Filter By:

Journal Check one or more journals to show results from those journals only.

Choose more journals

Article type Check one or more article types to show results from those article types only.
Subject Check one or more subjects to show results from those subjects only.
Date Choose a date option to show results from those dates only.

Custom date range

Clear all filters
Sort by:
Showing 1–22 of 22 results
Advanced filters: Author: Robbie G. Majzner Clear advanced filters
  • Chimeric antigen receptor (CAR) T cells engineered to overexpress the canonical AP-1 transcription factor c-Jun are resistant to T cell exhaustion, and provide enhanced therapeutic benefit in mouse tumour models.

    • Rachel C. Lynn
    • Evan W. Weber
    • Crystal L. Mackall
    Research
    Nature
    Volume: 576, P: 293-300
  • A phase I dose-escalation trial of GD2-CAR T cells in children and young adults with diffuse midline gliomas to assess the feasibility of manufacturing, safety and tolerability, and to preliminarily assess efficacy.

    • Robbie G. Majzner
    • Sneha Ramakrishna
    • Michelle Monje
    ResearchOpen Access
    Nature
    Volume: 603, P: 934-941
  • We evaluated the use of chimeric antigen receptor-modified T cells targeting GD2 (GD2-CART) for H3K27M+ diffuse midline glioma (DMG), finding that intravenous administration of GD2-CART, followed by intracranial infusions, induced tumour regressions and neurological improvements in patients with H3K27M-mutant pontine or spinal DMG.

    • Michelle Monje
    • Jasia Mahdi
    • Crystal Mackall
    ResearchOpen Access
    Nature
    Volume: 637, P: 708-715
  • Combination of TCR or CAR T cells expressing the engineered CD47 variant 47E with anti-CD47 antibody therapy results in synergistic antitumour efficacy due to T cell resistance to clearance by macrophages, while maintaining macrophage recruitment into the tumour microenvironment.

    • Sean A. Yamada-Hunter
    • Johanna Theruvath
    • Crystal L. Mackall
    ResearchOpen Access
    Nature
    Volume: 630, P: 457-465
  • Genomics analyses reveal that in vitro culture of CAR T cells can lead to reactivation of a latent herpesvirus, which might be involved in complications in patients receiving associated cell therapies.

    • Caleb A. Lareau
    • Yajie Yin
    • Ansuman T. Satpathy
    Research
    Nature
    Volume: 623, P: 608-615
  • Logic gating is used to develop a CAR T cell platform that is highly specific and allows the activity of T cells to be restricted to the encounter of two antigens, thus reducing on-target, off-tumour toxicity.

    • Aidan M. Tousley
    • Maria Caterina Rotiroti
    • Robbie G. Majzner
    Research
    Nature
    Volume: 615, P: 507-516
  • The combination of anti-GD2 and CD47 blockade mediates robust anti-tumor activity in mouse models of neuroblastoma, osteosarcoma and small-cell lung cancer by reorienting macrophage activity toward tumor cell phagocytosis.

    • Johanna Theruvath
    • Marie Menard
    • Robbie G. Majzner
    Research
    Nature Medicine
    Volume: 28, P: 333-344
  • A approach termed ‘receptor inhibition by phosphatase recruitment’ is described for attenuating both tonic and ligand-activated cell-surface receptor signalling.

    • Ricardo A. Fernandes
    • Leon Su
    • K. Christopher Garcia
    Research
    Nature
    Volume: 586, P: 779-784
  • Fry et al. report the first results from a human trial of a CD22-directed chimeric antigen receptor (CAR) T cell therapy providing evidence of efficacy in the treatment of pre–B cell acute lymphoblastic leukemia that is immunotherapy-naive or resistant to CD19-directed CAR T cells.

    • Terry J Fry
    • Nirali N Shah
    • Crystal L Mackall
    Research
    Nature Medicine
    Volume: 24, P: 20-28
  • The authors describe a localized toxicity syndrome that is associated with immunotherapy treatment for CNS tumors and propose a new grading scale—with the goal of promoting research and standardizing both reporting and management.

    • Jasia Mahdi
    • Jorg Dietrich
    • Michelle Monje
    Reviews
    Nature Medicine
    Volume: 29, P: 803-810
  • Chimeric antigen receptor (CAR) T cells are effective therapies for patients with relapsed and/or refractory B cell malignancies, partly owing to the ability to target B cell-specific antigens. However, CAR T cells targeting solid tumour antigens are likely to carry a higher risk of on-target, off-tumour toxicity (OTOT). Here, the authors summarize the available data on OTOT in the context of CAR T cells targeting solid tumour antigens and describe novel CAR T cell designs that might overcome such toxicities.

    • Christian L. Flugel
    • Robbie G. Majzner
    • Mohamed Abou-el-Enein
    Reviews
    Nature Reviews Clinical Oncology
    Volume: 20, P: 49-62
  • This Review Article provides an overview of chimeric antigen receptors (CARs) for T cells and discusses engineering strategies for the design of next-generation CAR-T therapies for haematologic and solid cancers.

    • Louai Labanieh
    • Robbie G. Majzner
    • Crystal L. Mackall
    Reviews
    Nature Biomedical Engineering
    Volume: 2, P: 377-391