Evidence map›Paper›PMID 11134278›Full record

ArticleJournal of virology2001

Immunogenicity and protective efficacy of oligomeric human immunodeficiency virus type 1 gp140.

P L Earl, W Sugiura, D C Montefiori, C C Broder, S A Lee, C Wild, J Lifson, B Moss

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

75 citing papers in PubMed, 142 citations in OpenAlex.

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  16. HIV-1 envelope trimer elicits more potent neutralizing antibody responses than monomeric gp120.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
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  18. Review
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15 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

8 authors at 5 institutions in 1 country.

P L EarlLaboratory of Viral Diseases, NIAID, National Institutes of Health, Bethesda, Maryland 20892-0455, USA. pearl@nih.gov
W Sugiura
D C Montefiori
C C Broder
S A Lee
C Wild
J Lifson
B Moss
National Institute of Allergy and Infectious Diseases · USNational Institutes of Health · USDuke University · USScience Applications International Corporation (United States) · USSensei Biotherapeutics (United States) · US

Funding

OPERATIONS &TECHNICAL SUPPORTN01CO056000 · CO · SCIENCE APPLICATIONS INTERNATIONAL CORP · PI FISCHINGER, PETER J · 1995 to 2000
$95.0M
Recombinant Vaccines for Prevention of AIDS and Other DiseasesZ01AI000416 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI MOSS, BERNARD · 1985 to 2008
$3.3M
PRIMATE IMMUNOLOGY LABORATORY FOR AIDS VACCINE R&DN01AI085343 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI LETVIN, NORMAN L · 1998 to 2000
$412k
NCI NIH HHS N01CO56000NIAID NIH HHS AI85343
6 · The paper itself

Abstract

The biologically active form of the human immunodeficiency virus type 1 (HIV-1) envelope (Env) glycoprotein is oligomeric. We previously described a soluble HIV-1 IIIB Env protein, gp140, with a stable oligomeric structure composed of uncleaved gp120 linked to the ectodomain of gp41 (P. L. Earl, C. C. Broder, D. Long, S. A. Lee, J. Peterson, S. Chakrabarti, R. W. Doms, and B. Moss, J. Virol. 68:3015-3026, 1994). Here we compared the antibody responses of rabbits to gp120 and gp140 that had been produced and purified in an identical manner. The gp140 antisera exhibited enhanced cross-reactivity with heterologous Env proteins as well as greater neutralization of HIV-1 compared to the gp120 antisera. To examine both immunogenicity and protective efficacy, we immunized rhesus macaques with oligomeric gp140. Strong neutralizing antibodies against a homologous virus and modest neutralization of heterologous laboratory-adapted isolates were elicited. No neutralization of primary isolates was observed. However, a substantial fraction of the neutralizing activity could not be blocked by a V3 loop peptide. After intravenous challenge with simian-HIV virus SHIV-HXB2, three of the four vaccinated macaques exhibited no evidence of virus replication.

Indexed as

Acquired Immunodeficiency SyndromeAIDS VaccinesAnimalsCross Reactionsenv Gene Products, Human Immunodeficiency VirusGene Products, envHIV-1HIV AntibodiesHIV Envelope Protein gp120HumansMacaca mulattaNeutralization TestsPeptide FragmentsRabbitsSimian Acquired Immunodeficiency SyndromeSimian Immunodeficiency VirusAIDS Vaccinesenv Gene Products, Human Immunodeficiency VirusGene Products, envgp140 envelope protein, Human immunodeficiency virus 1HIV AntibodiesHIV Envelope Protein gp120HIV envelope protein gp120 (305-321)Peptide Fragments

Identifiers

PMID11134278
PMCPMC113961
OpenAlexW2044465251

What OpenQuestion holds

Textmetadata
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.