Literature DB >> 33910219

Antibody Response to Coronavirus Disease 2019 (COVID-19) Messenger RNA Vaccination in Pregnant Women and Transplacental Passage Into Cord Blood.

Malavika Prabhu1, Elisabeth A Murphy, Ashley C Sukhu, Jim Yee, Sunidhi Singh, Dorothy Eng, Zhen Zhao, Laura E Riley, Yawei J Yang.   

Abstract

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Year:  2021        PMID: 33910219      PMCID: PMC8288193          DOI: 10.1097/AOG.0000000000004438

Source DB:  PubMed          Journal:  Obstet Gynecol        ISSN: 0029-7844            Impact factor:   7.661


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INTRODUCTION

Pregnant women were excluded from initial clinical trials for coronavirus disease 2019 (COVID-19) vaccines[1,2]; thus, the understanding of the immunologic response to vaccination in pregnancy and the transplacental transfer of maternal antibodies is limited.[3,4]

METHODS

Between January 28, 2021, and March 31, 2021, we studied 122 pregnant women with cord blood available at the time of birth at a single academic medical center. Women who self-reported receipt of one or both doses of a messenger RNA (mRNA)–based COVID-19 vaccine and gave birth to a singleton neonate (gestational age between 35 0/7 and 41 2/7 weeks) were included in the study. Semi-quantitative testing for antibodies against S-receptor binding domain[5,6] was performed on leftover clinical sera of maternal peripheral blood to identify antibodies mounted against the vaccine and on leftover clinical sera of cord blood to study passive immunity. Only women who tested negative for antibodies against the nucleocapsid protein antigen[7] were included to ensure antibodies were not the result of past severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. The relationship between immunoglobin (Ig)G antibody levels and time was studied using analysis of variance. The relationship between maternal and cord blood IgG levels and between IgG placental transfer (neonatal/maternal) ratio and time was studied using Pearson correlation analysis and linear regression. The study was approved by the Weill Cornell Medicine Institutional Review Board.

RESULTS

By the time of delivery, 55 pregnant women had received one dose of an mRNA vaccine and 67 had received both vaccine doses. Eighty-five women received the Pfizer-BioNTech vaccine, and 37 women received the Moderna vaccine. All women tested negative for SARS-CoV-2 infection using reverse-transcriptase polymerase chain reaction on nasopharyngeal swabs, and all women and neonates were asymptomatic at birth and until time of discharge. Eighty-seven pregnant women tested at birth produced an IgG response, 19 women produced both an IgM and IgG response, and 16 women had no detectable antibody response, the latter of whom were within 4 weeks of vaccine dose 1 (Fig. 1A). As the number of weeks elapsed, the number of women who mounted an antibody response and who conferred passive immunity to their neonates increased (Fig. 1A). All women and cord blood samples, except for one, had detectable IgG antibodies by 4 weeks after vaccine dose 1 (Fig. 1A). The one dyad with no transfer of antibodies to the neonate was 10 weeks from dose 1 and 6 weeks from dose 2. The earliest detection of antibodies in women occurred 5 days post–vaccine dose 1, and the earliest detection of antibodies in cord blood occurred 16 days post–vaccine dose 1. Forty-four percent (24/55) of cord blood samples from women who received only one vaccine dose had detectable IgG, whereas 99% (65/67) of cord blood samples from women who received both vaccine doses had detectable IgG.
Fig. 1.

Maternal antibody response to coronavirus disease 2019 (COVID-19) mRNA vaccination. A. Number of women who produced no antibody response, produced an antibody response but did not demonstrate passive immunity to their neonates, or produced an antibody response and also demonstrated passive immunity to their neonates. Time 0 is day of maternal vaccination dose 1. The earliest detection of antibodies in neonates (passive immunity) was at 16 days post–maternal dose 1. The one mother–neonate dyad with no transfer of antibodies to the neonate was at 10.14 weeks from dose 1 and 6 weeks from dose 2. B. Maternal immunoglobulin (Ig)G levels vs weeks elapsed since maternal vaccination dose 1 for women who received only one dose of the vaccine (n=55). Time point 0 is day of vaccination dose 1. C. Maternal IgG levels vs weeks elapsed since maternal vaccination dose 2 for women who received both doses of the vaccine (n=67). Time point 0 is day of vaccination dose 2. All positive serology cutoffs were 1 (dashed line). The relationship between IgG antibody levels and time was studied using analysis of variance with Tukey post hoc. Statistical analysis was performed using R 3.6.3, RStudio 1.1.463. ns, not significant.

Prabhu. COVID-19 Vaccination in Pregnancy. Obstet Gynecol 2021.

