Analysis of the transplacental transmission of SARS CoV-2 virus and antibody transfer according to the gestational age at maternal infection.
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
11 Feb 2024
11 Feb 2024
Historique:
received:
01
10
2023
accepted:
02
02
2024
medline:
12
2
2024
pubmed:
12
2
2024
entrez:
11
2
2024
Statut:
epublish
Résumé
To quantify transplacental transmission of SARS-CoV-2 virus and antibody transfer in pregnant women and their newborns according to the gestational age at maternal infection. A prospective observational multicenter study including pregnant women with a positive RT-PCR or a positive serology for SARS-CoV-2 and compatible symptoms, from April to December 2020, in 11 French maternities. The study was designed to obtain a systematic collection of mother-infant dyad's samples at birth. SARS-CoV-2 viral load was measured by RT-PCR. IgG and IgM antibodies against the SARS-CoV-2 spike protein were measured by enzyme-linked immunosorbent assay. Antibody concentrations and transplacental transfer ratios were analyzed according to the gestational age at maternal infection. The primary outcome was the rate of SARS CoV-2 materno-fetal transmission at birth. The secondary outcome was the quantification of materno-fetal antibody transfer. Maternal and neonatal outcomes at birth were additionally assessed. Among 165 dyads enrolled, one congenital infection was confirmed {n = 1 (0.63%) IC
Identifiants
pubmed: 38342940
doi: 10.1038/s41598-024-53580-5
pii: 10.1038/s41598-024-53580-5
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
3458Informations de copyright
© 2024. The Author(s).
Références
Vivanti, A. J. et al. Transplacental transmission of SARS-CoV-2 infection. Nat. Commun. 11(1), 3572 (2020).
pubmed: 32665677
pmcid: 7360599
doi: 10.1038/s41467-020-17436-6
Levy, A. et al. ACE2 expression and activity are enhanced during pregnancy. Am. J. Physiol-Regul. Integr. Comp. Physiol. 295(6), R1953–R1961 (2008).
pubmed: 18945956
doi: 10.1152/ajpregu.90592.2008
Mourad, M. et al. Placental response to maternal SARS-CoV-2 infection. Sci. Rep. 11(1), 14390 (2021).
pubmed: 34257394
pmcid: 8277865
doi: 10.1038/s41598-021-93931-0
Hoffmann, M. et al. SARS-CoV-2 cell entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor. Cell. 181(2), 271-280.e8 (2020).
pubmed: 32142651
pmcid: 7102627
doi: 10.1016/j.cell.2020.02.052
Mahyuddin, A. P. et al. Mechanisms and evidence of vertical transmission of infections in pregnancy including SARS-COV -2s. Prenat. Diagn. 40(13), 1655–1670 (2020).
pubmed: 32529643
pmcid: 7307070
doi: 10.1002/pd.5765
Chilamakuri, R. & Agarwal, S. COVID-19: Characteristics and therapeutics. Cells. 10(2), 206 (2021).
pubmed: 33494237
pmcid: 7909801
doi: 10.3390/cells10020206
SeyedHosseini, E. et al. The novel coronavirus Disease-2019 (COVID-19): Mechanism of action, detection and recent therapeutic strategies. Virology. 551, 1–9 (2020).
doi: 10.1016/j.virol.2020.08.011
Beesley, M. et al. COVID-19 and vertical transmission: assessing the expression of ACE2/TMPRSS2 in the human fetus and placenta to assess the risk of SARS-CoV-2 infection. BJOG Int. J. Obstetr. Gynaecol. 129(2), 256–266 (2021).
doi: 10.1111/1471-0528.16974
Zhou, J. et al. Is SARS-CoV-2 infection a risk factor for early pregnancy loss ACE2 and TMPRSS2 coexpression and persistent replicative infection in primitive trophoblast. J. Infect. Dis. 224(Supplement_6), S660–S669 (2021).
pubmed: 34293134
pmcid: 8411376
doi: 10.1093/infdis/jiab309
Rubio, R. et al. Maternal and neonatal immune response to SARS-CoV-2, IgG transplacental transfer and cytokine profile. Front. Immunol. 13, 999136 (2022).
pubmed: 36238312
pmcid: 9552073
doi: 10.3389/fimmu.2022.999136
Crovetto, F. et al. Impact of severe acute respiratory syndrome coronavirus 2 infection on pregnancy outcomes: a population-based study. Clin. Infect. Dis. 73(10), 1768–1775 (2021).
