Evidence map›Paper›PMID 25903343›Full record

ArticleJournal of virology2015

Nonneutralizing Antibodies Induced by the HIV-1 gp41 NHR Domain Gain Neutralizing Activity in the Presence of the HIV Fusion Inhibitor Enfuvirtide: a Potential Therapeutic Vaccine Strategy.

Qian Wang, Wenwen Bi, Xiaojie Zhu, Haoyang Li, Qianqian Qi, Fei Yu, Lu Lu, Shibo Jiang

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. The Role of MSCs and Cell Fusion in Tissue Regeneration.International journal of molecular sciences · 2021
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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

8 authors at 2 institutions in 2 countries.

Qian WangKey Lab of Medical Molecular Virology of MOE/MOH, Shanghai Medical College and Shanghai Public Health Clinical Center, Fudan University, Shanghai, China.
Wenwen BiKey Lab of Medical Molecular Virology of MOE/MOH, Shanghai Medical College and Shanghai Public Health Clinical Center, Fudan University, Shanghai, China.
Xiaojie ZhuKey Lab of Medical Molecular Virology of MOE/MOH, Shanghai Medical College and Shanghai Public Health Clinical Center, Fudan University, Shanghai, China.
Haoyang LiKey Lab of Medical Molecular Virology of MOE/MOH, Shanghai Medical College and Shanghai Public Health Clinical Center, Fudan University, Shanghai, China.
Qianqian QiKey Lab of Medical Molecular Virology of MOE/MOH, Shanghai Medical College and Shanghai Public Health Clinical Center, Fudan University, Shanghai, China Lindsley F. Kimball Research Institute, New York Blood Center, New York, New York, USA.
Fei YuKey Lab of Medical Molecular Virology of MOE/MOH, Shanghai Medical College and Shanghai Public Health Clinical Center, Fudan University, Shanghai, China.
Lu LuKey Lab of Medical Molecular Virology of MOE/MOH, Shanghai Medical College and Shanghai Public Health Clinical Center, Fudan University, Shanghai, China lul@fudan.edu.cn shibojiang@fudan.edu.cn.
Shibo JiangKey Lab of Medical Molecular Virology of MOE/MOH, Shanghai Medical College and Shanghai Public Health Clinical Center, Fudan University, Shanghai, China Lindsley F. Kimball Research Institute, New York Blood Center, New York, New York, USA lul@fudan.edu.cn shibojiang@fudan.edu.cn.
Shanghai Public Health Clinical Center · CNNew York Blood Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A key barrier against developing preventive and therapeutic human immunodeficiency virus (HIV) vaccines is the inability of viral envelope glycoproteins to elicit broad and potent neutralizing antibodies. However, in the presence of fusion inhibitor enfuvirtide, we show that the nonneutralizing antibodies induced by the HIV type 1 (HIV-1) gp41 N-terminal heptad repeat (NHR) domain (N63) exhibit potent and broad neutralizing activity against laboratory-adapted HIV-1 strains, including the drug-resistant variants, and primary HIV-1 isolates with different subtypes, suggesting the potential of developing gp41-targeted HIV therapeutic vaccines.

Indexed as

AnimalsAntibodies, NeutralizingEnfuvirtideHIV-1HIV AntibodiesHIV Envelope Protein gp41HIV Fusion InhibitorsHumansMiceNeutralization TestsPeptide FragmentsRabbitsAntibodies, NeutralizingEnfuvirtidegp41 protein, Human immunodeficiency virus 1HIV AntibodiesHIV Envelope Protein gp41HIV Fusion InhibitorsPeptide Fragments

Identifiers

PMID25903343
PMCPMC4468469
OpenAlexW2141299808

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.