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Abstract <p>Despite the success of immune checkpoint inhibitor (ICI) therapy, the problem of resistance makes the search for early response biomarkers critical. This study investigates the potential of monitoring autofluorescence of the NAD(P)H coenzyme in the T-lymphocyte subsets to assess early treatment efficacy. The ability of NAD(P)H FLIM to reflect sensitivity to ICI therapy was tested on the B16F0 mouse melanoma model and validated in the pilot study of the samples from melanoma patients during treatment. The&#xa0;mean fluorescence lifetime of NAD(P)H, τ<sub>m</sub>, showed the best correlation with subsequent clinical response and was identified as a sensitive marker of early lymphocyte activation following anti-PD-1 or combination therapy. In the patients who responded to treatment, an increase in τ<sub>m</sub> was observed, associated with metabolic reprogramming toward enhanced biosynthetic and bioenergetic pathways, as confirmed by the standard molecular analysis. Thus, the proposed approach represents a promising solution for personalized monitoring of early immunotherapy efficacy.</p>

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Monitoring Early Efficacy of the Checkpoint Immunotherapy Based on Fluorescence Lifetime Imaging Microscopy of the Patient-Derived Lymphocyte Subsets

  • 期刊论文

  • 发表日期：

    2026年7月31日

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  • Diana V. Yuzhakova,
  • Anastasia I. Kononova,
  • Anna V. Izosimova,
  • Margarita M. Sazhina,
  • Ilya D. Shchechkin,
  • Artem M. Mozherov,
  • Pavel A. Bureev,
  • Dmitry A. Kuzmin,
  • Alena I. Gavrina,
  • Irina S. Shumskaya,
  • Sergey V. Gamayunov,
  • Marina V. Shirmanova

摘要

Abstract

Despite the success of immune checkpoint inhibitor (ICI) therapy, the problem of resistance makes the search for early response biomarkers critical. This study investigates the potential of monitoring autofluorescence of the NAD(P)H coenzyme in the T-lymphocyte subsets to assess early treatment efficacy. The ability of NAD(P)H FLIM to reflect sensitivity to ICI therapy was tested on the B16F0 mouse melanoma model and validated in the pilot study of the samples from melanoma patients during treatment. The mean fluorescence lifetime of NAD(P)H, τm, showed the best correlation with subsequent clinical response and was identified as a sensitive marker of early lymphocyte activation following anti-PD-1 or combination therapy. In the patients who responded to treatment, an increase in τm was observed, associated with metabolic reprogramming toward enhanced biosynthetic and bioenergetic pathways, as confirmed by the standard molecular analysis. Thus, the proposed approach represents a promising solution for personalized monitoring of early immunotherapy efficacy.