LNPs as delivery platform of Rituximab for SMZL

Zhengnong Huang, Zifu Tang, Xianwen Zhang
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Abstract

Splenic Marginal Zone Lymphoma (SMZL) is a low-grade B-cell non-Hodgkin lymphoma from which patients may suffer anemia, autoimmune disorder and splenomegaly respectively. Due to its chronic nature, it has been increasingly hard to identify and treat effectively. The study establishes an SMZL mouse model and explores the potential of enhancing Rituximab treatment using Lipid Nanoparticles (LNPs). Designed experiment includes how to establish the NFS.N mice model, characterization of the disease on mice and recovery standard of mice. First, SMZL mice model is establish followed by histology and immunocytochemistry investigation which looks directly at the mices lesion. Then flow cytology is carried out which looks at the expression level of IgM, IgK, CD23, CD45 etc., before bone marrow infiltration is carried out. A controlled experiment of three groups of mice is designed, including mice treated with conventional Rituximab, delivery with LNPs and delivering empty LNPs, respectively. The effect of LNPs on treating mice SMZL is investigated. And some expected results and analysis methods were also discussed alongside with recovery standard. This experiment aims to provide theoretical support to the development of more effective and targeted therapies for this specific type of lymphoma. However, this is only an design rigorous experimentation strengthens the scientific validity of these findings.
将 LNPs 作为利妥昔单抗治疗 SMZL 的给药平台
脾边缘区淋巴瘤(SMZL)是一种低级别B细胞非霍奇金淋巴瘤,患者可能分别患有贫血、自身免疫紊乱和脾肿大。由于它的慢性性质,越来越难以识别和有效治疗。本研究建立了SMZL小鼠模型,并探索使用脂质纳米颗粒(LNPs)增强利妥昔单抗治疗的潜力。设计的实验包括如何建立NFS.N小鼠模型、小鼠的疾病特征和小鼠的康复标准。首先,建立 SMZL 小鼠模型,然后进行组织学和免疫细胞化学研究,直接观察小鼠的病变。然后进行流式细胞术,观察 IgM、IgK、CD23、CD45 等的表达水平,最后进行骨髓浸润。我们设计了三组小鼠对照实验,包括分别使用传统利妥昔单抗、LNPs 给药和空 LNPs 给药的小鼠。研究了 LNPs 治疗小鼠 SMZL 的效果。同时还讨论了一些预期结果和分析方法,以及回收标准。本实验旨在为开发针对这种特殊类型淋巴瘤的更有效的靶向疗法提供理论支持。然而,这仅仅是一项设计严谨的实验,它加强了这些发现的科学性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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