Evidence map›Paper›PMID 28706183›Full record

ArticleScientific reports2017

Modulation of Interleukin-12 activity in the presence of heparin.

Srinivas Jayanthi, Bhanu Prasanth Koppolu, Khue G Nguyen, Sean G Smith, Barbara K Felber, Thallapuranam Krishnaswamy Suresh Kumar, David A Zaharoff

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

19 citing papers in PubMed, 33 citations in OpenAlex.

  1. Glycosaminoglycans as Polyelectrolytes: Charge, Interactions, and Applications.Chembiochem : a European journal of chemical biology · 2025
    Review
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  12. Single injection of IL-12 coacervate as an effective therapy against B16-F10 melanoma in mice.Journal of controlled release : official journal of the Controlled Release Society · 2020
    Article
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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 4 institutions in 1 country.

Srinivas JayanthiDepartment of Chemistry and Biochemistry, University of Arkansas, Fayetteville, AR, USA.
Bhanu Prasanth KoppoluDepartment of Biomedical Engineering, University of Arkansas, Fayetteville, AR, USA.
Khue G NguyenCell and Molecular Biology Program, University of Arkansas, Fayetteville, AR, USA.
Sean G SmithDepartment of Biomedical Engineering, University of Arkansas, Fayetteville, AR, USA.
Barbara K FelberHuman Retrovirus Pathogenesis Section, Vaccine Branch-National Cancer Institute, Frederick, MD, United States.
Thallapuranam Krishnaswamy Suresh KumarDepartment of Chemistry and Biochemistry, University of Arkansas, Fayetteville, AR, USA. sthalla@uark.edu.
David A ZaharoffDepartment of Biomedical Engineering, University of Arkansas, Fayetteville, AR, USA. david_zaharoff@ncsu.edu.ORCID 0000-0001-6885-6727
North Carolina State University · USUniversity of Arkansas at Fayetteville · USUniversity of North Carolina at Chapel Hill · USNational Cancer Institute · US

Funding

Prevention of AIDSZIABC010350 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI FELBER, BARBARA K · 2009 to 2025
$30.0M
Overall (pp. 40-62)P41GM103485 · NIGMS · CORNELL UNIVERSITY · PI CERIONE, RICHARD A. · 2012 to 2018
$15.5M
Posttranscriptional control of gene expressionZIABC010334 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI FELBER, BARBARA K · 2009 to 2025
$15.1M
Biopolymer-based strategies for local delivery of cytokine therapeuticsR01CA172631 · NCI · UNIVERSITY OF ARKANSAS AT FAYETTEVILLE · PI ZAHAROFF, DAVID · 2014 to 2018
$1.5M
Intravesical Chitosan/IL-12 Immunotherapy for Bladder CarcinomaR15CA176648 · NCI · UNIVERSITY OF ARKANSAS AT FAYETTEVILLE · PI ZAHAROFF, DAVID · 2014 to 2014
$417k
NCI NIH HHS R01 CA172631NCI NIH HHS R15 CA176648NIGMS NIH HHS P41 GM103485
6 · The paper itself

Abstract

Glycosaminoglycans (GAGs), especially heparin and heparan sulfate (HS), modulate the functions of numerous cytokines. The aims of this multidisciplinary research were to characterize heparin binding to interleukin-12 (IL-12) and determine the mechanism(s) by which heparin influences IL-12 bioactivity. Heparin and HS were found to bind human IL-12 (hIL-12) with low micromolar affinity and increase hIL-12 bioactivity by more than 6-fold. Conversely, other GAGs did not demonstrate significant binding, nor did their addition affect hIL-12 bioactivity. Biophysical studies demonstrated that heparin induced only minor conformational changes while size-exclusion chromatography and small angle X-ray scattering studies indicated that heparin induced dimerization of hIL-12. Heparin modestly protected hIL-12 from proteolytic degradation, however, this was not a likely mechanism for increased cytokine activity in vitro. Flow cytometry studies revealed that heparin increased the amount of hIL-12 bound to cell surfaces. Heparin also facilitated hIL-12 binding and signaling in cells in which both hIL-12 receptor subunits were functionally deleted. Results of this study demonstrate a new role for heparin in modulating the biological activity of IL-12.

Indexed as

Biophysical PhenomenaCell LineChromatography, GelFlow CytometryHeparan SulfateHeparinHumansImmunologic FactorsInterleukin-12Interleukin-12 Subunit p35Protein BindingProtein ConformationProtein MultimerizationScattering, Small AngleHeparan SulfateHeparinIL12A protein, humanImmunologic FactorsInterleukin-12Interleukin-12 Subunit p35

Identifiers

PMID28706183
PMCPMC5509706
OpenAlexW2730458643

What OpenQuestion holds

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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.