4.2 Review

ErbB-targeted CAR T-cell immunotherapy of cancer

Journal

IMMUNOTHERAPY
Volume 7, Issue 3, Pages 229-241

Publisher

FUTURE MEDICINE LTD
DOI: 10.2217/IMT.14.120

Keywords

cancer; chimeric antigen receptor; ErbB receptors; HER2; immunotherapy; T cells

Categories

Funding

  1. Breast Cancer Campaign
  2. Worldwide Cancer Research
  3. Leukaemia and Lymphoma Research
  4. Pancreatic Cancer UK
  5. Wellcome Trust
  6. Jon Moulton Charitable Foundation
  7. Experimental Cancer Medicine Center at King's College London
  8. National Institute for Health Research (NIHR) Biomedical Research Center based at Guy's and St Thomas' NHS Foundation Trust
  9. King's College London
  10. Pancreatic Cancer UK [2013 RIF - Maher] Funding Source: researchfish
  11. Worldwide Cancer Research [13-1017] Funding Source: researchfish

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Chimeric antigen receptor (CAR) based immunotherapy has been under development for the last 25 years and is now a promising new treatment modality in the field of cancer immunotherapy. The approach involves genetically engineering T cells to target malignant cells through expression of a bespoke fusion receptor that couples an HLA-independent antigen recognition domain to one or more intracellular T-cell activating modules. Multiple clinical trials are now underway in several centers to investigate CAR T-cell immunotherapy of diverse hematologic and solid tumor types. The most successful results have been achieved in the treatment of patients with B-cell malignancies, in whom several complete and durable responses have been achieved. This review focuses on the preclinical and clinical development of CAR T-cell immunotherapy of solid cancers, targeted against members of the ErbB family.

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