Maternal antibody response to coronavirus disease 2019 (COVID-19) mRNA vaccination. A. Number of women who produced no antibody response, produced an antibody response but did not demonstrate passive immunity to their neonates, or produced an antibody response and also demonstrated passive immunity to their neonates. Time 0 is day of maternal vaccination dose 1. The earliest detection of antibodies in neonates (passive immunity) was at 16 days post–maternal dose 1. The one mother–neonate dyad with no transfer of antibodies to the neonate was at 10.14 weeks from dose 1 and 6 weeks from dose 2. B. Maternal immunoglobulin (Ig)G levels vs weeks elapsed since maternal vaccination dose 1 for women who received only one dose of the vaccine (n=55). Time point 0 is day of vaccination dose 1. C. Maternal IgG levels vs weeks elapsed since maternal vaccination dose 2 for women who received both doses of the vaccine (n=67). Time point 0 is day of vaccination dose 2. All positive serology cutoffs were 1 (dashed line). The relationship between IgG antibody levels and time was studied using analysis of variance with Tukey post hoc. Statistical analysis was performed using R 3.6.3, RStudio 1.1.463. ns, not significant.

Prabhu. COVID-19 Vaccination in Pregnancy. Obstet Gynecol 2021. Maternal IgG levels were significantly higher, week by week, starting 2 weeks after the first vaccine dose (P=.005 and .019, respectively), as well as between the first and second weeks after the second vaccine dose (P=2e-07) (Fig. 1B and C). Maternal IgG levels were linearly associated with cord blood IgG levels (R=0.89, P<2.2e-16) (Fig. 2A). The placental transfer ratio correlated with the number of weeks elapsed since maternal vaccine dose 2 (R=0.8, P=2.6e-15) (Fig. 2B).
Fig. 2.

Neonatal antibody response to maternal coronavirus disease 2019 (COVID-19) mRNA vaccination. A. Cord blood immunoglobulin (Ig)G levels vs maternal IgG levels. Grey dots represent neonates born to mothers who received only one dose of the vaccine. All positive serology cutoffs were 1 (dashed gray line). The relationship between maternal and neonatal IgG levels was studied using Pearson correlation analysis and linear regression on log2-scaled serologic values. CIs are represented by shaded region (95% CI 0.80–0.97). Lower and upper prediction intervals are indicated with dotted red lines. B. Placental transfer ratio (neonatal IgG/maternal IgG) vs weeks elapsed since maternal vaccination dose 2 for 65 dyads containing mothers who received both vaccine doses. Time point 0 is day of vaccine dose 2. The relationship between IgG placental transfer ratio (neonatal/maternal) and time was studied using Pearson correlation analysis and linear regression on placental transfer ratio and time elapsed since dose 2 (weeks). CIs are represented by shaded region (95% CI 0.11–0.16). Lower and upper prediction intervals are indicated with dotted blue lines. Statistical analysis was performed using R 3.6.3, RStudio 1.1.463.

Prabhu. COVID-19 Vaccination in Pregnancy. Obstet Gynecol 2021.

Neonatal antibody response to maternal coronavirus disease 2019 (COVID-19) mRNA vaccination. A. Cord blood immunoglobulin (Ig)G levels vs maternal IgG levels. Grey dots represent neonates born to mothers who received only one dose of the vaccine. All positive serology cutoffs were 1 (dashed gray line). The relationship between maternal and neonatal IgG levels was studied using Pearson correlation analysis and linear regression on log2-scaled serologic values. CIs are represented by shaded region (95% CI 0.80–0.97). Lower and upper prediction intervals are indicated with dotted red lines. B. Placental transfer ratio (neonatal IgG/maternal IgG) vs weeks elapsed since maternal vaccination dose 2 for 65 dyads containing mothers who received both vaccine doses. Time point 0 is day of vaccine dose 2. The relationship between IgG placental transfer ratio (neonatal/maternal) and time was studied using Pearson correlation analysis and linear regression on placental transfer ratio and time elapsed since dose 2 (weeks). CIs are represented by shaded region (95% CI 0.11–0.16). Lower and upper prediction intervals are indicated with dotted blue lines. Statistical analysis was performed using R 3.6.3, RStudio 1.1.463.

Prabhu. COVID-19 Vaccination in Pregnancy. Obstet Gynecol 2021.

DISCUSSION

Messenger RNA–based COVID-19 vaccines in pregnant women lead to maternal antibody production as early as 5 days after the first vaccination dose and transplacental transfer of passive immunity to the neonate as early as 16 days after the first vaccination dose. The increasing levels of maternal IgG over time and the increasing placental IgG transfer ratio over time suggest that timing between vaccination and birth may be an important factor to consider in vaccination strategies of pregnant women. Given the variability in antibody transfer and lack of transfer to one neonate, further studies are needed to understand the factors that influence transplacental transfer of IgG antibodies, as well as the protective nature of these antibodies.
  32 in total

1.  Neutralizing antibody activity against SARS-CoV-2 variants in gestational age-matched mother-infant dyads after infection or vaccination.

