Evidence map›Paper›PMID 19016904›Full record

ArticleImmunology2009

The decrease of regulatory T cells correlates with excessive activation and apoptosis of CD8+ T cells in HIV-1-infected typical progressors, but not in long-term non-progressors.

Yanmei Jiao, JunLiang Fu, Shaojun Xing, Baoyun Fu, Zheng Zhang, Ming Shi, Xicheng Wang, Jiyuan Zhang, Lei Jin, Fubiao Kang and 2 more

Open access · greenAbstract read
In one paragraph

Article in Immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 7% 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

47 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.

  1. Guideline
  2. Trial
  3. Review
  4. Article
  5. Updates in the pathogenesis of SJS/TEN.Allergology international : official journal of the Japanese Society of Allergology · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Microbiome Dependent Regulation of TFrontiers in immunology · 2019
    Review
  17. Regulatory T cells: the ultimate HIV reservoir?Journal of virus eradication · 2018
    Article
  18. Article
  19. Article
  20. 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

12 authors at 4 institutions in 2 countries.

Yanmei JiaoDepartment of Infectious Diseases, Beijing You-an Hospital Affiliated to Capital Medical University, Beijing, China.
JunLiang Fu
Shaojun Xing
Baoyun Fu
Zheng Zhang
Ming Shi
Xicheng Wang
Jiyuan Zhang
Lei Jin
Fubiao Kang
Hao Wu
Fu-Sheng Wang
302 Military Hospital of China · CNNational Institute for Communicable Disease Control and Prevention · CNBeijing YouAn Hospital · CNMolina Center for Energy and the Environment · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Persistent HIV infection results in a decrease in absolute counts of CD4(+) CD25(+) regulatory T cells (Treg). To investigate the role of decreased Treg counts in the regulation of excessive activation and apoptosis of CD8(+) T cells in human immunodeficiency virus (HIV)-1 infection, we characterized Treg in 83 HIV-1-infected individuals, including 19 long-term non-progressors (LTNPs) and 51 typical progressors (TPs) who were treatment-naïve, and 13 AIDS patients on highly active antiretroviral therapy (HAART), of whom nine were complete responders (CRs) and the remaining four were non-responders (NRs) to the treatment. TPs but not LTNPs had a significant decrease in absolute counts of circulating Treg, which was inversely correlated with the activation and apoptosis of CD8(+) T cells. Efficient HAART was found to increase Treg counts in CR patients and temper the excessive activation and apoptosis of CD8(+) T cells. Moreover, isolated Treg significantly inhibited the spontaneous and anti-CD3-induced apoptosis of CD8(+) T cells in a dose-dependent manner in vitro. Thus, our findings indicate that the decrease in Treg closely correlates with the increase in apoptotic CD8(+) T cells and disease progression in chronic HIV-1 infection, and that Treg may play a key role in maintaining the balance between the amount and quality of CD8(+) T cells in HIV-1 infection. Manipulation of Treg function may be a promising strategy for immune therapy of this disease.

Indexed as

HIV-1AdultAnti-HIV AgentsAntiretroviral Therapy, Highly ActiveApoptosisCD4 Lymphocyte CountCD8-Positive T-LymphocytesChronic DiseaseDisease ProgressionFemaleHIV InfectionsHumansLymphocyte ActivationMaleMiddle AgedRNA, ViralAnti-HIV AgentsRNA, Viral

Identifiers

PMID19016904
PMCPMC2753909
OpenAlexW2007946126

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.