Evidence map›Paper›PMID 21720245›Full record

ReviewCurrent opinion in rheumatology2011

Effector T-cell subsets in systemic lupus erythematosus: update focusing on Th17 cells.

Min S Shin, Naeun Lee, Insoo Kang

Abstract readReview
In one paragraph

Review in Current opinion in rheumatology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

60 citing papers in PubMed, 124 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Vitamin A and Its Related Diseases.Food science & nutrition · 2025
    Review
  8. The roles of arginases and arginine in immunity.Nature reviews. Immunology · 2025
    Review
  9. Article
  10. Article
  11. Article
  12. Vascular damage in systemic lupus erythematosus.Nature reviews. Nephrology · 2024
    Review
  13. Review
  14. Article
  15. Th17/Treg Imbalance: Implications in Lung Inflammatory Diseases.International journal of molecular sciences · 2023
    Review
  16. Article
  17. Review
  18. Observational
  19. Review
  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 at 1 institution in 1 country.

Min S ShinDepartment of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut 06520, USA.
Naeun Lee
Insoo Kang
Yale University · US

Funding

YALE UNIVERSITY CLINICAL AND TRANSLATIONAL SCIENCE AWARD PROGRAMUL1RR024139 · NCRR · YALE UNIVERSITY · PI SHERWIN, ROBERT S · 2006 to 2011
$56.8M
Yale Autoimmunity Center of ExcellenceU19AI082713 · NIAID · YALE UNIVERSITY · PI CHO, JUDY H. · 2009 to 2013
$3.6M
Dissecting the role for IL-15 in CD8+ T cell homeostasis in human lupusR01AI075157 · NIAID · YALE UNIVERSITY · PI CRAFT, JOSEPH EDGAR · 2008 to 2012
$2.0M
Aging and IL-7-mediated CD8+ T Cell survivalR01AG028069 · NIA · YALE UNIVERSITY · PI KANG, INSOO · 2007 to 2011
$1.6M
Aging and IL-7-Mediated CD8+ T Cell SurvivalR56AG028069 · NIA · YALE UNIVERSITY · PI KANG, INSOO · 2015 to 2015
$416k
Studying the effects of vitamin D on FOXP3 and IL-17 expression in human CD4+ T cR21AT005241 · NCCIH · YALE UNIVERSITY · PI KANG, INSOO · 2009 to 2010
$412k
Investigating aging and membrane-associated T cell receptor signaling in human CDR21AG030834 · NIA · YALE UNIVERSITY · PI KANG, INSOO · 2007 to 2008
$268k
NCCIH NIH HHS AT 005241NCCIH NIH HHS R21 AT005241NCRR NIH HHS UL1 RR024139NIAID NIH HHS AI082713NIAID NIH HHS R01 AI075157NIAID NIH HHS U19 AI082713NIA NIH HHS AG028069NIA NIH HHS AG030834NIA NIH HHS R01 AG028069NIA NIH HHS R21 AG030834NIA NIH HHS R56 AG028069
6 · The paper itself

Abstract

purpose of reviewThe discovery of T helper (Th)17 cells that produce the proinflammatory cytokine IL-17 has substantially advanced our understanding of T-cell biology and autoimmunity. We will review recent findings on effector T cells, in particular Th17 cells, in lupus. RECENT

findingsStudies reported increased IL-17 levels in the circulation and tissues in human and murine lupus. Patients with systemic lupus erythematosus (SLE or lupus) had an increased frequency of Th17 cells in peripheral blood which correlated with disease activity. However, the frequency of IFN-γ-producing Th1 cells did not change in the same patients, suggesting a selective dysregulation of Th17 cells in SLE. In addition, patients with SLE had an increased frequency of IL-17-producing CD3CD4CD8 (double negative) T cells in the peripheral blood and kidneys. Similar findings were noticed in lupus-prone MRL/MP-lpr/lpr (MRL/lpr) mice. A recent study demonstrated that IL-17 could promote B-cell survival and differentiation into antibody-producing cells. This raises the possibility that IL-17 is implicated in the pathogenesis of SLE by promoting humoral immunity against self-antigen. SUMMARY: Emerging data show a body of evidence that IL-17 and Th17 cells may play a role in the pathogenesis of SLE. Further studies are warranted to dissect the mechanism for increased IL-17 production and the therapeutic implication of targeting this cytokine in SLE.

Indexed as

AnimalsCytokinesHumansInflammation MediatorsInterleukin-17Lupus Erythematosus, SystemicMiceMice, Inbred MRL lprTh17 CellsTh1 CellsT-Lymphocyte SubsetsCytokinesInflammation MediatorsInterleukin-17

Identifiers

PMID21720245
PMCPMC3489922
OpenAlexW2002308862

What OpenQuestion holds

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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.