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ORIGINAL RESEARCH article

Front. Cell. Infect. Microbiol.

Sec. Virus and Host

Volume 15 - 2025 | doi: 10.3389/fcimb.2025.1551602

Impact of Omicron BA.5 Infection on Maternal and Neonatal Outcomes

Provisionally accepted
Xiaoping Tang Xiaoping Tang 1,2*Lu Li Lu Li 1Ruitian Hou Ruitian Hou 1,2,3Zan Mai Zan Mai 4Li Liang Li Liang 4Zheng Li Zheng Li 4Bin Long Bin Long 4Lin Chen Lin Chen 4Ping Feng Ping Feng 4Baojun Yang Baojun Yang 4Lijie Yang Lijie Yang 4Lianhua Tang Lianhua Tang 4Peizhi Wang Peizhi Wang 4Fan Zhong Fan Zhong 4Mei Chu Mei Chu 4Huichao Liang Huichao Liang 4*
  • 1 Guangzhou Medical University, Guangzhou, China
  • 2 Guangzhou National Laboratory, Guangzhou, Guangdong, China
  • 3 Institute of Infectious Diseases, Eighth People's Hospital of Guangzhou, Guangzhou, China
  • 4 Guangzhou Eighth People's Hospital, Guangzhou, Guangdong Province, China

The final, formatted version of the article will be published soon.

    Introduction: Physiological and immunological adaptations during pregnancy may elevate the risk of adverse perinatal and neonatal outcomes associated with SARS-CoV-2 infection. This retrospective study aimed to explore the clinical characteristics of pregnant women and the maternal and neonatal outcomes during pregnancy following Omicron BA.5 variant infection. Methods: Clinical and laboratory data from 208 pregnant women with Omicron BA.5 infection were analyzed, including intrapartum and postpartum records of 24 infected parturients and their neonates, with comparisons made to uninfected controls. Multiple specimen types, including placental membranes and amniotic fluid, were collected for SARS-CoV-2 RNA detection. Results: Among 208 infected pregnant women, 91.8% (191/208) had received at least one dose of inactivated SARS-CoV-2 vaccine. BA.5 infection in pregnant women exhibited viral load, clearance time and symptom profiles comparable to the general population, with no severe or critical illness being found. No significant differences were noted between pregnant women over and under 35 years. BA.5 infection reduced the white blood cell counts but did not aggravate the hypercoagulability compared to the uninfected controls. Neonates of infected mothers showed a higher rate of intrauterine hypoxia than those controls. However, no SARS-CoV-2 RNA was detectable in any of the neonatal oropharyngeal swabs as well as maternal specimens, including placental membranes, amniotic fluid, vaginal secretions, breast milk, venous blood and ascites. Conclusion: This study demonstrates favorable maternal and neonatal outcomes in vaccinated pregnant women with BA.5 infection following timely medical intervention. Neonates born to infected mothers have an extremely low risk of vertical transmission. Nevertheless, enhanced prenatal care for pregnant women with COVID-19 remains essential to mitigate adverse neonatal outcomes.

    Keywords: Omicron BA.5, Pregnancy, neonate, Vertical transmission, Vaccination

    Received: 26 Dec 2024; Accepted: 04 Mar 2025.

    Copyright: © 2025 Tang, Li, Hou, Mai, Liang, Li, Long, Chen, Feng, Yang, Yang, Tang, Wang, Zhong, Chu and Liang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence:
    Xiaoping Tang, Guangzhou Medical University, Guangzhou, China
    Huichao Liang, Guangzhou Eighth People's Hospital, Guangzhou, 510000, Guangdong Province, China

    Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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