Evidence map›Paper›PMID 26814372›Full record

ReviewExpert review of vaccines2016

HIV Susceptibility of human antigen-specific CD4 T cells in AIDS pathogenesis and vaccine response.

Haitao Hu, Fengliang Liu, Jerome Kim, Silvia Ratto-Kim

Open access · greenAbstract readReview
In one paragraph

Review in Expert review of vaccines, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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

4 authors at 3 institutions in 2 countries.

Haitao Hua Department of Microbiology & Immunology and Sealy Center for Vaccine Development , University of Texas Medical Branch , Galveston , TX , USA.
Fengliang Liua Department of Microbiology & Immunology and Sealy Center for Vaccine Development , University of Texas Medical Branch , Galveston , TX , USA.
Jerome Kimb International Vaccine Institute , Seoul , Republic of Korea.
Silvia Ratto-Kimc U.S. Military HIV Research Program, Henry M. Jackson Foundation , Walter Reed Army Institute of Research , Silver Spring , MD , USA.
The University of Texas Medical Branch at Galveston · USHenry M. Jackson Foundation · USInternational Vaccine Institute · KR

Funding

Susceptibility of antigen-specific CD4 T cells to HIV: implications for HIV vacciR21AI110214 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI HU, HAITAO · 2014 to 2015
$403k
NIAID NIH HHS R21 AI110214
6 · The paper itself

Abstract

HIV causes infection and progressive depletion of human CD4 T cells. Emerging data have shown that antigen-specific CD4 T-cell subsets manifest differential susceptibility to HIV, potentially leading to pathogen-specific immune failure and opportunistic infections. This concept was recently explored in context of vectors utilized in HIV vaccine trials, and the data suggest that adenovirus type 5(Ad5)-specific CD4 T cells elicited by Ad5-HIV vaccine may be particularly susceptible to HIV, potentially rendering Ad5 vaccine recipients susceptible to HIV acquisition. We here examined recent data regarding the HIV susceptibility of antigen-specific CD4 T cells induced during infection or HIV vaccination and discussed its potential impact on HIV acquisition risk posed by HIV vaccination.

Indexed as

Disease SusceptibilityAIDS VaccinesCD4-Positive T-LymphocytesHIV InfectionsHumansAIDS Vaccinesantigen specificityCD4 T cellsHIV susceptibilityHIV vaccinepathogenesis

Identifiers

PMID26814372
PMCPMC4955395
OpenAlexW2270979736

What OpenQuestion holds

Textmetadata
LicenceTDM
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.