Evidence map›Paper›PMID 22641382›Full record

ArticleThe Journal of experimental medicine2012

Potent and broad neutralization of HIV-1 by a llama antibody elicited by immunization.

Laura E McCoy, Anna Forsman Quigley, Nika M Strokappe, Bianca Bulmer-Thomas, Michael S Seaman, Daniella Mortier, Lucy Rutten, Nikita Chander, Carolyn J Edwards, Robin Ketteler and 3 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06585891 (VRC 617), which is not on this map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
9.0field-weighted citation impact, top 2% 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.

NCT06585891 phase1completednot on this mapstarted 2024, after this paper: background citation

VRC 617: A Phase 1, Open-Label, Dose-Escalation Study to Evaluate Safety and Pharmacokinetics of a Human Bispecific Antibody, VRC-HIVMAB0121-00-AB (CAP256J3LS) Administered Intravenously or Subcutaneously to Healthy Adults

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2024 to 2025Enrolled24ConditionsHIV InfectionArmsVRC-HIVMAB0121-00-AB
3 · Its place in the literature

Who cites it

84 citing papers in PubMed, 113 citations in OpenAlex.

  1. Trial
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  3. Deletions in variable region 1 of the HIV envelope accelerate V3-glycan bNAb induction in SHIV-infected rhesus macaques.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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  7. Review
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  19. Ultrapotent Broadly Neutralizing Human-llama Bispecific Antibodies against HIV-1.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  20. Review

24 more citing papers are in PubMed but not listed here.

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

13 authors at 6 institutions in 3 countries.

Laura E McCoyWohl Virion Centre, University College London, London WC1E 6BT, England, UK.
Anna Forsman Quigley
Nika M Strokappe
Bianca Bulmer-Thomas
Michael S Seaman
Daniella Mortier
Lucy Rutten
Nikita Chander
Carolyn J Edwards
Robin Ketteler
David Davis
Theo Verrips
Robin A Weiss
MRC Laboratory for Molecular Cell Biology · GBUniversity College London · GBUtrecht University · NLBiomedical Primate Research Centre · NLHarvard University · USMedical Research Council · GB

Funding

Medical Research Council G0801176Medical Research Council MC_EX_G0800785
6 · The paper itself

Abstract

Llamas (Lama glama) naturally produce heavy chain-only antibodies (Abs) in addition to conventional Abs. The variable regions (VHH) in these heavy chain-only Abs demonstrate comparable affinity and specificity for antigens to conventional immunoglobulins despite their much smaller size. To date, immunizations in humans and animal models have yielded only Abs with limited ability to neutralize HIV-1. In this study, a VHH phagemid library generated from a llama that was multiply immunized with recombinant trimeric HIV-1 envelope proteins (Envs) was screened directly for HIV-1 neutralization. One VHH, L8CJ3 (J3), neutralized 96 of 100 tested HIV-1 strains, encompassing subtypes A, B, C, D, BC, AE, AG, AC, ACD, CD, and G. J3 also potently neutralized chimeric simian-HIV strains with HIV subtypes B and C Env. The sequence of J3 is highly divergent from previous anti-HIV-1 VHH and its own germline sequence. J3 achieves broad and potent neutralization of HIV-1 via interaction with the CD4-binding site of HIV-1 Env. This study may represent a new benchmark for immunogens to be included in B cell-based vaccines and supports the development of VHH as anti-HIV-1 microbicides.

Indexed as

AnimalsAntibodies, NeutralizingAntibody AffinityCamelids, New WorldCD4 Antigensenv Gene Products, Human Immunodeficiency VirusEpitopesHIV-1Immunoglobulin Variable RegionNeutralization TestsPeptide LibraryRecombinant ProteinsVaccines, DNAAntibodies, NeutralizingCD4 Antigensenv Gene Products, Human Immunodeficiency VirusEpitopesgp140 envelope protein, Human immunodeficiency virus 1Immunoglobulin Variable RegionPeptide LibraryRecombinant ProteinsVaccines, DNA

Identifiers

PMID22641382
PMCPMC3371729
OpenAlexW1985534966

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

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.