Evidence map›Paper›PMID 39224539›Full record

ArticleMedComm2024

Targeting chronic lymphocytic leukemia with B-cell activating factor receptor CAR T cells.

Yaqing Qie, Martha E Gadd, Qing Shao, Tommy To, Andrew Liu, Shuhua Li, Rocio Rivera-Valentin, Farah Yassine, Hemant S Murthy, Roxana Dronca and 3 more

Abstract read
In one paragraph

Article in MedComm, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Advancing Immunotherapy in Chronic Lymphocytic Leukemia.International journal of molecular sciences · 2026
    Review
  2. Article
  3. 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

13 authors.

Yaqing QieRegenerative Immunotherapy and CAR-T Translational Research Program Mayo Clinic Jacksonville Florida USA.
Martha E GaddRegenerative Immunotherapy and CAR-T Translational Research Program Mayo Clinic Jacksonville Florida USA.
Qing ShaoRegenerative Immunotherapy and CAR-T Translational Research Program Mayo Clinic Jacksonville Florida USA.
Tommy ToRegenerative Immunotherapy and CAR-T Translational Research Program Mayo Clinic Jacksonville Florida USA.
Andrew LiuDepartment of Cancer Biology Mayo Clinic Jacksonville Florida USA.
Shuhua LiRegenerative Immunotherapy and CAR-T Translational Research Program Mayo Clinic Jacksonville Florida USA.
Rocio Rivera-ValentinDepartment of Pediatric Hematology‑Oncology University of Florida-Jacksonville Jacksonville Florida USA.
Farah YassineDivision of Hematology and Medical Oncology Department of Internal Medicine Mayo Clinic Jacksonville Florida USA.
Hemant S MurthyDivision of Hematology and Medical Oncology Department of Internal Medicine Mayo Clinic Jacksonville Florida USA.
Roxana DroncaDivision of Hematology and Medical Oncology Department of Internal Medicine Mayo Clinic Jacksonville Florida USA.
Mohamed A Kharfan-DabajaDivision of Hematology and Medical Oncology Department of Internal Medicine Mayo Clinic Jacksonville Florida USA.
Hong QinRegenerative Immunotherapy and CAR-T Translational Research Program Mayo Clinic Jacksonville Florida USA.
Yan LuoRegenerative Immunotherapy and CAR-T Translational Research Program Mayo Clinic Jacksonville Florida USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The challenge of disease relapsed/refractory (R/R) remains a therapeutic hurdle in chimeric antigen receptor (CAR) T-cell therapy, especially for hematological diseases, with chronic lymphocytic leukemia (CLL) being particularly resistant to CD19 CAR T cells. Currently, there is no approved CAR T-cell therapy for CLL patients. In this study, we aimed to address this unmet medical need by choosing the B-cell activating factor receptor (BAFF-R) as a promising target for CAR design against CLL. BAFF-R is essential for B-cell survival and is consistently expressed on CLL tumors. Our research discovered that BAFF-R CAR T-cell therapy exerted the cytotoxic effects on both CLL cell lines and primary B cells derived from CLL patients. In addition, the CAR T cells exhibited cytotoxicity against CD19-knockout CLL cells that are resistant to CD19 CAR T therapy. Furthermore, we were able to generate BAFF-R CAR T cells from small blood samples collected from CLL patients and then demonstrated the cytotoxic effects of these patient-derived CAR T cells against autologous tumor cells. Given these promising results, BAFF-R CAR T-cell therapy has the potential to meet the long-standing need for an effective treatment on CLL patients.

Indexed as

BAFF‐RB‐cell malignanciesCAR T cellschronic lymphocytic leukemiaimmunotherapy

Identifiers

PMID39224539
PMCPMC11366826

What Socratic holds

Textmetadata
LicenceCC BY
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.