Evidence map›Paper›PMID 27363286›Full record

ArticleRetrovirology2016

Major influence of CD4 count at the initiation of cART on viral and immunological reservoir constitution in HIV-1 infected patients.

Anne-Emmanuelle Depincé-Berger, Delphine Vergnon-Miszczycha, Alexandre Girard, Anne Frésard, Elisabeth Botelho-Nevers, Claude Lambert, Emilie Del Tedesco, Christian Genin, Bruno Pozzetto, Frédéric Lucht and 3 more

Open access · goldAbstract read
In one paragraph

Article in Retrovirology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

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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

13 authors at 2 institutions in 1 country.

Anne-Emmanuelle Depincé-BergerGroupe Immunité des Muqueuses et Agents Pathogènes - GIMAP EA 3064, CIC 1408, Faculté de Médecine J. Lisfranc, Université de Saint-Etienne, Université de Lyon, 42023, Saint-Étienne Cedex 02, France.
Delphine Vergnon-MiszczychaGroupe Immunité des Muqueuses et Agents Pathogènes - GIMAP EA 3064, CIC 1408, Faculté de Médecine J. Lisfranc, Université de Saint-Etienne, Université de Lyon, 42023, Saint-Étienne Cedex 02, France.
Alexandre GirardGroupe Immunité des Muqueuses et Agents Pathogènes - GIMAP EA 3064, CIC 1408, Faculté de Médecine J. Lisfranc, Université de Saint-Etienne, Université de Lyon, 42023, Saint-Étienne Cedex 02, France.
Anne FrésardService de Maladies Infectieuses et Tropicales, Centre Hospitalo-Universitaire, Saint-Étienne, France.
Elisabeth Botelho-NeversGroupe Immunité des Muqueuses et Agents Pathogènes - GIMAP EA 3064, CIC 1408, Faculté de Médecine J. Lisfranc, Université de Saint-Etienne, Université de Lyon, 42023, Saint-Étienne Cedex 02, France.
Claude LambertGroupe Immunité des Muqueuses et Agents Pathogènes - GIMAP EA 3064, CIC 1408, Faculté de Médecine J. Lisfranc, Université de Saint-Etienne, Université de Lyon, 42023, Saint-Étienne Cedex 02, France.
Emilie Del TedescoService d'Hépato-Gastroentérologie, Centre Hospitalo-Universitaire, Saint-Étienne, France.
Christian GeninGroupe Immunité des Muqueuses et Agents Pathogènes - GIMAP EA 3064, CIC 1408, Faculté de Médecine J. Lisfranc, Université de Saint-Etienne, Université de Lyon, 42023, Saint-Étienne Cedex 02, France.
Bruno PozzettoGroupe Immunité des Muqueuses et Agents Pathogènes - GIMAP EA 3064, CIC 1408, Faculté de Médecine J. Lisfranc, Université de Saint-Etienne, Université de Lyon, 42023, Saint-Étienne Cedex 02, France.
Frédéric LuchtGroupe Immunité des Muqueuses et Agents Pathogènes - GIMAP EA 3064, CIC 1408, Faculté de Médecine J. Lisfranc, Université de Saint-Etienne, Université de Lyon, 42023, Saint-Étienne Cedex 02, France.
Xavier RoblinGroupe Immunité des Muqueuses et Agents Pathogènes - GIMAP EA 3064, CIC 1408, Faculté de Médecine J. Lisfranc, Université de Saint-Etienne, Université de Lyon, 42023, Saint-Étienne Cedex 02, France.
Thomas BourletGroupe Immunité des Muqueuses et Agents Pathogènes - GIMAP EA 3064, CIC 1408, Faculté de Médecine J. Lisfranc, Université de Saint-Etienne, Université de Lyon, 42023, Saint-Étienne Cedex 02, France. thomas.bourlet@chu-st-etienne.fr.
Stéphane PaulGroupe Immunité des Muqueuses et Agents Pathogènes - GIMAP EA 3064, CIC 1408, Faculté de Médecine J. Lisfranc, Université de Saint-Etienne, Université de Lyon, 42023, Saint-Étienne Cedex 02, France.
Centre Hospitalier Universitaire de Saint-Étienne · FRUniversité Claude Bernard Lyon 1 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA persistent immune activation is observed in gut during HIV-1 infection, which is not completely reversed by a combined antiretroviral therapy (cART). The impact of the time of cART initiation may highly influence the size of the viral reservoir and the ratio of CD4(+)/CD8(+) T cells in the gut. In this study, we analyzed the characteristics of HIV rectal reservoir of long-term treated patients, regarding their blood CD4(+) T cells count at the time of cART initiation.

resultsTwenty-four consenting men were enrolled: 9 exhibiting a CD4(+) T cells count >350/mm(3) ("high-level CD4 group") and 15 < 350/mm(3) ("low-level CD4 group") in blood, at the start of cART. An immunophenotypical analysis of T and B cells subpopulations was performed in blood and rectal biopsies. HIV cell-associated DNA loads and qualitative intra-cellular RNA were determined in both compartments. The ratio of CD4(+)/CD8(+) T cells was significantly decreased in the blood but not in the rectum of the "low-level CD4 group" of patients. The alteration in β7(+) CD4(+) T cells homing was higher in this group and was correlated to a low ratio of CD4(+)/CD8(+) T cells in blood. An initiation of cART in men exhibiting a low-level CD4 count was also associated with an alteration of B cells maturation. HIV blood and gut DNA reservoirs were significantly lower in the "high-level CD4 group" of men. A high HIV DNA level was associated to a detectable intracellular HIV RNA in rectum.

conclusionsAn early initiation of cART could significantly preserve gut immunity and limit the viral reservoir constitution.

Indexed as

CD4 Lymphocyte CountHIV-1Viral LoadAdultAnti-HIV AgentsAntiretroviral Therapy, Highly ActiveCD4-CD8 RatioDNA, ViralGastrointestinal TractHIV InfectionsHumansMaleRectumRNA, ViralTime-to-TreatmentAnti-HIV AgentsDNA, ViralRNA, ViralcARTGALTHIVHomingReservoir

Identifiers

PMID27363286
PMCPMC4929778
OpenAlexW2474003163

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.