Evidence map›Paper›PMID 31551033›Full record

ArticleLupus2019

T cell-specific STAT3 deficiency abrogates lupus nephritis.

N Yoshida, F He, V C Kyttaris

Open access · greenAbstract readComparative Study
In one paragraph

Article in Lupus, 2019. 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
1.8field-weighted citation impact, top 15% 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

22 citing papers in PubMed, 28 citations in OpenAlex.

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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.

N YoshidaDivision of Rheumatology, Beth Israel Deaconess Medical Center, Division of Rheumatology, Boston, USA.
F HeDivision of Rheumatology, Beth Israel Deaconess Medical Center, Division of Rheumatology, Boston, USA.
V C KyttarisDivision of Rheumatology, Beth Israel Deaconess Medical Center, Division of Rheumatology, Boston, USA.ORCID https://orcid.org/0000-0001-7652-3826
Beth Israel Deaconess Medical Center · US

Funding

The Role of Interleukin 23 in LupusR01AR060849 · NIAMS · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KYTTARIS, VASILEIOS CHRISTOS · 2012 to 2016
$1.9M
NIAMS NIH HHS R01 AR060849
6 · The paper itself

Abstract

Signal transducer and activator of transcription (STAT) 3 is a regulator of T-cell responses to external stimuli, such as pro-inflammatory cytokines and chemokines. We have previously shown that STAT3 is activated (phosphorylated) at high levels in systemic lupus erythematosus (SLE) T cells and mediates chemokine-induced migration and T:B cell interactions. Stattic, a small molecular STAT3 inhibitor, can partially ameliorate lupus nephritis in mice. To understand the role of STAT3 better in T-cell pathophysiology in lupus nephritis and its potential as a treatment target, we silenced its expression in T cells using a cd4-driven CRE-Flox model. We found that lupus-prone mice that do not express STAT3 in T cells did not develop lymphadenopathy, splenomegaly, or glomerulonephritis. Moreover, the production of anti-dsDNA antibodies was decreased in these mice compared to controls. To dissect the mechanism, we also used a nephrotoxic serum model of nephritis. In this model, T cell-specific silencing of STAT3 resulted in amelioration of nephrotoxic serum-induced kidney damage. Taken together, our results suggest that in mouse models of autoimmune nephritis, T cell-specific silencing of STAT3 can hamper their ability to help B cells to produce autoantibodies and induce cell tissue infiltration. We propose that STAT3 inhibition in T cells represents a novel approach in the treatment of SLE and lupus nephritis in particular.

Indexed as

AnimalsAutoantibodiesChemokinesCyclic S-OxidesCytokinesHumansLupus Erythematosus, SystemicLupus NephritisMiceMice, KnockoutSTAT3 Transcription FactorT-LymphocytesAutoantibodiesChemokinesCyclic S-OxidesCytokinesSTAT3 protein, humanSTAT3 Transcription Factorstatticmurine lupusnephritisSLESTAT3T cells

Identifiers

PMID31551033
PMCPMC6791775
OpenAlexW2975203734

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.