Evidence map›Paper›PMID 28239376›Full record

ArticleFrontiers in immunology2017

A Mature NK Profile at the Time of HIV Primary Infection Is Associated with an Early Response to cART.

Françoise Gondois-Rey, Antoine Chéret, Françoise Mallet, Ghislain Bidaut, Samuel Granjeaud, Camille Lécuroux, Mickaël Ploquin, Michaela Müller-Trutwin, Christine Rouzioux, Véronique Avettand-Fenoël and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 21% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Harnessing Natural Killer Cell Innate and Adaptive Traits in HIV Infection.Frontiers in cellular and infection microbiology · 2020
    Review
  14. Article
  15. Article
  16. NKG2CClinical & translational immunology · 2017
    Article
  17. 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

15 authors at 8 institutions in 2 countries.

Françoise Gondois-ReyCNRS, INSERM, Institut Paoli-Calmettes, CRCM, Immunity and Cancer Team, Aix Marseille Univ , Marseille , France.
Antoine ChéretAPHP, Hôpital Bicêtre, Internal Medecin Unit, Le Kremlin-Bicêtre, France; U1184, Paris-Sud Univ, Le Kremlin-Bicêtre, France; CEA, DSV/iMETI, IDMIT, Fontenay-aux-Roses, France; INSERM U1184, ImVA "Immunology of Chronic Viral Infections and Autoimmune Diseases", Le Kremlin-Bicêtre, France; Institut Pasteur, HIV, Inflammation and Persistance Unit, Paris, France; Virology Laboratory, APHP CHU Necker-Enfants Malades, Paris, France.
Françoise MalletCNRS, INSERM, Institut Paoli-Calmettes, CRCM, Immunity and Cancer Team, Aix Marseille Univ , Marseille , France.
Ghislain BidautCNRS, INSERM, Institut Paoli-Calmettes, CRCM, CiBi Platform, Aix Marseille Univ , Marseille , France.
Samuel GranjeaudCNRS, INSERM, Institut Paoli-Calmettes, CRCM, CiBi Platform, Aix Marseille Univ , Marseille , France.
Camille LécurouxU1184, Paris-Sud Univ, Le Kremlin-Bicêtre, France; CEA, DSV/iMETI, IDMIT, Fontenay-aux-Roses, France; INSERM U1184, ImVA "Immunology of Chronic Viral Infections and Autoimmune Diseases", Le Kremlin-Bicêtre, France.
Mickaël PloquinInstitut Pasteur, HIV, Inflammation and Persistance Unit , Paris , France.
Michaela Müller-TrutwinInstitut Pasteur, HIV, Inflammation and Persistance Unit , Paris , France.
Christine RouziouxVirology Laboratory, APHP CHU Necker-Enfants Malades, Paris, France; EA 7327 Paris Descartes University, Paris, France.
Véronique Avettand-FenoëlVirology Laboratory, APHP CHU Necker-Enfants Malades, Paris, France; EA 7327 Paris Descartes University, Paris, France.
Andrea De MariaDipartimento di Scienze della Salute and Centro di Eccellenza per la Ricerca Biomedica, Università di Genova, Genova, Italy; Clinica Malattie Infettive, IRCCS Azienda Ospedaliera Universitaria San Martino - Istituto Nazionale per la Ricerca sul Cancro, Genova, Italy.
Gilles PialouxAPHP, Hôpital Tenon, Infectious Diseases Unit , Paris , France.
Cécile GoujardAPHP, Hôpital Bicêtre, Internal Medecin Unit , Le Kremlin-Bicêtre , France.
Laurence MeyerINSERM, CESP U1018, Epidemiology and population health, APHP, Hôpital Bicêtre, Paris 11 Univ , Le Kremlin-Bicêtre , France.
Daniel OliveCNRS, INSERM, Institut Paoli-Calmettes, CRCM, Immunity and Cancer Team, Aix Marseille Univ , Marseille , France.
Assistance Publique – Hôpitaux de Paris · FRInserm · FRBicêtre Hospital · FRCentre National de la Recherche Scientifique · FRInstitut Pasteur · FRInfectious Disease Models and Innovative Therapies · FRUniversité Paris-Sud · FRUniversity of Genoa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural killer (NK) cells are major effectors of the innate immune response. Despite an overall defect in their function associated with chronic human immunodeficiency virus (HIV) infection, their role in primary HIV infection is poorly understood. We investigated the modifications of the NK cell compartment in patients from the ANRS-147-Optiprim trial, a study designed to examine the benefits of intensive combination antiretroviral therapy (cART) in patients with acute or early primary HIV infection. Multiparametric flow cytometry combined with bioinformatics analyses identified the NK phenotypes in blood samples from 30 primary HIV-infected patients collected at inclusion and after 3 months of cART. NK phenotypes were revealed by co-expression of CD56/CD16/NKG2A/NKG2C and CD57, five markers known to delineate stages of NK maturation. Three groups of patients were formed according to their distributions of the 12 NK cell phenotypes identified. Their virological and immunological characteristics were compared along with the early outcome of cART. At inclusion, HIV-infected individuals could be grouped into those with predominantly immature/early differentiated NK cells and those with predominantly mature NK cells. Several virological and immunological markers were improved in patients with mature NK profiles, including lower HIV viral loads, lower immune activation markers on NK and dendritic cell (DC), lower levels of plasma IL-6 and IP-10, and a trend to normal DC counts. Whereas all patients showed a decrease of viremia higher than 3 log

Indexed as

cARTHIVmemory-like NKNK cells maturationprimary infection

Identifiers

PMID28239376
PMCPMC5300971
OpenAlexW2587354014

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.