Evidence map›Paper›PMID 33306199›Full record

ReviewClinical and experimental immunology2021

E3 ubiquitin ligase Casitas B lineage lymphoma-b and its potential therapeutic implications for immunotherapy.

D Jafari, M J Mousavi, S Keshavarz Shahbaz, L Jafarzadeh, S Tahmasebi, J Spoor, A Esmaeilzadeh

Open access · bronzeAbstract readReview
In one paragraph

Review in Clinical and experimental immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
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  11. CRISPR-Cas9-Based Gene Knockout of Immune Checkpoints in Expanded NK Cells.International journal of molecular sciences · 2023
    Article
  12. Review
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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 5 institutions in 2 countries.

D JafariDepartment of Immunology, School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran.ORCID 0000-0002-7822-5096
M J MousaviDepartment of Hematology, Faculty of Allied medicine, Bushehr University of Medical Sciences, Bushehr, Iran.ORCID 0000-0003-4849-6706
S Keshavarz ShahbazDepartment of Immunology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.ORCID 0000-0001-7333-5969
L JafarzadehDepartment of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
S TahmasebiDepartment of Immunology, School of public health, Tehran University of Medical Sciences, Tehran, Iran.ORCID 0000-0002-8598-1922
J SpoorErasmus University Medical Centre, Erasmus University Rotterdam, Rotterdam, the Netherlands.
A EsmaeilzadehDepartment of Immunology, School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran.ORCID 0000-0002-5402-3967
Tehran University of Medical Sciences · IRZanjan University of Medical Sciences · IRBushehr University of Medical Sciences · IRErasmus University Rotterdam · NLMashhad University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The distinction of self from non-self is crucial to prevent autoreactivity and ensure protection from infectious agents and tumors. Maintaining the balance between immunity and tolerance of immune cells is strongly controlled by several sophisticated regulatory mechanisms of the immune system. Among these, the E3 ligase ubiquitin Casitas B cell lymphoma-b (Cbl-b) is a newly identified component in the ubiquitin-dependent protein degradation system, which is thought to be an important negative regulator of immune cells. An update on the current knowledge and new concepts of the relevant immune homeostasis program co-ordinated by Cbl-b in different cell populations could pave the way for future immunomodulatory therapies of various diseases, such as autoimmune and allergic diseases, infections, cancers and other immunopathological conditions. In the present review, the latest findings are comprehensively summarized on the molecular structural basis of Cbl-b and the suppressive signaling mechanisms of Cbl-b in physiological and pathological immune responses, as well as its emerging potential therapeutic implications for immunotherapy in animal models and human diseases.

Indexed as

AnimalsAutoimmune DiseasesHomeostasisHumansHypersensitivityImmune SystemImmunotherapyNeoplasmsProto-Oncogene Proteins c-cblUbiquitinProto-Oncogene Proteins c-cblUbiquitinCbl-bimmunotherapyubiquitinationubiquitin-binding protein

Identifiers

PMID33306199
PMCPMC7944365
OpenAlexW3112338673

What Socratic 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 Socratic graph.