Vaccine value profile for invasive non-typhoidal Salmonella disease.


Journal

Vaccine
ISSN: 1873-2518
Titre abrégé: Vaccine
Pays: Netherlands
ID NLM: 8406899

Informations de publication

Date de publication:
25 Jul 2024
Historique:
received: 02 10 2022
revised: 12 04 2024
accepted: 14 04 2024
medline: 14 7 2024
pubmed: 14 7 2024
entrez: 13 7 2024
Statut: ppublish

Résumé

Invasive non-typhoidal Salmonella (iNTS) disease is an under-recognized high-burden disease causing major health and socioeconomic issues in sub-Saharan Africa (sSA), predominantly among immune-naïve infants and young children, including those with recognized comorbidities such as HIV infection. iNTS disease is primarily caused by Salmonella enterica serovar Typhimurium sequence type (ST) 313 and 'African-restricted clades' of Salmonella Enteritidis ST11 that have emerged across the African continent as a series of epidemics associated with acquisition of new antimicrobial resistance. Due to genotypes with a high prevalence of antimicrobial resistance and scarcity of therapeutic options, these NTS serovars are designated by the World Health Organization as a priority pathogen for research and development of interventions, including vaccines, to address and reduce NTS associated bacteremia and meningitis in sSA. Novel and traditional vaccine technologies are being applied to develop vaccines against iNTS disease, and the results of the first clinical trials in the infant target population should become available in the near future. The "Vaccine Value Profile" (VVP) addresses information related predominantly to invasive disease caused by Salmonella Enteritidis and Salmonella Typhimurium prevalent in sSA. Information is included on stand-alone iNTS disease candidate vaccines and candidate vaccines targeting iNTS disease combined with another invasive serotype, Salmonella Typhi, that is also common across sSA. Out of scope for the first version of this VVP is a wider discussion on either diarrheagenic NTS disease (dNTS) also associated with Salmonella Enteritidis and Salmonella Typhimurium or the development of a multivalent Salmonella vaccines targeting key serovars for use globally. This VVP for vaccines to prevent iNTS disease is intended to provide a high-level, holistic assessment of the information and data that are currently available to inform the potential public health, economic, and societal value of pipeline vaccines and vaccine-like products. Future versions of this VVP will be updated to reflect ongoing activities such as vaccine development strategies and a "Full Vaccine Value Assessment" that will inform the value proposition of an iNTS disease vaccine. This VVP was developed by a working group of subject matter experts from academia, non-profit organizations, public private partnerships, and multi-lateral organizations, and in collaboration with stakeholders from the World Health Organization African Region. All contributors have extensive expertise on various elements of the iNTS disease VVP and collectively aimed to identify current research and knowledge gaps. The VVP was developed using only existing and publicly available information.

Identifiants

pubmed: 39003017
pii: S0264-410X(24)00470-5
doi: 10.1016/j.vaccine.2024.04.045
pii:
doi:

Substances chimiques

Salmonella Vaccines 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

S101-S124

Informations de copyright

Copyright © 2024. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: LBM and MJS report financial support and administrative support by the World Health Organization. LBM was an independent consultant during VVP development; she is currently employed by the US Pharmacopeial Convention. CSM and JAC received support through the received funding from the EU Horizon 2020 research and innovation programme under the project Vacc-iNTS (grant agreement number 815439).VM was employed by the International Vaccines Institute during VVP development; he is currently employed by the World Health Organization. All other authors declare no conflicts of interest.

Auteurs

Laura B Martin (LB)

Independent Consultant, USA. Electronic address: LauraBMartin@vacc4impact.science.

Bieke Tack (B)

Department of Clinical Sciences, Institute of Tropical Medicine Antwerp, Belgium and Department of Microbiology, Immunology and Transplantation, KU Leuven, Belgium. Electronic address: btack@itg.be.

Christian S Marchello (CS)

Centre for International Health, University of Otago, New Zealand. Electronic address: Christian.Marchello@otago.ac.nz.

Michael J Sikorski (MJ)

Center for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, USA. Electronic address: michael.sikorski@som.umaryland.edu.

Ellis Owusu-Dabo (E)

Kwame Nkrumah University of Science and Technology, Ghana. Electronic address: Eowusu-Dabo.chs@knust.edu.gh.

Tonney Nyirenda (T)

University of Malawi - College of Medicine, Malawi. Electronic address: TNyirenda@medcol.mw.

Vittal Mogasale (V)

International Vaccine Institute, Republic of Korea. Electronic address: mogasalev@who.int.

John A Crump (JA)

Centre for International Health, University of Otago, New Zealand. Electronic address: john.crump@otago.ac.nz.

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Classifications MeSH