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. 2022 Oct 12:13:1015002.
doi: 10.3389/fimmu.2022.1015002. eCollection 2022.

SARS-CoV-2 specific antibody trajectories in mothers and infants over two months following maternal infection

Affiliations

SARS-CoV-2 specific antibody trajectories in mothers and infants over two months following maternal infection

Melanie A Martin et al. Front Immunol. .

Abstract

Infants exposed to caregivers infected with SARS-CoV-2 may have heightened infection risks relative to older children due to their more intensive care and feeding needs. However, there has been limited research on COVID-19 outcomes in exposed infants beyond the neonatal period. Between June 2020 - March 2021, we conducted interviews and collected capillary dried blood spots from 46 SARS-CoV-2 infected mothers and their infants (aged 1-36 months) for up to two months following maternal infection onset (COVID+ group, 87% breastfeeding). Comparative data were also collected from 26 breastfeeding mothers with no known SARS-CoV-2 infection or exposures (breastfeeding control group), and 11 mothers who tested SARS-CoV-2 negative after experiencing symptoms or close contact exposure (COVID- group, 73% breastfeeding). Dried blood spots were assayed for anti-SARS-CoV-2 S-RBD IgG and IgA positivity and anti-SARS-CoV-2 S1 + S2 IgG concentrations. Within the COVID+ group, the mean probability of seropositivity among infant samples was lower than that of corresponding maternal samples (0.54 and 0.87, respectively, for IgG; 0.33 and 0.85, respectively, for IgA), with likelihood of infant infection positively associated with the number of maternal symptoms and other household infections reported. COVID+ mothers reported a lower incidence of COVID-19 symptoms among their infants as compared to themselves and other household adults, and infants had similar PCR positivity rates as other household children. No samples returned by COVID- mothers or their infants tested antibody positive. Among the breastfeeding control group, 44% of mothers but none of their infants tested antibody positive in at least one sample. Results support previous research demonstrating minimal risks to infants following maternal COVID-19 infection, including for breastfeeding infants.

Keywords: COVID-19; IgA; IgG; breastfeeding; infancy; pediatric.

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Conflict of interest statement

KL is employed by Traverse Science. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Individual maternal IgG and IgA S/CO trajectories (dashed, colored lines) over two months following maternal infection onset or enrollment, and loess smooth curves (solid, colored lines) fit for each enrollment group: COVID+ (n = 36, nobs = 116); COVID- (n = 6, nobs = 18); BF control group, (n = 20, nobs = 50, excluding samples collected post-vaccination). S/CO=1.0 (solid black line), S/CO=2.0 (dashed black line). Y-axis is truncated at S/CO = 10; samples with S/CO between 10-20 not shown (IgG nsubj = 12, nobs = 19; IgA nsubj = 6, nobs = 4).
Figure 2
Figure 2
Individual infant IgG and IgA S/CO trajectories (dashed, colored lines) with group-level loess smoothes (solid, colored lines) over two months following maternal infection onset or enrollment, by maternal study group: COVID+ (n = 25, nobs = 66); COVID- (n = 7, nobs = 18); and BF control group, excluding samples collected post-maternal vaccination (n = 15, nobs = 35), S/CO=1.0 (solid black line), S/CO=2.0 (dashed black line). Y-axis is truncated at S/CO = 10; samples with S/CO between 10-20 not shown (IgG nsubj = 3, nobs = 11; IgA nsubj = 2, nobs = 3).
Figure 3
Figure 3
Predicted mean probability (with 95% credible intervals) of IgG and IgA seropositivity across all samples collected from COVID+ mothers (n = 36, nobs = 116) and their exposed infants (n = 25, nobs = 66). IgG infant = 0.54 [0.33 – 0.74], IgG maternal = 0.87 [0.76 – 0.95]. IgA infant = 0.33 [0.17 – 0.52]; IgA maternal = 0.85 [0.72 – 0.93].
Figure 4
Figure 4
Mean estimated probabilities (95% credible intervals) of IgG and IgA seropositivity (S/CO ≥1) in samples collected from COVID+ mothers (n = 36, nobs = 116) and their exposed infants (n = 25, nobs = 66) in the two months following maternal infection onset.
Figure 5
Figure 5
Predicted IgG S1 and S2 concentration (with 95% credible intervals) in COVID+ mothers (n = 26, nobs= 66) and exposed infants (n = 9, nobs=17) over two months following maternal infection onset.

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References

    1. Castagnoli R, Votto M, Licari A, Brambilla I, Bruno R, Perlini S, et al. . Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in children and adolescents: A systematic review. JAMA Pediatr (2020) 174(9):882–9. doi: 10.1001/jamapediatrics.2020.1467 - DOI - PubMed
    1. Viner RM, Mytton OT, Bonell C, Melendez-Torres GJ, Ward J, Hudson L, et al. . Susceptibility to SARS-CoV-2 infection among children and adolescents compared with adults: A systematic review and meta-analysis. JAMA Pediatr (2020) 175(2):143–56. doi: 10.1001/jamapediatrics.2020.4573 - DOI - PMC - PubMed
    1. Götzinger F, Santiago-García B, Noguera-Julián A, Lanaspa M, Lancella L, Calò Carducci FI, et al. . COVID-19 in children and adolescents in Europe: a multinational, multicentre cohort study. Lancet Child Adolesc Health (2020) 4(9):653–61. doi: 10.1016/S2352-4642(20)30177-2 - DOI - PMC - PubMed
    1. Rudan I, Adeloye D, Katikireddi SV, Murray J, Simpson C, Shah SA, et al. . The COVID-19 pandemic in children and young people during 2020-2021: Learning about clinical presentation, patterns of spread, viral load, diagnosis and treatment. J Glob Health (2021) 11:01010. doi: 10.7189/jogh.11.01010 - DOI - PMC - PubMed
    1. Chou J, Thomas PG, Randolph AG. Immunology of SARS-CoV-2 infection in children. Nat Immunol (2022) 23(2):177–85. doi: 10.1038/s41590-021-01123-9 - DOI - PMC - PubMed

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