Literature DB >> 32218162

HSP70/IL-2 Treated NK Cells Effectively Cross the Blood Brain Barrier and Target Tumor Cells in a Rat Model of Induced Glioblastoma Multiforme (GBM).

Farzaneh Sharifzad1,2, Soura Mardpour2, Saeid Mardpour3, Esmaeil Fakharian1,4, Adeleh Taghikhani2,5, Amirhossein Sharifzad6, Sahar Kiani2, Yasaman Heydarian2, Marek J Łos7,8, Zahra Azizi9, Saeid Ghavami10,11, Amir Ali Hamidieh12, Marzieh Ebrahimi2.   

Abstract

Natural killer (NK) cell therapy is one of the most promising treatments for Glioblastoma Multiforme (GBM). However, this emerging technology is limited by the availability of sufficient numbers of fully functional cells. Here, we investigated the efficacy of NK cells that were expanded and treated by interleukin-2 (IL-2) and heat shock protein 70 (HSP70), both in vitro and in vivo. Proliferation and cytotoxicity assays were used to assess the functionality of NK cells in vitro, after which treated and naïve NK cells were administrated intracranially and systemically to compare the potential antitumor activities in our in vivo rat GBM models. In vitro assays provided strong evidence of NK cell efficacy against C6 tumor cells. In vivo tracking of NK cells showed efficient homing around and within the tumor site. Furthermore, significant amelioration of the tumor in rats treated with HSP70/Il-2-treated NK cells as compared to those subjected to nontreated NK cells, as confirmed by MRI, proved the efficacy of adoptive NK cell therapy. Moreover, results obtained with systemic injection confirmed migration of activated NK cells over the blood brain barrier and subsequent targeting of GBM tumor cells. Our data suggest that administration of HSP70/Il-2-treated NK cells may be a promising therapeutic approach to be considered in the treatment of GBM.

Entities:  

Keywords:  MRI cell tracking; NK cell therapy; blood brain barrier; fluorescent cell tracking; glioblastoma multiforme; rat model

Mesh:

Substances:

Year:  2020        PMID: 32218162      PMCID: PMC7178276          DOI: 10.3390/ijms21072263

Source DB:  PubMed          Journal:  Int J Mol Sci        ISSN: 1422-0067            Impact factor:   5.923


  58 in total

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