Evidence map›Paper›PMID 41168273›Full record

ArticleScientific reports2025

NT-I7, a novel long-acting interleukin-7, promotes anti-PD-1 efficacy in an autologous humanized melanoma model.

Yee Peng Phoon, Alexandra A Wolfarth, Pauline Funchain, Jennifer S Ko, Donghoon Choi, Eliska Dedkova, Daniela Duarte Bateman, Jessica Corvin, Jan J Melenhorst, Brian R Gastman

Erratum issuedAbstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Yee Peng PhoonCenter for Immunotherapy & Precision Immuno-Oncology, Cleveland Clinic, 9500 Euclid Ave, Cleveland, OH, 44195, USA.
Alexandra A WolfarthNeoImmuneTech, Inc., Rockville, MD, 20850, USA.
Pauline FunchainStanford Cancer Institute, Stanford, CA, USA.
Jennifer S KoAnatomic Pathology, Cleveland Clinic, Cleveland, OH, 44195, USA.
Donghoon ChoiNeoImmuneTech, Inc., Rockville, MD, 20850, USA.
Eliska DedkovaCenter for Immunotherapy & Precision Immuno-Oncology, Cleveland Clinic, 9500 Euclid Ave, Cleveland, OH, 44195, USA.
Daniela Duarte BatemanCenter for Immunotherapy & Precision Immuno-Oncology, Cleveland Clinic, 9500 Euclid Ave, Cleveland, OH, 44195, USA.
Jessica CorvinCenter for Immunotherapy & Precision Immuno-Oncology, Cleveland Clinic, 9500 Euclid Ave, Cleveland, OH, 44195, USA.
Jan J MelenhorstCenter for Immunotherapy & Precision Immuno-Oncology, Cleveland Clinic, 9500 Euclid Ave, Cleveland, OH, 44195, USA. melenhj@ccf.org.
Brian R GastmanCenter for Immunotherapy & Precision Immuno-Oncology, Cleveland Clinic, 9500 Euclid Ave, Cleveland, OH, 44195, USA. brian.gastman@iovance.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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

Indexed as

Immune Checkpoint InhibitorsInterleukin-7MelanomaProgrammed Cell Death 1 ReceptorAnimalsAntibodies, Monoclonal, HumanizedCell Line, TumorDisease Models, AnimalFemaleHumansImmunotherapyMiceT-LymphocytesXenograft Model Antitumor AssaysAntibodies, Monoclonal, HumanizedIL7 protein, humanImmune Checkpoint InhibitorsInterleukin-7PDCD1 protein, humanpembrolizumabProgrammed Cell Death 1 ReceptorAutologous humanized melanoma mouse modelEfineptakin alfaIL-7ImmunotherapyMelanomaNT-I7rhIL-7-hyFc

Identifiers

PMID41168273
PMCPMC12575847

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Registered trials

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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 OpenQuestion graph.