Peter B. Gilbert

Dr. Peter B. Gilbert

orcid

Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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7 January 2022 in Science
Verified
Journal Article
Open access
PGPeter B. Gilbert
Peter B. Gilbert
DMDavid C. Montefiori
David C. Montefiori
AMAdrian B. McDermott
Adrian B. McDermott
YFYouyi Fong
Youyi Fong
DBDavid Benkeser
David Benkeser
UTUnited States Government (USG)/CoVPN Biostatistics Team
United States Government (USG)/CoVPN Biostatistics Team
Antibody levels predict vaccine efficacy: Symptomatic COVID-19 infection can be prevented by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines. A “correlate of protection” is a molecular biomarker to measure how much immunity is needed to fight infection and is key for successful global immunization programs. Gilbert et al . determined that antibodies are the correlate of protection in vaccinated individuals enrolled in the Moderna COVE phase 3 clinical trial (see the Perspective by Openshaw). By measuring binding and neutralizing antibodies against the viral spike protein, the authors found that the levels of both antibodies correlated with the degree of vaccine efficacy. The higher the antibody level, the greater the protection afforded by the messenger RNA (mRNA) vaccine. Antibody levels that predict mRNA vaccine efficacy can therefore be used to guide vaccine regimen modifications and support regulatory approvals for a broader spectrum of the population. —PNK

19 November 2015 in New England Journal of Medicine
Verified
Journal Article
Closed access
PDF file
DNDaniel E. Neafsey
Daniel E. Neafsey
MJMichal Juraska
Michal Juraska
TBTrevor Bedford
Trevor Bedford
DBDavid Benkeser
David Benkeser
CVClarissa Valim
Clarissa Valim
DWDyann F. Wirth
Dyann F. Wirth
The RTS,S/AS01 vaccine targets the circumsporozoite protein of Plasmodium falciparum and has partial protective efficacy against clinical and severe malaria disease in infants and children. We investigated whether the vaccine efficacy was specific to certain parasite genotypes at the circumsporozoite protein locus. We used polymerase chain reaction–based next-generation sequencing of DNA extracted from samples from 4985 participants to survey circumsporozoite protein polymorphisms. We evaluated the effect that polymorphic positions and haplotypic regions within the circumsporozoite protein had on vaccine efficacy against first episodes of clinical malaria within 1 year after vaccination. In the per-protocol group of 4577 RTS,S/AS01-vaccinated participants and 2335 control-vaccinated participants who were 5 to 17 months of age, the 1-year cumulative vaccine efficacy was 50.3% (95% confidence interval [CI], 34.6 to 62.3) against clinical malaria in which parasites matched the vaccine in the entire circumsporozoite protein C-terminal (139 infections), as compared with 33.4% (95% CI, 29.3 to 37.2) against mismatched malaria (1951 infections) (P=0.04 for differential vaccine efficacy). The vaccine efficacy based on the hazard ratio was 62.7% (95% CI, 51.6 to 71.3) against matched infections versus 54.2% (95% CI, 49.9 to 58.1) against mismatched infections (P=0.06). In the group of infants 6 to 12 weeks of age, there was no evidence of differential allele-specific vaccine efficacy. These results suggest that among children 5 to 17 months of age, the RTS,S vaccine has greater activity against malaria parasites with the matched circumsporozoite protein allele than against mismatched malaria. The overall vaccine efficacy in this age category will depend on the proportion of matched alleles in the local parasite population; in this trial, less than 10% of parasites had matched alleles. (Funded by the National Institutes of Health and others.)

4 November 2020 in Science Translational Medicine
Verified
Journal Article
Open access
PDF file
BHBarton F. Haynes
Barton F. Haynes
LCLawrence Corey
Lawrence Corey
PFPrabhavathi Fernandes
Prabhavathi Fernandes
PGPeter B. Gilbert
Peter B. Gilbert
PHPeter J. Hotez
Peter J. Hotez
AAAnn Arvin
Ann Arvin
Prior vaccine development experiences do not raise concerns about vaccine-associated enhanced disease for COVID-19 vaccine candidates.

24 November 2008 in Biometrics
Verified
Journal Article
Closed access
PDF file
PGPeter B. Gilbert
Peter B. Gilbert
MHMichael G. Hudgens
Michael G. Hudgens

16 October 2017 in Biometrika
Verified
Journal Article
Closed access
DBD Benkeser
D Benkeser
MCM Carone
M Carone
MLM J Van Der Laan
M J Van Der Laan
PGPeter B. Gilbert
Peter B. Gilbert
Summary: Doubly robust estimators are widely used to draw inference about the average effect of a treatment. Such estimators are consistent for the effect of interest if either one of two nuisance parameters is consistently estimated. However, if flexible, data-adaptive estimators of these nuisance parameters are used, double robustness does not readily extend to inference. We present a general theoretical study of the behaviour of doubly robust estimators of an average treatment effect when one of the nuisance parameters is inconsistently estimated. We contrast different methods for constructing such estimators and investigate the extent to which they may be modified to also allow doubly robust inference. We find that while targeted minimum loss-based estimation can be used to solve this problem very naturally, common alternative frameworks appear to be inappropriate for this purpose. We provide a theoretical study and a numerical evaluation of the alternatives considered. Our simulations highlight the need for and usefulness of these approaches in practice, while our theoretical developments have broad implications for the construction of estimators that permit doubly robust inference in other problems.

26 August 2003 in Biometrics
Verified
Journal Article
Closed access
PDF file
PGPeter B. Gilbert
Peter B. Gilbert
RBRonald J. Bosch
Ronald J. Bosch
MHMichael G. Hudgens
Michael G. Hudgens