Evidence map›Paper›PMID 21852682›Full record

ReviewAmerican journal of respiratory cell and molecular biology2011

Arc of a vicious circle: pathways activated by Mycobacterium tuberculosis that target the HIV-1 long terminal repeat.

James V Falvo, Shahin Ranjbar, Luke D Jasenosky, Anne E Goldfeld

Abstract readReview
In one paragraph

Review in American journal of respiratory cell and molecular biology, 2011. 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
1.4field-weighted citation impact, top 20% 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, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. TheFuture virology · 2020
    Review
  6. Article
  7. Article
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  11. Review
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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

4 authors at 1 institution in 1 country.

James V FalvoImmune Disease Institute and Program in Cellular and Molecular Medicine, Children’s Hospital Boston, MA, USA. falvo@idi.harvard.edu
Shahin Ranjbar
Luke D Jasenosky
Anne E Goldfeld
Boston Children's Hospital · US

Funding

Checkpoints of TNF Gene RegulationR01GM076685 · NIGMS · IMMUNE DISEASE INSTITUTE, INC. · PI GOLDFELD, ANNE · 2006 to 2019
$5.2M
GENETIC FACTORS AND SUSCEPTIBILITY TO TUBERCULOSISR01HL059838 · NHLBI · IMMUNE DISEASE INSTITUTE, INC. · PI GOLDFELD, ANNE · 1997 to 2006
$3.8M
HIV-1 regulation by MTb: pathogen and host factorR01AI065285 · NIAID · IMMUNE DISEASE INSTITUTE, INC. · PI GOLDFELD, ANNE · 2005 to 2009
$2.1M
HIV-1 regulation by MTb: pathogen and host factorR56AI065285 · NIAID · IMMUNE DISEASE INSTITUTE, INC. · PI GOLDFELD, ANNE · 2010 to 2010
$525k
Clade-specific regulation of HIV-1 by M tuberculosisR21AI060433 · NIAID · IMMUNE DISEASE INSTITUTE, INC. · PI GOLDFELD, ANNE · 2004 to 2004
$473k
NHLBI NIH HHS R01 HL059838NIAID NIH HHS AI065285NIAID NIH HHS R01 AI065285NIAID NIH HHS R21 AI060433NIAID NIH HHS R21AI060433NIAID NIH HHS R56 AI065285NIGMS NIH HHS R01 GM076685NIGMS NIH HHS R01GM076685PHS HHS 059838
6 · The paper itself

Abstract

In this review, we examine how a subset of signal transduction cascades initiated by Mycobacterium tuberculosis (Mtb) infection modulates transcription mediated by the human immunodeficiency virus type 1 long terminal repeat (HIV-1 LTR). We describe two distinct phases of signaling that target transcription factors known to bind the HIV-1 LTR, and thus drive viral transcription and replication, in cells of the Mtb-infected host. First, Mtb-derived molecules, including cell wall components and DNA, interact with a number of host pattern recognition receptors. Second, cytokines and chemokines secreted in response to Mtb infection initiate signal transduction cascades through their cognate receptors. Given the variation in cell wall components among distinct clinical Mtb strains, the initial pattern recognition receptor interaction leading to direct LTR activation and differential cytokine and chemokine production is likely to be an important aspect of Mtb strain-specific regulation of HIV-1 transcription and replication. Improved understanding of these molecular mechanisms in the context of bacterial and host genetics should provide key insights into the accelerated viral replication and disease progression characteristic of HIV/TB coinfection.

Indexed as

HIV InfectionsTuberculosisAnimalsCytokinesHIV-1HIV Long Terminal RepeatHumansMycobacterium tuberculosisReceptors, Pattern RecognitionSignal TransductionTranscription FactorsTranscription, GeneticVirus ReplicationCytokinesReceptors, Pattern RecognitionTranscription Factors

Identifiers

PMID21852682
PMCPMC3262667
OpenAlexW2095194311

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.