Inter-individual and inter-regional variability of breast milk antibody reactivity to bacterial lipopolysaccharides

Front Immunol. 2024 Sep 6:15:1404192. doi: 10.3389/fimmu.2024.1404192. eCollection 2024.

Abstract

Breast milk is a vital source of nutrients, prebiotics, probiotics, and protective factors, including antibodies, immune cells and antimicrobial proteins. Using bacterial lipopolysaccharide arrays, we investigated the reactivity and specificity of breast milk antibodies towards microbial antigens, comparing samples from rural Kenya and urban Switzerland. Results showed considerable variability in antibody reactivity both within and between these locations. Kenyan breast milk demonstrated broad reactivity to bacterial lipopolysaccharides, likely due to increased microbial exposure. Antibodies primarily recognized the O-antigens of lipopolysaccharides and showed strong binding to specific carbohydrate motifs. Notably, antibodies against specific Escherichia coli O-antigens showed cross-reactivity with parasitic pathogens like Leishmania major and Plasmodium falciparum, thus showing that antibodies reacting against lipopolysaccharide O-antigens can recognize a wide range of antigens beyond bacteria. The observed diversity in antigen recognition highlights the significance of breast milk in safeguarding infants from infections, particularly those prevalent in specific geographic regions. The findings also offer insights for potential immunobiotic strategies to augment natural antibody-mediated defense against diverse pathogens.

Keywords: O-antigen; antigen mimicry; glycan; infection; lactation; microarray; natural protection.

MeSH terms

  • Adult
  • Antibodies, Bacterial / immunology
  • Cross Reactions / immunology
  • Escherichia coli / immunology
  • Female
  • Humans
  • Kenya
  • Lipopolysaccharides* / immunology
  • Milk, Human* / chemistry
  • Milk, Human* / immunology
  • O Antigens / immunology
  • Switzerland

Substances

  • Lipopolysaccharides
  • Antibodies, Bacterial
  • O Antigens

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by the Swiss National Foundation grant 310030_212231 and partially by the Spanish Ministry of Science and Innovation grant (PID2022-137031OB-I00) and the Program on the Molecular Mechanisms of Malaria (Fundación Ramón Areces) to LI.