Evidence map›Paper›PMID 24434272›Full record

ArticleClinical immunology (Orlando, Fla.)2014

Peripheral CD27-CD21- B-cells represent an exhausted lymphocyte population in hepatitis C cirrhosis.

Hiroyoshi Doi, Shiroh Tanoue, David E Kaplan

Abstract read
In one paragraph

Article in Clinical immunology (Orlando, Fla.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

39 citing papers in PubMed, 58 citations in OpenAlex.

  1. Review
  2. Human CD21Journal of human immunity · 2026
    Review
  3. FcRL1, a New B-Cell-Activating Co-Receptor.International journal of molecular sciences · 2025
    Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
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  11. Review
  12. Article
  13. Article
  14. Deep Phenotyping of CD11cFrontiers in immunology · 2021
    Article
  15. Article
  16. Article
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  18. Observational
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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

3 authors at 2 institutions in 1 country.

Hiroyoshi DoiDivision of Gastroenterology, Department of Medicine, University of Pennsylvania, USA.
Shiroh TanoueDivision of Gastroenterology, Department of Medicine, University of Pennsylvania, USA.
David E KaplanMedicine and Research Services, Philadelphia VA Medical Center, Philadelphia, PA, USA; Division of Gastroenterology, Department of Medicine, University of Pennsylvania, USA. Electronic address: dakaplan@mail.med.upenn.edu.
University of Pennsylvania · USPhiladelphia VA Medical Center · US

Funding

B-Cell Dysregulation in Cirrhosis due to Chronic Hepatitis C InfectionI01CX000981 · VA · PHILADELPHIA VA MEDICAL CENTER · PI KAPLAN, DAVID E · 2014 to 2019
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CSRD VA I01 CX000981
6 · The paper itself

Abstract

unlabelledHepatitis C cirrhosis is associated with a profound disappearance of memory B-cells. We sought to determine if this loss is associated with the expansion of the CD27(-)CD21(-) tissue-like memory B-cells with features of B-cell exhaustion. To this end, we quantified the frequency of CD27(-)CD21(-) B-cells in healthy, non-cirrhotic HCV-infected, and cirrhotic patients. We examined the expression of putative inhibitory receptors, the proliferative and immunoglobulin-secreting capacity of CD27/CD21-defined B-cell subsets upon B-cell receptor and/or CD40 stimulation. We found that CD27(-)CD21(-) B-cells are significantly increased in frequency relative to healthy donors in HCV-infected patients. CD27(-)CD21(-) B-cells were hypoproliferative relative to naïve and resting memory B-cells upon agonistic stimulation, but retained similar capacity for antibody secretion.

conclusionCD27(-)CD21(-) tissue-like memory B-cells with exhausted proliferation circulate at increased frequency in cirrhotic and non-cirrhotic HCV-infected patients. This B-cell subset does not appear anergic, exhibiting immunoglobulin-secreting capacity on CD40 agonism indistinguishable from other CD27/CD21-defined B-cell subsets.

Indexed as

AdultAgedAntibody FormationB-Lymphocyte SubsetsFemaleHepatitis CHumansImmunophenotypingLiver CirrhosisLymphocyte ActivationMaleMiddle AgedPhenotypeReceptors, Antigen, B-CellReceptors, Complement 3dTumor Necrosis Factor Receptor Superfamily, Member 7Receptors, Antigen, B-CellReceptors, Complement 3dTumor Necrosis Factor Receptor Superfamily, Member 7AnergyB-cellCD21Hepatitis CHumanLymphocyte

Identifiers

PMID24434272
PMCPMC4580910
OpenAlexW2047231661

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.