Evidence map›Paper›PMID 24270546›Full record

ArticleNature medicine2013

Subinfectious hepatitis C virus exposures suppress T cell responses against subsequent acute infection.

Su-Hyung Park, Naga Suresh Veerapu, Eui-Cheol Shin, Angélique Biancotto, J Philip McCoy, Stefania Capone, Antonella Folgori, Barbara Rehermann

Open access · greenAbstract read
In one paragraph

Article in Nature medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 45 citations in OpenAlex.

  1. Trial
  2. Trial
  3. TInternational journal of molecular sciences · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Intrahepatic TFrontiers in pharmacology · 2020
    Review
  10. Review
  11. Article
  12. HLA variation and disease.Nature reviews. Immunology · 2018
    Review
  13. Article
  14. Review
  15. Review
  16. Adaptive immunity in the liver.Cellular & molecular immunology · 2016
    Review
  17. Article
  18. Review
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Su-Hyung ParkImmunology Section, Liver Diseases Branch, NIDDK, National Institutes of Health (NIH), Department of Health and Human Services, Bethesda, Maryland, USA.
Naga Suresh Veerapu
Eui-Cheol Shin
Angélique Biancotto
J Philip McCoy
Stefania Capone
Antonella Folgori
Barbara Rehermann
National Institutes of Health · USNational Heart Lung and Blood Institute · USNational Institute of Diabetes and Digestive and Kidney Diseases · US

Funding

Flow Cytometry Core FacilityZICHL005905 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI DAGUR, PRADEEP · 2009 to 2025
$32.3M
Regulation of hepatic and systemic immune responsesZIADK054508 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI REHERMANN, BARBARA · 2009 to 2025
$22.1M
Intramural NIH HHS ZIA DK054508
6 · The paper itself

Abstract

Hepatitis C virus (HCV) is endemic in many countries due to its high propensity for establishing persistence. The presence of HCV-specific T cells in subjects repeatedly exposed to HCV who test negative for HCV RNA and antibodies and who do not have any history of HCV infection has been interpreted as T cell-mediated protection. Here, we show in nonhuman primates that repeated exposure to human plasma with trace amounts of HCV induced HCV-specific T cells without seroconversion and systemic viremia but did not protect upon subsequent HCV challenge. Rather, HCV-specific recall and de novo T cell responses, as well as intrahepatic T cell recruitment and interferon-γ (IFN-γ) production, were suppressed upon HCV challenge, concomitant with quantitative and qualitative changes in regulatory T cells (T(reg) cells) that occurred after subinfectious HCV exposure and increased after HCV challenge. In vitro T(reg) cell depletion restored HCV-specific T cell responses. Thus, T cells primed by trace amounts of HCV do not generate effective recall responses upon subsequent HCV infection. Subinfectious HCV exposure predisposes to T(reg) cell expansion, which suppresses effector T cells during subsequent infection. Strategies to reverse this exposure-induced immune suppression should be examined to aid in the development of T cell-based vaccines against HCV and other endemic pathogens.

Indexed as

Acute DiseaseAnimalsCell ProliferationHepacivirusHepatitis CHepatitis C, ChronicImmune ToleranceInterferon-gammaLymphocyte ActivationPan troglodytesSeverity of Illness IndexT-LymphocytesViremiaInterferon-gamma

Identifiers

PMID24270546
PMCPMC4196667
OpenAlexW2061008627

What OpenQuestion holds

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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.