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Glycerol monolaurate inhibition of human B cell activation
Journal article   Open access   Peer reviewed

Glycerol monolaurate inhibition of human B cell activation

Micaela G Fosdick, Shannon Loftus, Isabella Phillips, Zeb R Zacharias and Jon C D Houtman
Scientific reports, Vol.12(1), pp.13506-13506
08/05/2022
DOI: 10.1038/s41598-022-17432-4
PMCID: PMC9355977
PMID: 35931746
url
https://doi.org/10.1038/s41598-022-17432-4View
Published (Version of record) Open Access

Abstract

Glycerol monolaurate (GML) is a naturally occurring antimicrobial agent used commercially in numerous products and food items. GML is also used as a homeopathic agent and is being clinically tested to treat several human diseases. In addition to its anti-microbial function, GML suppresses immune cell proliferation and inhibits primary human T cell activation. GML suppresses T cell activation by altering membrane dynamics and disrupting the formation of protein clusters necessary for intracellular signaling. The ability of GML to disrupt cellular membranes suggests it may alter other cell types. To explore this possibility, we tested how GML affects human B cells. We found that GML inhibits BCR-induced cytokine production, phosphorylation of signaling proteins, and protein clustering, while also changing cellular membrane dynamics and dysregulating cytoskeleton rearrangement. Although similar, there are also differences between how B cells and T cells respond to GML. These differences suggest that unique intrinsic features of a cell may result in differential responses to GML treatment. Overall, this study expands our understanding of how GML impacts the adaptive immune response and contributes to a broader knowledge of immune modulating monoglycerides.

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