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

被引:17
|
作者
Capolla, Sara [1 ]
Mezzaroba, Nelly [1 ]
Zorzet, Sonia [1 ]
Tripodo, Claudio [2 ]
Mendoza-Maldonado, Ramiro [3 ]
Granzotto, Marilena [4 ]
Vita, Francesca [1 ]
Spretz, Ruben [5 ]
Larsen, Gustavo [5 ,6 ]
Noriega, Sandra [5 ]
Mansilla, Eduardo [7 ]
Dal Bo, Michele [8 ]
Gattei, Valter [8 ]
Pozzato, Gabriele [4 ]
Nunez, Luis [5 ,6 ]
Macor, Paolo [1 ,9 ]
机构
[1] Univ Trieste, Dept Life Sci, I-34127 Trieste, Italy
[2] Univ Palermo, Dept Human Pathol, I-90133 Sicily, Italy
[3] Natl Lab Consorzio Interuniv Biotecnol CIB, Mol Oncol Unit, I-34012 Trieste, Italy
[4] Univ Trieste, Dipartimento Univ Clin Sci Med Chirurg & Salute, I-34149 Trieste, Italy
[5] LNK Chemsolut LLC, Lincoln, NE 68521 USA
[6] Biotarget Inc, Chicago, IL 60637 USA
[7] Minist Hlth, Ctr Unico Coordinador Ablac & Implante Prov Bueno, La Plata, Buenos Aires, Argentina
[8] IRCCS, Ctr Riferimento Oncol, Clin & Expt Oncohematol Unit, I-33081 Aviano, Italy
[9] Callerio Fdn Onlus, Inst Biol Res, I-34127 Trieste, Italy
基金
美国国家卫生研究院;
关键词
chronic lymphocytic leukemia; immune targeted nanoparticles; treatment; xenograft model; CHRONIC LYMPHOCYTIC-LEUKEMIA; HYDROXYCHLOROQUINE; DIAGNOSIS; CELLS; XENOGRAFT; SURVIVAL; CYCLOPHOSPHAMIDE; BIODISTRIBUTION; STRATEGIES; RESISTANCE;
D O I
10.1007/s12274-015-0935-3
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
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 side-effects 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.
引用
收藏
页码:537 / 548
页数:12
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