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Int Immunopharmacol ; 51: 57-65, 2017 Oct.
Article in English | MEDLINE | ID: mdl-28802902

ABSTRACT

Pseudomonas aeruginosa-mannose sensitive hemagglutinin (PA-MSHA) injection serves as immunological adjuvant in clinical treatment of cancer patients. In present study, we investigated whether PA-MSHA injection enhanced the anti-tumor efficacy of CIK cells. Twenty patients with malignancies were enrolled in this retrospective clinical trial. They were divided into two groups: 10 patients received PA-MSHA treated CIK cells transfusion combined with chemotherapy, and other patients accepted CIK cells and chemotherapy. The efficacy of PA-MSHA treated CIK cells was also observed in vitro and in vivo. With PA-MSHA treatment CIK cells exhibited enhanced proliferation but decreased expression of inhibitory cell surface markers such as Tim-3 and PD-1. Particularly in CIK cells, PA-MSHA promoted the extrusion of pro-inflammatory cytokines like IFN-γ. Of 10 patients with PA-MSHA treated CIK cells and chemotherapy, two patients reached partial remissions, 7 patients had stable disease and the other one had progressive disease. Some of these patients experienced fever after cell infusion. 8 patients with CIK cells showed stable disease and 2 patients had progressive disease. Moreover, the side effects were small in patients with CIK treatment. Our data indicated that PA-MSHA improves the functions of CIK cells and shed new light on developing more potent therapeutic approaches for malignancies.


Subject(s)
Cancer Vaccines/immunology , Colonic Neoplasms/therapy , Cytokine-Induced Killer Cells/immunology , Fimbriae Proteins/administration & dosage , Immunotherapy, Adoptive/methods , Lung Neoplasms/therapy , Ovarian Neoplasms/therapy , Pseudomonas aeruginosa/immunology , Adult , Aged , Cells, Cultured , Colonic Neoplasms/immunology , Combined Modality Therapy , Cytokine-Induced Killer Cells/transplantation , Drug Therapy , Female , Humans , Interferon-gamma/metabolism , Lung Neoplasms/immunology , Male , Middle Aged , Ovarian Neoplasms/immunology , Remission Induction , Retrospective Studies
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