ArticleProceedings of the National Academy of Sciences of the United States of America2026
FcγRIIB functions as an IgG transporter in the mammary gland.
Article in Proceedings of the National Academy of Sciences of the United States of America, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
2 citing papers in PubMed.
- Myelin Oligodendrocyte Glycoprotein Antibodies in Breast Milk in a Lactating Woman With Severe Enterovirus-Associated MOGAD.Neurology(R) neuroimmunology & neuroinflammation · 2026Article
- Nutritional dynamics and untargeted metabolomics reveal breed and lactation-dependent shifts in goat milk composition: from colostrum to mature milk.Food chemistry: X · 2026Article
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Authors and funding
20 authors.
Funding
Abstract
In mammals, passive acquisition of maternal immunoglobulins is essential for neonatal immune development and defense against infections. IgG, a central mediator of humoral immunity, is maternally transferred via distinct mechanisms depending on placental structure in placental mammals. In humans (hemochorial placenta), IgG is prenatally transported across the placenta, whereas in large domestic animals such as pigs and cows (epitheliochorial/connective chorionic placenta), IgG is exclusively transferred postnatally via colostrum and absorbed in the neonatal intestine. Rodents (allantoic chorionic placenta) employ both pathways. Critically, IgG must traverse multiple tissue barriers-including the placenta, mammary gland, and neonatal intestine-to reach the circulation of newborns. While FcRn is known to facilitate IgG transport in the placenta and neonatal intestine, the mechanisms underlying IgG secretion into milk remain unclear. Here, we identify FcγRIIB as the key transporter mediating maternal IgG transfer across the mammary gland in mammals. Using constitutive and conditional knockout mice, we demonstrate that FcγRIIB deficiency impairs mammary IgG transfer, whereas its overexpression enhances milk IgG levels. Strikingly, in pigs, FcγRIIB is highly upregulated in mammary tissue prepartum, and its disruption abolishes IgG accumulation in colostrum. Our work opens avenues for improving neonatal immunity through targeted modulation of FcγRIIB-mediated IgG transport.
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