Evidence map›Paper›PMID 30384610›Full record

ArticleJournal of medicinal chemistry2018

Synthetic HIV V3 Glycopeptide Immunogen Carrying a N334 N-Glycan Induces Glycan-Dependent Antibodies with Promiscuous Site Recognition.

Hui Cai, Rou-Shu Zhang, Jared Orwenyo, John Giddens, Qiang Yang, Celia C LaBranche, David C Montefiori, Lai-Xi Wang

Abstract read
In one paragraph

Article in Journal of medicinal chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

17 citing papers in PubMed, 25 citations in OpenAlex.

  1. Trial
  2. ACS central science · 2025
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Recent Advances in the Chemical Biology ofMolecules (Basel, Switzerland) · 2021
    Review
  11. Review
  12. Article
  13. Article
  14. Chemoenzymatic Synthesis of HIV-1 Glycopeptide Antigens.Methods in molecular biology (Clifton, N.J.) · 2020
    Article
  15. Glycans in drug discovery.MedChemComm · 2019
    Review
  16. Review
  17. Review
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

8 authors at 2 institutions in 1 country.

Hui CaiDepartment of Chemistry and Biochemistry , University of Maryland , College Park , Maryland 20742 , United States.ORCID 0000-0002-5394-8167
Rou-Shu ZhangDepartment of Chemistry and Biochemistry , University of Maryland , College Park , Maryland 20742 , United States.
Jared OrwenyoDepartment of Chemistry and Biochemistry , University of Maryland , College Park , Maryland 20742 , United States.
John GiddensDepartment of Chemistry and Biochemistry , University of Maryland , College Park , Maryland 20742 , United States.
Qiang YangDepartment of Chemistry and Biochemistry , University of Maryland , College Park , Maryland 20742 , United States.
Celia C LaBrancheDepartment of Surgery , Duke University Medical Center , Durham , North Carolina 27705 , United States.
David C MontefioriDepartment of Surgery , Duke University Medical Center , Durham , North Carolina 27705 , United States.
Lai-Xi WangDepartment of Chemistry and Biochemistry , University of Maryland , College Park , Maryland 20742 , United States.ORCID 0000-0003-4293-5819
University of Maryland, College Park · USDuke Medical Center · US

Funding

Synthetic HIV Vaccine Targeting Glycopeptide Neutralizing EpitopesR01AI113896 · NIAID · UNIV OF MARYLAND, COLLEGE PARK · PI WANG, LAI-XI · 2014 to 2018
$2.3M
NIAID NIH HHS R01 AI113896
6 · The paper itself

Abstract

The N332 high-mannose glycan on the HIV-1 gp120 V3-loop is the target of many bNAbs. About 17% HIV isolates carry the N332 to N334 mutation, but the antibody recognition of the N334 N-glycan and its immunogenicity are not well characterized. Here we report the chemoenzymatic synthesis, antigenicity, and immunogenicity of the V3 N334 glycopeptides from HIV-1 A244 gp120, a key component in the partially successful Thai clinical trials. We found that synthetic V3 glycopeptide carrying a N334 high-mannose glycan could be recognized by bNAb PGT128 and PGT126 but not by 10-1074. Rabbit immunization with the synthetic three-component A244 glycopeptide immunogen elicited substantial glycan-dependent antibodies with broad reactivity to various HIV-1 gp120/gp140 carrying N332 or N334 glycosylation sites. These results indicated that the N334 site is vulnerable and the A244 V3 glycopeptide represents a valuable immunogen for further HIV-1 vaccine studies.

Indexed as

Amino Acid SequenceAnimalsAntibodies, ViralBinding SitesChemistry Techniques, Syntheticenv Gene Products, Human Immunodeficiency VirusFemaleGlycopeptidesGlycosylationHIV Envelope Protein gp120ImmunizationModels, MolecularPolysaccharidesProtein ConformationRabbitsSubstrate SpecificityAntibodies, Viralenv Gene Products, Human Immunodeficiency VirusGlycopeptidesgp120 protein, Human immunodeficiency virus 1gp140 envelope protein, Human immunodeficiency virus 1HIV Envelope Protein gp120Polysaccharides

Identifiers

PMID30384610
PMCPMC6283719
OpenAlexW2899006185

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.