Evidence map›Paper›PMID 41290542›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Single-Cell Dissection Reveals Immune Dysregulation After CD5 or CD7-Directed Chimeric Antigen Receptor T-Cell Therapy.

Yuechen Luo, Haixiao Zhang, Kaiting Tang, Yiming Wang, Huajiang Dong, Wei Qi, Lingling Shan, Yue Tan, Liping Zhao, Jun Shi and 3 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 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. 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.

Yuechen LuoState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, 300020, China.
Haixiao ZhangState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, 300020, China.
Kaiting TangState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, 300020, China.
Yiming WangNovogene Co., Ltd., Beijing, 100015, China.
Huajiang DongLogistics University of Chinese People's Armed Police Forces, Tianjin, 300309, China.
Wei QiNovogene Co., Ltd., Beijing, 100015, China.
Lingling ShanState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, 300020, China.
Yue TanState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, 300020, China.
Liping ZhaoState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, 300020, China.
Jun ShiState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, 300020, China.
Erlie JiangState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, 300020, China.
Jing PanState Key Laboratory of Experimental Hematology, Department of Hemato-oncology and Immunotherapy, Beijing GoBroad Hospital, Beijing, 102206, China.
Xiaoming FengState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, 300020, China.ORCID https://orcid.org/0009-0009-7675-3600

Funding

CAMS Innovation Fund for Medical Sciences 2021-I2M-1-041CAMS Innovation Fund for Medical Sciences 2022-I2M-JB-015National Defense Science and Technology Innovation ZZKY20222420National Key R&D Program of China 2021YFA1100703National Natural Science Foundation of China 82370221Tianjin Municipal Science and Technology Commission Grant 23JCYBJC00190
6 · The paper itself

Abstract

CD5- and CD7-directed chimeric antigen receptor T-cell (5CAR and 7CAR) therapies for T-cell malignancies carry the risk of life-threatening infection. Although depletion of target-positive lymphocytes is expected, the contribution of residual cell dysfunction to infection risk remains unclear. This work uses single-cell sequencing to investigate immune dysregulation after 5CAR or 7CAR therapy in patients with T-cell acute lymphoblastic leukemia. 5CAR induces marked T-cell exhaustion linked to CD5 loss and B lymphocyte-induced maturation protein 1 upregulation. This is accompanied by reduced frequency and diversity of Epstein-Barr virus (EBV)-associated T-cell receptors, potentially contributing to the high incidence of severe EBV infection. 5CAR therapy also impairs B-cell function and diversity while enhancing natural killer cell function and monocyte activation. In contrast, 7CAR reduces the frequency and diversity of multiple pathogen-associated T-cell receptors, but causes less T-cell exhaustion. 7CAR also substantially impairs innate immunity by decreasing monocyte activation and eliminating dendritic cells, which may contribute to the high risk of infection. Thus, unlike CD19 and CD22 CAR therapy, which primarily affects B cells, 5CAR and 7CAR therapies result in broad dysregulation across multiple immune cell types, providing a basis for infection prevention and safer CAR-T therapy.

Indexed as

Antigens, CD7CD5 AntigensImmunotherapy, AdoptiveReceptors, Chimeric AntigenB-LymphocytesHumansSingle-Cell AnalysisT-LymphocytesAntigens, CD7CD5 AntigensReceptors, Chimeric AntigenCAR T cellsimmunodeficiencysingle‐cell sequencing

Identifiers

PMID41290542
PMCPMC12884813

What OpenQuestion 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 OpenQuestion graph.