Evidence map›Paper›PMID 31345930›Full record

Trial reportThe Journal of experimental medicine2019

Detection and activation of HIV broadly neutralizing antibody precursor B cells using anti-idiotypes.

Tara Bancroft, Blair L DeBuysscher, Connor Weidle, Allison Schwartz, Abigail Wall, Matthew D Gray, Junli Feng, Holly R Steach, Kristin S Fitzpatrick, Mesfin M Gewe and 9 more

Abstract readClinical Trial
In one paragraph

Trial report in The Journal of experimental medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed, 16 citations in OpenAlex.

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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

19 authors at 1 institution in 1 country.

Tara BancroftVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Blair L DeBuysscherVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Connor WeidleVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Allison SchwartzVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Abigail WallVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Matthew D GrayVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA.ORCID 0000-0002-4260-9784
Junli FengVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Holly R SteachVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Kristin S FitzpatrickVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA.ORCID 0000-0001-8086-5239
Mesfin M GeweBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Patrick D SkogDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA.ORCID 0000-0002-5759-5071
Colleen Doyle-CooperDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA.ORCID 0000-0002-1208-1165
Takayuki OtaDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA.
Roland K StrongVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
David NemazeeDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA.ORCID 0000-0002-4769-6311
Marie PanceraVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Leonidas StamatatosVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA lstamata@fredhutch.org.ORCID 0000-0002-1106-7097
Andrew T McGuireVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA amcguire@fredhutch.org.ORCID 0000-0003-1841-6859
Justin J TaylorVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA jtaylor3@fredhutch.org.ORCID 0000-0001-9718-2901
Infectious Disease Research Institute · US

Funding

Recombinant HIV-1 Env glycoprotein immunogens and antibodies production and structural characterizationP01AI138212 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI MCGUIRE, ANDREW · 2019 to 2023
$9.2M
Knock-in mice expressing germline-reverted broadly neutralizing HIV antibodiesR01AI073148 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI NEMAZEE, DAVID · 2007 to 2023
$8.2M
Monitoring the development of anti-Env Abs during HIV infectionR01AI081625 · NIAID · SEATTLE BIOMEDICAL RESEARCH INSTITUTE · PI STAMATATOS, LEONIDAS · 2010 to 2020
$5.8M
Immune Tolerance in Non-Clonal Immune SystemsR37AI059714 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI NEMAZEE, DAVID · 2014 to 2020
$3.5M
Identification and Analysis of HIV-specific Naive B cells in HIV-unexposed IndividualsR01AI122912 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI TAYLOR, JUSTIN J · 2016 to 2020
$2.7M
Molecular Medicine Training ProgramT32GM095421 · NIGMS · UNIVERSITY OF WASHINGTON · PI HAWN, THOMAS R, LILES, W. CONRAD · 2011 to 2020
$1.6M
Germline-targeting anti-idiotype antibodies as novel HIV-1 immunogensR21AI127249 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI MCGUIRE, ANDREW · 2016 to 2017
$484k
NIAID NIH HHS P01 AI138212NIAID NIH HHS R01 AI073148NIAID NIH HHS R01 AI081625NIAID NIH HHS R01 AI122912NIAID NIH HHS R21 AI127249NIAID NIH HHS R37 AI059714NIGMS NIH HHS T32 GM095421
6 · The paper itself

Abstract

Many tested vaccines fail to provide protection against disease despite the induction of antibodies that bind the pathogen of interest. In light of this, there is much interest in rationally designed subunit vaccines that direct the antibody response to protective epitopes. Here, we produced a panel of anti-idiotype antibodies able to specifically recognize the inferred germline version of the human immunodeficiency virus 1 (HIV-1) broadly neutralizing antibody b12 (iglb12). We determined the crystal structure of two anti-idiotypes in complex with iglb12 and used these anti-idiotypes to identify rare naive human B cells expressing B cell receptors with similarity to iglb12. Immunization with a multimerized version of this anti-idiotype induced the proliferation of transgenic murine B cells expressing the iglb12 heavy chain in vivo, despite the presence of deletion and anergy within this population. Together, our data indicate that anti-idiotypes are a valuable tool for the study and induction of potentially protective antibodies.

Indexed as

AdultAnimalsAntibodies, Anti-IdiotypicAntibodies, NeutralizingFemaleHIV-1HIV AntibodiesHIV InfectionsHumansMaleMiceMice, TransgenicPrecursor Cells, B-LymphoidAntibodies, Anti-IdiotypicAntibodies, NeutralizingHIV Antibodies

Identifiers

PMID31345930
PMCPMC6780997
OpenAlexW2964267167

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

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.