Evidence map›Paper›PMID 34832642›Full record

ArticlePathogens (Basel, Switzerland)2021

Short- and Long-Term Immunological Responses in Chronic HCV/HIV Co-Infected Compared to HCV Mono-Infected Patients after DAA Therapy.

Stefania Farcomeni, Sonia Moretti, Caterina Fimiani, Lucia Fontanelli Sulekova, Fenicia Vescio, Leonardo Sernicola, Maria T Maggiorella, Anna Lisa Remoli, Orietta Picconi, Luciana Mosca and 6 more

Open access · goldAbstract read
In one paragraph

Article in Pathogens (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 46% 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, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Review
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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

16 authors at 4 institutions in 1 country.

Stefania FarcomeniNational HIV/AIDS Research Center, Istituto Superiore di Sanità, 00161 Rome, Italy.
Sonia MorettiNational HIV/AIDS Research Center, Istituto Superiore di Sanità, 00161 Rome, Italy.
Caterina FimianiDepartment of Public Health and Infectious Diseases, "Sapienza" University of Rome, 00161 Rome, Italy.
Lucia Fontanelli SulekovaDepartment of Translation and Precision Medicine, "Sapienza" University of Rome, 00161 Rome, Italy.
Fenicia VescioDepartment of Infectious Diseases, Istituto Superiore di Sanità, 00161 Rome, Italy.
Leonardo SernicolaNational HIV/AIDS Research Center, Istituto Superiore di Sanità, 00161 Rome, Italy.
Maria T MaggiorellaNational HIV/AIDS Research Center, Istituto Superiore di Sanità, 00161 Rome, Italy.
Anna Lisa RemoliDepartment of Infectious Diseases, Istituto Superiore di Sanità, 00161 Rome, Italy.
Orietta PicconiNational HIV/AIDS Research Center, Istituto Superiore di Sanità, 00161 Rome, Italy.
Luciana MoscaDepartment of Biochemical Sciences, "Sapienza" University of Rome, 00161 Rome, Italy.ORCID 0000-0003-2748-9021
Rozenn EsvanDepartment of Public Health and Infectious Diseases, "Sapienza" University of Rome, 00161 Rome, Italy.ORCID 0000-0001-6127-0045
Elisa BiliottiDepartment of Clinical Medicine, Policlinico Umberto I, "Sapienza" University of Rome, 00161 Rome, Italy.
Massimo CiccozziMedical Statistics and Molecular Epidemiology Unit, University Campus Bio-Medico of Rome, 00161 Rome, Italy.
Marco SgarbantiDepartment of Infectious Diseases, Istituto Superiore di Sanità, 00161 Rome, Italy.ORCID 0000-0002-0433-5110
Gloria TalianiChronic Infectious Diseases Unit, Policlinico Umberto I, "Sapienza" University of Rome, 00161 Rome, Italy.
Alessandra BorsettiNational HIV/AIDS Research Center, Istituto Superiore di Sanità, 00161 Rome, Italy.ORCID 0000-0002-5401-135X
Istituto Superiore di Sanità · ITSapienza University of Rome · ITPoliclinico Umberto I · ITUniversità Campus Bio-Medico · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDirect-acting antivirals (DAAs) treatment, although highly efficacious for the treatment of hepatitis C virus (HCV) infection, may not completely reconstitute the HCV-mediated dysregulated immune system, especially in patients co-infected with human immunodeficiency virus (HIV) and HCV.

objectivesWe aimed to evaluate the impact of HCV eradication following DAA therapy on the immune system and liver disease improvement through comparative monitoring of 10 HCV mono-infected and 10 HCV/HIV co-infected patients under combined antiretroviral therapy (cART). Early and late longitudinal phenotypic changes in peripheral blood mononuclear cell (PBMC) subsets, T-cell activation, differentiation and exhaustion, as well as inflammatory biomarkers, indoleamine 2-3 dioxygenase (IDO) activity, and liver stiffness, APRI and FIB-4 scores were assessed. MATERIALS AND

methodsSamples were obtained at baseline (T0), week 1 (T1), week 2 (T2), week 12 (T3, end of treatment, EOT), and month 9 (T4, end of follow-up, 36 weeks post EOT).

resultsAll patients achieved a sustained virological response (SVR 12) after DAA treatment. Overall, changes of the T-cell immune phenotypes were greater in HCV/HIV co-infected than in HCV mono-infected, due to an increase in CD4+ and CD8+ T-cell percentages and of CD8+ T-cell activation and memory markers, in particular at the end of follow-up. On the other end, HCV mono-infected showed changes in the activation profile and in the memory CD4+ T-cell compartment. In HCV/HIV co-infected, a decrease in the IDO activity by DAA treatment was observed; conversely, in HCV mono-infected, it resulted unmodified. Regarding inflammatory mediators, viral suppression was associated with a reduction in IP-10 levels, while interferon regulatory factor (IRF)-7, interferon (IFN)-β, and interferon (IFN)-γ levels were downregulated during therapy and increased post therapy. A decrease in liver stiffness, APRI, and FIB-4 scores was also observed.

conclusionsOur study suggests that, although patients achieved HCV eradication, the immune activation state in both HCV mono-infected and HCV/HIV co-infected patients remains elevated for a long time after the end of DAA therapy, despite an improvement of liver-specific outcomes, meanwhile highlighting the distinct immunophenotypic and inflammatory biomarker profile between the groups of patients.

Indexed as

DAA direct-acting antiviralsHCV/HIV coinfectionHCV infectionimmune activationindoleamine 2-3 dioxygenase (IDO) activityinterferon-stimulated gene (ISG) expression

Identifiers

PMID34832642
PMCPMC8623367
OpenAlexW3213872952

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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.