Evidence map›Paper›PMID 23283958›Full record

ArticleJournal of virology2013

Evolution of CD8+ T cell responses after acute PARV4 infection.

Ruth Simmons, Colin Sharp, Jordana Levine, Paul Bowness, Peter Simmonds, Andrea Cox, Paul Klenerman

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Parvovirus 4 in Individuals with Severe Hemophilia A and Matched Control Group.International journal of hematology-oncology and stem cell research · 2021
    Article
  2. Article
  3. The (gradual) rise of memory inflation.Immunological reviews · 2018
    Review
  4. Article
  5. Review
  6. Human Parvoviruses.Clinical microbiology reviews · 2017
    Review
  7. T cell responses to cytomegalovirus.Nature reviews. Immunology · 2016
    Review
  8. Article
  9. Article
  10. 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

7 authors at 4 institutions in 2 countries.

Ruth SimmonsNuffield Department of Medicine, University of Oxford, Oxford, UK.
Colin Sharp
Jordana Levine
Paul Bowness
Peter Simmonds
Andrea Cox
Paul Klenerman
Johns Hopkins University · USUniversity of Edinburgh · GBUniversity of Oxford · GBJohn Radcliffe Hospital · GB

Funding

Scientific CoreU19AI088791 · NIAID · JOHNS HOPKINS UNIVERSITY · PI COX, ANDREA L · 2010 to 2020
$8.2M
Pathogenesis of HIV and HCV in Hemophilia: HGDSR01HD041224 · NICHD · CHILDREN'S HOSPITAL LOS ANGELES · PI GOMPERTS, EDWARD DAVID · 2001 to 2004
$2.8M
RECEPTOR BINDING AND CORONAVIRUS PATHOGENESISF32AI008879 · NIAID · U.S. UNIFORMED SERVICES UNIV OF HLTH SCI · PI WESSNER, DAVID R · 1994 to 1995
–
Medical Research Council MC_U137884185NIAID NIH HHS 1U19AI08879NIAID NIH HHS F32 AI008879NIAID NIH HHS U19 AI088791NICHD NIH HHS R01 HD041224NICHD NIH HHS R01 HD41224Wellcome Trust 091663Wellcome Trust 095831Wellcome Trust WT091663MA
6 · The paper itself

Abstract

PARV4 is a small DNA human virus that is strongly associated with hepatitis C virus (HCV) and HIV infections. The immunologic control of acute PARV4 infection has not been previously described. We define the acute onset of PARV4 infection and the characteristics of the acute-phase and memory immune responses to PARV4 in a group of HCV- and HIV-negative, active intravenous drug users. Ninety-eight individuals at risk of blood-borne infections were tested for PARV4 IgG. Gamma interferon enzyme-linked immunosorbent spot assays, intracellular cytokine staining, and a tetrameric HLA-A2-peptide complex were used to define the T cell populations responding to PARV4 peptides in those individuals who acquired infection during the study. Thirty-five individuals were found to be PARV4 seropositive at the end of the study, eight of whose baseline samples were found to be seronegative. Persistent and functional T cell responses were detected in the acute infection phase. These responses had an active, mature, and cytotoxic phenotype and were maintained several years after infection. Thus, PARV4 infection is common in individuals exposed to blood-borne infections, independent of their HCV or HIV status. Since PARV4 elicits strong, broad, and persistent T cell responses, understanding of the processes responsible may prove useful for future vaccine design.

Indexed as

CD8-Positive T-LymphocytesCytokinesEnzyme-Linked Immunospot AssayHumansParvoviridae InfectionsParvovirusSubstance Abuse, IntravenousCytokines

Identifiers

PMID23283958
PMCPMC3592128
OpenAlexW2137986259

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.