Authors:  Yusuke Matsui; Lin Li; Mary Prahl; Arianna G Cassidy; Nida Ozarslan; Yarden Golan; Veronica J Gonzalez; Christine Y Lin; Unurzul Jigmeddagva; Megan A Chidboy; Mauricio Montano; Taha Y Taha; Mir M Khalid; Bharath Sreekumar; Jennifer M Hayashi; Pei-Yi Chen; G Renuka Kumar; Lakshmi Warrier; Alan Hb Wu; Dongli Song; Priya Jegatheesan; Daljeet S Rai; Balaji Govindaswami; Jordan Needens; Monica Rincon; Leslie Myatt; Ifeyinwa V Asiodu; Valerie J Flaherman; Yalda Afshar; Vanessa L Jacoby; Amy P Murtha; Joshua F Robinson; Melanie Ott; Warner C Greene; Stephanie L Gaw
Journal:  JCI Insight       Date:  2022-06-22

Review 2.  Vaccine Protection Through Placenta and Breastfeeding: The Unmet Topic in COVID-19 Pandemic.

Authors:  Ariane Laguila Altoé; Anna Paula Marques Mambriz; Daniela Maira Cardozo; Joana Maira Valentini Zacarias; Jeane Eliete Laguila Visentainer; Larissa Danielle Bahls-Pinto
Journal:  Front Immunol       Date:  2022-06-03       Impact factor: 8.786

3.  Placental pathology in women vaccinated and unvaccinated against SARS-CoV-2.

Authors:  Marie C Smithgall; Elisabeth A Murphy; Nina Schatz-Siemers; Cathleen Matrai; Jiangling Tu; Rebecca N Baergen; Yawei J Yang
Journal:  Am J Obstet Gynecol       Date:  2022-06-28       Impact factor: 10.693

4.  Maternal immune response and placental antibody transfer after COVID-19 vaccination across trimester and platforms.

Authors:  Caroline G Atyeo; Lydia L Shook; Sara Brigida; Rose M De Guzman; Stepan Demidkin; Cordelia Muir; Babatunde Akinwunmi; Arantxa Medina Baez; Maegan L Sheehan; Erin McSweeney; Madeleine D Burns; Ruhi Nayak; Maya K Kumar; Chinmay D Patel; Allison Fialkowski; Dana Cvrk; Ilona T Goldfarb; Lael M Yonker; Alessio Fasano; Alejandro B Balazs; Michal A Elovitz; Kathryn J Gray; Galit Alter; Andrea G Edlow
Journal:  Nat Commun       Date:  2022-06-28       Impact factor: 17.694

5.  Scientific Evidence Supporting Coronavirus Disease 2019 (COVID-19) Vaccine Efficacy and Safety in People Planning to Conceive or Who Are Pregnant or Lactating.

Authors:  Guillermina Girardi; Andrew A Bremer
Journal:  Obstet Gynecol       Date:  2022-01-01       Impact factor: 7.661

Review 6.  Global Perspectives on Immunization Against SARS-CoV-2 During Pregnancy and Priorities for Future Research: An International Consensus Paper From the World Association of Infectious Diseases and Immunological Disorders.

Authors:  Bahaa Abu-Raya; Shabir A Madhi; Saad B Omer; Gayatri Amirthalingam; Michelle L Giles; Katie L Flanagan; Petra Zimmermann; Miguel O'Ryan; Marco A Safadi; Vassiliki Papaevangelou; Kirsten Maertens; Nasamon Wanlapakorn; Vicens Diaz-Brito; Eline Tommelein; Susanna Esposito
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Review 7.  An update on COVID-19 and pregnancy.

Authors:  Denise J Jamieson; Sonja A Rasmussen
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Review 8.  COVID-19 Vaccination in Pregnancy and Lactation: Current Research and Gaps in Understanding.

Authors:  Lydia L Shook; Parisa N Fallah; Jason N Silberman; Andrea G Edlow
Journal:  Front Cell Infect Microbiol       Date:  2021-09-16       Impact factor: 5.293

9.  Safety of COVID-19 vaccines, their components or their platforms for pregnant women: A rapid review.

Authors:  Agustín Ciapponi; Ariel Bardach; Agustina Mazzoni; Tomás Alconada; Steven Anderson; Fernando J Argento; Jamile Ballivian; Karin Bok; Daniel Comandé; Emily Erbelding; Erin Goucher; Beate Kampmann; Ruth Karron; Flor M Munoz; María Carolina Palermo; Edward P K Parker; Federico Rodriguez Cairoli; María Victoria Santa; Andy Stergachis; Gerald Voss; Xu Xiong; Natalia Zamora; Sabra Zaraa; Mabel Berrueta; Pierre M Buekens
Journal:  medRxiv       Date:  2021-06-06

10.  Obstetric Outpatient Management During the COVID-19 Pandemic: Prevention, Treatment of Mild Disease, and Vaccination.

Authors:  Naima T Joseph; Emily S Miller
Journal:  Clin Obstet Gynecol       Date:  2022-03-01       Impact factor: 2.190

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