Evidence map›Paper›PMID 39794549›Full record

SynthesisMolecular biotechnology2026

CRISPR/Cas9 System as a Promising Therapy in Thalassemia and Sickle Cell Disease: A Systematic Review of Clinical Trials.

Rehab Ahmed, Wafa N Alghamdi, Fetun R Alharbi, Huda D Alatawi, Kawthar M Alenezi, Turki F Alanazi, Nehal M Elsherbiny

Abstract readSystematic Review
PubMed Publisher
In one paragraph

Synthesis in Molecular biotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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.

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

2 citing papers in PubMed.

  1. Article
  2. Review
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.

Rehab AhmedDivision of Microbiology, Immunology and Biotechnology, Department of Natural Products and Alternative Medicine, Faculty of Pharmacy, University of Tabuk, Tabuk, Saudi Arabia.
Wafa N AlghamdiPharm D Program, Faculty of Pharmacy, University of Tabuk, Tabuk, 71491, Saudi Arabia.
Fetun R AlharbiPharm D Program, Faculty of Pharmacy, University of Tabuk, Tabuk, 71491, Saudi Arabia.
Huda D AlatawiPharm D Program, Faculty of Pharmacy, University of Tabuk, Tabuk, 71491, Saudi Arabia.
Kawthar M AleneziPharm D Program, Faculty of Pharmacy, University of Tabuk, Tabuk, 71491, Saudi Arabia.
Turki F AlanaziPharm D Program, Faculty of Pharmacy, University of Tabuk, Tabuk, 71491, Saudi Arabia.
Nehal M ElsherbinyDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Tabuk, Tabuk, Saudi Arabia. nelsherbiny@ut.edu.sa.ORCID http://orcid.org/0000-0001-5167-3377

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clustered, regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated protein (Cas) system is a new gene editing tool that represents a revolution in gene therapy. This study aimed to review the clinical trials conducted to evaluate the efficacy and safety of the CRISPR/Cas9 system in treating thalassemia and sickle cell disease (SCD). We searched relevant literature using "CRISPR Cas", "thalassemia", "sickle cell" and "clinical trial" as subject terms in PubMed, Cochrane, Web of Science, and Google Scholar up to December 3rd, 2023. Following the PIO format (Patients, Intervention, Outcome), PRISMA guidelines were followed in the study selection, data extraction, and quality assessment processes. Out of 110 publications, 6 studies met our eligibility criteria with a total of 115 patients involved. CRISPR/Cas9 system was used to disrupt BCL11A gene enhancer in 4 studies and to disrupt γ-globin gene promoters in 2 studies. Patients demonstrated significant activation of fetal hemoglobin, elevated total hemoglobin, transfusion independence in thalassemia, and repression of vaso-occlusive episodes in SCD. Using CRISPR/Cas9 system to directly disrupt genes provides a safe and potential one-time functional cure for thalassemia and SCD, suggesting CRISPR/Cas9 as a potential therapeutic tool for the treatment of inherited hematological disorders.

Indexed as

Anemia, Sickle CellCRISPR-Cas SystemsGene EditingGenetic TherapyThalassemiaClinical Trials as Topicgamma-GlobinsHumansRepressor ProteinsBCL11A protein, humangamma-GlobinsRepressor ProteinsCRISPR/Cas9 systemFetal hemoglobinSickle cell diseaseThalassemiaTherapy

Identifiers

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.