Evidence map›Paper›PMID 36591309›Full record

ReviewFrontiers in immunology2022

The emerging role of regulatory cell-based therapy in autoimmune disease.

Farbod Ghobadinezhad, Nasim Ebrahimi, Fatemeh Mozaffari, Neda Moradi, Sheida Beiranvand, Mehran Pournazari, Fatemeh Rezaei-Tazangi, Roya Khorram, Maral Afshinpour, Rob A Robino and 2 more

Open access · goldAbstract readReview
In one paragraph

Review 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 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
6.5field-weighted citation impact, top 2% 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

45 citing papers in PubMed, 81 citations in OpenAlex.

  1. Review
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  8. Review
  9. [Rheumatic disease spectrum and immunological profile of anti-PM/Scl antibodies in idiopathic inflammatory myopathies].Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2025
    Article
  10. Review
  11. Article
  12. Article
  13. Tumor-educated cells in tumor microenvironment: Key drivers of immunotherapy resistance.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2025
    Article
  14. Article
  15. Expanding the engineered Treg multiverse.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  16. Review
  17. Generation of Human Chimeric Antigen Receptor Regulatory T Cells.Journal of visualized experiments : JoVE · 2025
    Article
  18. Review
  19. Review
  20. 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

12 authors at 10 institutions in 2 countries.

Farbod GhobadinezhadStudent Research Committee, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Nasim EbrahimiDivision of Genetics, Department of Cell and Molecular Biology and Microbiology, Faculty of Biological Science and Technology, University of Isfahan, Isfahan, Iran.
Fatemeh MozaffariDepartment of Nutrition, School of Medicine, Zabol University of Medical Sciences, Zabol, Iran.
Neda MoradiDivision of Biotechnology, Department of Cell and Molecular Biology and Microbiology, Nourdanesh Institute of Higher Education, University of Meymeh, Isfahan, Iran.
Sheida BeiranvandDepartment of Biology, Faculty of Basic Sciences, Islamic Azad University, Shahrekord, Iran.
Mehran PournazariClinical Research Development Center, Imam Reza Hospital, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Fatemeh Rezaei-TazangiDepartment of Anatomy, School of Medicine, Fasa University of Medical Sciences, Fasa, Iran.
Roya KhorramBone and Joint Diseases Research Center, Department of Orthopedic Surgery, Shiraz University of Medical Sciences, Shiraz, Iran.
Maral AfshinpourDepartment of Chemistry and Biochemistry, South Dakota State University, Brookings, SD, United States.
Rob A RobinoDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC, United States.
Amir Reza ArefDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, United States.
Leonardo M R FerreiraDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC, United States.
Kermanshah University of Medical Sciences · IRMedical University of South Carolina · USFasa University of Medical Sciences · IRHarvard University · USIslamic Azad University of Shahrekord · IRNourDanesh Institute of Higher EducationShiraz University of Medical Sciences · IRSouth Dakota State University · USUniversity of Isfahan · IRZabol University of Medical Sciences · IR

Funding

The Human Islet Distribution Coordinating Center (UC4)UC4DK098085 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI EVANS-MOLINA, CARMELLA, NILAND, JOYCE CAROL · 2012 to 2017
$25.6M
Renewal of the Human Islet Research Enhancement Center (HIREC) for the Type-1-Diabetes-Focused Human Islet Research Network (HIRN).U24DK104162 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI John S. Kaddis, Joyce Carol Niland · 2019 to 2026
$12.3M
South Carolina Clinical & Translational Research Institute (SCTR)TL1TR001451 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI FEGHALI-BOSTWICK, CAROL A. · 2015 to 2024
$4.6M
Rapid, single-step precision engineering and pre-clinical evaluation of chimeric antigen receptor Regulatory T cells for Type 1 diabetesR43DK133029 · NIDDK · INDEE, INC · PI PAWELL, RYAN · 2022 to 2022
$310k
NCATS NIH HHS TL1 TR001451NIDDK NIH HHS R43 DK133029NIDDK NIH HHS U24 DK104162NIDDK NIH HHS UC4 DK098085
6 · The paper itself

Abstract

Autoimmune disease, caused by unwanted immune responses to self-antigens, affects millions of people each year and poses a great social and economic burden to individuals and communities. In the course of autoimmune disorders, including rheumatoid arthritis, systemic lupus erythematosus, type 1 diabetes mellitus, and multiple sclerosis, disturbances in the balance between the immune response against harmful agents and tolerance towards self-antigens lead to an immune response against self-tissues. In recent years, various regulatory immune cells have been identified. Disruptions in the quality, quantity, and function of these cells have been implicated in autoimmune disease development. Therefore, targeting or engineering these cells is a promising therapeutic for different autoimmune diseases. Regulatory T cells, regulatory B cells, regulatory dendritic cells, myeloid suppressor cells, and some subsets of innate lymphoid cells are arising as important players among this class of cells. Here, we review the roles of each suppressive cell type in the immune system during homeostasis and in the development of autoimmunity. Moreover, we discuss the current and future therapeutic potential of each one of these cell types for autoimmune diseases.

Indexed as

Autoimmune DiseasesImmunity, InnateAutoantigensAutoimmunityHumansLymphocytesAutoantigensadoptive cell therapyautoimmunityIL-10-producing cellimmune suppressive cellsregulatory B cellregulatory immune cellsregulatory T celltolerogenic dendritic cell

Identifiers

PMID36591309
PMCPMC9795194
OpenAlexW4311479028

What OpenQuestion holds

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LicenceCC BY
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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.