Evidence map›Paper›PMID 26161861›Full record

ArticlePloS one2015

Vγ9Vδ2 T-Cell Polyfunctionality Is Differently Modulated in HAART-Treated HIV Patients according to CD4 T-Cell Count.

Rita Casetti, Gabriele De Simone, Alessandra Sacchi, Alessandra Rinaldi, Domenico Viola, Chiara Agrati, Veronica Bordoni, Eleonora Cimini, Nicola Tumino, Francesca Besi and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact, top 99% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. γδT Cells Are Required for CD8Frontiers in immunology · 2021
    Article
  5. Article
  6. Article
  7. Boosting the Immune System for HIV Cure: A γδ T Cell Perspective.Frontiers in cellular and infection microbiology · 2020
    Review
  8. Review
  9. 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

11 authors at 1 institution in 1 country.

Rita CasettiLaboratory of Cellular Immunology, "Lazzaro Spallanzani" National Institute for Infectious Diseases IRCCS, Rome, Italy.
Gabriele De SimoneLaboratory of Cellular Immunology, "Lazzaro Spallanzani" National Institute for Infectious Diseases IRCCS, Rome, Italy.
Alessandra SacchiLaboratory of Cellular Immunology, "Lazzaro Spallanzani" National Institute for Infectious Diseases IRCCS, Rome, Italy.
Alessandra RinaldiLaboratory of Cellular Immunology, "Lazzaro Spallanzani" National Institute for Infectious Diseases IRCCS, Rome, Italy.
Domenico ViolaLaboratory of Cellular Immunology, "Lazzaro Spallanzani" National Institute for Infectious Diseases IRCCS, Rome, Italy.
Chiara AgratiLaboratory of Cellular Immunology, "Lazzaro Spallanzani" National Institute for Infectious Diseases IRCCS, Rome, Italy.
Veronica BordoniLaboratory of Cellular Immunology, "Lazzaro Spallanzani" National Institute for Infectious Diseases IRCCS, Rome, Italy.
Eleonora CiminiLaboratory of Cellular Immunology, "Lazzaro Spallanzani" National Institute for Infectious Diseases IRCCS, Rome, Italy.
Nicola TuminoLaboratory of Cellular Immunology, "Lazzaro Spallanzani" National Institute for Infectious Diseases IRCCS, Rome, Italy.
Francesca BesiLaboratory of Cellular Immunology, "Lazzaro Spallanzani" National Institute for Infectious Diseases IRCCS, Rome, Italy.
Federico MartiniLaboratory of Cellular Immunology, "Lazzaro Spallanzani" National Institute for Infectious Diseases IRCCS, Rome, Italy.
Istituto Nazionale per le Malattie Infettive Lazzaro Spallanzani · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alteration of γδ T-cell distribution and function in peripheral blood is among the earliest defects during HIV-infection. We asked whether the polyfunctional response could also be affected, and how this impairment could be associated to CD4 T-cell count. To this aim, we performed a cross-sectional study on HIV-infected individuals. In order to evaluate the polyfunctional-Vγ9Vδ2 T-cell response after phosphoantigen-stimulation, we assessed the cytokine/chemokine production and cytotoxicity by flow-cytometry in HAART-treated-HIV+ persons and healthy-donors. During HIV-infection Vγ9Vδ2-polyfunctional response quality is affected, since several Vγ9Vδ2 T-cell subsets resulted significantly lower in HIV+ patients in respect to healthy donors. Interestingly, we found a weak positive correlation between Vγ9Vδ2 T-cell-response and CD4 T-cell counts. By dividing the HIV+ patients according to CD4 T-cell count, we found that Low-CD4 patients expressed a lower number of two Vγ9Vδ2 T-cell subsets expressing MIP-1β in different combinations with other molecules (CD107a/IFNγ) in respect to High-CD4 individuals. Our results show that the Vγ9Vδ2 T-cell-response quality in Low-CD4 patients is specifically affected, suggesting a direct link between innate Vγ9Vδ2 T-cells and CD4 T-cell count. These findings suggest that Vγ9Vδ2 T-cell quality may be indirectly influenced by HAART therapy and could be included in a new therapeutical strategy which would perform an important role in fighting HIV infection.

Indexed as

Antiretroviral Therapy, Highly ActiveAdaptor Proteins, Signal TransducingAdultCD4-Positive T-LymphocytesChronic DiseaseFemaleFlow CytometryHIV InfectionsHumansInterferon-gammaLymphocyte CountLysosomal-Associated Membrane Protein 1MaleReceptors, Antigen, T-Cell, gamma-deltaT-Lymphocyte SubsetsAdaptor Proteins, Signal TransducingInterferon-gammaLysosomal-Associated Membrane Protein 1MAPKAP1 protein, humanReceptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID26161861
PMCPMC4498914
OpenAlexW793188790

What OpenQuestion holds

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LicenceCC BY
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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.