Evidence map›Paper›PMID 36574685›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2023

Humanized V(D)J-rearranging and TdT-expressing mouse vaccine models with physiological HIV-1 broadly neutralizing antibody precursors.

Sai Luo, Changbin Jing, Adam Yongxin Ye, Sven Kratochvil, Christopher A Cottrell, Ja-Hyun Koo, Aimee Chapdelaine Williams, Lucas Vieira Francisco, Himanshu Batra, Edward Lamperti and 9 more

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.1field-weighted citation impact, top 12% of its field
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

26 citing papers in PubMed, 25 citations in OpenAlex.

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  8. Recurrent SARS-CoV-2 Omicron broadly neutralizing humanized antibodies in different single human VProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  9. Nanoparticle Immunoadjuvant Complexes Augment Germinal Center Responses to Vaccination.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
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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 5 institutions in 1 country.

Sai LuoHHMI, Boston Children's Hospital, Boston, MA 02115.ORCID 0000-0002-7362-5445
Changbin JingHHMI, Boston Children's Hospital, Boston, MA 02115.
Adam Yongxin YeHHMI, Boston Children's Hospital, Boston, MA 02115.
Sven KratochvilThe Ragon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology and Harvard University, Cambridge, MA 02139.
Christopher A CottrellDepartment of Immunology and Microbiology, The Scripps Research Institute, La Jolla, San Diego, CA 92037.ORCID 0000-0002-3364-3083
Ja-Hyun KooThe Ragon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology and Harvard University, Cambridge, MA 02139.
Aimee Chapdelaine WilliamsHHMI, Boston Children's Hospital, Boston, MA 02115.ORCID 0000-0001-9402-4326
Lucas Vieira FranciscoHHMI, Boston Children's Hospital, Boston, MA 02115.
Himanshu BatraHHMI, Boston Children's Hospital, Boston, MA 02115.
Edward LampertiThe Ragon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology and Harvard University, Cambridge, MA 02139.
Oleksandr KalyuzhniyDepartment of Immunology and Microbiology, The Scripps Research Institute, La Jolla, San Diego, CA 92037.ORCID 0000-0002-5273-1951
Yuxiang ZhangHHMI, Boston Children's Hospital, Boston, MA 02115.
Alessandro BarbieriDepartment of Laboratory Medicine, Boston Children's Hospital, Boston, MA 02115.
John P ManisDepartment of Laboratory Medicine, Boston Children's Hospital, Boston, MA 02115.
Barton F HaynesDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710.
William R SchiefThe Ragon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology and Harvard University, Cambridge, MA 02139.ORCID 0000-0002-1120-0150
Facundo D BatistaThe Ragon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology and Harvard University, Cambridge, MA 02139.ORCID 0000-0002-1130-9463
Ming TianHHMI, Boston Children's Hospital, Boston, MA 02115.
Frederick W AltHHMI, Boston Children's Hospital, Boston, MA 02115.
Boston Children's Hospital · USRagon Institute of MGH, MIT and Harvard · USScripps Research Institute · USDuke University · USHarvard University · US

Funding

Identification of neutralizing epitopes on SARS-CoV-2 spike for design of vaccines and small-molecule antiviralsUM1AI144462 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI BURTON, DENNIS R. · 2019 to 2025
$201.6M
Nonhuman primate studies for development of a prototype HIV vaccine that induces broadly neutralizing antibodiesUM1AI144371 · NIAID · DUKE UNIVERSITY · PI HAYNES, BARTON F. · 2019 to 2025
$190.4M
Support Component D/Vaccine Discovery, Concept to ClinicUM1AI100663 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI AHMED, RAFI · 2012 to 2018
$131.5M
Virus and Antibody Gene Sequencing CoreP01AI131251 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI Kevin Wiehe · 2017 to 2026
$40.7M
Structure/function studies of immunogen recognition by anti-HIV antibody b12P01AI094419 · NIAID · SEATTLE BIOMEDICAL RESEARCH INSTITUTE · PI STAMATATOS, LEONIDAS · 2011 to 2015
$10.6M
Modeling and correcting human SCID using patient-derived iPS cellsR01AI100887 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI MANIS, JOHN P · 2012 to 2020
$4.5M
NIAID NIH HHS P01 AI094419NIAID NIH HHS P01 AI131251NIAID NIH HHS R01 AI100887NIAID NIH HHS UM1 AI100663NIAID NIH HHS UM1 AI144371NIAID NIH HHS UM1 AI144462
6 · The paper itself

Abstract

Antibody heavy chain (HC) and light chain (LC) variable region exons are assembled by V(D)J recombination. V(D)J junctional regions encode complementarity-determining-region 3 (CDR3), an antigen-contact region immensely diversified through nontemplated nucleotide additions ("N-regions") by terminal deoxynucleotidyl transferase (TdT). HIV-1 vaccine strategies seek to elicit human HIV-1 broadly neutralizing antibodies (bnAbs), such as the potent CD4-binding site VRC01-class bnAbs. Mice with primary B cells that express receptors (BCRs) representing bnAb precursors are used as vaccination models. VRC01-class bnAbs uniformly use human HC V

Indexed as

HIV-1HIV InfectionsHIV SeropositivityVaccinesAnimalsAntibodies, NeutralizingBroadly Neutralizing AntibodiesComplementarity Determining RegionsDNA NucleotidylexotransferaseHIV AntibodiesHumansMiceAntibodies, NeutralizingBroadly Neutralizing AntibodiesComplementarity Determining RegionsDNA NucleotidylexotransferaseHIV AntibodiesVaccinesHIV-1 vaccinehumanized mouse modelterminal deoxynucleotidyl transferaseVRC01-class broadly neutralizing antibody

Identifiers

PMID36574685
PMCPMC9910454
OpenAlexW4313251644

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.