Evidence map›Paper›PMID 35419004›Full record

ArticleFrontiers in immunology2022

Reduction of Cell Surface T-Cell Receptor by Non-Mitogenic CD3 Antibody to Mitigate Murine Lupus.

Masashi Morita, Masayuki Mizui, Satoshi Masuyama, George C Tsokos, Yoshitaka Isaka

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 47% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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

5 authors at 2 institutions in 2 countries.

Masashi MoritaDepartment of Nephrology, Osaka University Graduate School of Medicine, Suita, Japan.
Masayuki MizuiDepartment of Nephrology, Osaka University Graduate School of Medicine, Suita, Japan.
Satoshi MasuyamaDepartment of Nephrology, Osaka University Graduate School of Medicine, Suita, Japan.
George C TsokosDivision of Rheumatology, Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, United States.
Yoshitaka IsakaDepartment of Nephrology, Osaka University Graduate School of Medicine, Suita, Japan.
Osaka University · JPHarvard University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T-cells are critically involved in the pathogenesis of systemic lupus erythematosus. Although treatment with the anti-CD3 antibody has been reported to be effective in several autoimmune disease animal models including lupus, the immunosuppressive mechanisms remain obscure because of its pleiotropic

Indexed as

Lupus Erythematosus, SystemicLupus NephritisReceptors, Antigen, T-CellAnimalsAutoantibodiesCD3 ComplexFemaleMaleMiceMice, Inbred NZBT-LymphocytesAutoantibodiesCD3 ComplexReceptors, Antigen, T-Cell145-2C11autoantibodyautoimmunityFc regionlupus nephritisNZB/W F1systemic lupus erythematosusTCR (T-cell receptor)

Identifiers

PMID35419004
PMCPMC8995471
OpenAlexW4221129714

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.