Clinical characteristics and antibody responses to Omicron variants among pregnant women in China during the December 2022-April 2023 COVID-19 pandemic wave.

Publication date: Apr 01, 2026

Clinical characteristics and humoral immune responses in pregnant women following natural SARS-CoV-2 Omicron infection remain unclear, particularly in those previously receiving inactivated vaccines, which may induce immune imprinting and affect cross-neutralization against emerging Omicron subvariants. This cross-sectional investigation was conducted in Zhejiang Province between December 2022 and April 2023. A total of 223 pregnant women with a gestational age of at least six weeks and 31 healthy non-pregnant women were recruited as research subjects and controls. Serum specimens were collected to determine anti-RBD IgG levels by ELISA, alongside pseudovirus neutralizing antibody titers against the prototype strain and Omicron BA. 4/5, XBB. 1.5 subvariants. Relevant clinical information was gathered through questionnaires, and multivariate regression analysis was applied to identify influencing factors of immune response characteristics. Acute COVID-19 symptom profiles were comparable between pregnant women and non-pregnant healthy women (P > 0. 05). Among questionnaire respondents, pregnant individuals had markedly prolonged symptom recovery, with a notably higher proportion taking over one week to recover (73. 0% vs. 23. 1%, P = 0. 045), and presented a significantly higher medical consultation rate (73. 0% vs. 15. 4%, P

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Concepts Keywords
April Adult
China Antibodies, Neutralizing
Pregnancy Antibodies, Neutralizing
Pseudovirus Antibodies, Viral
Antibodies, Viral
Antibody Formation
antibody response
China
clinical characteristics
Coronavirus Infections
COVID-19
COVID-19
Cross-Sectional Studies
Female
Humans
Immunoglobulin G
Immunoglobulin G
inactivated vaccine
omicron
Pandemics
Pregnancy
pregnancy
Pregnancy Complications, Infectious
SARS-CoV-2
Spike Glycoprotein, Coronavirus
Spike Glycoprotein, Coronavirus
Young Adult

Semantics

Type Source Name
disease MESH COVID-19 pandemic
disease MESH infection
disease MESH strain
pathway REACTOME SARS-CoV-2 Infection
drug DRUGBANK Coenzyme M
pathway REACTOME Reproduction
disease MESH Infectious Disease
pathway REACTOME Infectious disease
disease MESH severe acute respiratory syndrome
disease MESH clinical progression
disease MESH breakthrough infection
disease MESH ADCC
disease MESH PBS
disease MESH Coronavirus Infections
disease MESH Pregnancy Complications Infectious

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