Evidence map›Paper›PMID 24298980›Full record

ArticleClinical and experimental immunology2014

T cells from chronic bone infection show reduced proliferation and a high proportion of CD28⁻ CD4 T cells.

G Kumar, P-M Roger, M Ticchioni, C Trojani, R Bernard de Dompsur, N Bronsard, M Carles, E Bernard

Open access · greenAbstract read
In one paragraph

Article in Clinical and experimental immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

14 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Senescent CD4International journal of molecular sciences · 2022
    Review
  6. Metatranscriptome sequencing identifiesFrontiers in microbiology · 2022
    Article
  7. Article
  8. Article
  9. Article
  10. From Crosstalk between Immune and Bone Cells to Bone Erosion in Infection.International journal of molecular sciences · 2019
    Review
  11. Increased Fragility Fracture Rates in Older Men With Osteomyelitis.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2019
    Article
  12. Review
  13. Observational
  14. 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

8 authors at 2 institutions in 1 country.

G KumarUnité 576, Institut National de la Santé et de la Recherche Médicale, Hopital L'Archet 1, Centre Hospitalier Universitaire de Nice, Université de Nice Sophia-Antipolis, Nice, France.
P-M Roger
M Ticchioni
C Trojani
R Bernard de Dompsur
N Bronsard
M Carles
E Bernard
Centre Hospitalier Universitaire de Nice · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic bone infection is associated with bone resorption. From animal studies, CD3/CD28-activated T cells are known to enhance osteoclastogenesis and bone resorption. Because CD28 is expressed constitutively on T cells and its expression is down-regulated by chronic exposure to the inflammatory environment, we characterized co-stimulatory molecule expression on T cells from chronically infected patients. We used cytofluorometric techniques to phenotypically characterize T cells, its co-stimulatory molecules and perforin secretion from infected and non-infected human bones. Chronic bone infection was defined as infection lasting for more than a month. We show a higher T cell activation [human leucocyte antigen D-related (HLA-DR⁺)] in infected compared to non-infected bones: median being 16 versus 7%, P = 0·009 for CD4 T cells, and 33 versus 15%, P = 0·038 for CD8 T cells, respectively. However, T cell proliferation (Ki67⁺) was lower for CD8 T cells in infected bones: 26 versus 34%, P = 0·045. In contrast, we detected no difference in apoptosis and regulatory T cells. In infected bone, we found higher CD28-negative CD4⁺ T cells compared to non-infected bone: 20 versus 8%, respectively (P = 0·005); this T cell subset had higher CD11b expression and perforin secretion. Chronically infected human bones are characterized by an increase of CD28-negative CD4⁺ T cells, indicating long-term activated cells with cytotoxic ability. Therefore, this alteration of co-stimulatory molecules may modify interactions with osteoclasts and impact bone resorption.

Indexed as

Cell ProliferationAdultAgedBacterial InfectionsCD28 AntigensCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesChronic DiseaseFemaleFlow CytometryHLA-DR AntigensHumansLymphocyte ActivationLymphocyte CountMaleMiddle AgedCD28 AntigensHLA-DR AntigensPerforinapoptosisbacterialcell proliferationregulatory T cellsT cells

Identifiers

PMID24298980
PMCPMC3958153
OpenAlexW1521797630

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.