Evidence map›Paper›PMID 17005700›Full record

ArticleJournal of virology2006

Naive T-cell depletion related to infection by X4 human immunodeficiency virus type 1 in poor immunological responders to highly active antiretroviral therapy.

Pierre Delobel, Marie-Thérèse Nugeyre, Michelle Cazabat, Karine Sandres-Sauné, Christophe Pasquier, Lise Cuzin, Bruno Marchou, Patrice Massip, Rémi Cheynier, Françoise Barré-Sinoussi and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 12% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 60 citations in OpenAlex.

  1. Pooled it
  2. The Three Pioneers in the Discovery of the Human Immunodeficiency Virus.Infectious diseases & clinical microbiology · 2025
    Article
  3. Article
  4. Review
  5. Article
  6. Observational
  7. Review
  8. Observational
  9. Article
  10. Article
  11. Frontiers in immunology · 2018
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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 2 institutions in 1 country.

Pierre DelobelLaboratoire de Virologie EA2046-IFR30, Centre Hospitalier Universitaire, TSA 40031, 31059 Toulouse cedex 9, France.
Marie-Thérèse Nugeyre
Michelle Cazabat
Karine Sandres-Sauné
Christophe Pasquier
Lise Cuzin
Bruno Marchou
Patrice Massip
Rémi Cheynier
Françoise Barré-Sinoussi
Jacques Izopet
Nicole Israël
Centre Hospitalier Universitaire de Toulouse · FRInstitut Pasteur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The reasons for poor CD4+ T-cell recovery in some human immunodeficiency virus (HIV)-infected subjects despite effective highly active antiretroviral therapy (HAART) remain unclear. We recently reported that CXCR4-using (X4) HIV-1 could be gradually selected in cellular reservoirs during sustained HAART. Because of the differential expression of HIV-1 coreceptors CCR5 and CXCR4 on distinct T-cell subsets, the residual replication of R5 and X4 viruses could have different impacts on T-cell homeostasis during immune reconstitution on HAART. We examined this hypothesis and the mechanisms of CD4+ T-cell restoration by comparing the virological and immunological features of 15 poor and 15 good immunological responders to HAART. We found a high frequency of X4 viruses in the poor immunological responders. But the levels of intrathymic proliferation of the two groups were similar regardless of whether they were infected by R5 or X4 virus. The frequency of recent thymic emigrants in the poor immunological responders was also similar to that found in the good immunological responders, despite their reduced numbers of naïve CD4+ T cells. Our data, rather, suggest that the naïve T-cell compartment is drained by a high rate of mature naïve cell loss in the periphery due to bystander apoptosis or activation-induced differentiation. X4 viruses could play a role in the depletion of naïve T cells in poor immunological responders to HAART by triggering persistent T-cell activation and bystander apoptosis via gp120-CXCR4 interactions.

Indexed as

Antiretroviral Therapy, Highly ActiveAdultCD4 Lymphocyte CountCD4-Positive T-LymphocytesFlow CytometryHIV-1HIV Envelope Protein gp160HIV InfectionsHumansLymphocyte ActivationMiddle AgedMolecular Sequence DataReceptors, CXCR4Sequence Analysis, DNAThymus GlandT-Lymphocyte SubsetsHIV Envelope Protein gp160Receptors, CXCR4

Identifiers

PMID17005700
PMCPMC1617280
OpenAlexW2105415723

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.