Evidence map›Paper›PMID 29443657›Full record

ReviewJournal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research2018

IL-2 and Beyond in Cancer Immunotherapy.

John M Wrangle, Alicia Patterson, C Bryce Johnson, Daniel J Neitzke, Shikhar Mehrotra, Chadrick E Denlinger, Chrystal M Paulos, Zihai Li, David J Cole, Mark P Rubinstein

Open access · greenAbstract readReview
In one paragraph

Review in Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 5% 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.

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

74 citing papers in PubMed, 1 synthesis or guideline pooled it, 126 citations in OpenAlex.

  1. Pooled it
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  9. IL-15: from discovery to FDA approval.Journal of hematology & oncology · 2025
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14 more citing papers are in PubMed but not listed here.

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

10 authors at 1 institution in 1 country.

John M Wrangle1 Department of Medicine, Medical University of South Carolina , Charleston, South Carolina.
Alicia Patterson2 Department of Surgery, Medical University of South Carolina , Charleston, South Carolina.
C Bryce Johnson2 Department of Surgery, Medical University of South Carolina , Charleston, South Carolina.
Daniel J Neitzke2 Department of Surgery, Medical University of South Carolina , Charleston, South Carolina.
Shikhar Mehrotra2 Department of Surgery, Medical University of South Carolina , Charleston, South Carolina.
Chadrick E Denlinger2 Department of Surgery, Medical University of South Carolina , Charleston, South Carolina.
Chrystal M Paulos3 Department of Microbiology and Immunology, Medical University of South Carolina , Charleston, South Carolina.
Zihai Li3 Department of Microbiology and Immunology, Medical University of South Carolina , Charleston, South Carolina.
David J Cole2 Department of Surgery, Medical University of South Carolina , Charleston, South Carolina.
Mark P Rubinstein2 Department of Surgery, Medical University of South Carolina , Charleston, South Carolina.
Medical University of South Carolina · US

Funding

TCR TRANSDUCED CDB T CELLS FOR ADOPTIVE IMMUNOTHERAPYP01CA154778 · NCI · LOYOLA UNIVERSITY CHICAGO · PI NISHIMURA, MICHAEL I. · 2011 to 2015
$15.4M
NCI NIH HHS P01 CA154778
6 · The paper itself

Abstract

The development of the T- and natural killer (NK) cell growth factor IL-2 has been a sentinel force ushering in the era of immunotherapy in cancer. With the advent of clinical grade recombinant IL-2 in the mid-1980s, oncologists could for the first time directly manipulate lymphocyte populations with systemic therapy. By itself, recombinant IL-2 can induce clinical responses in up to 15% of patients with metastatic cancer or renal cell carcinoma. When administered with adoptively transferred tumor-reactive lymphocytes, IL-2 promotes T cell engraftment and response rates of up to 50% in metastatic melanoma patients. Importantly, these IL-2-driven responses can yield complete and durable responses in a subset of patients. However, the use of IL-2 is limited by toxicity and concern of the expansion of T regulatory cells. To overcome these limitations and improve response rates, other T cell growth factors, including IL-15 and modified forms of IL-2, are in clinical development. Administering T cell growth factors in combination with other agents, such as immune checkpoint pathway inhibitors, may also improve efficacy. In this study, we review the development of T- and NK cell growth factors and highlight current combinatorial approaches based on these reagents.

Indexed as

ImmunotherapyAnimalsHumansInterleukin-2NeoplasmsInterleukin-2adoptive cellular therapyIL-15IL-2T cells

Identifiers

PMID29443657
PMCPMC5815463
OpenAlexW2791130871

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.