Immune evasion pathways and the design of dendritic cell-based cancer vaccines.
Publication
, Journal Article
Hanks, BA
Published in: Discov Med
February 2016
Emerging data is suggesting that the process of dendritic cell (DC) tolerization is an important step in tumorigenesis. Our understanding of the networks within the tumor microenvironment that functionally tolerize DC function is evolving while methods for genetically manipulating DC populations in situ continue to develop. A more intimate understanding of the paracrine signaling pathways which mediate immune evasion by subverting DC function promises to provide novel strategies for improving the clinical efficacy of DC-based cancer vaccines. This will likely require a better understanding of both the antigen expression profile and the immune evasion network of the tumor and its associated stromal tissues.
Duke Scholars
Published In
Discov Med
EISSN
1944-7930
Publication Date
February 2016
Volume
21
Issue
114
Start / End Page
135 / 142
Location
United States
Related Subject Headings
- Neoplasms
- Models, Biological
- Immune Evasion
- Humans
- Dendritic Cells
- Cancer Vaccines
Citation
APA
Chicago
ICMJE
MLA
NLM
Hanks, B. A. (2016). Immune evasion pathways and the design of dendritic cell-based cancer vaccines. Discov Med, 21(114), 135–142.
Hanks, Brent A. “Immune evasion pathways and the design of dendritic cell-based cancer vaccines.” Discov Med 21, no. 114 (February 2016): 135–42.
Hanks BA. Immune evasion pathways and the design of dendritic cell-based cancer vaccines. Discov Med. 2016 Feb;21(114):135–42.
Hanks, Brent A. “Immune evasion pathways and the design of dendritic cell-based cancer vaccines.” Discov Med, vol. 21, no. 114, Feb. 2016, pp. 135–42.
Hanks BA. Immune evasion pathways and the design of dendritic cell-based cancer vaccines. Discov Med. 2016 Feb;21(114):135–142.
Published In
Discov Med
EISSN
1944-7930
Publication Date
February 2016
Volume
21
Issue
114
Start / End Page
135 / 142
Location
United States
Related Subject Headings
- Neoplasms
- Models, Biological
- Immune Evasion
- Humans
- Dendritic Cells
- Cancer Vaccines