A new approach for the treatment of CLL using chlorambucil/hydroxychloroquine-loaded anti-CD20 nanoparticles

被引:0
|
作者
Sara Capolla
Nelly Mezzaroba
Sonia Zorzet
Claudio Tripodo
Ramiro Mendoza-Maldonado
Marilena Granzotto
Francesca Vita
Ruben Spretz
Gustavo Larsen
Sandra Noriega
Eduardo Mansilla
Michele Dal Bo
Valter Gattei
Gabriele Pozzato
Luis Núñez
Paolo Macor
机构
[1] University of Trieste,Department of Life Sciences
[2] University of Palermo,Department of Human Pathology
[3] National Laboratory Consorzio Interuniversitatio per le Biotecnologie (CIB),Molecular Oncology Unit
[4] University of Trieste,Dipartimento Universitario Clinico di Scienze mediche, Chirurgiche e della Salute
[5] LNK Chemsolutions LLC,Centro Ùnico Coordinador de Ablacion e Implante Provincia de Buenos Aires (C.U.C.A.I.B.A.)
[6] Bio-Target Inc.,Clinical and Experimental Onco
[7] Ministry of Health,Hematology Unit, Centro di Riferimento Oncologico
[8] Istituto di Ricerca e Cura a Carattere Scientifico (I.R.C.C.S.),Callerio Foundation Onlus
[9] Institutes of Biological Researches,undefined
来源
Nano Research | 2016年 / 9卷
关键词
chronic lymphocytic leukemia; immune targeted nanoparticles; treatment; xenograft model;
D O I
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中图分类号
学科分类号
摘要
Current approaches for the treatment of chronic lymphocytic leukemia (CLL) have greatly improved the prognosis for survival, but some patients remain refractive to these therapeutic regimens. Hence, in addition to reducing the long-term sideeffects of therapeutics for all leukemia patients, there is an urgent need for novel therapeutic strategies for difficult-to-treat leukemia cases. Due to the cytotoxicity of drugs, the major challenge currently is to deliver the therapeutic agents to neoplastic cells while preserving the viability of non-malignant cells. In this study, we propose a therapeutic approach in which high doses of hydroxychloroquine and chlorambucil were loaded into biodegradable polymeric nanoparticles coated with an anti-CD20 antibody.We first demonstrated the ability of the nanoparticles to target and internalize in tumor B-cells. Moreover, these nanoparticles could kill not only p53-mutated/deleted leukemia cells expressing a low amount of CD20, but also circulating primary cells isolated from chronic lymphocytic leukemia patients. The safety of these nanoparticles was also demonstrated in healthy mice, and their therapeutic effects were shown in a new model of aggressive leukemia. These results showed that anti-CD20 nanoparticles containing hydroxychloroquine and chlorambucil can be effective in controlling aggressive leukemia and provided a rationale for adopting this approach for the treatment of other B-cell disorders.
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页码:537 / 548
页数:11
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