In addition to altered T cells subpopulation (significantly more Th1 and Th17 cells), increased proinflammatory cytokines such as IFN-, IL2, IL6, TNF-, MCP-1, and MIP-1 also point to the role of an autoimmune reaction in PD pathogenesis [210, 211]
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Over the past years, our comprehensive knowledge about the molecular biology of NSCLC has been rapidly enriching, which has promoted the discovery of driver genes in NSCLC and directed FDA-approved targeted therapies
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