CTA1-DD is an effective adjuvant for targeting anti-chlamydial immunity to the murine genital mucosa

被引:35
作者
Cunningham, Kelly A. [1 ]
Carey, Alison J. [1 ]
Lycke, Nils [2 ]
Timms, Peter [1 ]
Beagley, Kenneth W. [1 ]
机构
[1] Queensland Univ Technol, Inst Hlth & Biomed Innovat, Brisbane, Qld 4059, Australia
[2] Univ Gothenburg, Dept Microbiol & Immunol, Mucosal Immunol & Vaccine Res Ctr, Inst Biomed, S-40530 Gothenburg, Sweden
关键词
Chlamydia; CTA1-DD; Mucosal adjuvant; OUTER-MEMBRANE PROTEIN; INFLUENZA VACCINE; PROTECTIVE IMMUNITY; IMMUNIZATION; INFECTION; TRACT; CHALLENGE; INDUCTION; MICE; VP6;
D O I
10.1016/j.jri.2009.04.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Chlamydia trachomatis is a significant human pathogen with potentially severe disease sequelae in the genital tract, including infertility. A successful vaccine will need to effectively target immunity to the genital mucosa. Intranasal immunisation with cholera toxin (CT) can target immunity to the genital tract, but has the potential to cause neurological side effects. CTA1-DD is a non-toxic potent mucosal adjuvant which combines the enzymatic properties of CT, with a B cell targeting moiety. Here, we demonstrate that intranasal immunisation with CTA1-DD and chlamydial Major Outer Membrane Protein (MOMP) results in the induction of neutralising systemic and mucosal antibodies. and reduces the level of chlamydial shedding following intravaginal challenge with Chlamydia muridarum. Thus, CTA1-DD is an effective adjuvant for vaccine development against Chlamydia trachomatis, and possibly also a range of other genital pathogens. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:34 / 38
页数:5
相关论文
共 22 条
[1]
Agren LC, 1997, J IMMUNOL, V158, P3936
[2]
The nontoxic CTA1-DD adjuvant enhances protective immunity against Helicobacter pylori infection following mucosal immunization [J].
Akhiani, AA ;
Stensson, A ;
Schön, K ;
Lycke, N .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 2006, 63 (02) :97-105
[3]
In silico identification and in vivo analysis of a novel T-cell antigen from Chlamydia, NrdB [J].
Barker, Christopher J. ;
Beagley, Kenneth W. ;
Hafner, Louise M. ;
Timms, Peter .
VACCINE, 2008, 26 (10) :1285-1296
[4]
Chlamydia trachomatis infection:: incidence, health costs and prospects for vaccine development [J].
Beagley, KW ;
Timms, P .
JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2000, 48 (01) :47-68
[5]
The level of protection against rotavirus shedding in mice following immunization with a chimeric VP6 protein is dependent on the route and the coadministered adjuvant [J].
Choi, AH ;
McNeal, MM ;
Flint, JA ;
Basu, M ;
Lycke, NY ;
Clements, JD ;
Bean, JA ;
Davis, HL ;
McCluskie, MJ ;
VanCott, JL ;
Ward, RL .
VACCINE, 2002, 20 (13-14) :1733-1740
[6]
Poly-immunoglobulin Receptor-Mediated Transport of IgA into the Male Genital Tract is Important for Clearance of Chlamydia muridarum Infection [J].
Cunningham, Kelly A. ;
Carey, Alison J. ;
Finnie, Jane M. ;
Bao, Shisan ;
Coon, Charmere ;
Jones, Russell ;
Wijburg, Odilia ;
Strugnell, Richard A. ;
Timms, Peter ;
Beagley, Kenneth W. .
AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2008, 60 (05) :405-414
[7]
Male genital tract chlamydial infection: implications for pathology and infertility [J].
Cunningham, Kelly A. ;
Beagley, Kenneth W. .
BIOLOGY OF REPRODUCTION, 2008, 79 (02) :180-189
[8]
The universal influenza vaccine M2e-HBc administered intranasally in combination with the adjuvant CTA1-DD provides complete protection [J].
De Filette, M ;
Ramne, A ;
Birkett, A ;
Lycke, N ;
Löwenadler, B ;
Jou, WM ;
Saelens, X ;
Fiers, W .
VACCINE, 2006, 24 (05) :544-551
[9]
CTA1-M2e-DD: A novel mucosal adjuvant targeted influenza vaccine [J].
Eliasson, Dubravka Grdic ;
El Bakkouri, Karim ;
Schoen, Karin ;
Ramne, Anna ;
Festjens, Els ;
Lowenadler, Bjorn ;
Fiers, Walter ;
Saelens, Xavier ;
Lycke, Nits .
VACCINE, 2008, 26 (09) :1243-1252
[10]
The cholera toxin-derived CTA1-DD vaccine adjuvant administered intranasally does not cause inflammation or accumulate in the nervous tissues [J].
Eriksson, AM ;
Schön, KM ;
Lycke, NY .
JOURNAL OF IMMUNOLOGY, 2004, 173 (05) :3310-3319