Evidence map›Paper›PMID 35765110›Full record

ArticleJournal of experimental & clinical cancer research : CR2022

Expanding anti-CD38 immunotherapy for lymphoid malignancies.

Xu Wang, Xinfang Yu, Wei Li, Praveen Neeli, Ming Liu, Ling Li, Mingzhi Zhang, Xiaosheng Fang, Ken H Young, Yong Li

Abstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Daratumumab for CD20Journal of cellular and molecular medicine · 2025
    Article
  5. Article
  6. Viral oncogenesis in cancer: from mechanisms to therapeutics.Signal transduction and targeted therapy · 2025
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. The Role of NADPharmaceuticals (Basel, Switzerland) · 2024
    Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  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

10 authors.

Xu WangDepartment of Medicine, Baylor College of Medicine, Houston, TX, USA.
Xinfang YuDepartment of Medicine, Baylor College of Medicine, Houston, TX, USA.
Wei LiDepartment of Medicine, Baylor College of Medicine, Houston, TX, USA.
Praveen NeeliDepartment of Medicine, Baylor College of Medicine, Houston, TX, USA.
Ming LiuNational Clinical Research Center for Respiratory Disease, State Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Health, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 510120, China.
Ling LiDepartment of Oncology, Lymphoma Diagnosis and Treatment Center of Henan Province, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Mingzhi ZhangDepartment of Oncology, Lymphoma Diagnosis and Treatment Center of Henan Province, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Xiaosheng FangDepartment of Pathology, Division of Hematopathology, Duke University Medical Center, Durham, NC, USA.
Ken H YoungDepartment of Pathology, Division of Hematopathology, Duke University Medical Center, Durham, NC, USA.
Yong LiDepartment of Medicine, Baylor College of Medicine, Houston, TX, USA. yong.li@bcm.edu.ORCID http://orcid.org/0000-0001-8838-1714

Funding

Cancer Prevention and Research Institute of Texas RR190043
6 · The paper itself

Abstract

backgroundLymphoid neoplasms, including multiple myeloma (MM), non-Hodgkin lymphoma (NHL), and NK/T cell neoplasms, are a major cause of blood cancer morbidity and mortality. CD38 (cyclic ADP ribose hydrolase) is a transmembrane glycoprotein expressed on the surface of plasma cells and MM cells. The high expression of CD38 across MM and other lymphoid malignancies and its restricted expression in normal tissues make CD38 an attractive target for immunotherapy. CD38-targeting antibodies, like daratumumab, have been approved for the treatment of MM and tested against lymphoma and leukemia in multiple clinical trials.

methodsWe generated chimeric antigen receptor (CAR) T cells targeting CD38 and tested its cytotoxicity against multiple CD38

resultsCD38-CAR T cells dramatically inhibited the growth of CD38

conclusionsThese findings may expand anti-CD38 immunotherapy to a broad spectrum of lymphoid malignancies and call for the incorporation of ATRA into daratumumab or other anti-CD38 immunological agents for cancer therapy.

Indexed as

LymphomaLymphoma, B-CellMultiple MyelomaADP-ribosyl Cyclase 1AdultAnimalsHumansImmunotherapyMiceXenograft Model Antitumor AssaysADP-ribosyl Cyclase 1All-trans retinoic acidCAR TCD38DaratumumabMultiple myelomaNon-Hodgkin lymphoma

Identifiers

PMID35765110
PMCPMC9237984

What OpenQuestion holds

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Registered trials

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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.