Therapeutic Cancer Vaccines represent a promising approach to cancer treatment that harnesses the body's immune system to target and destroy cancer cells. Unlike traditional preventive vaccines, which aim to prevent infectious diseases, therapeutic cancer vaccines are designed to stimulate the immune system to recognize and attack tumor cells specifically.
The concept behind therapeutic cancer vaccines is to train the immune system to recognize cancer cells as foreign or abnormal and mount a targeted immune response against them. These vaccines typically contain tumor-associated antigens or neoantigens, which are proteins present on the surface of cancer cells but not on normal cells. By presenting these antigens to the immune system, therapeutic cancer vaccines aim to prime immune cells, such as T cells, to recognize and attack tumor cells bearing the same antigens. Several types of therapeutic cancer vaccines have been developed, including peptide vaccines, dendritic cell vaccines, and whole-cell vaccines. Peptide vaccines contain short fragments of tumor-associated antigens, while dendritic cell vaccines involve harvesting immune cells called dendritic cells from the patient, loading them with tumor antigens, and then reinfusing them into the patient to stimulate an immune response. Whole-cell vaccines are made from whole tumor cells or genetically modified tumor cells, which are then used to stimulate an immune response.
Therapeutic cancer vaccines have shown promise in clinical trials for various types of cancer, including melanoma, prostate cancer, breast cancer, and lung cancer. While therapeutic cancer vaccines have not yet achieved widespread success as a standalone treatment, they have demonstrated efficacy in combination with other cancer therapies, such as chemotherapy, radiation therapy, and immune checkpoint inhibitors.
Title : Prophylactic and molecular approaches for mitigating human influenza A viruses: i. Evaluating influenza vaccine effectiveness in the older population ii. Down-regulation of influenza virus genes with novel sirna-chimeric-ribozyme constructs
Madhu Khanna, University of Delhi, India
Title : Homology analysis of MPXV and VACV peptides underscores the need to consider both MPXV clades for vaccine development
Lara Isis Teodoro, Mayo Clinic, United States
Title : Development of a novel multi-component vaccine to address the burden of otitis media in high-risk populations
Ayesha Zahid, Griffith University, Australia
Title : High seroprevalence of RSV antibodies in adults indicates potential undetected transmission and requires further public health assessment
Lara Isis Teodoro, Mayo Clinic, United States
Title : The role of immunity in the pathogenesis of SARS-COV-2 and in the protection generated by COVID-19 in different age groups
Ahmed Abdulazeez, BHRUT Trust, United Kingdom
Title : New biomarkers in leishmania major vaccine development
Negar Seyed, Pasteur Institute of Iran, Iran (Islamic Republic of)
Title : Tubercular disease in children: Optimizing treatment strategies through disease insights
Elena Chiappini, University of Florence, Italy
Title : Approaches towards developing and establishing a biomanufacturing research & development, and manufacturing industry in Zimbabwe: A review of the need, potential funding sources, policy development and implementation
Elliot Nyagumbo, Midlands State University, Zimbabwe
Title : Racial disparities in pediatric pneumonia in Brazil: The role of structural racism forging inequalities in acess to vaccines
Livia Daflon Silva, Federal University of State of Rio de Janeiro, Brazil
Title : Capillary electrophoresis for adjuvanted multivalent recombinant vaccine purity determination
Ashley Prout, Merck, United States