Evidence map›Paper›PMID 37215124›Full record

ReviewFrontiers in immunology2023

Targeted CD7 CAR T-cells for treatment of T-Lymphocyte leukemia and lymphoma and acute myeloid leukemia: recent advances.

Jile Liu, Yi Zhang, Ruiting Guo, Yifan Zhao, Rui Sun, Shujing Guo, Wenyi Lu, Mingfeng Zhao

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07432100 (Clinical Study on the Safety, Efficacy and Pharmacokinetics of Universal CLL1 Chimeric Antigen Receptor T-Cell in Relapsed/Refractory Acute Myeloid Leukemia), which is not on this map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
6.4field-weighted citation impact, top 3% 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.

NCT07432100 phase1not yet recruitingnot on this mapstarted 2026, after this paper: background citation

Clinical Study on the Safety, Efficacy and Pharmacokinetics of Universal CLL1 Chimeric Antigen Receptor T-Cell in Relapsed/Refractory Acute Myeloid Leukemia

TypeinterventionalSponsorMingfeng ZhaoRan2026 to 2028Enrolled20ConditionsAcute Myeloid Leukemia, Chimeric Antigen Receptor T-cell, Universal CLL1 CAR-TArmsuniversal CLL1 CAR-T cells
3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Delivery platforms forFrontiers in immunology · 2026
    Review
  9. Article
  10. Article
  11. CAR-T cell therapy for cancer: current challenges and future directions.Signal transduction and targeted therapy · 2025
    Review
  12. CAR-T cell therapy for treatment of acute myeloid leukemia, advances and outcomes.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. 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

8 authors at 3 institutions in 1 country.

Jile LiuDepartment of Hematology, First Center Clinic College of Tianjin Medical University, Tianjin, China.
Yi ZhangDepartment of Hematology, First Center Clinic College of Tianjin Medical University, Tianjin, China.
Ruiting GuoDepartment of Hematology, First Center Clinic College of Tianjin Medical University, Tianjin, China.
Yifan ZhaoDepartment of Hematology, First Center Clinic College of Tianjin Medical University, Tianjin, China.
Rui SunDepartment of Hematology, School of Medicine, Nankai University, Tianjin, China.
Shujing GuoDepartment of Hematology, First Center Clinic College of Tianjin Medical University, Tianjin, China.
Wenyi LuDepartment of Hematology, Tianjin First Central Hospital, Tianjin, China.
Mingfeng ZhaoDepartment of Hematology, Tianjin First Central Hospital, Tianjin, China.
Tianjin Medical University · CNTianjin First Center Hospital · CNNankai University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The high expression of CD7 targets in T-cell acute lymphoblastic leukemia (T-ALL) and T-lymphoma has attracted considerable attention from researchers. However, because CD7 chimeric antigen receptor (CAR) T-cells undergo fratricide, CD7 CAR T-cells develop an exhaustion phenotype that impairs the effect of CAR T-cells. There have been significant breakthroughs in CD7-targeted CAR T-cell therapy in the past few years. The advent of gene editing, protein blockers, and other approaches has effectively overcome the adverse effects of conventional methods of CD7 CAR T-cells. This review, in conjunction with recent advances in the 64

Indexed as

Immunotherapy, AdoptiveLeukemia, Myeloid, AcuteLymphomaPrecursor T-Cell Lymphoblastic Leukemia-LymphomaHumansT-LymphocytesAmerican society of hematologybase editingCD7 CAR T-cell therapynatural selection CD7 CAR T-cellsprotein blocker

Identifiers

PMID37215124
PMCPMC10196106
OpenAlexW4377565151

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.