Department of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA, USA.
Department of Chemistry and Biochemistry, Brigham Young University, UT, USA.
Curr Opin Immunol. 2019 Aug;59:65-71. doi: 10.1016/j.coi.2019.03.004. Epub 2019 Apr 28.
High-affinity binding of antibodies provides for increased specificity and usually higher effector functions in vivo. This goal, well documented in cancer immunotherapy, is very relevant to vaccines as well, and has particularly significant application toward glycan antigens. The inability to elicit high-affinity antibodies has limited potential applications of glycan-based immunogens, giving rise to insufficient population coverage due to low titers and short duration of protection. That such vaccines have achieved widespread use in spite of these shortcomings highlights the surpassing importance of glycans as prophylactic immunological targets. New advances in the combination of synthetic chemistry, bioconjugation, and mechanistic immunology offer the possibility to vastly expand the number of potential molecular targets in cancer and infectious diseases by opening a wider world of carbohydrate structures to immunological recognition and high-affinity response.
抗体的高亲和力结合提供了更高的特异性,并通常在体内具有更高的效应功能。这一目标在癌症免疫治疗中已有充分的记录,与疫苗也非常相关,并且在糖抗原方面具有特别重要的应用。由于滴度低和保护持续时间短,无法诱导高亲和力抗体,限制了基于聚糖的免疫原的潜在应用,导致人群覆盖率不足。尽管存在这些缺点,这些疫苗仍得到广泛应用,这突出表明糖作为预防性免疫靶标具有非常重要的意义。合成化学、生物缀合和机制免疫学的新进展为通过将更广泛的碳水化合物结构引入免疫识别和高亲和力反应,为癌症和传染病中的潜在分子靶标数量的大幅增加提供了可能性。