Evaluation of Systemic and Mucosal Immune Responses Induced by a Nasal Powder Delivery System in Conjunction with an OVA Antigen in Cynomolgus Monkeys

被引:7
作者
Torikai, Yusuke [1 ,2 ]
Sasaki, Yuji [3 ]
Sasaki, Keita [2 ]
Kyuno, Akifumi [2 ]
Haruta, Shunji [2 ]
Tanimoto, Akihide [1 ]
机构
[1] Kagoshima Univ, Dept Mol & Cellular Pathol, Grad Sch Med & Dent Sci, 8-35-1 Sakuragaoka, Kagoshima 8508544, Japan
[2] Shin Nippon Biomed Labs Ltd, TR Co, R&D Dept, 2438 Miyanoura, Kagoshima 8911394, Japan
[3] Shin Nippon Biomed Labs Ltd, Dept Pathol Drug & Safety Res Labs, 2438 Miyanoura, Kagoshima 8911394, Japan
关键词
Controlled delivery; Controlled release; Drug delivery system; Formulation; Immunogenicity; Mucoadhesive; Mucosal vaccination; Powder technology; Nasal drug delivery; Vaccine; LYMPHOID-TISSUE NALT; INFLUENZA VACCINES; IGA;
D O I
10.1016/j.xphs.2020.11.023
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
An immune response for a nasal ovalbumin (OVA) powder formulation with an applied nasal delivery platform technology, consisting of a powdery nasal carrier and a device, was evaluated in monkeys with similar upper respiratory tracts and immune systems to those of humans, in order to assess the appli-cability to a vaccine antigen. Nasal distribution and retention studies using a 3D nasal cavity model and manganese-enhanced MRI were conducted by administering nasal dye and manganese powder for-mulations with the applied technology. Systemic and mucosal immune responses for the nasal OVA powder formulation were evaluated by determining serum IgG and nasal wash IgA antibody titers. The nasal dye and manganese powder formulations showed wider distribution and longer retention time than did a nasal liquid formulation. The nasal OVA powder formulation also showed comparable and higher antigen-specific IgG antibody titer to an injection and nasal liquid formulation, respectively. Furthermore, antigen-specific IgA antibody response was detected only for the nasal OVA powder formulation. The present study suggests that the technology, originally designed for drug absorption, is promising for nasal vaccines, enabling both a mucosal immunity response as the first line of defense and systemic immunity response as a second line of defense against infection. (C) 2020 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:2038 / 2046
页数:9
相关论文
共 26 条
[1]  
Akiyoshi Y, 2018, 45 CONTR REL SOC ANN
[2]  
BRANDTZAEG P, 1981, CLIN EXP IMMUNOL, V44, P221
[3]   Live Attenuated Influenza Vaccine (FluMist®; Fluenz™) A Review of its Use in the Prevention of Seasonal Influenza in Children and Adults [J].
Carter, Natalie J. ;
Curran, Monique P. .
DRUGS, 2011, 71 (12) :1591-1622
[4]  
Chauhan H, 2018, ADDRESSING CHALLENGE
[5]   Nasal-associated lymphoid tissue (NALT):: frequency and localization in young children [J].
Debertin, AS ;
Tschernig, T ;
Tönjes, H ;
Kleemann, WJ ;
Tröger, HD ;
Pabst, R .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2003, 134 (03) :503-507
[6]   Preservation of the Immunogenicity of Dry-powder Influenza H5N1 Whole Inactivated Virus Vaccine at Elevated Storage Temperatures [J].
Geeraedts, Felix ;
Saluja, Vinay ;
ter Veer, Wouter ;
Amorij, Jean-Pierre ;
Frijlink, Henderik W. ;
Wilschut, Jan ;
Hinrichs, Wouter L. J. ;
Huckriede, Anke .
AAPS JOURNAL, 2010, 12 (02) :215-222
[7]   The nose revisited: A brief review of the comparative structure, function, and toxicologic pathology of the nasal epithelium [J].
Harkema, Jack R. ;
Carey, Stephan A. ;
Wagner, James G. .
TOXICOLOGIC PATHOLOGY, 2006, 34 (03) :252-269
[8]  
Haruta S, 2012, ONDRUGDELIVERY MAGAZ, P4
[9]   A novel dry powder influenza vaccine and intranasal delivery technology: induction of systemic and mucosal immune responses in rats [J].
Huang, J ;
Garmise, RJ ;
Crowder, TM ;
Mar, K ;
Hwang, CR ;
Hickey, AJ ;
Mikszta, JA ;
Sullivan, VJ .
VACCINE, 2004, 23 (06) :794-801
[10]   A post-marketing surveillance study of a human live-virus pandemic influenza A (H1N1) vaccine (Nasovac®) in India [J].
Kulkarni, Prasad S. ;
Raut, Sidram K. ;
Dhere, Rajeev M. .
HUMAN VACCINES & IMMUNOTHERAPEUTICS, 2013, 9 (01) :122-124