Does Maternal SARS-CoV-2 Infection or SARS-CoV-2 Vaccination Trigger an Inflammatory Response in the Fetus? A Prospective Cohort Study.


Journal

Gynecologic and obstetric investigation
ISSN: 1423-002X
Titre abrégé: Gynecol Obstet Invest
Pays: Switzerland
ID NLM: 7900587

Informations de publication

Date de publication:
2022
Historique:
received: 10 01 2022
accepted: 11 04 2022
pubmed: 22 6 2022
medline: 12 10 2022
entrez: 21 6 2022
Statut: ppublish

Résumé

SARS-CoV-2 infection triggers a significant maternal inflammatory response. There is a dearth of information regarding whether maternal SARS-CoV-2 infection at admission for delivery or SARS-CoV-2 vaccination triggers an inflammatory response in the fetus. This study aims at evaluating fetal inflammatory response to maternal SARS-CoV-2 infection or SARS-CoV-2 vaccination compared to control group. Design, Participants, Setting, and Methods: A prospective cohort study was performed with a total of 61 pregnant women who presented for delivery at a single medical center (William Beaumont Hospital, Royal Oak, MI). All mothers were tested for SARS-CoV-2 infection using polymerase chain reaction (PCR) on admission to labor and delivery unit. Three groups were evaluated: 22 pregnant with a positive SARS-CoV-2 test (case group), 23 pregnant women with a negative SARS-CoV-2 test (control group), and 16 pregnant women who had recent SAR-CoV-2 vaccination and a negative SARS-CoV-2 test (vaccine group). At delivery, cord blood was collected to determine the levels of IL-6, C-reactive protein (CRP), and SARS-CoV-2 nucleocapsid IgG and IgM antibodies. In all cases, the newborn had a negative PCR test or showed no clinical findings consistent with SARS-CoV-2 infection. Mean (SD) IL-6 level was not significantly different for the three groups: case group 9.00 ± 3.340 pg/mL, control group 5.19 ± 0.759 pg/mL, and vaccine group 7.11 ± 2.468 pg/mL (p value 0.855). Pairwise comparison also revealed no statistical difference for IL-6 concentrations with p values for case versus control, case versus vaccine, and control versus vaccine = 0.57, 0.91, and 0.74, respectively. Similarly, there was no statistically significant difference in the frequency of elevated IL-6 (>11 pg/mL) between groups (p value 0.89). CRP levels across the three groups were not statistically significant different (p value 0.634). Pairwise comparison of CRP levels among the different groups was also not statistically different. SARS-CoV-2 nucleocapsid IgG was positive in 12 out of 22 cord blood samples in the case group, 2 out of 23 of the control group (indicating old resolved maternal infection), and 0 out of 16 of the vaccine group. SARS-CoV-2 nucleocapsid IgM was negative in all cord blood samples of the case group, control group, and vaccine group. A total number of 61 mothers enrolled in the study which represents a relatively small number of patients. Most patients with positive SARS-CoV-2 PCR were mainly asymptomatic. In addition, our vaccine group received the mRNA-based vaccines (mRNA1273 and BNT162b2). We did not study fetal response to other SARS-CoV-2 vaccines. In our prospective cohort, neither IL-6 nor CRP indicated increased inflammation in the cord blood of newborns of SARS-CoV-2-infected or vaccinated mothers.

Identifiants

pubmed: 35728583
pii: 000525625
doi: 10.1159/000525625
doi:

Substances chimiques

Antibodies, Viral 0
COVID-19 Vaccines 0
Immunoglobulin G 0
Immunoglobulin M 0
Interleukin-6 0
RNA, Messenger 0
C-Reactive Protein 9007-41-4
BNT162 Vaccine N38TVC63NU

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

219-225

Informations de copyright

© 2022 S. Karger AG, Basel.

Auteurs

Ali Alhousseini (A)

William Beaumont Hospital, Royal Oak, Michigan, USA.
Oakland University William Beaumont School of Medicine, Royal Oak, Michigan, USA.
Sparrow Health System, Lansing, Michigan, USA.
Department of Obstetrics and Gynecology, Michigan State University, Lansing, Michigan, USA.

Onur Turkoglu (O)

William Beaumont Hospital, Royal Oak, Michigan, USA.
Oakland University William Beaumont School of Medicine, Royal Oak, Michigan, USA.

Sonia Sajja (S)

William Beaumont Hospital, Royal Oak, Michigan, USA.
Oakland University William Beaumont School of Medicine, Royal Oak, Michigan, USA.

Kurt Wharton (K)

William Beaumont Hospital, Royal Oak, Michigan, USA.
Oakland University William Beaumont School of Medicine, Royal Oak, Michigan, USA.

Jay Idler (J)

William Beaumont Hospital, Royal Oak, Michigan, USA.
Oakland University William Beaumont School of Medicine, Royal Oak, Michigan, USA.

Ray Bahado-Singh (R)

William Beaumont Hospital, Royal Oak, Michigan, USA.
Oakland University William Beaumont School of Medicine, Royal Oak, Michigan, USA.

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Classifications MeSH