Evidence map›Paper›PMID 36203573›Full record

ReviewFrontiers in immunology2022

IL12 immune therapy clinical trial review: Novel strategies for avoiding CRS-associated cytokines.

Zhiliang Jia, Dristhi Ragoonanan, Kris Michael Mahadeo, Jonathan Gill, Richard Gorlick, Elizabeth Shpal, Shulin Li

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
7.0field-weighted citation impact, top 2% 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

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 78 citations in OpenAlex.

  1. Pooled it
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  11. Therapeutic application of IL-12 for cancer therapy.Translational cancer research · 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

7 authors at 1 institution in 1 country.

Zhiliang JiaDepartment of Pediatric Research, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Dristhi RagoonananDepartment of Pediatric Research, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Kris Michael MahadeoDepartment of Pediatric Research, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Jonathan GillDepartment of Pediatric Research, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Richard GorlickDepartment of Pediatric Research, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Elizabeth ShpalDepartment of Stem Cell Transplantation and Cellular Therapy, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Shulin LiDepartment of Pediatric Research, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
The University of Texas MD Anderson Cancer Center · US

Funding

Gene-Product Auto-Targeting to Tumor VesselsR01CA120895 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LI, SHULIN · 2007 to 2025
$4.8M
Computerized Analysis of Mesothelioma on CT ScansR01CA102085 · NCI · UNIVERSITY OF CHICAGO · PI ARMATO, SAMUEL G. · 2006 to 2009
$1.5M
NCI NIH HHS R01 CA102085NCI NIH HHS R01 CA120895
6 · The paper itself

Abstract

Interleukin 12 (IL-12) is a naturally occurring cytokine that plays a key role in inducing antitumor immune responses, including induction of antitumor immune memory. Currently, no IL-12-based therapeutic products have been approved for clinical application because of its toxicities. On the basis of this review of clinical trials using primarily wild-type IL-12 and different delivery methods, we conclude that the safe utilization of IL-12 is highly dependent on the tumor-specific localization of IL-12 post administration. In this regard, we have developed a cell membrane-anchored and tumor-targeted IL-12-T (attIL12-T) cell product for avoiding toxicity from both IL-12 and T cells-induced cytokine release syndrome in peripheral tissues. A phase I trial using this product which seeks to avoid systemic toxicity and boost antitumor efficacy is on the horizon. Of note, this product also boosts the impact of CAR-T or TCR-T cell efficacy against solid tumors, providing an alternative approach to utilize CAR-T to overcome tumor resistance.

Indexed as

NeoplasmsReceptors, Chimeric AntigenCytokinesHumansInterleukin-12T-LymphocytesCytokinesInterleukin-12Receptors, Chimeric Antigenclinical trialCRScytokinesIL-12T cells

Identifiers

PMID36203573
PMCPMC9530253
OpenAlexW4297907002

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.