NGcGM3 Ganglioside: A Privileged Target for Cancer Vaccines

Author:

Fernandez Luis E.1,Gabri Mariano R.2,Guthmann Marcelo D.3,Gomez Roberto E.3,Gold Silvia4,Fainboim Leonardo5,Gomez Daniel E.2,Alonso Daniel F.2

Affiliation:

1. Vaccine Department, Center of Molecular Immunology, Havana 11600, Cuba

2. Laboratory of Molecular Oncology, Quilmes National University, Roque Saenz Peña 352, Bernal B1876BXD Buenos Aires, Argentina

3. Elea Laboratories, C1417AZE Buenos Aires, Argentina

4. Chemo-Romikin, C1061ABC Buenos Aires, Argentina

5. Division of Immunogenetics, José de San Martín Clinics Hospital, University of Buenos Aires, C1120AAF Buenos Aires, Argentina

Abstract

Active specific immunotherapy is a promising field in cancer research. N-glycolyl (NGc) gangliosides, and particularly NGcGM3, have received attention as a privileged target for cancer therapy. Many clinical trials have been performed with the anti-NGc-containing gangliosides anti-idiotype monoclonal antibody racotumomab (formerly known as 1E10) and the conjugated NGcGM3/VSSP vaccine for immunotherapy of melanoma, breast, and lung cancer. The present paper examines the role of NGc-gangliosides in tumor biology as well as the available preclinical and clinical data on these vaccine products. A brief discussion on the relevance of prioritization of cancer antigens in vaccine development is also included.

Funder

National Agency of Scientific and Technological Promotion

Publisher

Hindawi Limited

Subject

General Medicine,Immunology,Immunology and Allergy

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