Publication | Open Access
Carbohydrate-Monophosphoryl Lipid A Conjugates Are Fully Synthetic Self-Adjuvanting Cancer Vaccines Eliciting Robust Immune Responses in the Mouse
112
Citations
25
References
2011
Year
ImmunologyImmunoeditingImmunotherapeuticsImmunotherapySynthetic ImmunologyTumor-associated Carbohydrate AntigensTumor ImmunityCancer VaccinesAntibody EngineeringMucosal VaccinationTitermax GoldTherapeutic VaccinePolyvalent VaccineCell BiologyTumor MicroenvironmentBiomolecular EngineeringSynthetic Glycoconjugate VaccinesVaccinationVaccine DesignMedicine
Tumor-associated carbohydrate antigens (TACAs) are useful targets in the development of therapeutic cancer vaccines. However, a serious problem with them is the poor immunogenicity. To overcome the problem, a monophosphorylated derivative of Neisseria meningitidis lipid A was explored as a potential carrier molecule and built-in adjuvant for the construction of structurally defined fully synthetic glycoconjugate vaccines. Some paradigm-shifting discoveries about the monophosphoryl lipid A (MPLA)-TACA conjugates were that they elicited robust IgG antibody responses, indicating T cell-mediated immunity, without an external adjuvant and that an external adjuvant, e.g., Titermax Gold, actually reduced rather than promoted the immunological activity of the conjugates. The induced antibodies were proved to bind selectively to target tumor cells. MPLA was therefore demonstrated to be a powerful built-in immunostimulant and adjuvant for an all new design of fully synthetic glycoconjugate cancer vaccines.
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