# Dissecting infant and maternal antibody repertoires exposes the early onset of infant humoral immunity

**Authors:** Albert Bondt, Minjie Tan, Kelly A Dingess, Danique MH van Rijswijck, Yuexiao Chen, Shuai Zhu, Ye Tian, Tianhui Lin, Yuanzhen Zhang, Yanyi Huang, Guanbo Wang, Jing Zhu, Juanjuan Guo, Albert JR Heck

PMC · DOI: 10.1002/cti2.70073 · Clinical & Translational Immunology · 2026-01-11

## TL;DR

This study shows that newborns start producing their own antibodies a few months after birth, separate from antibodies received from their mothers.

## Contribution

The study demonstrates the ability to distinguish infant-produced IgA1 and IgG1 antibodies from maternal sources using mass spectrometry.

## Key findings

- Infant serum at T2 contains unique IgA1 and IgG1 antibody clones not found in maternal serum or breastmilk.
- Maternal IgG1 clones in infant serum are significantly reduced by T2, indicating the emergence of infant-produced antibodies.
- No evidence of milk antibodies entering the infant's bloodstream was found.

## Abstract

The early development of humoral immunity is important for long‐term protection of the newborn. Here, we set out to discern these infant‐produced antibodies from the vast background of maternal antibodies, which is challenging but essential to shed light on the infant‐produced repertoire.

Using IgA1 and IgG1 antibody clonal repertoire analysis by mass spectrometry, we compared matched maternal serum, maternal milk, and infant serum samples, both at birth (T1) and at 7–11 weeks after delivery (T2) in four mother–infant dyads.

We observed for both IgA1 and IgG1 unique infant‐produced antibody repertoires at T2. For IgA1 at T2, no substantial clonal overlap was found between infant serum and breastmilk. The serum IgG1 clonal repertoires were highly alike at birth for mother and infant, but at T2, the contribution of the maternal clonal population in the infant had been drastically reduced, and a large portion of the T2 IgG1 repertoire originated from the infant.

Newborns produce their own antibody repertoires as early as a few months after birth. From this small study, no convincing evidence is found for transfer of milk antibodies into the infant circulation.

Can we dissect the newborn's own humoral antibody repertoire from the bulk it receives from its mother through placenta (IgG) or through breastfeeding (IgA)? Yes we can! We show that both IgA1 and IgG1 showed unique, infant‐produced clones at 7–11 weeks after birth, not found in maternal serum or breastmilk.

## Linked entities

- **Proteins:** IGHA1 (immunoglobulin heavy constant alpha 1), Ighg1 (immunoglobulin heavy constant gamma 1 (G1m marker))

## Full-text entities

- **Genes:** IGHA1 (immunoglobulin heavy constant alpha 1) [NCBI Gene 3493] {aka IgA1}

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12790936/full.md

## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC12790936/full.md

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Source: https://tomesphere.com/paper/PMC12790936