Moving beyond Titers

被引:2
作者
Brooks, Benjamin D. [1 ,2 ]
Beland, Alexander [3 ]
Aguero, Gabriel [3 ]
Taylor, Nicholas [3 ]
Towne, Francina D. [3 ]
机构
[1] Rocky Vista Univ, Dept Biomed Sci, Ivins, UT 84738 USA
[2] Inovan Inc, Fargo, ND 58103 USA
[3] Rocky Vista Univ, Coll Osteopath Med, Parker, CO 80112 USA
关键词
vaccine non-responsiveness/poor durability/longevity; titers; immune repertoire sequencing; immunogenomics; HLA typing; B cell epitopes; epitope binning; immunogenicity; vaccine efficacy; COVID-19; vaccine development; ANTIBODY REPERTOIRE; COST; IDENTIFICATION; VACCINOMICS; CHALLENGES; INFLUENZA; COVID-19; VACCINES; INSIGHTS; BROAD;
D O I
10.3390/vaccines10050683
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Vaccination to prevent and even eliminate disease is amongst the greatest achievements of modern medicine. Opportunities remain in vaccine development to improve protection across the whole population. A next step in vaccine development is the detailed molecular characterization of individual humoral immune responses against a pathogen, especially the rapidly evolving pathogens. New technologies such as sequencing the immune repertoire in response to disease, immunogenomics/vaccinomics, particularly the individual HLA variants, and high-throughput epitope characterization offer new insights into disease protection. Here, we highlight the emerging technologies that could be used to identify variation within the human population, facilitate vaccine discovery, improve vaccine safety and efficacy, and identify mechanisms of generating immunological memory. In today's vaccine-hesitant climate, these techniques used individually or especially together have the potential to improve vaccine effectiveness and safety and thus vaccine uptake rates. We highlight the importance of using these techniques in combination to understand the humoral immune response as a whole after vaccination to move beyond neutralizing titers as the standard for immunogenicity and vaccine efficacy, especially in clinical trials.
引用
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页数:14
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