Novel IL-2-Poly(HPMA)Nanoconjugate Based Immunotherapy
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61389013%3A_____%2F15%3A00448356" target="_blank" >RIV/61389013:_____/15:00448356 - isvavai.cz</a>
Alternative codes found
RIV/61388971:_____/15:00448356
Result on the web
<a href="http://dx.doi.org/10.1166/jbn.2015.2114" target="_blank" >http://dx.doi.org/10.1166/jbn.2015.2114</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1166/jbn.2015.2114" target="_blank" >10.1166/jbn.2015.2114</a>
Alternative languages
Result language
angličtina
Original language name
Novel IL-2-Poly(HPMA)Nanoconjugate Based Immunotherapy
Original language description
Interleukin-2 (IL-2) possesses a strong stimulatory activity for activated T and NK cells and it is an attractive molecule for immunotherapy. Nevertheless, extremely short half-life and severe toxicities associated with high-dose IL-2 treatment are serious and limiting drawbacks. In order to increase IL-2 half-life in vivo, we covalently conjugated synthetic semitelechelic polymeric carrier based on N-(2-hydroxypropyl)methacrylamide (HPMA) to IL-2. Thus, we synthesized IL-2-poly(HPMA) conjugate containing 2-3 polymer chains per IL-2 molecule in average. Such conjugate has lower biologic activity in comparison to IL-2 in vitro. However, it exerts much higher activity than IL-2 in vivo as shown by expansion of memory CD8(+) T, NK, NKT, gamma delta T and Treg cells. Moreover, IL-2-poly(HPMA) extremely effectively potentiates CD8(+) T cell peptide-based vaccination. IL-2-poly(HPMA) shows also much longer half-time in circulation than IL-2 (similar to 4 h versus similar to 5 min). Collectively, modification of IL-2 with poly(HPMA) chains dramatically improves its potency and pharmacologic features in vivo, which have implications for immunotherapy. To our knowledge, this is the first proof-of-concept report of the use of polymer/protein modification of IL-2 to obtain more pronounced biological activity
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
EC - Immunology
OECD FORD branch
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Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2015
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Journal of Biomedical Nanotechnology
ISSN
1550-7033
e-ISSN
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Volume of the periodical
11
Issue of the periodical within the volume
9
Country of publishing house
US - UNITED STATES
Number of pages
12
Pages from-to
1662-1673
UT code for WoS article
000359391700013
EID of the result in the Scopus database
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