Evidence map›Paper›PMID 36172388›Full record

ArticleFrontiers in immunology2022

Treatment of aggressive T-cell lymphoma/leukemia with anti-CD4 CAR T cells.

Jia Feng, Haichan Xu, Andrew Cinquina, Zehua Wu, Wenli Zhang, Lihua Sun, Qi Chen, Lei Tian, Le Song, Kevin G Pinz and 5 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. In vivo CAR T cell therapy against angioimmunoblastic T cell lymphoma.Journal of experimental & clinical cancer research : CR · 2024
    Article
  6. Review
  7. Transcriptome Analysis in Mexican Adults with Acute Lymphoblastic Leukemia.International journal of molecular sciences · 2024
    Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. 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

15 authors.

Jia FengDepartment of Hematology, Peking University Shenzhen Hospital, Shenzhen, China.
Haichan XuDepartment of Hematology, Peking University Shenzhen Hospital, Shenzhen, China.
Andrew CinquinaiCell Gene Therapeutics LLC, Research & Development Division, Long Island High Technology Incubator, Stony Brook, NY, United States.
Zehua WuDepartment of Hematology, Peking University Shenzhen Hospital, Shenzhen, China.
Wenli ZhangDepartment of Hematology, Peking University Shenzhen Hospital, Shenzhen, China.
Lihua SunDepartment of Hematology, Peking University Shenzhen Hospital, Shenzhen, China.
Qi ChenDepartment of Hematology, Peking University Shenzhen Hospital, Shenzhen, China.
Lei TianDepartment of Hematology, Peking University Third Hospital, Beijing, China.
Le SongDepartment of Nuclear Medicine, Peking University Third Hospital, Beijing, China.
Kevin G PinziCell Gene Therapeutics LLC, Research & Development Division, Long Island High Technology Incubator, Stony Brook, NY, United States.
Masayuki WadaiCell Gene Therapeutics LLC, Research & Development Division, Long Island High Technology Incubator, Stony Brook, NY, United States.
Xun JiangiCell Gene Therapeutics LLC, Research & Development Division, Long Island High Technology Incubator, Stony Brook, NY, United States.
William M HanesiCell Gene Therapeutics LLC, Research & Development Division, Long Island High Technology Incubator, Stony Brook, NY, United States.
Yupo MaiCell Gene Therapeutics LLC, Research & Development Division, Long Island High Technology Incubator, Stony Brook, NY, United States.
Hongyu ZhangDepartment of Hematology, Peking University Shenzhen Hospital, Shenzhen, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T-cell lymphomas are aggressive lymphomas that often resist current therapy options or present with relapsed disease, making the development of more effective treatment regimens clinically important. Previously, we have shown that CD4 CAR can effectively target T-cell malignancies in preclinical studies. As IL-15 has been shown to strengthen the anti-tumor response, we have modified CD4 CAR to secrete an IL-15/IL-15sushi complex. These CD4-IL15/IL15sushi CAR T cells and NK92 cells efficiently eliminated CD4+ leukemic cell lines in co-culture assays. Additionally, CD4-IL15/IL15sushi CAR out-performed CD4 CAR in

Indexed as

LeukemiaLymphoma, T-CellClinical Trials, Phase I as TopicHumansImmunotherapy, AdoptiveInterleukin-15Killer Cells, NaturalInterleukin-15CAR T cellsCD4 CARhematopoietic cellsIL15/IL15sushiT-cell lymphoma

Identifiers

PMID36172388
PMCPMC9511023

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.