Evidence map›Paper›PMID 15867490›Full record

Trial reportAIDS (London, England)2005

Antigen-specific immune responses and liver histology in HIV and hepatitis C coinfection.

Camilla S Graham, Annalee Wells, Tun Liu, Kenneth E Sherman, Marion Peters, Raymond T Chung, Atul K Bhan, Janet Andersen, Margaret James Koziel, ACTG 5071 Study Team

Registry-linked trialAbstract readClinical TrialRandomized Controlled Trial
In one paragraph

Trial report in AIDS (London, England), 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00008463 (A Prospective, Multicenter, Phase II/III, Open-Label, Controlled, Randomized Trial Evaluating the Efficacy, Safety, and Tolerability of Interferon-alfa-2a Plus Ribavirin Versus PEG-interferon-alfa-2a Plus Ribavirin for Chronic Hepatitis C Virus), which is not on this map. Cited by 15 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 2 pooled it
2.0field-weighted citation impact, top 14% 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.

NCT00008463 phase2completednot on this map

A Prospective, Multicenter, Phase II/III, Open-Label, Controlled, Randomized Trial Evaluating the Efficacy, Safety, and Tolerability of Interferon-alfa-2a Plus Ribavirin Versus PEG-interferon-alfa-2a Plus Ribavirin for Chronic Hepatitis C Virus (HCV) Infection in Individuals Co-Infected With Human Immunodeficiency Virus-1 (HIV-1)

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2000 to 2006Enrolled132ConditionsHIV Infections, Hepatitis CArmsRibavirin, Interferon alfa-2a, Peginterferon alfa-2a
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 2 syntheses or guidelines pooled it, 32 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Plasma Inflammatory Biomarkers Associated with Advanced Liver Fibrosis in HIV-HCV-Coinfected Individuals.International journal of environmental research and public health · 2020
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Substance abuse, HIV-1 and hepatitis.Current HIV research · 2012
    Review
  11. Review
  12. Article
  13. Hepatitis infection in the treatment of opioid dependence and abuse.Substance abuse : research and treatment · 2008
    Review
  14. Article
  15. 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

10 authors at 4 institutions in 1 country.

Camilla S GrahamBeth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02115, USA. cgraham@bidmc.harvard.edu
Annalee Wells
Tun Liu
Kenneth E Sherman
Marion Peters
Raymond T Chung
Atul K Bhan
Janet Andersen
Margaret James Koziel
ACTG 5071 Study Team
GTx (United States) · USBeth Israel Deaconess Medical Center · USHarvard University · USUniversity of California, San Francisco · US

Funding

AIDS Clinical Trials Group NetworkU01AI068636 · NIAID · SOCIAL AND SCIENTIFIC SYSTEMS, INC. · PI KURITZKES, DANIEL R. · 2006 to 2010
$147.1M
HCV Genomic Variability in HIV Infected HemophiliacsR01AI049508 · NIAID · UNIVERSITY OF CINCINNATI · PI SHERMAN, KENNETH E · 2001 to 2004
$2.9M
T Lymphocyte Apoptosis in Hepatitis C PersistenceR01AI050752 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KOZIEL, MARGARET J · 2002 to 2006
$1.9M
Cellular Immunity to Hepatitis C Virus in HIVK08DA014495 · NIDA · BETH ISRAEL DEACONESS MEDICAL CENTER · PI GRAHAM, CAMILLA S · 2001 to 2005
$562k
CAN AND PKA ASSOCIATION IN BETA CELLS BY AKAP155R03DK056041 · NIDDK · OREGON HEALTH AND SCIENCE UNIVERSITY · PI LESTER, LINDA B · 1999 to 1999
–
NIAID NIH HHS AI49508NIAID NIH HHS R01 AI049508NIAID NIH HHS R01 AI050752NIAID NIH HHS U01 AI068636NIDA NIH HHS DA14495-01NIDA NIH HHS K08 DA014495NIDDK NIH HHS DK56041
6 · The paper itself

Abstract

objectiveTo test the hypothesis that antigen-specific interferon (IFN)gamma responses are correlated with milder liver disease in subjects coinfected with HIV-1 and hepatitis C virus (HCV).

designCellular immune responses were studied in a cohort with HIV/HCV coinfection (n = 107) who underwent liver biopsy.

methodsWe measured HCV-specific and recall responses in peripheral blood mononuclear cells using IFNgamma and interleukin (IL)-10 ELISpots, and correlated these immune responses with liver histology. The relationship of immunologic, virologic and clinical variables to inflammation and fibrosis was modeled using recursive partitioning.

resultsThere were significant negative correlations between inflammatory scores and IFNgamma production in response to the HCV proteins core, NS5 and summed HCV responses. Lower fibrosis scores were also correlated with higher IFNgamma production in response to NS5 and summed HCV proteins. Higher IFNgamma production in response to Candida was significantly associated with lower inflammatory and fibrosis scores. In multivariable models, factors associated with severe fibrosis were lower IFNgamma responses to Candida and summed HCV proteins. Factors associated with severe inflammation were detectable HIV viral load and lower HCV viral load, while predictors of mild inflammation included undetectable HIV viral load and higher IFNgamma response to Candida.

conclusionsIn this cohort of subjects coinfected with HIV and HCV, antigen-specific IFNgamma responses are correlated with milder inflammation and fibrosis. Immunological responses best predicted severity of fibrosis, while clinical variables and recall antigen responses best predicted severity of inflammation.

Indexed as

AdolescentAdultAnti-HIV AgentsAntiretroviral Therapy, Highly ActiveCandidaFemaleFibrosisHepacivirusHepatitis C AntigensHepatitis C, ChronicHIV-1HIV InfectionsHumansImmunologic MemoryInflammationInterferon-gammaAnti-HIV AgentsHepatitis C AntigensInterferon-gammaInterleukin-10

Identifiers

PMID15867490
PMCPMC4050654
OpenAlexW2090513927

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.