Eosinophil and Mast Cell Siglecs: From Biology to Drug Target
Overview
Affiliations
Mast cells and eosinophils are innate immune cells involved in both acute and chronic inflammatory responses. Siglecs are a family of cell surface receptors that share sialic acid binding activity. Over the past 20 years, our knowledge of the expression and function of Siglecs on cells of the immune system and others has greatly expanded, as has our understanding of their signaling, ligands, and possible roles in disease pathophysiology. Because of this, Siglecs have garnered interest as potential drug targets using strategies ranging from biologics to ligand-directed nanoparticles. This mini-review will highlight the state of our knowledge regarding human eosinophil and mast cell Siglecs, their biology, what they recognize, tools developed for in vitro and preclinical experimentation, and the status of ongoing efforts to develop drugs that engage eosinophil and mast cell Siglecs for potential therapeutic benefit.
Mechanistic and Therapeutic Implications of Protein and Lipid Sialylation in Human Diseases.
Zhong X, DAntona A, Rouse J Int J Mol Sci. 2024; 25(22).
PMID: 39596031 PMC: 11594235. DOI: 10.3390/ijms252211962.
Sialic acid in the regulation of blood cell production, differentiation and turnover.
Irons E, Gc S, Lau J Immunology. 2024; 172(4):517-532.
PMID: 38503445 PMC: 11223974. DOI: 10.1111/imm.13780.
Wang Y, Peng Y, Long R, Shi P, Zhang Y, Kong D Comput Struct Biotechnol J. 2023; 21:4159-4171.
PMID: 37675287 PMC: 10477811. DOI: 10.1016/j.csbj.2023.08.014.
Siglecs as potential targets of therapy in human mast cell- and/or eosinophil-associated diseases.
OSullivan J, Youngblood B, Schleimer R, Bochner B Semin Immunol. 2023; 69:101799.
PMID: 37413923 PMC: 10528103. DOI: 10.1016/j.smim.2023.101799.
Siglec-9 is an inhibitory receptor on human mast cells in vitro.
Miralda I, Samanas N, Seo A, Foronda J, Sachen J, Hui Y J Allergy Clin Immunol. 2023; 152(3):711-724.e14.
PMID: 37100120 PMC: 10524464. DOI: 10.1016/j.jaci.2023.04.007.