Evidence map›Paper›PMID 31479428›Full record

ArticleThe Journal of clinical investigation2019

Mechanisms of reactivation of latent tuberculosis infection due to SIV coinfection.

Allison N Bucşan, Ayan Chatterjee, Dhiraj K Singh, Taylor W Foreman, Tae-Hyung Lee, Breanna Threeton, Melanie G Kirkpatrick, Mushtaq Ahmed, Nadia Golden, Xavier Alvarez and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
5.0field-weighted citation impact, top 3% 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

56 citing papers in PubMed, 70 citations in OpenAlex.

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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

15 authors at 5 institutions in 1 country.

Allison N BucşanTulane National Primate Research Center, Covington, Louisiana, USA.
Ayan ChatterjeeSouthwest National Primate Research Center, Texas Biomedical Research Institute, San Antonio, Texas, USA.
Dhiraj K SinghSouthwest National Primate Research Center, Texas Biomedical Research Institute, San Antonio, Texas, USA.
Taylor W ForemanTulane National Primate Research Center, Covington, Louisiana, USA.
Tae-Hyung LeeSouthwest National Primate Research Center, Texas Biomedical Research Institute, San Antonio, Texas, USA.
Breanna ThreetonTulane National Primate Research Center, Covington, Louisiana, USA.
Melanie G KirkpatrickTulane National Primate Research Center, Covington, Louisiana, USA.
Mushtaq AhmedDepartment of Molecular Microbiology, Washington University in St. Louis School of Medicine, St. Louis, Missouri, USA.
Nadia GoldenTulane National Primate Research Center, Covington, Louisiana, USA.
Xavier AlvarezTulane National Primate Research Center, Covington, Louisiana, USA.
James A HoxieHematology-Oncology Division, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
Smriti MehraTulane National Primate Research Center, Covington, Louisiana, USA.
Jyothi RengarajanEmory Vaccine Center and.
Shabaana A KhaderDepartment of Molecular Microbiology, Washington University in St. Louis School of Medicine, St. Louis, Missouri, USA.
Deepak KaushalTulane National Primate Research Center, Covington, Louisiana, USA.
Tulane University · USTexas Biomedical Research Institute · USWashington University in St. Louis · USEmory University · USUniversity of Pennsylvania · US

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
Tulane NPRC SPF Sheltered Outdoor Enclosure ExpansionP51OD011104 · OD · TULANE UNIVERSITY OF LOUISIANA · PI L Lee HAMM · 2012 to 2026
$142.4M
The Southwest National Primate Research Center Supplement- Infrastructure improvements of ABSL2 holding areasP51OD011133 · OD · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI Larry S. Schlesinger · 2012 to 2026
$129.7M
Viral Testing CoreU42OD010442 · OD · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI Smriti Mehra · 2012 to 2026
$35.6M
ROLE OF INDUCIBLE BRONCHUS ASSOCIATED LYMPHOID TISSUE IN LATENT TUBERCULOSISR01AI111914 · NIAID · WASHINGTON UNIVERSITY · PI KAUSHAL, DEEPAK, KHADER, SHABAANA A. · 2015 to 2025
$11.1M
Immune Correlates of Protection from TBR01AI134240 · NIAID · TULANE UNIVERSITY OF LOUISIANA · PI KAUSHAL, DEEPAK · 2017 to 2022
$4.8M
Perturbation of antigen-specific T cell responses in latent TB/SIV co-infectionR01AI111943 · NIAID · TULANE UNIVERSITY OF LOUISIANA · PI KAUSHAL, DEEPAK, RENGARAJAN, JYOTHI · 2015 to 2019
$3.9M
Impact of concurrent HIV and latent TB therapies on Mtb-specific immune function-Diversity SupplementR01AI123047 · NIAID · TULANE UNIVERSITY OF LOUISIANA · PI KAUSHAL, DEEPAK, RENGARAJAN, JYOTHI · 2017 to 2020
$3.9M
COMMON IMMUNE CORRELATES OF RISK OF TB DISEASE IN ANIMAL MODELS AND HUMANSR01AI123780 · NIAID · WASHINGTON UNIVERSITY · PI KAUSHAL, DEEPAK, KHADER, SHABAANA A. · 2016 to 2019
$2.9M
NIAID NIH HHS R01 AI111914NIAID NIH HHS R01 AI111943NIAID NIH HHS R01 AI123047NIAID NIH HHS R01 AI123780NIAID NIH HHS R01 AI134240NIH HHS P51 OD011104NIH HHS P51 OD011132NIH HHS P51 OD011133NIH HHS U42 OD010442
6 · The paper itself

Abstract

HIV is a major driver of tuberculosis (TB) reactivation. Depletion of CD4+ T cells is assumed to be the basis behind TB reactivation in individuals with latent tuberculosis infection (LTBI) coinfected with HIV. Nonhuman primates (NHPs) coinfected with a mutant simian immunodeficiency virus (SIVΔGY) that does not cause depletion of tissue CD4+ T cells during infection failed to reactivate TB. To investigate the contribution of CD4+ T cell depletion relative to other mechanisms of SIV-induced reactivation of LTBI, we used CD4R1 antibody to deplete CD4+ T cells in animals with LTBI without lentiviral infection. The mere depletion of CD4+ T cells during LTBI was insufficient in generating reactivation of LTBI. Instead, direct cytopathic effects of SIV resulting in chronic immune activation, along with the altered effector T cell phenotypes and dysregulated T cell homeostasis, were likely mediators of reactivation of LTBI. These results revealed important implications for TB control in HIV-coinfected individuals.

Indexed as

AnimalsCD4-Positive T-LymphocytesCoinfectionHomeostasisLatent TuberculosisLentivirusLymphocyte DepletionMacaca mulattaMutationMycobacterium tuberculosisPhenotypeSimian Acquired Immunodeficiency SyndromeSimian Immunodeficiency VirusAIDS/HIVInfectious diseaseT cellsTuberculosis

Identifiers

PMID31479428
PMCPMC6877319
OpenAlexW2971962589

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.