2021
DOI: 10.1007/s11912-021-01130-x
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A New Generation of Vaccines in the Age of Immunotherapy

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Cited by 14 publications
(6 citation statements)
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“…Additionally, the high cost of biologics, and particularly patient-specific cellular therapeutics must also be considered. There are a broad range of potential modalities that can be locally delivered, and within these modalities a variety of agents with similar targets or mechanisms of action, with many more in pre-clinical or early phase clinical trials (24,26,27). The varied formulations and compatibilities of potentially useful therapeutics must be considered if they are to be coadministered through indwelling catheters.…”
Section: Potential Drawbacks To Intra-cavitary Therapeuticsmentioning
confidence: 99%
“…Additionally, the high cost of biologics, and particularly patient-specific cellular therapeutics must also be considered. There are a broad range of potential modalities that can be locally delivered, and within these modalities a variety of agents with similar targets or mechanisms of action, with many more in pre-clinical or early phase clinical trials (24,26,27). The varied formulations and compatibilities of potentially useful therapeutics must be considered if they are to be coadministered through indwelling catheters.…”
Section: Potential Drawbacks To Intra-cavitary Therapeuticsmentioning
confidence: 99%
“…Also, the human papilloma virus E6/E7 antigen for Hpv associated tumors, the carcinoembryonic antigen (CEA) for colorectal and pancreatic cancers, and many more. [ 62 ] Non‐replicative Adenovirus vectors can have multiple applications in cancer therapy. That is feasible by delivering suicide genes, [ 63 ] by transferring pro‐drug‐converting enzymes to target tissues, [ 64 ] and by delivering immune‐regulatory genes to stimulate anti‐tumor response.…”
Section: Genome Engineering Technologies For Cancer Treatmentmentioning
confidence: 99%
“…The DNA vaccine pVAX1-MAGEA3-sPD1 is based on the MAGE-A3 antigen, enhanced with soluble PD-1 (sPD1). A series of DNA plasmids encoding MAGE-A3, and the extracellular domain of murine PD-1 (sPD1) was developed and showed immunogenicity and tumor growth inhibition in mice [ 65 ].…”
Section: Platforms Developed For Vaccine Therapymentioning
confidence: 99%