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. 2023 Jan-Dec:19:17455057231190955.
doi: 10.1177/17455057231190955.

Severe acute respiratory syndrome coronavirus 2 seroprevalence and longitudinal antibody response following natural infection in pregnancy: A prospective cohort study

Affiliations

Severe acute respiratory syndrome coronavirus 2 seroprevalence and longitudinal antibody response following natural infection in pregnancy: A prospective cohort study

Alison L Drake et al. Womens Health (Lond). 2023 Jan-Dec.

Abstract

Background: Antenatal care provides unique opportunities to assess severe acute respiratory syndrome coronavirus 2 seroprevalence and antibody response duration after natural infection detected during pregnancy; transplacental antibody transfer may inform peripartum and neonatal protection. We estimated seroprevalence and durability of antibodies from natural infection (anti-nucleocapsid immunoglobulin G) among pregnant people, and evaluated transplacental transfer efficiency.

Objective and design: We conducted a cross-sectional study to measure severe acute respiratory syndrome coronavirus 2 seroprevalence, and a prospective cohort study to longitudinally measure anti-nucleocapsid immunoglobulin G responses and transplacental transfer of maternally derived anti-nucleocapsid antibodies.

Methods: We screened pregnant people for the seroprevalence study between 9 December 2020 and 19 June 2021 for anti-nucleocapsid immunoglobulin G in Seattle, Washington. We enrolled anti-nucleocapsid immunoglobulin G positive people from the seroprevalence study or identified through medical records with positive reverse transcription polymerase chain reaction or antigen positive results in a prospective cohort between 9 December 2020 and 9 August 2022.

Results: In the cross-sectional study (N = 1284), 5% (N = 65) tested severe acute respiratory syndrome coronavirus 2 anti-nucleocapsid immunoglobulin G positive, including 39 (60%) without prior positive reverse transcription polymerase chain reaction results and 42 (65%) without symptoms. In the prospective cohort study (N = 107 total; N = 65 from the seroprevalence study), 86 (N = 80%) had anti-nucleocapsid immunoglobulin G positive results during pregnancy. Among 63 participants with delivery samples and prior anti-nucleocapsid positive results, 29 (46%) were anti-nucleocapsid immunoglobulin G negative by delivery. Of 34 remaining anti-nucleocapsid immunoglobulin G positive at delivery with paired cord blood, 19 (56%) had efficient transplacental anti-nucleocapsid immunoglobulin G antibody transfer. Median time from first anti-nucleocapsid immunoglobulin G positive to below positive antibody threshold was 19 weeks and did not differ by prior positive reverse transcription polymerase chain reaction status.

Conclusions: Maternally derived severe acute respiratory syndrome coronavirus 2 antibodies to natural infection may wane before delivery. Vaccines are recommended for pregnant persons to reduce severe illness and confer protection to infants.

Keywords: SARS-CoV-2; antibody; natural infection; pregnancy; seroprevalence; transplacental transfer.

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Conflict of interest statement

The author(s) declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: JAE reports serving as a consultant for Sanofi Pasteur, AstraZeneca, Meissa Vaccines, Pfizer, and Moderna and has received grant support from Pfizer, GlaxoSmithKline, AstraZeneca, Moderna and Merck. ABK reports serving as an unpaid consultant for GlaxoSmith-Kline and as a consultant for Pfizer and has received grant support from Pfizer and Merck. ALD, JNE, MCA, EAW, BAR, ALG and SML received grant support from Merck.

Figures

Figure 1.
Figure 1.
Flowchart of pregnant people enrolled in prospective cohort study with a history of SARS-CoV-2 infection (from seroprevalence study or identified through the medical system) as having a prior positive RT-PCR or antigen test. IgG+ if Abbott index ⩾ 1.4 except two people with IgG+ results from the seroprevalence study not enrolled in the prospective cohort who were tested for IgG with the DiaSorin Liaison SARS-CoV-2 S1/S2 IgG assay in a commercial laboratory. aIgG+ includes any person with an IgG+ sample at baseline or follow-up.
Figure 2.
Figure 2.
Time to anti-N IgG below positive threshold among pregnant people with serologic evidence of prior SARS-CoV-2 infection. (a) Time from anti-N IgG+ to anti-N IgG below positive threshold (n = 68). (b) Time from infection to anti-N IgG below positive threshold (n = 85). Anti-N IgG index below positive threshold based on Abbott index < 1.4.
Figure 3.
Figure 3.
Abbott anti-N IgG index and timing among pregnant people with a history of SARS-CoV-2 infection among those with ⩾ 2 samples available. (a) Time since first anti-N IgG+ (n = 68). (b) Time since RT-PCR+ (or antigen +) (n = 71). (c) Time since infection (n = 81). Dashed line represents Abbott index for positive threshold (log10 transformed value of 1.4). Thick line represents lowess smoother; excludes samples collected at or after SARS-CoV-2 infection. aFirst sample collected following reinfection with SARS-CoV-2, confirmed with subsequent RT-PCR+ or antigen positive result (n = 3).
Figure 4.
Figure 4.
IgG index among paired maternal cord blood samples among participants with anti-N IgG positive results at delivery (n = 34 pairs). Transplacental transfer ratio (infant anti-N IgG index/maternal delivery anti-N IgG index) is ⩾ 1 for circles on or above the diagonal line (dark gray), < 1 for circles below the diagonal line (light gray); circles below the horizontal dashed line (threshold for anti-N IgG positive ⩾ 1.4) represents cord blood samples below the anti-N IgG positive threshold (light gray).

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