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Sökning: onr:"swepub:oai:DiVA.org:uu-337075" > Enhanced stimulatio...

Enhanced stimulation of human tumor-specific T cells by dendritic cells matured in the presence of interferon-gamma and multiple toll-like receptor agonists

Lövgren, Tanja (författare)
Karolinska Institutet,Uppsala universitet,Klinisk immunologi,Karolinska Institute; Karolinska University Hospital
Sarhan, Dhifaf (författare)
Karolinska Institutet
Truxova, Iva (författare)
Karolinska Inst, Dept Oncol Pathol, Canc Ctr Karolinska, Stockholm, Sweden.
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Choudhary, Bhavesh (författare)
Karolinska Inst, Dept Oncol Pathol, Canc Ctr Karolinska, Stockholm, Sweden.
Maas, Roeltje (författare)
Karolinska Inst, Dept Oncol Pathol, Canc Ctr Karolinska, Stockholm, Sweden.
Melief, Jeroen (författare)
Karolinska Institutet
Nystrom, Maria (författare)
Karolinska Inst, Dept Oncol Pathol, Canc Ctr Karolinska, Stockholm, Sweden.
Edback, Ulrika (författare)
Karolinska Inst, Dept Oncol Pathol, Canc Ctr Karolinska, Stockholm, Sweden.
Vermeij, Renee (författare)
Karolinska Inst, Dept Oncol Pathol, Canc Ctr Karolinska, Stockholm, Sweden.
Scurti, Gina (författare)
Loyola Univ Chicago, Dept Surg, Maywood, IL USA.
Nishimura, Michael (författare)
Loyola Univ Chicago, Dept Surg, Maywood, IL USA.
Masucci, Giuseppe (författare)
Karolinska Institutet
Karlsson-Parra, Alex (författare)
Uppsala universitet,Klinisk immunologi
Lundqvist, Andreas (författare)
Karolinska Institutet
Adamson, Lars (författare)
Karolinska Institutet
Kiessling, Rolf (författare)
Karolinska Institutet
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 (creator_code:org_t)
2017-06-10
2017
Engelska.
Ingår i: Cancer Immunology and Immunotherapy. - : SPRINGER. - 0340-7004 .- 1432-0851. ; 66:10, s. 1333-1344
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Dendritic cell (DC) vaccines have been demonstrated to elicit immunological responses in numerous cancer immunotherapy trials. However, long-lasting clinical effects are infrequent. We therefore sought to establish a protocol to generate DC with greater immunostimulatory capacity. Immature DC were generated from healthy donor monocytes by culturing in the presence of IL-4 and GM-CSF and were further differentiated into mature DC by the addition of cocktails containing different cytokines and toll-like receptor (TLR) agonists. Overall, addition of IFN gamma and the TLR7/8 agonist R848 during maturation was essential for the production of high levels of IL-12p70 which was further augmented by adding the TLR3 agonist poly I:C. In addition, the DC matured with IFN gamma, R848, and poly I:C also induced upregulation of several other pro-inflammatory and Th1-skewing cytokines/chemokines, co-stimulatory receptors, and the chemokine receptor CCR7. For most cytokines and chemokines the production was even further potentiated by addition of the TLR4 agonist LPS. Concurrently, upregulation of the anti-inflammatory cytokine IL-10 was modest. Most importantly, DC matured with IFN gamma, R848, and poly I:C had the ability to activate IFN gamma production in allogeneic T cells and this was further enhanced by adding LPS to the cocktail. Furthermore, epitope-specific stimulation of TCR-transduced T cells by peptide- or whole tumor lysate-loaded DC was efficiently stimulated only by DC matured in the full maturation cocktail containing IFN gamma and the three TLR ligands R848, poly I:C, and LPS. We suggest that this cocktail is used for future clinical trials of anti-cancer DC vaccines.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

Cancer
Dendritic cell-vaccine
IFN gamma
R848
Poly I:C
LPS

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