Scientific rationale for developing potent RBD-based vaccines targeting COVID-19

被引:99
作者
Kleanthous, Harry [1 ]
Silverman, Judith Maxwell [2 ]
Makar, Karen W. [1 ]
Yoon, In-Kyu [3 ]
Jackson, Nicholas [3 ]
Vaughn, David W. [1 ]
机构
[1] Bill & Melinda Gates Fdn, Seattle, WA USA
[2] Bill & Melinda Gates Med Res Inst, Seattle, WA USA
[3] Coalit Epidem Preparedness Innovat, Greater London, England
关键词
RECEPTOR-BINDING DOMAIN; NEUTRALIZING ANTIBODIES; NANOPARTICLE VACCINES; SARS-COV-2; IMMUNITY; IMMUNOGENICITY; SPIKE; ELICITATION; RESPONSES; EFFICACY;
D O I
10.1038/s41541-021-00393-6
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 of the global population against COVID-19 is a great scientific, logistical, and moral challenge. Despite the rapid development and authorization of several full-length Spike (S) protein vaccines, the global demand outweighs the current supply and there is a need for safe, potent, high-volume, affordable vaccines that can fill this gap, especially in low- and middle-income countries. Whether SARS-CoV-2 S-protein receptor-binding domain (RBD)-based vaccines could fill this gap has been debated, especially with regards to its suitability to protect against emerging viral variants of concern. Given a predominance for elicitation of neutralizing antibodies (nAbs) that target RBD following natural infection or vaccination, a key biomarker of protection, there is merit for selection of RBD as a sole vaccine immunogen. With its high-yielding production and manufacturing potential, RBD-based vaccines offer an abundance of temperature-stable doses at an affordable cost. In addition, as the RBD preferentially focuses the immune response to potent and recently recognized cross-protective determinants, this domain may be central to the development of future pan-sarbecovirus vaccines. In this study, we review the data supporting the non-inferiority of RBD as a vaccine immunogen compared to full-length S-protein vaccines with respect to humoral and cellular immune responses against both the prototype pandemic SARS-CoV-2 isolate and emerging variants of concern.
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页数:10
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