ArticleScientific reports2025
NT-I7, a novel long-acting interleukin-7, promotes anti-PD-1 efficacy in an autologous humanized melanoma model.
Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.
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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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Who cites it
2 citing papers in PubMed.
- Therapeutic Resistance in Melanoma: Molecular Mechanisms and Emerging Pharmaceutical Strategies.Pharmaceuticals (Basel, Switzerland) · 2026Review
- Systemic treatment for a young patient with stage IV melanoma: A case report.Oncology letters · 2026Article
Corrections and comments
- Erratum issued
Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Despite recent advancements in immunotherapy, most cancer patients still struggle to achieve sustained benefits, highlighting the need for new treatment strategies. In the past, lack of available models to assess immunotherapeutic combinations hampered development. In this new study, we utilized a novel all-autologous humanized melanoma mouse model to assess the efficacy of NT-I7 (human-reagent grade, efineptakin alfa), a long-acting human IL-7. Given that NT-I7 has been shown to enhance T cell proliferation and survival in both humans and mice, we hypothesized that NT-I7 would improve the engraftment of patient immune cells and the effectiveness of anti-PD-1 therapy in our humanized melanoma model, which was reported to accurately mimic actual clinical outcome, providing more precise assessment of clinical efficacy and relevance. Our findings indicate that NT-I7 significantly enhances T cell engraftment. We discovered a synergistic effect between NT-I7 and anti-PD-1 (Pembrolizumab) that notably augments immunotherapeutic efficacy through the expansion of T
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