免疫原性
表位
抗原
抗体
癌症疫苗
免疫系统
免疫学
免疫
抗体效价
免疫
肽疫苗
癌症
病毒学
效价
免疫疗法
医学
生物
内科学
作者
Barbara Richichi,Baptiste Thomas,Michele Fiore,Rosa Bosco,Huma Qureshi,Cristina Nativi,Olivier Renaudet,Lbachir BenMohamed
标识
DOI:10.1002/anie.201406897
摘要
Abstract Tumor‐associated carbohydrate antigens (TACAs) are key components of cancer vaccines. A variety of vaccines based on native TACAs such as α‐Tn have shown immunogenicity and protection in preclinical animal studies, however, their weak immunogenicity, low in vivo instability, and poor bioavailability, have discouraged their further evaluations in clinical studies. A new improved vaccine prototype is reported. It is composed of four clustered Tn‐antigen mimetics and a immunogenic peptide epitope that are conjugated to a cyclopeptide carrier. The immunization of mice with this vaccine 1) was safe, 2) induced a strong and long‐lasting Tn‐specific response with IgM/IgG antibodies able to recognize native carbohydrate antigens; 3) produced high titers of IgG1, IgG2a, and IgG3 antibodies; and 4) produced a significant antibody‐dependent regression of tumors and conferred protection. Altogether, these findings pave the way for the clinical development of safe and effective therapeutic vaccines against Tn‐expressing cancers.
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