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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, 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.

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