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Vaccine Comparison

Contusugene ladenovec IDD-3
Vaccine Information Vaccine Information
  • Product Name: Ad-p53; Ad5CMV-p53 Gene
  • Vaccine Ontology ID: VO_0007594
  • Type: Other
  • Status: Clinical trial
  • Host Species for Licensed Use: Human
  • Host Species as Laboratory Animal Model: Human
  • Antigen: p53
  • human TP53 (P53) gene engineering:
    • Type: Recombinant protein preparation
    • Detailed Gene Information: Click Here.
  • Description: A replication-defective adenoviral-CMV vector that encodes a wild-type p53 gene. Ad5CMV-p53 induces tumor cells that have been transfected with the vector to produce wild-type p53, a tumor suppressor gene that is deleted or mutated in a significant number of cancers. In transfected tumor cells, the wild-type p-53 gene product exerts an antitumor effect by blocking cell cycle progression at the G1/S regulation point, activating DNA repair proteins in the presence of DNA damage, and initiating apoptosis when DNA damage is irreparable. (NCI04) (NCIT_C2471).
  • Vaccine Ontology ID: VO_0007619
  • Type: Dendritic cell
  • Status: Clinical trial
  • Preparation: The vaccine (IDD-3) consisted 8 doses of autologous monocyte-derived matured DC generated in serum-free medium with granulocyte macrophage colony stimulating factor (GM-CSF) and interleukin-13 (IL-13), pulsed with lysates of three allogeneic melanoma cell lines, and matured with interferon gamma (Ribas et al., 2010).
  • Immunization Route: Intramuscular injection (i.m.)
  • Description: The administration of matured DC loaded with tumor lysates has significant immunogenicity and antitumor activity in patients with limited metastatic melanoma (Ribas et al., 2010).
Host Response Host Response

Baboon Response

  • Description: A clinical trial on this vaccine is reported with the ClinicalTrials.gov Identifier: NCT03544723 (Clinical trial NCT03544723).

Baboon Response

  • Vaccine Immune Response Type: VO_0003057
  • Immune Response: (90%) had detectable TAA-specific CD8+ T cells in peripheral blood. 19/26 of patients with boosted/induced immune responses post-treatment to a single pool or multiple pools of TAA-derived peptides. 3/26 patients with stable immune response to one (or more) pool; and 4/26 patients with decreased immune response to one (or more) pool (Ribas et al., 2010).
References References
Clinical trial NCT03544723: Safety and Efficacy of p53 Gene Therapy Combined With Immune Checkpoint Inhibitors in Solid Tumors [https://clinicaltrials.gov/ct2/show/NCT03544723]
NCIT_C2471: [https://ncit.nci.nih.gov/ncitbrowser/ConceptReport.jsp?dictionary=NCI_Thesaurus&code=C2471]