# Immune response in breastmilk of Black women to SARS-CoV-2 infection and vaccination against COVID-19

**Authors:** Maeve O. Smith, Jessica Price, Ryan Baker, Halle Neely, Dominique Alfandari, Kimarie Bugg, Lindiwe Sibeko, Kathleen F. Arcaro

PMC · DOI: 10.3389/fnut.2025.1703784 · Frontiers in Nutrition · 2026-01-12

## TL;DR

This study explores immune responses in breastmilk of Black women to SARS-CoV-2 infection and vaccination, highlighting variability and the need for diverse representation in research.

## Contribution

The study addresses gaps in understanding immune responses in breastmilk of Black lactating women and includes analysis of mammary epithelium permeability.

## Key findings

- Breastmilk and blood samples from all participants showed anti-SARS-CoV-2 antibodies, but saliva samples showed variability.
- Mammary epithelium permeability correlated with cytokine concentrations like IL-1β, IL-6, and IL-8.

## Abstract

In the United States, Black lactating women are underrepresented in health-related studies. This underrepresentation is a concern when interpreting results from studies of the immune response to SARS-CoV-2 in breastmilk because we know that individuals vary greatly in their response to both infection and vaccination. Additionally, few studies of the immune response in human milk include analysis of mammary epithelium permeability, despite the knowledge that elevated permeability can alter constituents in milk. To address these gaps, we enrolled local Black breastfeeding mothers during a 3-day breastfeeding conference in New Orleans to assess the immune response in milk to infection or vaccination with SARS-CoV-2.

3 weeks prior to the ROSE Black Breastfeeding & Birth Justice Summit of 25–27 August 2022, we advertised for “Black breastfeeding moms to participate in a health study of the special benefits of breastmilk during COVID-19.” Consented participants (n = 16) received kits with instructions to collect bilateral milk samples, dried blood spots (DBS), and saliva. Concentrations of anti-SARS-CoV-2 antibodies against both the Wuhan and Omicron variants were determined in milk, DBS, and saliva using the ELISA test. The concentration of a panel of cytokines was determined in milk, and the permeability of the mammary gland was assessed.

Among the 16 lactating women who provided samples, 8 had a positive COVID-19 test within the previous 19 months, and 12 had received an mRNA-based COVID-19 vaccine within the previous 16 months. Milk and maternal blood spots from all participants were positive for all anti-SARS-CoV-2 antibody classes tested, while only a subset of saliva samples were positive for all anti-SARS-CoV-2 antibody classes. A significant correlation was found between mammary epithelium permeability and concentrations of IL-1β, IL-6, and IL-8 cytokines.

Results from this small pilot study supported the need to include a diverse population in breastmilk studies, as the immune response in milk varied greatly among individuals. Future studies assessing the response to infections and vaccinations in lactating women should include analysis of milk from both breasts, as well as assessment of mammary epithelium permeability.

## Linked entities

- **Proteins:** IL1B (interleukin 1 beta), IL6 (interleukin 6), CXCL8 (C-X-C motif chemokine ligand 8)
- **Diseases:** SARS-CoV-2 (MONDO:0100096), COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** COVID-19 (MESH:D000086382), infection (MESH:D007239)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12833877/full.md

## References

58 references — full list in the complete paper: https://tomesphere.com/paper/PMC12833877/full.md

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Source: https://tomesphere.com/paper/PMC12833877