Publication | Open Access
Antitumor Humoral and T Cell Responses by Mucin-1 Conjugates of Bacteriophage Qβ in Wild-type Mice
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Citations
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References
2018
Year
Wild-type MiceHumoral ResponseImmunologyImmunoeditingImmunodominanceImmunologic MechanismAntigen ProcessingCd4 T Cell ResponsesImmunotherapeuticsImmunotherapySynthetic ImmunologyTumor ImmunologyTumor ImmunityAntibody EngineeringIgg TitersImmunoengineeringImmune SurveillanceMuc1 PeptidesHumoral ImmunityT Cell ImmunityQβ-muc1 ConjugatesMucin-1 ConjugatesCell BiologyCellular Immune ResponseMedicineBacteriophage QβViral Immunity
Mucin-1 (MUC1) is one of the top ranked tumor associated antigens. In order to generate effective anti-MUC1 immune responses as potential anticancer vaccines, MUC1 peptides and glycopeptides have been covalently conjugated to bacteriophage Qβ. Immunization of mice with these constructs led to highly potent antibody responses with IgG titers over one million, which are among the highest anti-MUC1 IgG titers reported to date. Furthermore, the high IgG antibody levels persisted for more than six months. The constructs also elicited MUC1 specific cytotoxic T cells, which can selectively kill MUC1 positive tumor cells. The unique abilities of Qβ-MUC1 conjugates to powerfully induce both antibody and cytotoxic T cell immunity targeting tumor cells bode well for future translation of the constructs as anticancer vaccines.
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