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Sökning: L773:2162 4011 > (2015-2019) > Cancer vaccine base...

Cancer vaccine based on a combination of an infection-enhanced adenoviral vector and pro-inflammatory allogeneic DCs leads to sustained antigen-specific immune responses in three melanoma models

Fotaki, Grammatiki (författare)
Uppsala universitet,Science for Life Laboratory, SciLifeLab,Klinisk immunologi
Jin, Chuan, 1986- (författare)
Uppsala universitet,Klinisk immunologi,Science for Life Laboratory, SciLifeLab
Kerzeli, Iliana Kyriaki (författare)
Uppsala universitet,Klinisk immunologi,Science for Life Laboratory, SciLifeLab
visa fler...
Ramachandran, Mohanraj, 1988- (författare)
Uppsala universitet,Klinisk immunologi,Science for Life Laboratory, SciLifeLab
Martikainen, Minttu-Maria (författare)
Uppsala universitet,Institutionen för immunologi, genetik och patologi,Science for Life Laboratory, SciLifeLab
Karlsson-Parra, Alex (författare)
Uppsala universitet,Klinisk immunologi,Science for Life Laboratory, SciLifeLab,Immunicum AB, Gothenburg
Yu, Di, 1985- (författare)
Uppsala universitet,Klinisk immunologi,Science for Life Laboratory, SciLifeLab
Essand, Magnus (författare)
Uppsala universitet,Klinisk immunologi,Science for Life Laboratory, SciLifeLab
visa färre...
 (creator_code:org_t)
2018
2018
Engelska.
Ingår i: Oncoimmunology. - 2162-4011 .- 2162-402X. ; 7:3
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Autologous patient-derived dendritic cells (DCs) modified ex vivo to present tumor-associated antigens (TAAs) are frequently used as cancer vaccines. However, apart from the stringent logistics in producing DCs on a patient basis, accumulating evidence indicate that ex vivo engineered DCs are poor in migration and in fact do not directly present TAA epitopes to naïve T cells in vivo. Instead, it is proposed that bystander host DCs take up material from vaccine-DCs, migrate and subsequently initiate antitumor T-cell responses. We used mouse models to examine the possibility of using pro-inflammatory allogeneic DCs (alloDCs) to activate host DCs and enable them to promote antigen-specific T-cell immunity. We found that alloDCs were able to initiate host DC activation and migration to draining lymph node leading to T-cell activation. The pro-inflammatory milieu created by alloDCs also led to recruitment of NK cells and neutrophils at the site of injection. Vaccination with alloDCs combined with Ad5M(gp100), an infection-enhanced adenovirus encoding the human melanoma-associated antigen gp100 resulted in generation of CD8+ T cells with a T-cell receptor (TCR) specific for the gp10025-33 epitope (gp100-TCR+). Ad5M(gp100)-alloDC vaccination in combination with transfer of gp100-specific pmel-1 T cells resulted in prolonged survival of B16-F10 melanoma-bearing mice and altered the composition of the tumor microenvironment (TME). We hereby propose that alloDCs together with TAA- or neoepitope-encoding Ad5M can become an “off-the-shelf” cancer vaccine, which can reverse the TME-induced immunosuppression and induce host cellular anti-tumor immune responses in patients without the need of a time-consuming preparation step of autologous DCs.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Immunologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Immunology in the medical area (hsv//eng)

Nyckelord

adjuvants
Allogeneic dendritic cells
cell-based immunotherapy
tumor microenvironment
tumor-associated antigen

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

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