Effective nasal influenza vaccine delivery using chitosan

被引:139
作者
Read, RC
Naylor, SC
Potter, CW
Bond, J
Jabbal-Gill, I
Fisher, A
Illum, L
Jennings, R
机构
[1] Univ Sheffield, Sch Med, Div Genom Med, Acad Unit Infect & Immun, Sheffield S10 2RX, S Yorkshire, England
[2] Durg Delivery & Clin Res Ctr Ltd, W Pharmaceut Serv, Albert Einstein Ctr, Nottingham NG7 2TN, England
关键词
nasal influenza vaccination; chitosan; serum haemagglutination inhibition;
D O I
10.1016/j.vaccine.2005.04.021
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Nasal influenza vaccination may prove to be a good alternative to parenteral injection because of the enhancement of the mucosal immune response and the ease of vaccine administration. This study investigated the use of chitosan, a bioadhesive polymer, as a nasal delivery system with inactivated, subunit influenza vaccine. Subjects received nasally 15 or 7.5 mu g of the standard inactivated trivalent influenza vaccine with chitosan or 15 mu g of the same vaccine intramuscularly. Serum haemagglutination inhibition (HI) titres for all three vaccine components were measured prior to. and at time points up to 14 weeks after dosing. Serum HI titres following intranasal vaccination with the nasal chitosan-influenza vaccine met the criteria set by the Committee for Proprietary Medicinal Products in terms of seroprotection rate, seroconversion rate and mean fold increase of HI titre for at least one of the three antigens in the vaccination schedules used. These data show that nasal immunisation with chitosan plus trivalent inactivated influenza is a potentially effective, easily-administered form of vaccination. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4367 / 4374
页数:8
相关论文
共 46 条
[1]   REDUCTION IN MORTALITY ASSOCIATED WITH INFLUENZA VACCINE DURING 1989-90 EPIDEMIC [J].
AHMED, AEH ;
NICHOLSON, KG ;
NGUYENVANTAM, JS .
LANCET, 1995, 346 (8975) :591-595
[2]  
[Anonymous], 1997, NOT GUID HARM REQ IN
[3]  
Askonas B, 1982, BASIC APPLIED INFLUE
[4]   Carbohydrate biopolymers enhance antibody responses to mucosally delivered vaccine antigens [J].
Bacon, A ;
Makin, J ;
Sizer, PJ ;
Jabbal-Gill, I ;
Hinchcliffe, M ;
Illum, L ;
Chatfield, S ;
Roberts, M .
INFECTION AND IMMUNITY, 2000, 68 (10) :5764-5770
[5]   Modulation of immune response to group C meningococcal conjugate vaccine given intranasally to mice together with the LTK63 mucosal adjuvant and the trimethyl chitosan delivery system [J].
Baudner, BC ;
Morandi, M ;
Giuliani, MM ;
Verhoef, JC ;
Junginger, HE ;
Costantino, P ;
Rappuoli, R ;
Del Giudice, G .
JOURNAL OF INFECTIOUS DISEASES, 2004, 189 (05) :828-832
[6]   The concomitant use of the LTK63 mucosal adjuvant and of chitosan-based delivery system enhances the immunogenicity and efficacy of intranasally administered vaccines [J].
Baudner, BC ;
Giuliani, MM ;
Verhoef, JC ;
Rappuoli, R ;
Junginger, HE ;
Del Giudice, G .
VACCINE, 2003, 21 (25-26) :3837-3844
[7]  
BENAHMEIDA ETS, 1993, VACCINE, V11, P1302
[8]   Safety and immunogenicity of adjuvanted and unadjuvanted subunit influenza vaccines administered intranasally to healthy adults [J].
Boyce, TG ;
Hsu, HH ;
Sannella, EC ;
Coleman-Dockery, SD ;
Baylis, E ;
Zhu, YW ;
Barchfeld, O ;
DiFrancesco, A ;
Paranandi, M ;
Culley, B ;
Neuzil, KM ;
Wright, PF .
VACCINE, 2000, 19 (2-3) :217-226
[9]  
COUCH RB, 1997, J INFECT DIS, V176, P38
[10]   Adjuvants - A classification and review of their modes of action [J].
Cox, JC ;
Coulter, AR .
VACCINE, 1997, 15 (03) :248-256