4.2 Review

Anti-GD2 mAbs and next-generation mAb-based agents for cancer therapy

Journal

IMMUNOTHERAPY
Volume 8, Issue 9, Pages 1097-1117

Publisher

FUTURE MEDICINE LTD
DOI: 10.2217/imt-2016-0021

Keywords

cancer immunotherapy; monoclonal antibodies; neuroblastoma

Categories

Funding

  1. Hyundai Hope on Wheels Grant
  2. Midwest Athletes Against Childhood
  3. Stand Up 2 Cancer
  4. The St. Baldrick's Foundation
  5. American Association of Cancer Research
  6. University of Wisconsin-Madison Carbone Cancer Center
  7. Public Health Service Grants from the National Cancer Institute [CA21115, CA23318, CA66636, CA180820, CA180794, CA21076, CA180799, CA14958, CA180816, CA166105, CA197078]
  8. The Advanced Opportunity Fellowship through SciMed Graduate Research Scholars
  9. Molecular Bioscience Training Grant (MBTG) at University of Wisconsin - Madison [T32 GM07215]
  10. Howard Hughes Medical Scholars Fellowship Program

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Tumor-specific monoclonal antibodies (mAbs) have demonstrated efficacy in the clinic, becoming an important approach for cancer immunotherapy. Due to its limited expression on normal tissue, the GD2 disialogangloside expressed on neuroblastoma cells is an excellent candidate for mAb therapy. In 2015, dinutuximab (an anti-GD2 mAb) was approved by the US FDA and is currently used in a combination immunotherapeutic regimen for the treatment of children with high-risk neuroblastoma. Here, we review the extensive preclinical and clinical development of anti-GD2 mAbs and the different mechanisms by which they mediate tumor cell killing. In addition, we discuss different mAb-based strategies that capitalize on the targeting ability of anti-GD2 mAbs to potentially deliver, as monotherapy, or in combination with other treatments, improved antitumor efficacy.

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