Evidence map›Paper›PMID 25754122›Full record

ArticleCancer immunology, immunotherapy : CII2015

Intravesical chitosan/interleukin-12 immunotherapy induces tumor-specific systemic immunity against murine bladder cancer.

Sean G Smith, Bhanu Prasanth Koppolu, Sruthi Ravindranathan, Samantha L Kurtz, Lirong Yang, Matthew D Katz, David A Zaharoff

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.4field-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

27 citing papers in PubMed, 47 citations in OpenAlex.

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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 2 institutions in 1 country.

Sean G SmithDepartment of Biomedical Engineering, University of Arkansas, 120 John A. White, Jr. Engineering Hall, Fayetteville, AR, 72701, USA.
Bhanu Prasanth Koppolu
Sruthi Ravindranathan
Samantha L Kurtz
Lirong Yang
Matthew D Katz
David A Zaharoff
University of Arkansas at Fayetteville · USUniversity of Arkansas for Medical Sciences · US

Funding

Biopolymer-based strategies for local delivery of cytokine therapeuticsR01CA172631 · NCI · UNIVERSITY OF ARKANSAS AT FAYETTEVILLE · PI ZAHAROFF, DAVID · 2014 to 2018
$1.5M
Chitosan-based Delivery and Immunopotentiation of Cancer VaccinesK22CA131567 · NCI · UNIVERSITY OF ARKANSAS AT FAYETTEVILLE · PI ZAHAROFF, DAVID · 2010 to 2012
$505k
Intravesical Chitosan/IL-12 Immunotherapy for Bladder CarcinomaR15CA176648 · NCI · UNIVERSITY OF ARKANSAS AT FAYETTEVILLE · PI ZAHAROFF, DAVID · 2014 to 2014
$417k
NCI NIH HHS K22 CA131567NCI NIH HHS K22CA131567NCI NIH HHS R01 CA172631NCI NIH HHS R01CA172631NCI NIH HHS R15 CA176648NCI NIH HHS R15CA176649
6 · The paper itself

Abstract

Bladder cancer is a highly recurrent disease in need of novel, durable treatment strategies. This study assessed the ability of an intravesical immunotherapy composed of a coformulation of the biopolymer chitosan with interleukin-12 (CS/IL-12) to induce systemic adaptive tumor-specific immunity. Intravesical CS/IL-12 immunotherapy was used to treat established orthotopic MB49 and MBT-2 bladder tumors. All mice receiving intravesical CS/IL-12 immunotherapy experienced high cure rates of orthotopic disease. To investigate the durability and extent of the resultant adaptive immune response, cured mice were rechallenged both locally (intravesically) and distally. Cured mice rejected 100 % of intravesical tumor rechallenges and 50-100 % of distant subcutaneous rechallenges in a tumor-specific manner. The ability of splenocytes from cured mice to lyse targets in a tumor-specific manner was assessed in vitro, revealing that lytic activity of splenocytes from cured mice was robust and tumor specific. Protective immunity was durable, lasting for at least 18 months after immunotherapy. In an advanced bladder cancer model, intravesical CS/IL-12 immunotherapy controlled simultaneous orthotopic and subcutaneous tumors in 70 % of treated mice. Intravesical CS/IL-12 immunotherapy creates a robust and durable tumor-specific adaptive immune response against bladder cancer. The specificity, durability, and potential of this therapy to treat both superficial and advanced disease are deserving of consideration for clinical translation.

Indexed as

Administration, IntravesicalAnimalsCell Line, TumorChitosanDose-Response Relationship, ImmunologicFemaleImmunotherapyInterleukin-12MiceMice, Inbred C3HMice, Inbred C57BLRandom AllocationUrinary Bladder NeoplasmsChitosanInterleukin-12

Identifiers

PMID25754122
PMCPMC4458215
OpenAlexW2087754237

What OpenQuestion holds

Textmetadata
LicenceTDM
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.