Evidence map›Paper›PMID 31904583›Full record

Trial reportThe Journal of clinical investigation2020

CD4+ T cell restoration and control of hepatitis C virus replication after childbirth.

Samantha L Coss, Almudena Torres-Cornejo, Mona R Prasad, Melissa Moore-Clingenpeel, Arash Grakoui, Georg M Lauer, Christopher M Walker, Jonathan R Honegger

Open access · bronzeAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in The Journal of clinical investigation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Lymphocyte Landscape after ChronicInternational journal of molecular sciences · 2020
    Review
  14. Adaptive Immune Response against Hepatitis C Virus.International journal of molecular sciences · 2020
    Review
  15. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 1 country.

Samantha L CossThe Ohio State University College of Medicine, Columbus, Ohio, USA.
Almudena Torres-CornejoDivision of Gastroenterology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Mona R PrasadThe Ohio State University College of Medicine, Columbus, Ohio, USA.
Melissa Moore-ClingenpeelAbigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, Ohio, USA.
Arash GrakouiEmory University, Atlanta, Georgia, USA.
Georg M LauerDivision of Gastroenterology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Christopher M WalkerThe Ohio State University College of Medicine, Columbus, Ohio, USA.
Jonathan R HoneggerThe Ohio State University College of Medicine, Columbus, Ohio, USA.
The Ohio State University · USMassachusetts General Hospital · USNationwide Children's Hospital · USEmory University · US

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
YNPRC NHP CLINICAL MEDICINE RESIDENCY PROGRAM - SUPPLEMENTP51RR000165 · NCRR · EMORY UNIVERSITY · PI RENGARAJAN, JYOTHI · 1985 to 2011
$114.0M
The OSU Center for Clinical and Translational Science: Advancing Today's Discoveries to Improve HealthUL1TR002733 · NCATS · OHIO STATE UNIVERSITY · PI RINGEL, MATTHEW D · 2018 to 2022
$28.9M
Persistent hepatitis C virus replication and T cell immunity in pregnancyR01AI096882 · NIAID · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI WALKER, CHRISTOPHER M. · 2012 to 2022
$5.7M
Mechanisms of hepatitis C virus persistenceR01AI070101 · NIAID · EMORY UNIVERSITY · PI GRAKOUI, ARASH · 2006 to 2016
$3.9M
Child Health Research Career Development AwardK12HD043372 · NICHD · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI BRADY, MICHAEL THOMAS · 2003 to 2012
$3.8M
Dynamics of antigen specific B and Tfh responses during acute and chronic HCVR01AI136533 · NIAID · EMORY UNIVERSITY · PI GRAKOUI, ARASH · 2018 to 2022
$3.8M
T cell Immunity and the Outcome of Acute HCV InfectionR01AI126890 · NIAID · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI GRAKOUI, ARASH, WALKER, CHRISTOPHER M. · 2016 to 2020
$3.7M
T cell compartmentalization and antiviral responseR01AI124680 · NIAID · EMORY UNIVERSITY · PI GRAKOUI, ARASH, ZHU, CHENG · 2016 to 2020
$3.2M
CD4+ T Cells in Acute Versus Chronic HCV InfectionR01AI105035 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI LAUER, GEORG MICHAEL · 2013 to 2017
$2.3M
NICHD Institutional Training for Pediatricians (T32)T32HD043003 · NICHD · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI BARNARD, JOHN A · 2003 to 2014
$1.7M
Immune Control and Evadion during Acute HCV InfectionU01AI131314 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI LAUER, GEORG MICHAEL · 2016 to 2020
$1.4M
NCATS NIH HHS UL1 TR002733NCRR NIH HHS P51 RR000165NIAID NIH HHS R01 AI070101NIAID NIH HHS R01 AI096882NIAID NIH HHS R01 AI105035NIAID NIH HHS R01 AI124680NIAID NIH HHS R01 AI126890NIAID NIH HHS R01 AI136533NIAID NIH HHS R56 AI096882NIAID NIH HHS U01 AI131314NICHD NIH HHS K12 HD043372NICHD NIH HHS T32 HD043003NIH HHS P51 OD011132
6 · The paper itself

Abstract

Chronic hepatitis C virus (HCV) infection is characterized by persistent high-level viremia and defective cellular immunity, including a lack of functional HCV-specific CD4+ T cells. We previously described an exceptional period of viral control that occurs in some chronically infected women after childbirth. Here, we investigated whether reduced HCV replication after pregnancy is associated with recovery of CD4+ T cell immunity. Class II tetramer analysis revealed significantly greater frequencies of circulating HCV-specific CD4+ T cells at 3 months postpartum in women with concurrent declines in viremia compared with those with stable viremia. These HCV-specific CD4+ T cells had an effector-memory phenotype. Inhibitory coreceptor expression on these cells corresponded to the degree of viral control. Circulating CD4+ T cells produced IL-2 and IFN-γ after HCV antigen stimulation, demonstrating Th1 functionality. These data provide direct evidence that the profound loss of HCV-specific CD4+ T cell help that results in chronic infection is reversible following pregnancy, and this recovery of CD4+ T cells is associated with at least transient control of persistent viral replication.

Indexed as

ParturitionAdultFemaleHepacivirusHepatitis C, ChronicHumansInterferon-gammaInterleukin-2PregnancyPregnancy Complications, InfectiousTh1 CellsVirus ReplicationIFNG protein, humanIL2 protein, humanInterferon-gammaInterleukin-2HepatitisImmunologyInfectious diseaseT cells

Identifiers

PMID31904583
PMCPMC6994162
OpenAlexW2998001287

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.