Evidence map›Paper›PMID 29523966›Full record

ArticleMedical microbiology and immunology2018

Soluble CD163 and soluble CD14 plasma levels but not cellular HIV-DNA decrease during successful interferon-free anti-HCV therapy in HIV-1-HCV co-infected patients on effective combined anti-HIV treatment.

Saverio G Parisi, Samantha Andreis, Carlo Mengoli, Nicola Menegotto, Silvia Cavinato, Renzo Scaggiante, Massimo Andreoni, Giorgio Palù, Monica Basso, Anna Maria Cattelan

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Article in Medical microbiology and immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

14 citing papers in PubMed, 23 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

10 authors at 3 institutions in 1 country.

Saverio G ParisiDepartment of Molecular Medicine, University of Padova, Via Gabelli 63, 35100, Padova, Italy. saverio.parisi@unipd.it.
Samantha AndreisDepartment of Molecular Medicine, University of Padova, Via Gabelli 63, 35100, Padova, Italy.
Carlo MengoliDepartment of Molecular Medicine, University of Padova, Via Gabelli 63, 35100, Padova, Italy.
Nicola MenegottoDepartment of Molecular Medicine, University of Padova, Via Gabelli 63, 35100, Padova, Italy.
Silvia CavinatoInfectious Diseases Unit, Padova Hospital, Via Giustiniani, 2, 35128, Padova, Italy.
Renzo ScaggianteInfectious Diseases Unit, Padova Hospital, Via Giustiniani, 2, 35128, Padova, Italy.
Massimo AndreoniClinical Infectious Diseases, Tor Vergata University, Viale Oxford, 81, 00133, Rome, Italy.
Giorgio PalùDepartment of Molecular Medicine, University of Padova, Via Gabelli 63, 35100, Padova, Italy.
Monica BassoDepartment of Molecular Medicine, University of Padova, Via Gabelli 63, 35100, Padova, Italy.
Anna Maria CattelanInfectious Diseases Unit, Padova Hospital, Via Giustiniani, 2, 35128, Padova, Italy.
University of Padua · ITSanta Maria Nuova Hospital · ITUniversity of Rome Tor Vergata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Soluble CD163, soluble CD14 and cellular HIV-1-DNA levels reflect two different aspects of HIV infection: immune activation and the reservoir of infected cells. The aim of this study was to describe their relationships in a cohort of HIV-HCV co-infected patients successfully treated for both HCV and HIV infections. Fifty-five patients were recruited and studied prior to the start of direct-acting antivirals (DAAs) (T0), at week 12 of DAA treatment (T1) and 24 weeks after T0 (T2). The subjects were classified as having undetectable plasma HIV viraemia (UV) or low-level viraemia (LLV) in the 18 months before T2. Plasma levels of sCD163 and of sCD14 were comparable in patients with UV and in subjects with LVL at T0, T1 and T2. The HIV DNA level was positively correlated with LLV but not with sCD163 and sCD14 levels; these two markers of inflammation were positively correlated (p = 0.017). Soluble CD163 and sCD14 decreased over time from T0 to T2 (p = 0.000 and p = 0.034, respectively). In conclusion, the significant decrease in sCD163 and sCD14 levels in patients cured of HCV infection, regardless of the presence of LLV, suggests a main role for HCV in immune activation in HIV-HCV co-infected patients.

Indexed as

AdultAgedAged, 80 and overAntigens, CDAntigens, Differentiation, MyelomonocyticAntiviral AgentsCD163 AntigenCoinfectionDNA, ViralFemaleHepatitis C, ChronicHIV InfectionsHumansLipopolysaccharide ReceptorsMaleMiddle AgedAntigens, CDAntigens, Differentiation, MyelomonocyticAntiviral AgentsCD163 AntigenDNA, ViralLipopolysaccharide ReceptorsReceptors, Cell SurfaceCellular HIV-DNADirect-acting antiviralsHIV-1–HCV coinfectionsCD14sCD163

Identifiers

PMID29523966
OpenAlexW2790436620

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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.