Characterization and utility of two monoclonal antibodies to cholera toxin B subunit

• Published in: Scientific reports Vol. 13; no. 1; p. 4305
• Main Authors: Verjan Garcia, Noel, Santisteban Celis, Ian Carlosalberto, Dent, Matthew, Matoba, Nobuyuki
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 15.03.2023; Nature Publishing Group; Nature Portfolio
• Subjects: 631/1647/664/1257; 631/1647/664/1467; 631/1647/664/2228; 631/250/2152/2153/1291; 631/250/347; 631/61; Adjuvants, Immunologic; Animals; Antibodies, Monoclonal; Caco-2 Cells; Cholera; Cholera Toxin - metabolism; Cholera toxin B subunit; Colon; Cyclic AMP; E coli; Enzyme-linked immunosorbent assay; Epithelial cells; Escherichia coli; Flow cytometry; Heat-labile enterotoxin; Humanities and Social Sciences; Humans; Immunohistochemistry; Immunomodulation; Leukocytes; Localization; Mice; Monoclonal antibodies; Mucosa; multidisciplinary; Oral administration; Science; Science (multidisciplinary); Surface plasmon resonance; Toxins; Waterborne diseases
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-023-30834-2

Cholera toxin B subunit (CTB) is a potent immunomodulator exploitable in mucosal vaccine and immunotherapeutic development. To aid in the characterization of pleiotropic biological functions of CTB and its variants, we generated a panel of anti-CTB monoclonal antibodies (mAbs). By ELISA and surface plasmon resonance, two mAbs, 7A12B3 and 9F9C7, were analyzed for their binding affinities to cholera holotoxin (CTX), CTB, and EPICERTIN: a recombinant CTB variant possessing mucosal healing activity. Both 7A12B3 and 9F9C7 bound efficiently to CTX, CTB, and EPICERTIN with equilibrium dissociation constants at low to sub-nanomolar concentrations but bound weakly, if at all, to Escherichia coli heat-labile enterotoxin B subunit. In a cyclic adenosine monophosphate assay using Caco2 human colon epithelial cells, the 7A12B3 mAb was found to be a potent inhibitor of CTX, whereas 9F9C7 had relatively weak inhibitory activity. Meanwhile, the 9F9C7 mAb effectively detected CTB and EPICERTIN bound to the surface of Caco2 cells and mouse spleen leukocytes by flow cytometry. Using 9F9C7 in immunohistochemistry, we confirmed the preferential localization of EPICERTIN in colon crypts following oral administration of the protein in mice. Collectively, these mAbs provide valuable tools to investigate the biological functions and preclinical development of CTB variants.