Evidence map›Paper›PMID 23636058›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2013

Blockade of programmed death-1 in young (New Zealand Black x New Zealand White)F1 mice promotes the suppressive capacity of CD4+ regulatory T cells protecting from lupus-like disease.

Maida Wong, Antonio La Cava, Bevra H Hahn

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 16% 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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 78 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Armored human CAR TScience advances · 2025
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  6. PD-L1International journal of molecular sciences · 2025
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  10. The effect of PD-1/PD-L1 signaling axis on the interaction between CD19Advances in rheumatology (London, England) · 2023
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
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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.

Maida WongDivision of Rheumatology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA. maidawong@mednet.ucla.edu
Antonio La Cava
Bevra H Hahn
University of California, Los Angeles · US

Funding

MECHANISMS OF IMMUNE TOLERANCE INDUCED IN MURINE LUPUSR37AI046776 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HAHN, BEVRA H · 2000 to 2009
$3.9M
Role of Leptin in Systemic Lupus ErythematosusR01AR053239 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LA CAVA, ANTONIO · 2006 to 2010
$1.6M
Academic Training in RheumatologyT32AR053463 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SINGH, RAM RAJ · 2007 to 2011
$1.1M
NIAID NIH HHS AI46776NIAID NIH HHS R37 AI046776NIAMS NIH HHS AR053463NIAMS NIH HHS AR53239NIAMS NIH HHS R01 AR053239NIAMS NIH HHS T32 AR053463
6 · The paper itself

Abstract

Programmed death-1 (PD-1) usually acts as a negative signal for T cell activation, and its expression on CD8(+)Foxp3(+) T cells is required for their suppressive capacity. In this study, we show that PD-1 signaling is required for the maintenance of functional regulatory CD4(+)CD25(+)Foxp3(+) regulatory T cells (CD4(+) T(reg)) that can control autoimmunity in (New Zealand Black × New Zealand White)F1 lupus mice. PD-1 signaling induced resistance to apoptosis and prolonged the survival of CD4(+) T(reg). In vivo, the blockade of PD-1 with a neutralizing Ab reduced PD-1 expression on CD4(+) T(reg) (PD1(lo)CD4(+) T(reg)). PD1(lo)CD4(+) T(reg) had an increased ability to promote B cell apoptosis and to suppress CD4(+) Th as compared with CD4(+) T(reg) with elevated PD-1 expression (PD1(hi)CD4(+) T(reg)). When PD-1 expression on CD4(+) T(reg) was blocked in vitro, PD1(lo)CD4(+) T(reg) suppressed B cell production of IgG and anti-dsDNA Ab. Finally, in vitro studies showed that the suppressive capacity of CD4(+) T(reg) depended on PD-1 expression and that a fine-tuning of the expression of this molecule directly affected cell survival and immune suppression. These results indicate that PD-1 expression has multiple effects on different immune cells that directly contribute to a modulation of autoimmune responses.

Indexed as

Adaptive ImmunityAnimalsAntibodies, MonoclonalAntibodies, NeutralizingAutoantibodiesCD4 AntigensDisease ProgressionFemaleGene Expression RegulationImmune ToleranceInterleukin-2Interleukin-2 Receptor alpha SubunitInterleukin-6Lupus Erythematosus, SystemicMiceMice, Inbred NZBAntibodies, MonoclonalAntibodies, NeutralizingAutoantibodiesCD4 AntigensInterleukin-2Interleukin-2 Receptor alpha SubunitInterleukin-6Programmed Cell Death 1 ReceptorTransforming Growth Factor beta

Identifiers

PMID23636058
PMCPMC3700538
OpenAlexW2097527928

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.