Evidence map›Paper›PMID 30666652›Full record

ReviewJournal of cellular physiology2019

Decreased number and impaired function of type 1 regulatory T cells in autoimmune diseases.

Xi Jia, Tianyu Zhai, Bing Wang, Qiuming Yao, Qian Li, Kaida Mu, Jin-An Zhang

Abstract readReview
In one paragraph

Review in Journal of cellular physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
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  6. CD4 T-Cell Subsets and the Pathophysiology of Inflammatory Bowel Disease.International journal of molecular sciences · 2023
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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

7 authors at 3 institutions in 1 country.

Xi JiaDepartment of Endocrinology, Jinshan Hospital of Fudan University, Shanghai, China.ORCID 0000-0001-6956-3416
Tianyu ZhaiDepartment of Endocrinology, Zhongshan Hospital of Fudan University, Shanghai, China.
Bing WangDepartment of Endocrinology, Jinshan Hospital of Fudan University, Shanghai, China.
Qiuming YaoDepartment of Endocrinology, Jinshan Hospital of Fudan University, Shanghai, China.
Qian LiDepartment of Endocrinology, Jinshan Hospital of Fudan University, Shanghai, China.
Kaida MuDepartment of Endocrinology, Shanghai University of Medicine & Health Sciences Affiliated Zhoupu Hospital, Shanghai, China.
Jin-An ZhangDepartment of Endocrinology, Shanghai University of Medicine & Health Sciences Affiliated Zhoupu Hospital, Shanghai, China.
Jinshan Hospital of Fudan University · CNShanghai University of Medicine and Health Sciences · CNSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type 1 regulatory T (Tr1) cell is a special type of T regulatory cells with surface molecular markers such as lymphocyte-activation gene 3 and CD49b. A key property of Tr1 cells is the capability to produce high-level interleukin 10 (IL-10) upon activation, in a FOXP3-independent manner. The immunosuppressive function of IL-10 producing Tr1 cells has been extensively studied for many years. Autoimmune diseases (AIDs) are conditions in which the immune system breaks down and starts to attack the body. AIDs include inflammatory bowel disease, rheumatoid arthritis, multiple sclerosis (MS), type 1 diabetes mellitus, Greaves' disease, and so forth. In recent years, more and more studies have documented that the number of Tr1 cells is decreased and the function is inhibited in a variety of AIDs, among which MS is the most widely studied. The protocol for engineering Tr1 cell therapy has been established and is gradually being used in clinical practice in recent years. Tr1 cell therapy has been proven to be safe and effective, but it is mainly involved in myeloid leukemia, graft versus host disease currently. Its therapeutic role in AIDs still needs to be further explored. In this study, we will summarize the research advances of Tr1 cells in AIDs, which will provide useful information for treating AIDs through Tr1 cell therapy in the future.

Indexed as

Acquired Immunodeficiency SyndromeAutoimmune DiseasesCell- and Tissue-Based TherapyCells, CulturedForkhead Transcription FactorsGraft vs Host DiseaseHumansInterleukin-10Leukemia, MyeloidT-Lymphocytes, RegulatoryForkhead Transcription FactorsFOXP3 protein, humanIL10 protein, humanInterleukin-10autoimmune diseasesIL-10immunotolerancemultiple sclerosistype 1 regulatory cells

Identifiers

PMID30666652
PMCPMC13484160
OpenAlexW2912889009

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.