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Scientific rationale for developing potent RBD-based vaccines targeting COVID-19.
Kleanthous, Harry; Silverman, Judith Maxwell; Makar, Karen W; Yoon, In-Kyu; Jackson, Nicholas; Vaughn, David W.
  • Kleanthous H; Bill and Melinda Gates Foundation, Seattle, WA, USA.
  • Silverman JM; Bill and Melinda Gates Medical Research Institute, Seattle, WA, USA.
  • Makar KW; Bill and Melinda Gates Foundation, Seattle, WA, USA.
  • Yoon IK; Coalition for Epidemic Preparedness Innovations, Greater London, UK.
  • Jackson N; Coalition for Epidemic Preparedness Innovations, Greater London, UK. nick.jackson@cepi.net.
  • Vaughn DW; Bill and Melinda Gates Foundation, Seattle, WA, USA.
NPJ Vaccines ; 6(1): 128, 2021 Oct 28.
Article in English | MEDLINE | ID: covidwho-1545613
ABSTRACT
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.

Full text: Available Collection: International databases Database: MEDLINE Type of study: Randomized controlled trials Topics: Vaccines / Variants Language: English Journal: NPJ Vaccines Year: 2021 Document Type: Article Affiliation country: S41541-021-00393-6

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Randomized controlled trials Topics: Vaccines / Variants Language: English Journal: NPJ Vaccines Year: 2021 Document Type: Article Affiliation country: S41541-021-00393-6