Life SciencesImmunologyOncologyCancer ImmunologyCellular ImmunologyImmunotherapyAntitumor T Cell ResponsesCancer ImmunotherapyCancer VaccinesCytokines In Tumor ImmunityDendritic Cell BiologyImmuno-oncology BiomarkersClinical Outcome MeasurementCytokine Biomarkers In CancerImmune Biomarkers In CancerNon-small Cell Lung Cancer ImmunotherapyPeripheral Blood Immune BiomarkersPeripheral Blood Lymphocyte AnalysisPhase Iii Clinical TrialsRandomized Clinical Trials
AIM: To investigate the quantitative and functional status of peripheral blood lymphocytes in patients with non-small cell lung cancer during DC-vaccine therapy and identify the most informative immunological parameters which are associated with clinical outcome. MATERIALS AND METHODS: The study was conducted within the framework of randomized phase III clinical trial of DC-vaccine efficacy in patients with non-small cell lung cancer. Quantitative composition of peripheral blood lymphocytes was determined by flow cytometry. Cytokines mRNA expression level was estimated using real-time RT-PCR. RESULTS: In our study the most pronounced changes in the immune system have been defined after fourth DC-vaccine injection. Immunologic features such as reduction the MIP-1α mRNA expression level, increasing the RANTES mRNA expression level and NK-cells count, retention CD4/CD8 ratio at physiological level were associated with favorable clinical outcome after DC-immunotherapy. CONCLUSIONS: Immunological markers established in our investigation can be used for estimation of DC-immunotherapy efficiency. The results of our research are very promising, but these data should be confirmed in further studies with a large cohort of patients.
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Evolution of end points for cancer immunotherapy trials
Axel Hoos · Annals of Oncology · 2012 · 101 citations
Life Sciences, Immunology, Oncology +14
MIP-1α and MIP-1β differentially mediate mucosal and systemic adaptive immunity
James W. Lillard, Udai P. Singh, Prosper N. Boyaka et al. · Blood · 2003 · 99 citations · Full text