pubmed: 33556958
doi: 10.1093/cid/ciab104
Villar, J. et al. Maternal and neonatal morbidity and mortality among pregnant women with and without COVID-19 infection: The INTERCOVID multinational cohort study. JAMA Pediatr. 175(8), 817 (2021).
pubmed: 33885740
doi: 10.1001/jamapediatrics.2021.1050
Fabre, M. et al. Frequent placental SARS-CoV-2 in patients with COVID-19-associated hypertensive disorders of pregnancy. Fetal. Diagn. Ther. 48(11–12), 801–811 (2021).
pubmed: 34794139
doi: 10.1159/000520179
Fallach, N. et al. Pregnancy outcomes after SARS-CoV-2 infection by trimester: A large, population-based cohort study. PLOS ONE. 17(7), e0270893 (2022).
pubmed: 35857758
pmcid: 9299339
doi: 10.1371/journal.pone.0270893
Ciapponi, A. et al. COVID-19 and pregnancy: An umbrella review of clinical presentation, vertical transmission, and maternal and perinatal outcomes. PLOS ONE. 16(6), e0253974 (2021).
pubmed: 34185807
pmcid: 8241118
doi: 10.1371/journal.pone.0253974
Juan, J. et al. Effect of coronavirus disease 2019 (COVID-19) on maternal, perinatal and neonatal outcome: systematic review. Ultrasound. Obstet. Gynecol. 56(1), 15–27 (2020).
pubmed: 32430957
pmcid: 7276742
doi: 10.1002/uog.22088
Mannar, D. et al. SARS-CoV-2 omicron variant: Antibody evasion and cryo-EM structure of spike protein-ACE2 complex. Science. 375(6582), 760–764 (2022).
pubmed: 35050643
pmcid: 9799367
doi: 10.1126/science.abn7760
Rangchaikul, P. & Venketaraman, V. SARS-CoV-2 and the immune response in pregnancy with delta variant considerations. Infect. Dis. Rep. 13(4), 993–1008 (2021).
pubmed: 34940401
pmcid: 8700906
doi: 10.3390/idr13040091
Wang, S. et al. A Case report of neonatal 2019 coronavirus disease in China. Clin. Infect. Dis. 71(15), 853–857 (2020).
pubmed: 32161941
doi: 10.1093/cid/ciaa225
Shah, P. S., Diambomba, Y., Acharya, G., Morris, S. K. & Bitnun, A. Classification system and case definition for SARS-CoV-2 infection in pregnant women, fetuses, and neonates. Acta Obstet. Gynecol. Scand. 99(5), 565–568 (2020).
pubmed: 32277845
doi: 10.1111/aogs.13870
Schwartz, D. A. An analysis of 38 pregnant women with COVID-19, their newborn infants, and maternal-fetal transmission of SARS-CoV-2: Maternal Coronavirus infections and pregnancy outcomes. Arch. Pathol. Lab. Med. 144(7), 799–805 (2020).
pubmed: 32180426
doi: 10.5858/arpa.2020-0901-SA
Edlow, A. G. et al. Assessment of maternal and neonatal SARS-CoV-2 viral load, transplacental antibody transfer, and placental pathology in pregnancies during the COVID-19 pandemic. JAMA Netw. Open. 3(12), e2030455 (2020).
pubmed: 33351086
pmcid: 7756241
doi: 10.1001/jamanetworkopen.2020.30455
Walker, K. et al. Maternal transmission of SARS-COV-2 to the neonate, and possible routes for such transmission: a systematic review and critical analysis. R Coll. Obstet. Gynaecol. 127(11), 1324–1336 (2020).
Bwire, G. M., Njiro, B. J., Mwakawanga, D. L., Sabas, D. & Sunguya, B. F. Possible vertical transmission and antibodies against SARS-CoV-2 among infants born to mothers with COVID-19: A living systematic review. J. Med. Virol. 93(3), 1361–1369 (2021).
pubmed: 33090535
doi: 10.1002/jmv.26622
Kotlyar, A. M. et al. Vertical transmission of coronavirus disease 2019: A systematic review and meta-analysis. Am. J. Obstet. Gynecol. 224(1), 35-53.e3 (2021).
