Frontiers in Immunology (Dec 2022)

Innate immune function during antineoplastic treatment is associated with 12-months survival in non-small cell lung cancer

  • Heidi Ryssel,
  • Heidi Ryssel,
  • Heidi Ryssel,
  • Kristian Egebjerg,
  • Susanne Dam Nielsen,
  • Susanne Dam Nielsen,
  • Jens Lundgren,
  • Jens Lundgren,
  • Mette Pøhl,
  • Seppo W. Langer,
  • Seppo W. Langer,
  • Andreas Kjaer,
  • Andreas Kjaer,
  • Andreas Kjaer,
  • Sisse Rye Ostrowski,
  • Sisse Rye Ostrowski,
  • Barbara Malene Fischer,
  • Barbara Malene Fischer,
  • Barbara Malene Fischer

DOI
https://doi.org/10.3389/fimmu.2022.1024224
Journal volume & issue
Vol. 13

Abstract

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IntroductionThe immune system has proven to be a key player in the progression as well as containment of cancer with new treatment strategies based on immunotherapy targeting this interaction. Assessing immune function could reveal critical information about the immune response to therapeutic interventions, revealing predictive biomarkers for tailored care and precision medicine.MethodsWe investigated immune function in 37 patients with inoperable non-small cell lung cancer (NSCLC) undergoing treatment with PD-L1 immune checkpoint inhibitor (ICI), chemotherapy (CT) or chemo-radiotherapy (CT/RT). Blood samples before (day 0) and during therapy (day 7, 21 and 80) were investigated by a standardized immunoassay, TruCulture®.ResultsOutcomes revealed a developing innate immune response induced by both immunotherapy and chemotherapy. NSCLC-patients displayed evidence of chronic innate immune activation and exhaustion prior to treatment. This pattern was particularly pronounced during treatment in patients dying within 12-months follow-up. Compared to treatment with CT, ICI demonstrated a higher ex vivo-stimulated release of proinflammatory cytokines.DiscussionThese preliminary findings may pave the way for tailored treatment and immune-monitoring.

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