| Literature DB >> 26155408 |
Norma Bloy1, Aitziber Buqué1, Fernando Aranda2, Francesca Castoldi3, Alexander Eggermont4, Isabelle Cremer5, Catherine Sautès-Fridman5, Jitka Fucikova6, Jérôme Galon7, Radek Spisek6, Eric Tartour8, Laurence Zitvogel9, Guido Kroemer10, Lorenzo Galluzzi11.
Abstract
One type of anticancer vaccine relies on the administration of DNA constructs encoding one or multiple tumor-associated antigens (TAAs). The ultimate objective of these preparations, which can be naked or vectored by non-pathogenic viruses, bacteria or yeast cells, is to drive the synthesis of TAAs in the context of an immunostimulatory milieu, resulting in the (re-)elicitation of a tumor-targeting immune response. In spite of encouraging preclinical results, the clinical efficacy of DNA-based vaccines employed as standalone immunotherapeutic interventions in cancer patients appears to be limited. Thus, efforts are currently being devoted to the development of combinatorial regimens that allow DNA-based anticancer vaccines to elicit clinically relevant immune responses. Here, we discuss recent advances in the preclinical and clinical development of this therapeutic paradigm.Entities:
Keywords: AFP, α-fetoprotein; APC, antigen-presenting cell; CDR, complementarity-determining region; CEA, carcinoembryonic antigen; CIN, cervical intraepithelial neoplasia; CTLA4, cytotoxic T lymphocyte protein 4; DAMP, damage-associated molecular pattern; DC, dendritic cell; FDA, Food and Drug Administration; GM-CSF, granulocyte macrophage colony-stimulating factor; GX-188E; HCC, hepatocellular carcinoma; HNSCC, head and neck squamous cell carcinoma; HPV, human papillomavirus; IL, interleukin; OS, overall survival; OVA, ovalbumin; PAP, prostate acid phosphatase; SCGB2A2, secretoglobin, family 2A, member 2; SOX2, SRY (sex determining region Y)-box 2; T, brachyury homolog; TAA, tumor-associated antigen; TLR, Toll-like receptor; TRA, tumor rejection antigen; Treg, regulatory T cell; VGX-3100; WT1, Wilms tumor 1; adjuvants; dendritic cell; electroporation; mucosal immunity
Year: 2015 PMID: 26155408 PMCID: PMC4485755 DOI: 10.1080/2162402X.2015.1026531
Source DB: PubMed Journal: Oncoimmunology ISSN: 2162-4011 Impact factor: 8.110