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用基于纳米乳剂佐剂配制的商用三价流感疫苗对雪貂进行鼻内免疫。

Intranasal immunization of ferrets with commercial trivalent influenza vaccines formulated in a nanoemulsion-based adjuvant.

作者信息

Hamouda Tarek, Sutcliffe Joyce A, Ciotti Susan, Baker James R

机构信息

NanoBio Corp., 2311 Green Road, Suite A, Ann Arbor, MI 48105, USA.

出版信息

Clin Vaccine Immunol. 2011 Jul;18(7):1167-75. doi: 10.1128/CVI.00035-11. Epub 2011 May 4.

DOI:10.1128/CVI.00035-11
PMID:21543588
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3147313/
Abstract

NB-1008 is a surfactant-stabilized soybean oil-in-water nanoemulsion (NE) adjuvant with influenza virus antigen incorporated into the NE by simple mixing. Intranasal administration of the antigen with NE adjuvant efficiently produces both mucosal and serum antibody responses as well as a robust cellular Th1 immune response. To demonstrate the adjuvant effect of the W(80)5EC NE, a killed commercial influenza vaccine for intramuscular administration (Fluzone or Fluvirin) was mixed with the W(80)5EC NE adjuvant and administered intranasally to naïve ferrets. After a single intranasal immunization, the adjuvanted influenza vaccine elicited elevated serum hemagglutination inhibition (HAI) geometric mean titers (GMTs) ranging from 196 to 905 for the three hemagglutinin (HA) antigens present in the vaccine, which are approximately 19- to 90-fold higher titers at 1/50 the standard intramuscular commercial nonadjuvanted influenza vaccine dose. Seroconversion rates of 67% to 100% were achieved against each of the three viral strains present. The adjuvanted nasal influenza vaccine also produced significant cross immunity to five other H3N2 influenza virus strains not present in the vaccine and produced sterile immunity after challenge with homologous live virus. No safety issues were observed in 249 ferrets receiving the adjuvanted influenza vaccine. These findings demonstrate the ability of W(80)5EC NE to adjuvant nasally administered influenza vaccine and provide a basis for studying the intranasal W(80)5EC-adjuvanted influenza vaccine in humans.

摘要

NB - 1008是一种由表面活性剂稳定的水包油型大豆纳米乳剂(NE)佐剂,通过简单混合将流感病毒抗原掺入NE中。经鼻给予抗原与NE佐剂可有效产生黏膜和血清抗体反应以及强大的细胞Th1免疫反应。为证明W(80)5EC NE的佐剂效果,将一种用于肌肉注射的商业化流感灭活疫苗(Fluzone或Fluvirin)与W(80)5EC NE佐剂混合,并经鼻给予未接触过抗原的雪貂。单次经鼻免疫后,佐剂化流感疫苗针对疫苗中存在的三种血凝素(HA)抗原引发的血清血凝抑制(HAI)几何平均滴度(GMT)升高,范围为196至905,这在标准肌肉注射商业化无佐剂流感疫苗剂量的1/50时,滴度约高19至90倍。针对疫苗中存在的三种病毒株,血清转化率达到67%至100%。佐剂化鼻用流感疫苗还对疫苗中不存在的其他五种H3N2流感病毒株产生了显著的交叉免疫,并在用同源活病毒攻击后产生了无菌免疫。在249只接受佐剂化流感疫苗的雪貂中未观察到安全问题。这些发现证明了W(80)5EC NE作为经鼻给予流感疫苗佐剂的能力,并为在人体中研究经鼻W(80)5EC佐剂化流感疫苗提供了基础。

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Nasal immunization with a recombinant HIV gp120 and nanoemulsion adjuvant produces Th1 polarized responses and neutralizing antibodies to primary HIV type 1 isolates.用重组HIV gp120和纳米乳剂佐剂进行鼻腔免疫可产生Th1极化反应以及针对原发性HIV-1分离株的中和抗体。
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