pubmed: 32739398
doi: 10.1016/j.ajog.2020.07.049
Flannery, D. D. et al. Assessment of maternal and neonatal cord blood SARS-CoV-2 antibodies and placental transfer ratios. JAMA Pediatr. 175(6), 594 (2021).
pubmed: 33512440
doi: 10.1001/jamapediatrics.2021.0038
Houhou-Fidouh, N. et al. Preliminary results on transmission of SARS-CoV-2 antibodies to the fetus and serum neutralizing activity. Int. J. Gynaecol. Obstet. Off. Organ. Int. Fed. Gynaecol. Obstet. 158(2), 476–478 (2022).
doi: 10.1002/ijgo.14185
Song, D. et al. Passive and active immunity in infants born to mothers with SARS-CoV-2 infection during pregnancy: Prospective cohort study. BMJ Open. 11(7), e053036 (2021).
pubmed: 34234001
pmcid: 8264915
doi: 10.1136/bmjopen-2021-053036
Matsui, Y. et al. Neutralizing antibody activity against SARS-CoV-2 variants in gestational age-matched mother-infant dyads after infection or vaccination. JCI Insight. 7(12), e157354 (2022).
pubmed: 35579965
pmcid: 9309042
doi: 10.1172/jci.insight.157354
Brebant, D. et al. Transplacental transfer of anti-SARS-CoV-2 neutralizing antibodies in comparison to other pathogens total antibodies. J. Clin. Virol. Off. Publ. Pan. Am. Soc. Clin. Virol. 165, 105495 (2023).
doi: 10.1016/j.jcv.2023.105495
Rottenstreich, M. et al. Covid-19 vaccination during the third trimester of pregnancy: rate of vaccination and maternal and neonatal outcomes, a multicentre retrospective cohort study. Int. J. Obstetr. Gynaecol. 8, 248 (2021).
Biguenet, A. et al. SARS-CoV-2 respiratory viral loads and association with clinical and biological features. J. Med. Virol. 93(3), 1761–1765 (2021).
pubmed: 32889755
doi: 10.1002/jmv.26489
Lassi, Z. S. et al. A systematic review and meta-analysis of data on pregnant women with confirmed COVID-19: Clinical presentation, and pregnancy and perinatal outcomes based on COVID-19 severity. J. Glob. Health. 11, 05018 (2021).
pubmed: 34221361
pmcid: 8248750
doi: 10.7189/jogh.11.05018
Jafari, M. et al. Clinical characteristics and outcomes of pregnant women with COVID-19 and comparison with control patients: A systematic review and meta-analysis. Rev. Med. Virol. 31(5), 1–16 (2021).
pubmed: 33387448
doi: 10.1002/rmv.2208
Ward, J. D. et al. The clinical impact of maternal COVID-19 on mothers, their infants, and placentas with an analysis of vertical transfer of maternal SARS-CoV-2-specific IgG antibodies. Placenta. 123, 12–23 (2022).
pubmed: 35512490
pmcid: 9057562
doi: 10.1016/j.placenta.2022.04.006
Karimi, H., Mansouri, V. & Rezaei, N. Vertical transmission and maternal passive immunity post-SARS-CoV-2. Fut. Virol. 18(13), 895–912 (2023).
doi: 10.2217/fvl-2023-0089
Nielsen, S. Y. et al. Transplacental transfer of SARS-CoV-2 antibodies: a cohort study. Eur. J. Clin. Microbiol. Infect. Dis. 42(3), 277–285 (2023).
pubmed: 36692603
pmcid: 9872727
doi: 10.1007/s10096-023-04553-5
González-Mesa, E. et al. Transmitted fetal immune response in cases of SARS-CoV-2 infections during pregnancy. Diagnostics. 12(2), 245 (2022).
pubmed: 35204335
pmcid: 8870756
doi: 10.3390/diagnostics12020245
Trinité, B. et al. SARS-CoV-2 infection elicits a rapid neutralizing antibody response that correlates with disease severity. Sci. Rep. 11(1), 2608 (2021).
pubmed: 33510275
pmcid: 7843981
doi: 10.1038/s41598-021-81862-9
Timircan, M. et al. Exploring pregnancy outcomes associated with SARS-CoV-2 infection. Medicina 57(8), 796 (2021).
pubmed: 34441002
pmcid: 8400058
doi: 10.3390/medicina57080796
Ville, Y. The placenta in COVID -19 infection in pregnancy. BJOG Int. J. Obstet. Gynaecol. 129(8), 1375–1375 (2022).
