Does Anybody Want an Injectable Rotavirus Vaccine, and Why? Understanding the Public Health Value Proposition of Next-Generation Rotavirus Vaccines.

combination vaccines cost-effectiveness gastroenteritis product preferences rotavirus value proposition

Journal

Vaccines
ISSN: 2076-393X
Titre abrégé: Vaccines (Basel)
Pays: Switzerland
ID NLM: 101629355

Informations de publication

Date de publication:
20 Jan 2022
Historique:
received: 12 11 2021
revised: 05 01 2022
accepted: 17 01 2022
entrez: 26 2 2022
pubmed: 27 2 2022
medline: 27 2 2022
Statut: epublish

Résumé

Routine infant immunization with live, oral rotavirus vaccines (LORVs) has had a major impact on severe gastroenteritis disease. Nevertheless, in high morbidity and mortality settings rotavirus remains an important cause of disease, partly attributable to the sub-optimal clinical efficacy of LORVs in those settings. Regardless of the precise immunological mechanism(s) underlying the diminished efficacy, the introduction of injectable next-generation rotavirus vaccines (iNGRV), currently in clinical development, could offer a potent remedy. In addition to the potential for greater clinical efficacy, precisely how iNGRVs are delivered (multiple doses to young infants; alongside LORVs or as a booster; co-formulated with Diphtheria-Tetanus-Pertussis (DTP)-containing vaccines), their pricing, and their storage and cold chain characteristics could each have major implications on the resultant health outcomes, on cost-effectiveness as well as on product preferences by national stakeholders and healthcare providers. To better understand these implications, we critically assessed whether there is a compelling public health value proposition for iNGRVs based on potential (but still hypothetical) vaccine profiles. Our results suggest that the answer is highly dependent on the specific use cases and potential attributes of such novel vaccines. Notably, co-formulation of iNGRVs with similar or greater efficacy than LORVs with a DTP-containing vaccine, such as DTP-Hib-HepB, scored especially high on potential impact, cost-effectiveness, and strength of preference by national stakeholders and health care providers in lower and middle income countries.

Identifiants

pubmed: 35214608
pii: vaccines10020149
doi: 10.3390/vaccines10020149
pmc: PMC8880741
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Subventions

Organisme : Bill & Melinda Gates Foundation
ID : OPP 1203883
Pays : United States

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Auteurs

William P Hausdorff (WP)

Center for Vaccine Innovation and Access, PATH, 455 Massachusetts Ave NW, Washington, DC 20001, USA.
Faculty of Medicine, Université Libre de Bruxelles, 1070 Brussels, Belgium.

Jessica Price (J)

Center for Vaccine Innovation and Access, PATH, 2201 Westlake Ave, Suite 200, Seattle, WA 98121, USA.

Frédéric Debellut (F)

Center for Vaccine Innovation and Access, PATH, Rue de Varembé 7, 1202 Geneva, Switzerland.

Jessica Mooney (J)

Center for Vaccine Innovation and Access, PATH, 2201 Westlake Ave, Suite 200, Seattle, WA 98121, USA.

Andrew A Torkelson (AA)

Linksbridge SPC, 808 5th Ave N, Seattle, WA 98109, USA.

Khatuna Giorgadze (K)

Linksbridge SPC, 808 5th Ave N, Seattle, WA 98109, USA.

Clint Pecenka (C)

Center for Vaccine Innovation and Access, PATH, 2201 Westlake Ave, Suite 200, Seattle, WA 98121, USA.

Classifications MeSH