Evidence map›Paper›PMID 41550947›Full record

ReviewFrontiers in immunology2025

IL-7: a potential next-generation adjuvant for immune cell therapies.

Richard S Hotchkiss, John F DiPersio, Cassian Yee, Russell K Pachynski, Marcel R M Van Den Brink

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. 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

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

5 authors.

Richard S HotchkissDepartment of Anesthesiology, Medicine, and Surgery, Washington University School of Medicine, St. Louis, MO, United States.
John F DiPersioDepartment of Medicine, Washington University School of Medicine, St Louis, MO, United States.
Cassian YeeDepartment of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Russell K PachynskiDepartment of Medicine, Washington University School of Medicine, St Louis, MO, United States.
Marcel R M Van Den BrinkCity of Hope Los Angeles and National Medical Center, Duarte, CA, United States.

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
Targeting the Bone Marrow Microenvironment In Acute Lymphocytic LeukemiaP50CA171963 · NCI · WASHINGTON UNIVERSITY · PI Daniel C Link · 2013 to 2026
$31.6M
Thymic and Peripheral Aspects of T Cell Aging and RejuvenationP01AG052359 · NIA · UNIVERSITY OF ARIZONA · PI Bonnie LaFleur · 2017 to 2026
$23.5M
Cancer Immunotherapy Trials Network Central Operations and Statistical CenterUM1CA154967 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI DAVIDSON, NANCY ELLEN · 2017 to 2022
$20.7M
Cancer Immunotherapy Trials Network Central Operations and Statistical CenterU01CA154967 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI CHEEVER, MARTIN ALEXANDER · 2010 to 2017
$16.8M
Optimizing Hematopoietic Stem Cell Transplantation For The Treatment Of Hematological MalignanciesR35CA210084 · NCI · WASHINGTON UNIVERSITY · PI John F. Dipersio · 2017 to 2026
$7.8M
Enhancing Innate and Adaptive Immunity to Improve Sepsis SurvivalR35GM126928 · NIGMS · WASHINGTON UNIVERSITY · PI Richard Samuel Hotchkiss · 2018 to 2026
$4.7M
NCI NIH HHS P30 CA015704NCI NIH HHS P50 CA171963NCI NIH HHS R35 CA210084NCI NIH HHS U01 CA154967NCI NIH HHS UM1 CA154967NIA NIH HHS P01 AG052359NIGMS NIH HHS R35 GM126928
6 · The paper itself

Abstract

Cell-based immune therapies ranging from CAR-T cells to tumor infiltrating lymphocytes (TILs) and endogenous T-cell products, have produced unprecedented clinical responses in hematologic malignancies and are currently under active investigation for solid tumors. Nevertheless, several key challenges continue to limit the durability and breadth of clinical benefit. IL-7 is a pleiotropic cytokine that increases both the number and function of lymphocytes. Although not yet clinically approved, IL-7 has been used in over 620 adult and pediatric patients for a variety of reasons including, for example, to hasten bone marrow recovery after allogenic stem cell transplantation, to reverse lymphopenia due to HIV and idiopathic etiologies, to treat patients with various malignancies, and to boost vaccine responses. IL-7 is generally well-tolerated and effective in producing a

Indexed as

Adjuvants, ImmunologicImmunotherapy, AdoptiveInterleukin-7AnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell MovementCytokine Release SyndromeEpitopes, T-LymphocyteHumansNeoplasmsReceptors, Antigen, T-CellT-Cell ExhaustionAdjuvants, ImmunologicEpitopes, T-LymphocyteInterleukin-7Receptors, Antigen, T-Cellcancer therapycar-tchimeric antigen receptor T-cell immunotherapyIL-7immunotherapyTIL (tumor infiltrating lymphocytes)

Identifiers

PMID41550947
PMCPMC12808468

What Socratic holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.