Evidence map›Paper›PMID 17475702›Full record

ArticleThe British journal of ophthalmology2007

Pars planitis is associated with an increased frequency of effector-memory CD57+ T cells.

Miguel Pedroza-Seres, Marisela Linares, Stephanie Voorduin, Rojas-Ramos Enrique, Ricardo Lascurain, Yonathan Garfias, Maria Carmen Jimenez-Martinez

Open access · bronzeAbstract read
In one paragraph

Article in The British journal of ophthalmology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

10 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Clinical characteristics and treatment of pars planitis: an adalimumab experience.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2022
    Article
  4. Immune and myodegenerative pathomechanisms in inclusion body myositis.Annals of clinical and translational neurology · 2017
    Review
  5. Immunopathogenic Background of Pars Planitis.Archivum immunologiae et therapiae experimentalis · 2016
    Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. 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

7 authors at 4 institutions in 2 countries.

Miguel Pedroza-SeresResearch Unit and Uvea Department, Institute of Ophthalmology, Fundación Conde de Valenciana, Chimalpopoca 14, Col Obrera, CP 06800, México DF, México.
Marisela Linares
Stephanie Voorduin
Rojas-Ramos Enrique
Ricardo Lascurain
Yonathan Garfias
Maria Carmen Jimenez-Martinez
Ocular Proteomics (United States) · USInstitute of Ophthalmology · MXInstitute for Social Security and Services for State Workers · MXUniversidad Nacional Autónoma de México · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo evaluate the frequency, phenotype and the potential function of CD57+ T cell subsets in patients with pars planitis.

methodsCD4+CD57+ and CD8+CD57+ T cells were quantitated in peripheral blood from 15 patients with pars planitis and 15 healthy controls. To evaluate the phenotype and potential function of CD57+ T cell subsets CCR7, CD27, CD28, CD45RA, CD45RO, intracellular IFN-gamma, IL-4, perforin and granzyme-A expression were assessed by flow cytometry.

resultsCD57+ T cells subsets were increased in patients with pars planitis (p = 0.002). The majority of CD4+CD57+ T cells were CCR7-CD27-CD28-CD45RO+, while the most CD8+CD57+ T cells were CCR7-CD27-CD28-CD45RA+. The number of cells positive for intracellular IFN-gamma and IL-4 was higher in the CD57+ T cell populations. A greater number of CD8+CD57+ T cells than CD8+CD57- T cells were positive to perforin (p = 0.006) and granzyme-A (p = 0.01).

conclusionsCD57+ T cells had a phenotype associated with peripheral memory (CCR7-CD27-CD28-). Cytokine production by CD57+ T cells suggests that these cells may play a role in helper cell regulation. High expression of intracellular proteins involved in cytotoxicity suggests that CD8+CD57+ T cells may play an effector role. Taken together, this study proposes that CD57+ T cells function as memory-effector T cell subsets during pars planitis pathogenesis.

Indexed as

AdolescentCD28 AntigensCD4-Positive T-LymphocytesCD57 AntigensCD8-Positive T-LymphocytesChildFemaleGranzymesHumansImmunologic MemoryImmunophenotypingInterferon-gammaInterleukin-4Leukocyte Common AntigensMaleMembrane GlycoproteinsCCR7 protein, humanCD28 AntigensCD57 AntigensGranzymesInterferon-gammaInterleukin-4Leukocyte Common AntigensMembrane GlycoproteinsPerforinPore Forming Cytotoxic ProteinsReceptors, CCR7Receptors, ChemokineTumor Necrosis Factor Receptor Superfamily, Member 7

Identifiers

PMID17475702
PMCPMC2001003
OpenAlexW2044765390

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.