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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

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    EC - Immunology

  • OECD FORD branch

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

  • 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