Evidence map›Paper›PMID 30615119›Full record

Trial reportThe Journal of infectious diseases2019

Rapid Boosting of HIV-1 Neutralizing Antibody Responses in Humans Following a Prolonged Immunologic Rest Period.

Paul Spearman, Georgia D Tomaras, David C Montefiori, Ying Huang, Marnie L Elizaga, Guido Ferrari, S Munir Alam, Abby Isaacs, Hasan Ahmed, John Hural and 8 more

Abstract readClinical Trial
In one paragraph

Trial report in The Journal of infectious diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

Paul SpearmanDepartment of Pediatrics, Cincinnati Children's Hospital, Ohio.
Georgia D TomarasDepartment of Surgery, Duke University Medical Center, Durham, North Carolina.
David C MontefioriDepartment of Surgery, Duke University Medical Center, Durham, North Carolina.
Ying HuangVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Marnie L ElizagaVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Guido FerrariDepartment of Surgery, Duke University Medical Center, Durham, North Carolina.
S Munir AlamDepartment of Surgery, Duke University Medical Center, Durham, North Carolina.
Abby IsaacsVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Hasan AhmedDepartment of Biology, Emory University, Atlanta, Georgia.
John HuralVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
M Juliana McElrathVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Laissa OuedraogoDivision of AIDS, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland.
Michael PensieroDivision of AIDS, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland.
Chris ButlerDivision of AIDS, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland.
Spyros A KalamsDepartment of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee.
Edgar Turner OvertonDepartment of Medicine, University of Alabama at Birmingham, Cambridge, Massachusetts.
Susan W BarnettNovartis Vaccines, Cambridge, Massachusetts.
HVTN 088 Protocol Team and the NIH/NIAID HIV Vaccine Trials Network

Funding

LOC: HIV Vaccine Trials NetworkUM1AI068614 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Dan H. Barouch, Lawrence Corey · 2011 to 2026
$1175.6M
LC: HIV Vaccine Trials NetworkUM1AI068618 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Margaret Juliana McElrath · 2011 to 2026
$483.6M
SDMC: HIV Vaccine Trials NetworkUM1AI068635 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Peter B. Gilbert, Yunda Huang · 2011 to 2026
$385.9M
Social and Behavioral Sciences CoreP30AI064518 · NIAID · DUKE UNIVERSITY · PI Nwora Lance Okeke · 2005 to 2026
$50.5M
Vanderbilt HIV Clinical Trials Unit (CTU)UM1AI069439 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI David W Haas, Spyros A Kalams · 2012 to 2026
$33.1M
A-Z Clinical Trials UnitUM1AI069452 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Paul A. Goepfert · 2012 to 2026
$28.8M
Seattle Vaccine Trials UnitUM1AI069481 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Rachel Ann Bender Ignacio, Margaret Juliana McElrath · 2012 to 2026
$24.4M
NIAID NIH HHS N01AI25473NIAID NIH HHS P30 AI064518NIAID NIH HHS UM1 AI068614NIAID NIH HHS UM1 AI068618NIAID NIH HHS UM1 AI068635NIAID NIH HHS UM1 AI069439NIAID NIH HHS UM1 AI069452NIAID NIH HHS UM1 AI069481
6 · The paper itself

Abstract

backgroundThe durability and breadth of human immunodeficiency virus type 1 (HIV-1)-specific immune responses elicited through vaccination are important considerations in the development of an effective HIV-1 vaccine. Responses to HIV-1 envelope subunit protein (Env) immunization in humans are often described as short-lived.

methodsWe enrolled 16 healthy volunteers who had received priming with an HIV-1 subtype B Env vaccine given with MF59 adjuvant 5-17 years previously and 20 healthy unprimed volunteers. Three booster immunizations with a heterologous subtype C trimeric gp140 protein vaccine were administered to the primed group, and the same subtype C gp140 protein vaccination regimen was administered to the unprimed subjects.

resultsBinding antibodies and neutralizing antibodies to tier 1 viral isolates were detected in the majority of previously primed subjects. Remarkably, a single dose of protein boosted binding and neutralizing antibody titers in 100% of primed subjects following this prolonged immunologic rest period, and CD4+ T-cell responses were boosted in 75% of primed individuals.

conclusionsThese results demonstrate that HIV-1 protein immunogens can elicit durable memory T- and B-cell responses and that strong tier 1 virus neutralizing responses can be elicited by a single booster dose of protein following a long immunologic rest period. However, we found no evidence that cross-clade boosting led to a significantly broadened neutralizing antibody response.

Indexed as

Adjuvants, ImmunologicAdolescentAdultAntibodies, NeutralizingHIV-1HIV AntibodiesHIV InfectionsHumansImmunization, SecondaryMiddle AgedVaccinationYoung AdultAdjuvants, ImmunologicAntibodies, NeutralizingHIV AntibodiesHIV envelopeHIV vaccineneutralization breadthneutralizing antibodies

Identifiers

PMID30615119
PMCPMC6775047

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.