Evidence map›Paper›PMID 38203514›Full record

ReviewInternational journal of molecular sciences2023

Applications of Genome-Editing Technologies for Type 1 Diabetes.

Rana El Nahas, Mohammad Ameen Al-Aghbar, Laura Herrero, Nicholas van Panhuys, Meritxell Espino-Guarch

Registry-linked trialAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01630850 (Islet Transplantation in Patients With "Brittle" Type I Diabetes), which is not on this map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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.

NCT01630850 narecruitingnot on this map

Islet Transplantation in Patients With "Brittle" Type I Diabetes

TypeinterventionalSponsorUniversity of ChicagoRan2012 to 2030Enrolled20ConditionsDiabetes Mellitus, Type 1ArmsAllogenic islet cells (human, U. Chicago), Intraportal infusion of islet cells
3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Review
  2. Review
  3. eVLP-Mediated Cas9 Delivery for Preventing IBMIR in Islet Transplantation.Small (Weinheim an der Bergstrasse, Germany) · 2026
    Article
  4. Article
  5. Review
  6. Strategies for optimization of hypoglycemia rat models.Animal models and experimental medicine · 2025
    Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Precision Genome Engineering in Human Disease: Expanding Therapeutic Roles of CRISPR Technologies.Nigerian medical journal : journal of the Nigeria Medical Association
    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.

Rana El NahasLaboratory of Immunoregulation, Translational Medicine, Sidra Medicine, Doha P.O. Box 26999, Qatar.ORCID 0000-0002-7812-6127
Mohammad Ameen Al-AghbarLaboratory of Immunoregulation, Translational Medicine, Sidra Medicine, Doha P.O. Box 26999, Qatar.ORCID 0000-0002-0520-979X
Laura HerreroDepartment of Biochemistry and Physiology, School of Pharmacy and Food Sciences, Institute of Biomedicine of the University of Barcelona (IBUB), 08028 Barcelona, Spain.ORCID 0000-0003-4244-4673
Nicholas van PanhuysLaboratory of Immunoregulation, Translational Medicine, Sidra Medicine, Doha P.O. Box 26999, Qatar.
Meritxell Espino-GuarchLaboratory of Immunoregulation, Translational Medicine, Sidra Medicine, Doha P.O. Box 26999, Qatar.ORCID 0000-0002-7211-3229

Funding

Merck Health Foundation 2021SGR00367Sidra Medical and Research Center SDR400130Spanish Biomedical Research Centre in Physiopathology of Obesity and Nutrition CB06/03/0001Spanish Ministry of Science and Innovation (MCIN/AEI) PID2020-114953RB-C21
6 · The paper itself

Abstract

Type 1 diabetes (T1D) is a chronic autoimmune disease characterized by the destruction of insulin-producing pancreatic β-cells by the immune system. Although conventional therapeutic modalities, such as insulin injection, remain a mainstay, recent years have witnessed the emergence of novel treatment approaches encompassing immunomodulatory therapies, such as stem cell and β-cell transplantation, along with revolutionary gene-editing techniques. Notably, recent research endeavors have enabled the reshaping of the T-cell repertoire, leading to the prevention of T1D development. Furthermore, CRISPR-Cas9 technology has demonstrated remarkable potential in targeting endogenous gene activation, ushering in a promising avenue for the precise guidance of mesenchymal stem cells (MSCs) toward differentiation into insulin-producing cells. This innovative approach holds substantial promise for the treatment of T1D. In this review, we focus on studies that have developed T1D models and treatments using gene-editing systems.

Indexed as

Autoimmune DiseasesDiabetes Mellitus, Type 1HumansInsulinInsulin, Regular, HumanTechnologyInsulinInsulin, Regular, Humanautoimmune diseaseCRISPR–Cas9genome-editingtherapyType 1 diabetesβ-cell

Identifiers

PMID38203514
PMCPMC10778854

What OpenQuestion holds

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Registered trials

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.