Evidence map›Paper›PMID 18725326›Full record

ReviewAutoimmunity reviews2009

Therapeutic potential of CD8+ cytotoxic T lymphocytes in SLE.

I Puliaeva, R Puliaev, C S Via

Abstract readReview
In one paragraph

Review in Autoimmunity reviews, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Review
  2. CD8Rheumatology and immunology research · 2021
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Low-Dose IL-2 in the Treatment of Lupus.Current rheumatology reports · 2016
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review
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.

I PuliaevaPathology Department, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.
R Puliaev
C S Via

Funding

IMMUNOPATHOGENESIS OF LUPUSR01AI047466 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI VIA, CHARLES S. · 2001 to 2012
$3.2M
NIAID NIH HHS R01 AI047466
6 · The paper itself

Abstract

Recent evidence supports the idea that following a break in tolerance, CD8 cytotoxic T lymphocytes (CTL) may be an important but unrecognized mechanism for limiting expansion of autoreactive B cells. Failure of this mechanism could allow persistence of CD4 T cell driven polyclonal B cell activation resulting in clinical lupus. Although CD8 CTL failure may occur early in disease, work in mice supports the concept that therapeutic CTL enhancement may be both practical and beneficial in lupus. Devising such therapy for humans will first require an understanding of the in vivo mechanisms critical in CTL expansion and down regulation, particularly in the lupus setting which may differ from CTL generation in other clinical settings (e.g. tumors, infections).

Indexed as

Immunotherapy, AdoptiveAnimalsB-LymphocytesCD8-Positive T-LymphocytesHomeostasisHumansLupus Erythematosus, SystemicMiceMice, CongenicT-Lymphocytes, Cytotoxic

Identifiers

PMID18725326
PMCPMC3215296

What OpenQuestion holds

Textmetadata
LicenceTDM
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.