4.6 Article

An Optimized GD2-Targeting Retroviral Cassette for More Potent and Safer Cellular Therapy of Neuroblastoma and Other Cancers

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PLOS ONE
卷 11, 期 3, 页码 -

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PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0152196

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资金

  1. Neuroblastoma UK
  2. UK NIHR Biomedical Research Centre
  3. Wellcome Trust
  4. Great Ormond Street Hospital, Biomedical Research Centre
  5. Great Ormond Street Hospital Children's Charity
  6. Cancer Research UK [14779] Funding Source: researchfish
  7. Great Ormond Street Hospital Childrens Charity [V1243, W1006] Funding Source: researchfish
  8. National Institute for Health Research [CL-2009-18-011] Funding Source: researchfish
  9. Wellcome Trust [102803/Z/13/Z] Funding Source: researchfish
  10. Wellcome Trust [102803/Z/13/Z] Funding Source: Wellcome Trust

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Neuroblastoma is the commonest extra cranial solid cancer of childhood. Despite escalation of treatment regimens, a significant minority of patients die of their disease. Disialogan-glioside (GD2) is consistently expressed at high-levels in neuroblastoma tumors, which have been targeted with some success using therapeutic monoclonal antibodies. GD2 is also expressed in a range of other cancer but with the exception of some peripheral nerves is largely absent from non-transformed tissues. Chimeric Antigen Receptors (CARs) are artificial type I proteins which graft the specificity of a monoclonal antibody onto a T-cell. Clinical data with early CAR designs directed against GD2 have shown some promise in Neuroblastoma. Here, we describe a GD2-targeting CAR retroviral cassette, which has been optimized for CAR T-cell persistence, efficacy and safety.

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