Evaluating Use Cases for Human Challenge Trials in Accelerating SARS-CoV-2 Vaccine Development.

COVID-19 controlled human infection human challenge trial pandemic vaccine evaluation

Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
16 02 2021
Historique:
received: 26 05 2020
accepted: 02 07 2020
pubmed: 7 7 2020
medline: 20 2 2021
entrez: 7 7 2020
Statut: ppublish

Résumé

Human challenge trials (HCTs) have been proposed as a means to accelerate SARS-CoV-2 vaccine development. We identify and discuss 3 potential use cases of HCTs in the current pandemic: evaluating efficacy, converging on correlates of protection, and improving understanding of pathogenesis and the human immune response. We outline the limitations of HCTs and find that HCTs are likely to be most useful for vaccine candidates currently in preclinical stages of development. We conclude that, while currently limited in their application, there are scenarios in which HCTs would be extremely beneficial. Therefore, the option of conducting HCTs to accelerate SARS-CoV-2 vaccine development should be preserved. As HCTs require many months of preparation, we recommend an immediate effort to (1) establish guidelines for HCTs for COVID-19; (2) take the first steps toward HCTs, including preparing challenge virus and making preliminary logistical arrangements; and (3) commit to periodically re-evaluating the utility of HCTs.

Identifiants

pubmed: 32628748
pii: 5868014
doi: 10.1093/cid/ciaa935
pmc: PMC7454474
doi:

Substances chimiques

COVID-19 Vaccines 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

710-715

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Auteurs

Linh Chi Nguyen (LC)

Department of Politics and International Relations, University of Oxford, Oxford, United Kingdom.

Christopher W Bakerlee (CW)

Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts, USA.
Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, Massachusetts, USA.

T Greg McKelvey (TG)

ASAPP, Inc, NY, USA.

Sophie M Rose (SM)

Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.

Alexander J Norman (AJ)

Independent Scholar, Worthing, United Kingdom.

Nicholas Joseph (N)

Independent Scholar, Oakland, California, USA.

David Manheim (D)

Health and Risk Communication Research Center, School of Public Health, University of Haifa, Haifa, Israel.

Michael R McLaren (MR)

Department of Population Health and Pathobiology, North Carolina State University, Raleigh, North Carolina, USA.

Steven Jiang (S)

Harvard Law School, Cambridge, Massachusetts, USA.

Conor F Barnes (CF)

Independent Scholar, Kelowna, British Columbia, Canada.

Megan Kinniment (M)

Department of Physics, University of Oxford, Oxford, United Kingdom.

Derek Foster (D)

Rethink Priorities, Redwood City, California, USA.

Thomas C Darton (TC)

Department of Infection, Immunity, and Cardiovascular Disease, University of Sheffield, Sheffield, United Kingdom.

Josh Morrison (J)

Waitlist Zero, Brooklyn, New York, USA.

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