VO vaccine
disease MESH breakthrough infection
disease VO effectiveness
disease MESH COVID 19
disease VO population
disease VO USA
disease MESH Infectious Diseases
disease VO effective
disease VO Glycoprotein
drug DRUGBANK Coenzyme M
disease VO vaccinated
disease VO immunization
disease VO titer
disease IDO blood
disease IDO history
disease IDO assay
drug DRUGBANK Proline
disease VO antibody titer
disease VO vaccination dose
disease IDO production
disease IDO host
disease VO frequency
disease IDO cell
disease MESH mutation rate
disease VO time
disease VO gene
disease IDO infectivity
drug DRUGBANK Angiotensin II
drug DRUGBANK Calcium
disease VO manufacturer
disease MESH Emergency
drug DRUGBANK (S)-Des-Me-Ampa
disease VO vaccine efficacy
disease VO pregnant women
drug DRUGBANK Modafinil
disease VO unvaccinated

Original Article

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