Strong adjuvant properties of cholera toxin on gut mucosal immune responses to orally presented antigens

• Published in: Immunology Vol. 59; no. 2; pp. 301 - 308
• Main Authors: LYCKE, N, HOLMGREN, J
• Format: Journal Article
• Language: English
• Published: Oxford Blackwell 01-10-1986
• Subjects: Adenylyl Cyclases; Adjuvants, Immunologic; Administration, Oral; Animals; Antibody-Producing Cells - immunology; Antigens - administration & dosage; Antigens - immunology; Applied sciences; B-Lymphocytes - immunology; Cholera Toxin - immunology; Cyclic AMP; Dose-Response Relationship, Immunologic; Exact sciences and technology; Hemocyanins - immunology; Immunization; Immunologic Memory; Intestinal Mucosa - immunology; Mice; Other techniques and industries; T-Lymphocytes - immunology; Time Factors
• ISSN: 0019-2805; 1365-2567

There is a great need for substances that can act as adjuvants on local mucosal immune responses to perorally (p.o.) administered immunogens and which could be included in future oral vaccines. In this study we show that in mice cholera toxin (CT) is a potent adjuvant on enteric mucosal immune responses to related (cholera B subunit) as well as unrelated (KLH) antigens presented by the p.o. route. The adjuvant action of CT was dose-dependent and was achieved only when CT was given p.o. and together with the antigen. Both priming (memory induction) and boosting of the gut mucosal immune system by the oral route were greatly potentiated by CT. High numbers of specific antibody-producing cells as well as substantial mucosal memory in the lamina propria were stimulated by p.o. priming immunizations if CT adjuvant was included. Anamnestic responses could be elicited by a single p.o. booster immunization for at least 10 weeks and probably much longer. The adjuvant action of CT is suggested to involve activation of adenylate cyclase and cyclic AMP-mediated signals with differential effects on B and regulatory T intestinal lymphocytes. The adjuvant-active dose of CT, 100-500 ng, was lower than the immunogenic dose (2 micrograms) and much below the p.o. dose needed for detectable net fluid secretion in mouse intestine (5-10 micrograms). Cholera B subunit (10 micrograms) administered p.o. together with 500 ng of CT was 50 times more effective in stimulating gut mucosal anti-toxin responses compared with B subunit vaccine alone. Our results suggest that CT or substances that use similar adjuvant mechanisms may substantially increase the mucosal immunogenicity and efficacy of non-replicating oral vaccines.