Evidence map›Paper›PMID 15654834›Full record

ArticleClinical and experimental immunology2005

T cell repertoire in patients with stable scleroderma.

K P Tiev, J Abriol, M C Burland, D Antonelli, D Klatzmann, J Cabane, O Boyer

Abstract readComparative Study
In one paragraph

Article in Clinical and experimental immunology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. CD8International journal of molecular sciences · 2022
    Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Subset-specific alterations in frequencies and functional signatures of γδ T cells in systemic sclerosis patients.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2016
    Article
  9. Article
  10. Missing: a diagnostic technique to enumerate antigen-specific T cells.Critical reviews in oncology/hematology · 2012
    Review
  11. Review
  12. Article
  13. Oligoclonal CD4+ T cells in the lungs of patients with severe emphysema.American journal of respiratory and critical care medicine · 2005
    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

7 authors.

K P TievService de Médecine Interne, Hôpital Saint Antoine, Saint Antoine, Paris, France. kiet.tiev@sat.ap-hop-paris.fr
J Abriol
M C Burland
D Antonelli
D Klatzmann
J Cabane
O Boyer

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

At onset of systemic sclerosis (SSc), T cells have been found to oligoclonally expand in the skin, presumably in response to auto-antigens, but the T cell repertoire has not been evaluated at a later stage. To determine whether a perpetuating immune response contributes to the pathogenesis of stable SSc, the T cell repertoire was analysed in patients with diffuse (d) or limited (l) SSc, and compared to patients with primary Raynaud's phenomenon (RP) or healthy volunteers (Ctrl). The T cell repertoire (total, CD4 or CD8 sorted blood T cells) was analysed by qualitative and quantitative immunoscope (14 BV families analysed) in 11 untreated dSSc and 11 untreated lSSc, 10 RP and 11 Ctrl. To better detect in vivo activated cells, repertoire analysis was also performed on sorted CD4 T cells after in vitro culture with IL-2. In parallel, 6 skin biopsies from SSc patients were analysed. After 7-8 years of disease evolution, SSc patients did not show detectable clonal T cell expansions in the skin, even after tentative expansion from the biopsy with IL-2. Total T cell, sorted CD4 and CD8 T cell repertoires from the blood of patients with SSc did not show significant perturbation as compared to patients with RP and Ctrl. After IL-2 culture for 7 days, blood CD4 T cells from the patients did not preferentially expand as compared to RP and Ctrl. These findings suggest that antigen-driven immune responses may play a lesser role in established SSc than at disease onset.

Indexed as

Case-Control StudiesCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCells, CulturedChronic DiseaseFemaleHumansInterleukin-2Lymphocyte ActivationMaleMiddle AgedRaynaud DiseaseScleroderma, SystemicSkinT-Lymphocyte SubsetsInterleukin-2

Identifiers

PMID15654834
PMCPMC1809294

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.