Evidence map›Paper›PMID 39207859›Full record

ArticleThe Journal of clinical investigation2024

B cell-based therapy produces antibodies that inhibit glioblastoma growth.

Si Wang, Brandyn A Castro, Joshua L Katz, Victor Arrieta, Hinda Najem, Gustavo I Vazquez-Cervantes, Hanxiao Wan, Ian E Olson, David Hou, Mark Dapash and 18 more

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. B cells in cancer: functions, mechanisms and therapeutic advances.Signal transduction and targeted therapy · 2026
    Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Targeting Cancer: Microenvironment and Immunotherapy Innovations.International journal of molecular sciences · 2024
    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

28 authors.

Si WangDepartment of Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Brandyn A CastroDepartment of Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Joshua L KatzDepartment of Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Victor ArrietaDepartment of Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Hinda NajemDepartment of Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Gustavo I Vazquez-CervantesDepartment of Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Hanxiao WanDepartment of Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Ian E OlsonDepartment of Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
David HouDepartment of Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Mark DapashDepartment of Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Leah K BillinghamDepartment of Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Tzu-Yi ChiaDepartment of Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Chao WeiDepartment of Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Aida RashidiDepartment of Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Leonidas C PlataniasRobert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, Illinois, USA.
Kathleen McCortneyDepartment of Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Craig M HorbinskiDepartment of Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Roger StuppDepartment of Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Peng ZhangDepartment of Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Atique U AhmedDepartment of Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Adam M SonabendDepartment of Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Amy B HeimbergerDepartment of Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Maciej S LesniakDepartment of Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Cécile Riviere-CazauxDepartment of Neurological Surgery, Mayo Clinic, Rochester, Minnesotta, USA.
Terry BurnsDepartment of Neurological Surgery, Mayo Clinic, Rochester, Minnesotta, USA.
Jason MiskaDepartment of Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Mariafausta FischiettiRobert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, Illinois, USA.
Catalina Lee-ChangDepartment of Neurological Surgery, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Devalingam Mahalingam · 1993 to 2026
$153.9M
Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Lila J. Rutten · 1985 to 2026
$151.3M
STINGing GBM: A First-in- Man Clinical Trial in Surgical Resectable Recurrent GBMP50CA221747 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Hui Zhang · 2018 to 2026
$21.4M
TR&D 7: Cell Specific ProteomicsP41GM108569 · NIGMS · NORTHWESTERN UNIVERSITY · PI KELLEHER, NEIL L · 2015 to 2024
$13.6M
Therapeutic Targeting of Malignant Glioma Stem CellsR35CA197725 · NCI · UNIVERSITY OF CHICAGO · PI LESNIAK, MACIEJ S · 2015 to 2021
$6.2M
MSTP at Mayo Clinic RochesterT32GM145408 · NIGMS · MAYO CLINIC ROCHESTER · PI SCOTT H KAUFMANN, LISA A SCHIMMENTI · 2023 to 2026
$4.7M
Modulation of Microglia and T Cell Interactions in Malignant GliomaR01CA120813 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI HEIMBERGER, AMY BETH, RAO, GANESH · 2007 to 2025
$4.7M
Development of B-cell-based vaccine for GlioblastomaR37CA258426 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Catalina Lee Chang · 2021 to 2026
$2.2M
Glioma intelligence from behind enemy linesR37CA276851 · NCI · MAYO CLINIC ROCHESTER · PI Terry Burns · 2023 to 2026
$2.1M
Arginine Metabolism Regulates Myeloid Immune Suppression in GlioblastomaR01NS115955 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LESNIAK, MACIEJ S, MISKA, JASON · 2020 to 2024
$1.9M
The hypoxic niche in glioblastoma is maintained by myeloid produced creatineR01CA279686 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Jason Miska · 2023 to 2026
$1.5M
Stinging the Glioma Immune LandscapeR01NS120547 · NINDS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI HEIMBERGER, AMY BETH, RAO, ARVIND · 2020 to 2023
$1.1M
NCI NIH HHS P30 CA015083NCI NIH HHS P30 CA060553NCI NIH HHS P50 CA221747NCI NIH HHS R01 CA120813NCI NIH HHS R01 CA279686NCI NIH HHS R35 CA197725NCI NIH HHS R37 CA258426NCI NIH HHS R37 CA276851NIGMS NIH HHS P41 GM108569NIGMS NIH HHS T32 GM145408NIH HHS S10 OD025194NINDS NIH HHS R01 NS115955NINDS NIH HHS R01 NS120547
6 · The paper itself

Abstract

Glioblastoma (GBM) is a highly aggressive and malignant brain tumor with limited therapeutic options and a poor prognosis. Despite current treatments, the invasive nature of GBM often leads to recurrence. A promising alternative strategy is to harness the potential of the immune system against tumor cells. Our previous data showed that the BVax (B cell-based vaccine) can induce therapeutic responses in preclinical models of GBM. In this study, we aimed to characterize the antigenic reactivity of BVax-derived Abs and evaluate their therapeutic potential. We performed immunoproteomics and functional assays in murine models and samples from patients with GBM. Our investigations revealed that BVax distributed throughout the GBM tumor microenvironment and then differentiated into Ab-producing plasmablasts. Proteomics analyses indicated that the Abs produced by BVax had unique reactivity, predominantly targeting factors associated with cell motility and the extracellular matrix. Crucially, these Abs inhibited critical processes such as GBM cell migration and invasion. These findings provide valuable insights into the therapeutic potential of BVax-derived Abs for patients with GBM, pointing toward a novel direction for GBM immunotherapy.

Indexed as

Brain NeoplasmsGlioblastomaAnimalsAntibodies, NeoplasmB-LymphocytesCancer VaccinesCell Line, TumorCell MovementFemaleHumansImmunotherapyMaleMiceTumor MicroenvironmentAntibodies, NeoplasmCancer VaccinesBrain cancerCancer immunotherapyExtracellular matrixImmunologyOncology

Identifiers

PMID39207859
PMCPMC11473152

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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.