CCL5 as an adjuvant for cancer immunotherapy
- PMID: 20233026
- DOI: 10.1517/14712591003657128
CCL5 as an adjuvant for cancer immunotherapy
Abstract
Importance of the field: To date cancer immunotherapy has only achieved limited clinical efficacy, thus more efficient immunotherapeutic approaches need to be explored. The CC chemokine CCL5 plays a role in chemoattraction and activation of immune cells implying its potential clinical application as an adjuvant for boosting anti-tumor immunity, although an effect on carcinogenesis and tumor cell invasiveness is also reported to be associated with CCL5.
Areas covered in this review: Recent progress in exploiting CCL5 as an adjuvant for cancer prevention and treatment, and updated understanding on how CCL5 is involved in tumor invasiveness and carcinogenesis.
What the reader will gain: CCL5 represents a natural adjuvant for enhancing anti-tumor immune responses. However, animal experiments and clinical reports suggest that CCL5 plays a role in carcinogenesis and invasiveness of tumor cells. Therefore, a CCL5-based cancer therapeutic approach needs to avoid the CCL5-associated potential detrimental effects.
Take home message: CCL5 has a pre-eminent role in chemotaxis and activation of a wide spectrum of immune cells. CCL5 functions as an adjuvant to boost anti-tumor immunity by diverse protocols such as co-immunization of recombinant CCL5 protein with tumor-associated antigen, vaccination with CCL-5-expressing tumor cells, or viral vector delivery of CCL5 cDNA into growing tumor. CCL5 may also promote tumor cell survival, proliferation and invasion by different mechanisms.
Similar articles
-
Cancer-germline antigen vaccines and epigenetic enhancers: future strategies for cancer treatment.Expert Opin Biol Ther. 2010 Jul;10(7):1061-75. doi: 10.1517/14712598.2010.485188. Expert Opin Biol Ther. 2010. PMID: 20420535 Review.
-
Vaccines as early therapeutic interventions for cancer therapy: neutralising the immunosuppressive tumour environment and increasing T cell avidity may lead to improved responses.Expert Opin Biol Ther. 2010 May;10(5):735-48. doi: 10.1517/14712591003769790. Expert Opin Biol Ther. 2010. PMID: 20384522 Review.
-
Engineered CCR5 superagonist chemokine as adjuvant in anti-tumor DNA vaccination.Vaccine. 2008 Jun 19;26(26):3252-60. doi: 10.1016/j.vaccine.2008.04.003. Epub 2008 Apr 24. Vaccine. 2008. PMID: 18479788
-
Combinational adenovirus-mediated gene therapy and dendritic cell vaccine in combating well-established tumors.Cell Res. 2006 Mar;16(3):241-59. doi: 10.1038/sj.cr.7310032. Cell Res. 2006. PMID: 16541123 Review.
-
Antitumor vaccination: where we stand.Haematologica. 2000 Nov;85(11):1172-206. Haematologica. 2000. PMID: 11074658 Review.
Cited by
-
ATM Mutations Benefit Bladder Cancer Patients Treated With Immune Checkpoint Inhibitors by Acting on the Tumor Immune Microenvironment.Front Genet. 2020 Aug 14;11:933. doi: 10.3389/fgene.2020.00933. eCollection 2020. Front Genet. 2020. PMID: 32922441 Free PMC article.
-
CC Chemokines in a Tumor: A Review of Pro-Cancer and Anti-Cancer Properties of Receptors CCR5, CCR6, CCR7, CCR8, CCR9, and CCR10 Ligands.Int J Mol Sci. 2020 Oct 15;21(20):7619. doi: 10.3390/ijms21207619. Int J Mol Sci. 2020. PMID: 33076281 Free PMC article. Review.
-
Transfer of Cellular Content from the Allogeneic Cell-Based Cancer Vaccine DCP-001 to Host Dendritic Cells Hinges on Phosphatidylserine and Is Enhanced by CD47 Blockade.Cells. 2021 Nov 19;10(11):3233. doi: 10.3390/cells10113233. Cells. 2021. PMID: 34831455 Free PMC article.
-
Naming the Barriers between Anti-CCR5 Therapy, Breast Cancer and Its Microenvironment.Int J Mol Sci. 2022 Nov 16;23(22):14159. doi: 10.3390/ijms232214159. Int J Mol Sci. 2022. PMID: 36430633 Free PMC article. Review.
-
Prognostic and Predictive Potential of CCL5 Expression in Muscle-Invasive Bladder Cancer Patients.Int J Mol Sci. 2024 Jun 7;25(12):6325. doi: 10.3390/ijms25126325. Int J Mol Sci. 2024. PMID: 38928033 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials