Establishing Preferred Product Characterization for the Evaluation of RNA Vaccine Antigens.

antigen presenting cells capping dendritic cells product characteristics therapeutics

Journal

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

Informations de publication

Date de publication:
27 Sep 2019
Historique:
received: 29 08 2019
revised: 17 09 2019
accepted: 23 09 2019
entrez: 2 10 2019
pubmed: 2 10 2019
medline: 2 10 2019
Statut: epublish

Résumé

The preferred product characteristics (for chemistry, control, and manufacture), in addition to safety and efficacy, are quintessential requirements for any successful therapeutic. Messenger RNA vaccines constitute a relatively new alternative to traditional vaccine development platforms, and thus there is less clarity regarding the criteria needed to ensure regulatory compliance and acceptance. Generally, to identify the ideal product characteristics, a series of assays needs to be developed, qualified and ultimately validated to determine the integrity, purity, stability, and reproducibility of a vaccine target. Here, using the available literature, we provide a summary of the array of biophysical and biochemical assays currently used in the field to characterize mRNA vaccine antigen candidates. Moreover, we review various in vitro functional cell-based assays that have been employed to facilitate the early assessment of the biological activity of these molecules, including the predictive immune response triggered in the host cell. Messenger RNA vaccines can be produced rapidly and at large scale, and thus will particularly benefit from well-defined and well-characterized assays ultimately to be used for in-process, release and stability-indications, which will allow equally rapid screening of immunogenicity, efficacy, and safety without the need to conduct often lengthy and costly in vivo experiments.

Identifiants

pubmed: 31569760
pii: vaccines7040131
doi: 10.3390/vaccines7040131
pmc: PMC6963847
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Subventions

Organisme : Robert J. and Helen C. Kleberg Foundation
ID : n/a
Organisme : Texas Children's Hospital
ID : n/a

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Auteurs

Cristina Poveda (C)

Department of Pediatrics, National School of Tropical Medicine, Baylor College of Medicine, One Baylor Plaza, BCM113 Houston, TX 77030, USA. Cristina.Poveda@bcm.edu.
Texas Children's Hospital Center for Vaccine Development, Baylor College of Medicine, 1102 Bates Street, Houston, TX 77030, USA. Cristina.Poveda@bcm.edu.

Amadeo B Biter (AB)

Department of Pediatrics, National School of Tropical Medicine, Baylor College of Medicine, One Baylor Plaza, BCM113 Houston, TX 77030, USA. Amadeo.Biter@bcm.edu.
Texas Children's Hospital Center for Vaccine Development, Baylor College of Medicine, 1102 Bates Street, Houston, TX 77030, USA. Amadeo.Biter@bcm.edu.

Maria Elena Bottazzi (ME)

Texas Children's Hospital Center for Vaccine Development, Baylor College of Medicine, 1102 Bates Street, Houston, TX 77030, USA. bottazzi@bcm.edu.
Department of Pediatrics and Molecular Virology & Microbiology, National School of Tropical Medicine, Baylor College of Medicine, One Baylor Plaza, BCM113 Houston, TX 77030, USA. bottazzi@bcm.edu.
Department of Biology, College of Arts and Sciences, Baylor University, Waco, TX 76798, USA. bottazzi@bcm.edu.

Ulrich Strych (U)

Department of Pediatrics, National School of Tropical Medicine, Baylor College of Medicine, One Baylor Plaza, BCM113 Houston, TX 77030, USA. strych@bcm.edu.
Texas Children's Hospital Center for Vaccine Development, Baylor College of Medicine, 1102 Bates Street, Houston, TX 77030, USA. strych@bcm.edu.

Classifications MeSH