ArticleiScience2026
Ciclopirox reprograms effector responses and modulates Notch1 activation in activated human T cells.
Article in iScience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
11 authors.
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Abstract
Ciclopirox (CPX) is an FDA approved, broad-spectrum antifungal agent. The prodrug of CPX, fosciclopirox, was evaluated for safety and preliminary efficacy in patients with advanced solid tumors, including bladder cancer, and was found to inhibit cell proliferation, the γ-secretase complex, and Notch signaling. However, the effects of CPX on human T cell function have remained undefined. In this study, we investigated the impact of CPX on primary human T cell activation and their effector responses. CPX enhanced early activation markers and IL-2 production; yet, suppressed activation-driven expansion, altered cell cycle progression, and reduced effector functions, including IFN-γ production and cytotoxic granule expression,
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.