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Addition of histamine to interleukin 2 treatment augments type 1 T-cell responses in patients with melanoma in vivo: immunologic results from a randomized clinical trial of interleukin 2 with or without histamine (MP 104)

Asemissen, Anne Marie (författare)
Scheibenbogen, Carmen (författare)
Letsch, Anne (författare)
visa fler...
Hellstrand, Kristoffer, 1956 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för laboratoriemedicin, Avdelningen för klinisk virologi,Institute of Laboratory Medicine, Dept of Clinical Virology
Bergh Thorén, Fredrik, 1976 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för laboratoriemedicin, Avdelningen för klinisk virologi,Institute of Laboratory Medicine, Dept of Clinical Virology
Gehlsen, Kurt (författare)
Schmittel, Alexander (författare)
Thiel, Eckhard (författare)
Keilholz, Ulrich (författare)
visa färre...
 (creator_code:org_t)
2005
2005
Engelska.
Ingår i: Clin Cancer Res. - 1078-0432. ; 11:1, s. 290-7
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • PURPOSE: Preclinical investigations suggest that histamine dihydrochloride (HDC) protects T cells and natural killer cells from inhibition by monocyte-derived reactive oxygen metabolites and synergizes with interleukin (IL) 2 in inducing T-cell activation. Here, we investigate whether this mechanism is operational in patients with melanoma treated with HDC as an adjunct to IL-2. EXPERIMENTAL DESIGN: Melanoma patients having liver metastases were treated with IL-2 with or without HDC within a randomized, multicenter, phase III trial. The effect of HDC on type 1 and type 2 T-cell cytokine production was investigated in peripheral blood samples from 19 patients with the use of intracellular cytokine flow cytometry. Melanoma-specific T-cell responses were analyzed in eight HLA-A2-positive patients. RESULTS: Frequencies of CD3+ T cells producing IFN-gamma (type 1 T cells) in response to phorbol myristate acetate/ionomycin increased (median, 1.8-fold) in patients receiving IL-2 plus HDC but not in those receiving IL-2 alone (P < 0.01 for comparison between arms). In contrast, the number of IL-13-producing type 2 T cells that increased in patients after treatment with IL-2 was not modulated by HDC. Melanoma- and tyrosinase-specific IFN-gamma and IL-13-producing T cells were detected in two of four HLA-A2-positive patients with melanoma following treatment with HDC + IL-2. CONCLUSIONS: Treatment of patients with stage IV melanoma with HDC in combination with IL-2 increases type 1 T-cell responses and may promote induction of melanoma-specific T cells. These effects are of relevance for tumor immunotherapy and provide a potential mechanism for the clinical efficacy of HDC added to IL-2.

Nyckelord

Antigens
CD3/biosynthesis
Cell Line
Tumor
Chromatography
High Pressure Liquid
Cytokines/biosynthesis
Flow Cytometry
Histamine/ therapeutic use
Histocompatibility Testing
Humans
Interferon Type II/metabolism
Interleukin-13/metabolism
Interleukin-2/metabolism/ therapeutic use
K562 Cells
Leukocytes
Mononuclear/metabolism
Liver Neoplasms/ drug therapy/secondary
Lymphocyte Activation
Melanoma/ drug therapy/metabolism
Monocytes/metabolism
Neoplasm Metastasis
Peptides/chemistry
Reactive Oxygen Species
T-Lymphocytes/immunology/ metabolism
Time Factors
Treatment Outcome

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