doi: 10.1111/1471-0528.17162
Papageorghiou, A. T. et al. Preeclampsia and COVID-19: Results from the INTERCOVID prospective longitudinal study. Am. J. Obstet. Gynecol. 225(3), 289.e1-289.e17 (2021).
pubmed: 34187688
doi: 10.1016/j.ajog.2021.05.014
Zaigham, M. & Andersson, O. Maternal and perinatal outcomes with COVID-19: A systematic review of 108 pregnancies. Acta Obstet. Gynecol. Scand. 99(7), 823–829 (2020).
pubmed: 32259279
doi: 10.1111/aogs.13867
Girardelli, S., Mullins, E. & Lees, C. C. COVID-19 and pregnancy: Lessons from 2020. Early Hum. Dev. 162, 105460 (2021).
pubmed: 34538701
pmcid: 8408048
doi: 10.1016/j.earlhumdev.2021.105460
Yu, N. et al. Clinical features and obstetric and neonatal outcomes of pregnant patients with COVID-19 in Wuhan, China: a retrospective, single-centre, descriptive study. Lancet Infect. Dis. 20(5), 559–564 (2020).
pubmed: 32220284
pmcid: 7158904
doi: 10.1016/S1473-3099(20)30176-6
Chen, C. Y., Yu, C., Chang, C. C. & Lin, C. W. Comparison of a novel computerized analysis program and visual interpretation of cardiotocography. PloS One. 9(12), e112296 (2014).
pubmed: 25437442
pmcid: 4249819
doi: 10.1371/journal.pone.0112296
WHO. Definition and categorization of the timing of mother-to-child transmission of SARS-CoV-2. Scientific brief. 7 February 2021, COVID-19: Scientific briefs, Geneva: World Health Organization, 2021. www.who.int/publications/i/item/WHO-2019-nCoV-mother-to-child-transmission-2021.1 (last accessed 01/07/21) WHO reference number: WHO/2019-nCoV/mother-to-child_transmission/2021.1.
Timi, P. et al. Placental injury and antibody transfer after coronavirus disease 2019 in pregnancy. J. Infect. Dis. 227(7), 850–854 (2023).
pubmed: 35767286
doi: 10.1093/infdis/jiac270
Beharier, O. et al. Efficient maternal to neonatal transfer of antibodies against SARS-CoV-2 and BNT162b2 mRNA COVID-19 vaccine. J Clin Invest https://doi.org/10.1172/JCI150319 (2021).
doi: 10.1172/JCI150319
pubmed: 34596052
pmcid: 8483743
Atyeo, C. G. et al. Maternal immune response and placental antibody transfer after COVID-19 vaccination across trimester and platforms. Nat Commun. 13(1), 3571 (2022).
pubmed: 35764643
pmcid: 9239994
doi: 10.1038/s41467-022-31169-8
Marshall, N. E. et al. SARS-CoV-2 vaccine booster elicits robust prolonged maternal antibody responses and passive transfer to the offspring via the placenta and breastmilk. Am J Obstet Gynecol MFM. 5(2), 100830 (2023).
pubmed: 36462615
doi: 10.1016/j.ajogmf.2022.100830
Lubrano, C. et al. Immune response and transplacental antibody transfer in pregnant women after COVID-19 vaccination. J. Pers. Med. 13(4), 689 (2023).
pubmed: 37109075
pmcid: 10141882
doi: 10.3390/jpm13040689
Yang, Y., Xing, H. & Zhao, Y. Transplacental transmission of SARS-CoV-2 immunoglobulin G antibody to infants from maternal COVID-19 vaccine immunization before pregnancy. J Med Virol 95(1), e28296 (2023).
pubmed: 36367230
doi: 10.1002/jmv.28296
Zilver, S. J. M. et al. Vaccination from the early second trimester onwards gives a robust SARS-CoV-2 antibody response throughout pregnancy and provides antibodies for the neonate. Int. J. Infect. Dis. 130, 126–135 (2023).
pubmed: 36868302
pmcid: 9977072
doi: 10.1016/j.ijid.2023.02.022
Adhikari, E. H. et al. Diverging maternal and cord antibody functions from SARS-CoV-2 infection and vaccination in pregnancy. J. Infect. Dis. https://doi.org/10.1093/infdis/jiad421 (2023).
doi: 10.1093/infdis/jiad421
pubmed: 37815524