Evidence map›Paper›PMID 35031547›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2022

Long-Acting Recombinant Human Interleukin-7, NT-I7, Increases Cytotoxic CD8 T Cells and Enhances Survival in Mouse Glioma Models.

Jian L Campian, Subhajit Ghosh, Vaishali Kapoor, Ran Yan, Sukrutha Thotala, Arijita Jash, Tong Hu, Anita Mahadevan, Kasem Rifai, Logan Page and 7 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03687957 (Effect of rhIL-7-hyFc on Increasing Lymphocyte Counts in Patients With Newly Diagnosed Non-severe Lymphopenic Gliomas Following Radiation and Temozolomide), which is not on this map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 4% of its field
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.

NCT03687957 phase1 / phase2active not recruitingnot on this map

Effect of rhIL-7-hyFc on Increasing Lymphocyte Counts in Patients With Newly Diagnosed Non-severe Lymphopenic Gliomas Following Radiation and Temozolomide

TypeinterventionalSponsorWashington University School of MedicineRan2019 to 2028Enrolled42ConditionsGliomaArmsrhIL-7-hyFc, Placebo, Temozolomide, Radiation therapy
3 · Its place in the literature

Who cites it

53 citing papers in PubMed, 1 synthesis or guideline pooled it, 60 citations in OpenAlex.

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  7. CD8Science China. Life sciences · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 2 institutions in 1 country.

Jian L Campian *Department of Medicine, Division of Oncology, Washington University in St. Louis, St. Louis, Missouri.
Subhajit Ghosh *Department of Radiation Oncology, School of Medicine, Washington University in St. Louis, St. Louis, Missouri.
Vaishali KapoorDepartment of Radiation Oncology, School of Medicine, Washington University in St. Louis, St. Louis, Missouri.ORCID 0000-0002-7581-1487
Ran YanDepartment of Medicine, Division of Oncology, Washington University in St. Louis, St. Louis, Missouri.
Sukrutha Thotala *Department of Radiation Oncology, School of Medicine, Washington University in St. Louis, St. Louis, Missouri.
Arijita JashDepartment of Medicine, Division of Oncology, Washington University in St. Louis, St. Louis, Missouri.
Tong HuDepartment of Medicine, Division of Oncology, Washington University in St. Louis, St. Louis, Missouri.
Anita MahadevanDepartment of Radiation Oncology, School of Medicine, Washington University in St. Louis, St. Louis, Missouri.
Kasem RifaiDepartment of Radiation Oncology, School of Medicine, Washington University in St. Louis, St. Louis, Missouri.ORCID 0000-0002-4882-6018
Logan PageDepartment of Radiation Oncology, School of Medicine, Washington University in St. Louis, St. Louis, Missouri.ORCID 0000-0003-2507-5263
Byung Ha LeeNeoImmuneTech, Inc., Rockville, Maryland.
Sara Ferrando-MartinezNeoImmuneTech, Inc., Rockville, Maryland.
Alexandra A WolfarthNeoImmuneTech, Inc., Rockville, Maryland.ORCID 0000-0001-7902-8935
Se Hwan YangNeoImmuneTech, Inc., Rockville, Maryland.
Dennis HallahanDepartment of Medicine, Division of Oncology, Washington University in St. Louis, St. Louis, Missouri.
Milan G Chheda *Department of Medicine, Division of Oncology, Washington University in St. Louis, St. Louis, Missouri.
Dinesh ThotalaDepartment of Radiation Oncology, School of Medicine, Washington University in St. Louis, St. Louis, Missouri.ORCID 0000-0001-5355-6406
Washington University in St. Louis · USOncoImmune (United States) · US

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
Leveraging Zika virus and the immune system to treat glioblastomaR01NS117149 · NINDS · WASHINGTON UNIVERSITY · PI CHHEDA, MILAN GIRISH · 2021 to 2025
$2.1M
Understanding how ZFHX4 drives the glioblastoma tumor propagating cell stateR01NS107833 · NINDS · WASHINGTON UNIVERSITY · PI CHHEDA, MILAN GIRISH · 2018 to 2022
$1.7M
NCI NIH HHS P30 CA091842NIH HHS R01 NS117149NINDS NIH HHS R01 NS107833NINDS NIH HHS R01 NS117149
6 · The paper itself

Abstract

purposePatients with glioblastoma (GBM) are treated with radiotherapy (RT) and temozolomide (TMZ). These treatments may cause prolonged systemic lymphopenia, which itself is associated with poor outcomes. NT-I7 is a long-acting IL7 that expands CD4 and CD8 T-cell numbers in humans and mice. We tested whether NT-I7 prevents systemic lymphopenia and improves survival in mouse models of GBM. EXPERIMENTAL

designC57BL/6 mice bearing intracranial tumors (GL261 or CT2A) were treated with RT (1.8 Gy/day × 5 days), TMZ (33 mg/kg/day × 5 days), and/or NT-I7 (10 mg/kg on the final day of RT). We followed the mice for survival while serially analyzing levels of circulating T lymphocytes. We assessed regulatory T cells (Treg) and cytotoxic T lymphocytes in the tumor microenvironment, cervical lymph nodes, spleen, and thymus, and hematopoietic stem and progenitor cells in the bone marrow.

resultsGBM tumor-bearing mice treated with RT+NT-I7 increased T lymphocytes in the lymph nodes, thymus, and spleen, enhanced IFNγ production, and decreased Tregs in the tumor which was associated with a significant increase in survival. NT-I7 also enhanced central memory and effector memory CD8 T cells in lymphoid organs and tumor. Depleting CD8 T cells abrogated the effects of NT-I7. Furthermore, NT-I7 treatment decreased progenitor cells in the bone marrow.

conclusionsIn orthotopic glioma-bearing mice, NT-I7 mitigates RT-related lymphopenia, increases cytotoxic CD8 T lymphocytes systemically and in the tumor, and improves survival. A phase I/II trial to evaluate NT-I7 in patients with high-grade gliomas is ongoing (NCT03687957).

Indexed as

Brain NeoplasmsGlioblastomaGliomaLymphopeniaAnimalsCD8-Positive T-LymphocytesCell Line, TumorClinical Trials, Phase I as TopicClinical Trials, Phase II as TopicDisease Models, AnimalHumansImmunologic FactorsInterleukin-7MiceMice, Inbred C57BLRecombinant Fusion Proteinsefineptakin alfaImmunologic FactorsInterleukin-7Recombinant Fusion ProteinsTemozolomide

Identifiers

PMID35031547
PMCPMC13020687
OpenAlexW4205890454

What OpenQuestion holds

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Registered trials

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.