HER1-based vaccine: Simultaneous activation of humoral and cellular immune response
The human epidermal growth factor receptor 1 (HER1) is a tumor-associated antigen that has been validated as a clinical target for several passive, non-immune therapies currently approved for the treatment of epithelial tumors. HER1 is an oncogene that not only promotes tumor progression and surviva...
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Published in | Seminars in oncology Vol. 45; no. 1-2; pp. 75 - 83 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.01.2018
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Abstract | The human epidermal growth factor receptor 1 (HER1) is a tumor-associated antigen that has been validated as a clinical target for several passive, non-immune therapies currently approved for the treatment of epithelial tumors. HER1 is an oncogene that not only promotes tumor progression and survival, but also immune escape. Its overexpression in some epithelial malignancies has been correlated with a poor prognosis. We developed an approach to target HER1 by specific active immunotherapy, recognizing the extracellular domain of the receptor, using a combination of VSSP and Montanide ISA 51 as adjuvants. We summarize the results obtained with this vaccine in both the preclinical and clinical settings, emphasizing the importance of the induction of both humoral and cellular responses for the success of cancer vaccines as safe therapeutic alternatives for the treatment of cancer. |
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AbstractList | The human epidermal growth factor receptor 1 (HER1) is a tumor-associated antigen that has been validated as a clinical target for several passive, non-immune therapies currently approved for the treatment of epithelial tumors. HER1 is an oncogene that not only promotes tumor progression and survival, but also immune escape. Its overexpression in some epithelial malignancies has been correlated with a poor prognosis. We developed an approach to target HER1 by specific active immunotherapy, recognizing the extracellular domain of the receptor, using a combination of VSSP and Montanide ISA 51 as adjuvants. We summarize the results obtained with this vaccine in both the preclinical and clinical settings, emphasizing the importance of the induction of both humoral and cellular responses for the success of cancer vaccines as safe therapeutic alternatives for the treatment of cancer. |
Author | Hernández Fernández, Diana R. Sánchez Ramírez, Belinda Mazorra Herrera, Zaima Bergado Báez, Gretchen |
Author_xml | – sequence: 1 givenname: Gretchen surname: Bergado Báez fullname: Bergado Báez, Gretchen organization: Tumor Immunology Direction, Center of Molecular Immunology, La Habana, Cuba – sequence: 2 givenname: Diana R. surname: Hernández Fernández fullname: Hernández Fernández, Diana R. organization: Tumor Immunology Direction, Center of Molecular Immunology, La Habana, Cuba – sequence: 3 givenname: Zaima surname: Mazorra Herrera fullname: Mazorra Herrera, Zaima organization: Clinical Direction, Center of Molecular Immunology, La Habana, Cuba – sequence: 4 givenname: Belinda surname: Sánchez Ramírez fullname: Sánchez Ramírez, Belinda email: belinda@cim.sld.cu organization: Tumor Immunology Direction, Center of Molecular Immunology, La Habana, Cuba |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30318087$$D View this record in MEDLINE/PubMed |
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