Evidence map›Paper›PMID 16902147›Full record

Trial reportBlood2006

HIV-1-driven regulatory T-cell accumulation in lymphoid tissues is associated with disease progression in HIV/AIDS.

Jakob Nilsson, Adriano Boasso, Paula Andrea Velilla, Rui Zhang, Monica Vaccari, Genoveffa Franchini, Gene M Shearer, Jan Andersson, Claire Chougnet

Open access · bronzeAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Blood, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 181 papers.

0numbers the graph read from it
0cells of the map it votes in
181citing papers in PubMed
11.1field-weighted citation impact, top 1% 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

181 citing papers in PubMed, 326 citations in OpenAlex.

  1. Trial
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  8. Article
  9. Article
  10. Natural Resistance to HIV Infection: Role of Immune Activation.Immunity, inflammation and disease · 2025
    Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Impact ofFrontiers in microbiology · 2023
    Article
  17. CRISPR/Cas9-Mediated Insertion of HIV Long Terminal Repeat withinJournal of immunology (Baltimore, Md. : 1950) · 2022
    Article
  18. Review
  19. Review
  20. Preterm Birth in Women With HIV: The Role of the Placenta.Frontiers in global women's health · 2022
    Review

121 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

9 authors at 2 institutions in 1 country.

Jakob NilssonDivision of Molecular Immunology (ML#7021), Cincinnati Children's Hospital Medical Center, 3333 Burnet Ave, Cincinnati, OH 45229, USA.
Adriano Boasso
Paula Andrea Velilla
Rui Zhang
Monica Vaccari
Genoveffa Franchini
Gene M Shearer
Jan Andersson
Claire Chougnet
Karolinska Institutet · SEKarolinska University Hospital · SE

Funding

Understanding the Role of the Host Response in HIVSIV InfectionZIABC005688 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI FRANCHINI, GENOVEFFA · 2009 to 2012
$4.8M
Vaccine Modalities to Prevent HIV-I InfectionZ01BC005688 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI FRANCHINI, GENOVEFFA · 1996 to 2008
$4.2M
Immune ProtectionDysregulation in HIVAIDSZ01BC009267 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SHEARER, GENE · 1996 to 2008
$1.9M
Role of Regulatory T Cells in HIV InfectionR01AI068524 · NIAID · CINCINNATI CHILDRENS HOSP MED CTR · PI CHOUGNET, CLAIRE A. · 2006 to 2010
$1.8M
Immune ProtectionDysregulation in HIVAIDSZIABC009267 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SHEARER, GENE · 2009 to 2009
$347k
NIAID NIH HHS AI068524NIAID NIH HHS R01 AI068524
6 · The paper itself

Abstract

Regulatory T (Treg) cells accumulate in the lymphoid tissues of human immunodeficiency virus (HIV)-infected individuals, contributing to the inability of the immune system to control virus replication. We investigate here Treg-cell numbers and functional markers (FOXP3, CTLA-4, IDO, and TGF-beta1) in lymphoid tissues from untreated infected hosts with progressive or nonprogressive disease (HIV-infected humans and simian immunodeficiency virus [SIV]-infected macaques). We found that increased numbers of FOXP3(+) T cells as well as increased expression of Treg-cell-associated functional markers were detected only during progressive disease. Such increases were not correlated with immune activation. Of importance, a high-perforin/FOXP3 ratio was associated with nonprogressive disease, suggesting that the immune control of virus replication represents a balance between cell-mediated immune responses and Treg-cell-mediated counter regulation of such responses. Furthermore, using an in vitro model of Treg-cell-HIV interactions, we showed that exposure of Treg cells to HIV selectively promoted their survival via a CD4-gp120-dependent pathway, thus providing an underlying mechanism for the accumulation of Treg cells in infected hosts with active viral replication. Considered together, our findings imply that therapeutic manipulation of Treg-cell number and/or function could improve immune control of HIV infection.

Indexed as

Acquired Immunodeficiency SyndromeAdultAntigens, DifferentiationCell SurvivalCohort StudiesDisease ProgressionFemaleHIV-1HIV Envelope Protein gp120HumansLymphoid TissueMaleMiddle AgedSignal TransductionT-Lymphocytes, RegulatoryVirus ReplicationAntigens, DifferentiationHIV Envelope Protein gp120

Identifiers

PMID16902147
PMCPMC1895475
OpenAlexW1968276891

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.