Evidence map›Paper›PMID 39632397›Full record

ArticleThe FEBS journal2025

Depletion of Tregs from CD4

Yunyan Sun, Jinyan Liu, Dong Zhan, Jia Wei, Li XianShi, Rui Zhang, Ci Duan, Disi Zhang, Xiaorong Tang, Tuo Lin and 2 more

Abstract read
In one paragraph

Article in The FEBS journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the 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.

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

11 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
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  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. [CAR T cell therapy in acute lymphoblastic leukemia].Innere Medizin (Heidelberg, Germany) · 2025
    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

12 authors.

Yunyan SunDepartment of Hematology, Yunnan Cancer Hospital, The Third Affiliated Hospital of Kunming Medical University, Peking University Cancer Hospital Yunnan, Kunming, China.
Jinyan LiuDepartment of Hematology, Yunnan Cancer Hospital, The Third Affiliated Hospital of Kunming Medical University, Peking University Cancer Hospital Yunnan, Kunming, China.
Dong ZhanDepartment of Human Anatomy and Histology & Embrology, School of Basic Medical Sciences, Kunming Medical University, China.
Jia WeiDepartment of Hematology, Yunnan Cancer Hospital, The Third Affiliated Hospital of Kunming Medical University, Peking University Cancer Hospital Yunnan, Kunming, China.
Li XianShiDepartment of Hematology, Yunnan Cancer Hospital, The Third Affiliated Hospital of Kunming Medical University, Peking University Cancer Hospital Yunnan, Kunming, China.
Rui ZhangDepartment of Hematology, Yunnan Cancer Hospital, The Third Affiliated Hospital of Kunming Medical University, Peking University Cancer Hospital Yunnan, Kunming, China.
Ci DuanDepartment of Hematology, Yunnan Cancer Hospital, The Third Affiliated Hospital of Kunming Medical University, Peking University Cancer Hospital Yunnan, Kunming, China.
Disi ZhangDepartment of Hematology, Yunnan Cancer Hospital, The Third Affiliated Hospital of Kunming Medical University, Peking University Cancer Hospital Yunnan, Kunming, China.
Xiaorong TangDepartment of Hematology, Yunnan Cancer Hospital, The Third Affiliated Hospital of Kunming Medical University, Peking University Cancer Hospital Yunnan, Kunming, China.
Tuo LinYunnan College of Business Management, Kunming, China.
Limei LiYunnan College of Business Management, Kunming, China.
Xun LaiDepartment of Hematology, Yunnan Cancer Hospital, The Third Affiliated Hospital of Kunming Medical University, Peking University Cancer Hospital Yunnan, Kunming, China.ORCID 0000-0002-2775-0800

Funding

Kunming Joint Special Project 202001AC070202Kunming Joint Special Project 202001AC070617National Natural Science Foundation of China 8216010239Qiu Lu Gui Expert Workstation in Yunnan Province 202105AF150051The Joint Project of Kunming Medical University and Science and Technology Agency 202101AY070001-049Yunnan Fundamental Research Projects 202101AT070199
6 · The paper itself

Abstract

Chimeric antigen receptor T (CAR-T) cell therapy, which targets CD19 for hematological malignancies, represents a breakthrough in cancer immunotherapy. However, some patients may develop resistance to CAR-T treatment, underscoring the importance of optimizing CAR-T design to enhance responsiveness. Here, we investigated the impact of different subpopulations in anti-CD19 CAR-T cells on the tumoricidal effect. Different populations of anti-CD19 CAR-T cells were isolated by magnetic-activated cell sorting (MACS). Their lytic activities on the acute lymphocytic leukemia cell line SUP-B15 and diffuse large B-cell lymphoma EB-3 cell line were examined in a co-culture system. The anti-tumorigenic outcome of different CAR-T cell compositions was evaluated in a xenograft mouse model of EB-3 cells. CD8

Indexed as

Antigens, CD19CD4-Positive T-LymphocytesCD8-Positive T-LymphocytesImmunotherapy, AdoptiveLymphoma, Large B-Cell, DiffuseReceptors, Chimeric AntigenT-Lymphocytes, RegulatoryAnimalsCell Line, TumorHumansInterleukin-2Interleukin-2 Receptor alpha SubunitMiceXenograft Model Antitumor AssaysAntigens, CD19CD19 molecule, humanInterleukin-2Interleukin-2 Receptor alpha SubunitReceptors, Chimeric AntigenCAR‐TCD19cytotoxicTregstumoricial

Identifiers

PMID39632397
PMCPMC12001162

What OpenQuestion holds

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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.