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比较小型猪和家猪的补体激活相关假性过敏反应:一种可验证免疫毒性模型的基础。

Comparison of complement activation-related pseudoallergy in miniature and domestic pigs: foundation of a validatable immune toxicity model.

机构信息

School of Materials Science and Engineering, Nanyang Technological University, Singapore; Centre for Biomimetic Sensor Science, Nanyang Technological University, Singapore.

Nanomedicine Research and Education Center, Institute of Pathophysiology, Semmelweis University, Nagyvárad tér 4. Budapest, Hungary; SeroScience Ltd, Nagyvárad tér 4. Budapest, Hungary.

出版信息

Nanomedicine. 2016 May;12(4):933-943. doi: 10.1016/j.nano.2015.12.377. Epub 2016 Jan 6.


DOI:10.1016/j.nano.2015.12.377
PMID:26767512
Abstract

UNLABELLED: Complement activation-related pseudoallergy (CARPA) is an acute adverse immune reaction caused by many nanomedicines. There is a regulatory need for a sensitive and standardizable in vivo predictive assay. While domestic pigs are a sensitive animal model, miniature pigs are favored in toxicological studies yet their utility as a CARPA model has not yet been explored. Herein, we used liposomal doxorubicin and amphotericin B (Doxil/Caelyx and AmBisome), Cremophor EL and zymosan as CARPA triggers to induce reactions in miniature and domestic pigs, and compared the hemodynamic, hematological, biochemical, and skin alterations. The changes observed after administration of the test agents were very similar in both pig strains, suggesting that miniature pigs are a sensitive, reproducible, and, hence, validatable animal model for CARPA regulatory testing. FROM THE CLINICAL EDITOR: With the advances in nanomedicine research, many new agents are now tested for use in clinical setting. Nonetheless, complement activation-related pseudoallergy (CARPA) is a well known phenomenon which can be caused by nanoparticles. In this study, the authors looked at and compared the use of domestic pigs versus miniature pigs as experimental animals for toxicological studies. Their findings confirmed the possible use of miniature pigs for regulatory testing.

摘要

未加标签:补体激活相关假性过敏 (CARPA) 是由许多纳米药物引起的急性免疫不良反应。因此需要一种灵敏且可标准化的体内预测性检测方法。虽然家猪是一种敏感的动物模型,但小型猪在毒理学研究中更受欢迎,但它们作为 CARPA 模型的效用尚未得到探索。在此,我们使用脂质体阿霉素和两性霉素 B(Doxil/Caelyx 和 AmBisome)、聚氧乙烯蓖麻油和酵母聚糖作为 CARPA 触发物,在小型猪和家猪中诱导反应,并比较了血液动力学、血液学、生化和皮肤变化。两种猪种在给予试验药物后的变化非常相似,这表明小型猪是一种敏感、可重复且可验证的 CARPA 监管测试的动物模型。

临床编辑按:随着纳米医学研究的进展,许多新的药物现在正在进行临床试验。尽管如此,补体激活相关假性过敏 (CARPA) 是一种众所周知的现象,它可能是由纳米颗粒引起的。在这项研究中,作者研究并比较了使用家猪和小型猪作为毒理学研究的实验动物。他们的发现证实了小型猪可用于监管测试。

相似文献

[1]
Comparison of complement activation-related pseudoallergy in miniature and domestic pigs: foundation of a validatable immune toxicity model.

Nanomedicine. 2016-1-6

[2]
Liposome-induced complement activation and related cardiopulmonary distress in pigs: factors promoting reactogenicity of Doxil and AmBisome.

Nanomedicine. 2011-6-24

[3]
Features of complement activation-related pseudoallergy to liposomes with different surface charge and PEGylation: comparison of the porcine and rat responses.

J Control Release. 2014-8-19

[4]
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[5]
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Int J Nanomedicine. 2018-10-11

[6]
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[7]
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[8]
Complement Activation-Related Pathophysiological Changes in Anesthetized Rats: Activator-Dependent Variations of Symptoms and Mediators of Pseudoallergy.

Molecules. 2019-9-9

[9]
A porcine model of complement-mediated infusion reactions to drug carrier nanosystems and other medicines.

Adv Drug Deliv Rev. 2012-7-20

[10]
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Adv Drug Deliv Rev. 2011-7-14

引用本文的文献

[1]
Increased Cardiovascular Mortality in Hemodialysis: The Role of Chronic Inflammation, Complement Activation, and Non-Biocompatibility.

Toxins (Basel). 2025-7-10

[2]
Liposomal amphotericin B and complement activation-related pseudoallergy (CARPA).

Antimicrob Agents Chemother. 2025-3-5

[3]
Protein is expressed in all major organs after intravenous infusion of mRNA-lipid nanoparticles in swine.

Mol Ther Methods Clin Dev. 2024-8-6

[4]
Comirnaty-induced cardiopulmonary distress and other symptoms of complement-mediated pseudo-anaphylaxis in a hyperimmune pig model: Causal role of anti-PEG antibodies.

Vaccine X. 2024-5-23

[5]
Radiofrequency Combined with Intratumoral Immunotherapy: Preclinical Results and Safety in Metastatic Colorectal Carcinoma.

Pharmaceutics. 2024-2-23

[6]
Evaluation of the Acute Anaphylactoid Reactogenicity of Nanoparticle-Containing Medicines and Vaccines Using the Porcine CARPA Model.

Methods Mol Biol. 2024

[7]
Inter-Individual Variations: A Challenge for the Standardisation of Complement Activation Assays.

Int J Nanomedicine. 2023

[8]
Zymosan Particle-Induced Hemodynamic, Cytokine and Blood Cell Changes in Pigs: An Innate Immune Stimulation Model with Relevance to Cytokine Storm Syndrome and Severe COVID-19.

Int J Mol Sci. 2023-1-6

[9]
PEGylated Polyester Nanoparticles Trigger Adverse Events in a Large Animal Model of Trauma and in Naı̈ve Animals: Understanding Cytokine and Cellular Correlations with These Events.

ACS Nano. 2022-7-26

[10]
The Emerging Role of Ultrasonic Nanotechnology for Diagnosing and Treatment of Diseases.

Front Med (Lausanne). 2022-2-22

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