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IL-12: a promising adjuvant for cancer vaccination
- Source :
- Scopus-Elsevier, Cancer Immunology Immunotherapy, 52, 133-144. Springer Science+Business Media
- Publication Year :
- 2003
- Publisher :
- Springer Science and Business Media LLC, 2003.
-
Abstract
- The clinical development of interleukin 12 (IL-12) as a single agent for systemic cancer therapy has been hindered by its significant toxicity and disappointing anti-tumor effects. The lack of efficacy was accompanied by, and probably related to, the declining biological effects of IL-12 in the course of repeated administrations at doses approaching the maximum tolerated dose (MTD). Nevertheless, IL-12 remains a very promising immunotherapeutic agent because recent cancer vaccination studies in animal models and humans have demonstrated its powerful adjuvant properties. Therefore, IL-12 may re-enter the arena of cancer therapy. Here, we review the immune modulating characteristics of IL-12 considered responsible for the adjuvant effects, as well as the results of animal and human cancer vaccination studies with IL-12 applied as an adjuvant. In addition, we discuss how studies with systemic IL-12 in cancer patients, and several other lines of evidence, indicate that IL-12 may exert optimal adjuvant effects only at low dose levels. Therefore, the MTD may not constitute the maximum effective dose of IL-12 for adjuvant application.
- Subjects :
- Oncology
Cancer Research
medicine.medical_specialty
Time Factors
Maximum Tolerated Dose
T-Lymphocytes
medicine.medical_treatment
Immunology
Down-Regulation
Cancer Vaccines
Immune system
SDG 3 - Good Health and Well-being
Neoplasms
Internal medicine
medicine
Animals
Humans
Immunology and Allergy
Inflammation
Chemotherapy
Dose-Response Relationship, Drug
business.industry
Cancer
Dendritic Cells
Immunotherapy
medicine.disease
Interleukin-12
Effective dose (pharmacology)
Recombinant Proteins
Killer Cells, Natural
Vaccination
Chemotherapy, Adjuvant
Toxicity
business
Adjuvant
Subjects
Details
- ISSN :
- 14320851 and 03407004
- Volume :
- 52
- Database :
- OpenAIRE
- Journal :
- Cancer Immunology, Immunotherapy
- Accession number :
- edsair.doi.dedup.....4ea27922a414954adcb52d454e183d51
- Full Text :
- https://doi.org/10.1007/s00262-002-0356-5