Abstract
Studies have shown that photodynamic therapy (PDT) causes or enhances an antitumor immune response. Moving from a mouse model in lung cancer to a translational approach, researchers are conducting an ongoing observational study to determine whether the immune response in patients with lung cancer treated with PDT is mediated by a T-cell phenotype, which may result in decreased tumor size and potentially improve survival. Preliminary findings focus on certain inflammatory cytokines that may be predictive of these T-cell phenotypes, such as interleukin (IL)-12, IL-4, T-regulatory cells, and T helper 17 cells. Correlation of the immunobiology of PDT associated with outcomes and surrogate markers may allow clinicians to predict improvement in patients treated with PDT and improve prognostic counseling. © JNCCN - Journal of the National Comprehensive Cancer Network.
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CITATION STYLE
Moffatt-Bruce, S. (2012). The immunobiology of photodynamic therapy: The potential for therapeutic intervention in lung cancer. JNCCN Journal of the National Comprehensive Cancer Network. Harborside Press. https://doi.org/10.6004/jnccn.2012.0169
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