Development of lactococcal GEM-based pneumococcal vaccines

被引:91
作者
Audouy, Sandrine A. L.
van Selm, Saskia
van Roosmalen, Maarten L.
Post, Eduard
Kanninga, Rolf
Neef, Jolanda
Estevao, Silvia
Nieuwenhuis, Edward E. S.
Adrian, Peter V.
Leenhouts, Kees
Hermans, Peter W. M.
机构
[1] Radboud Univ Nijmegen Med Ctr, Lab Pediat Infect Dis, NL-6500 HB Nijmegen, Netherlands
[2] Erasmus MC, Pediat Lab, Rotterdam, Netherlands
[3] BiOMaDe Technol Fdn, Groningen, Netherlands
关键词
nasal vaccine; Streptococcus pneumoniae; Gram-positive Enhancer Matrix (GEM);
D O I
10.1016/j.vaccine.2006.09.026
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We report the development of a novel protein-based nasal vaccine against Streptococcus pneumoniae, in which three pneumococcal proteins were displayed on the surface of a non-recombinant, killed Lactococcus lactis-derived delivery system, called Gram-positive Enhancer Matrix (GEM). The GEM particles induced the production of the proinflammatory cytokine tumour necrosis factor-alpha (TNF-alpha) by macrophages as well as the maturation of dendritic cells. The pneumococcal proteins IgA1 protease (IgA1p), putative proteinase maturation protein A (PpmA) and streptococcal lipoprotein A (SlrA) were anchored in trans to the surface of the GEM particles after recombinant production of the antigens in L. lactis as hybrids with a lactococcal cell wall binding domain, named Protein Anchor domain (PA). Intranasal immunisation with the SlrA-IgAlp or trivalent vaccine combinations without additional adjuvants showed significant protection against fatal pneumococcal pneumonia in mice. The GEM-based trivalent vaccine is a potential pneumococcal vaccine candidate that is expected to be easy to administer, safe and affordable to produce. (C) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2497 / 2506
页数:10
相关论文
共 52 条
[1]   Development of antibodies against pneumococcal proteins α-enolase, immunoglobulin A1 protease, streptococcal lipoprotein rotamase A, and putative proteinase maturation protein A in relation to pneumococcal carriage and Otitis Media [J].
Adrian, PV ;
Bogaert, DB ;
Oprins, M ;
Rapola, S ;
Lahdenkari, M ;
Kilpi, T ;
de Groot, R ;
Käyhty, H ;
Hermans, PWM .
VACCINE, 2004, 22 (21-22) :2737-2742
[2]   IMMUNIZATION OF MICE WITH PNEUMOLYSIN TOROID CONFERS A SIGNIFICANT DEGREE OF PROTECTION AGAINST AT LEAST 9 SEROTYPES OF STREPTOCOCCUS-PNEUMONIAE [J].
ALEXANDER, JE ;
LOCK, RA ;
PEETERS, CCAM ;
POOLMAN, JT ;
ANDREW, PW ;
MITCHELL, TJ ;
HANSMAN, D ;
PATON, JC .
INFECTION AND IMMUNITY, 1994, 62 (12) :5683-5688
[3]   Proinflammatory responses in the murine brain after intranasal delivery of cholera toxin: Implications for the use of AB toxins as adjuvants in intranasal vaccines [J].
Armstrong, ME ;
Lavelle, EC ;
Loscher, CE ;
Lynch, MA ;
Mills, KHG .
JOURNAL OF INFECTIOUS DISEASES, 2005, 192 (09) :1628-1633
[4]   Lactococcus lactis GEM particles displaying pneumococcal antigens induce local and systemic immune responses following intranasal immunization [J].
Audouy, Sandrine A. L. ;
van Roosmalen, Maarten L. ;
Neef, Jolanda ;
Kanninga, Rolf ;
Post, Eduard ;
van Deemter, Marielle ;
Metselaar, Heidi ;
van Selm, Saskia ;
Robillard, George T. ;
Leenhouts, Kees J. ;
Hermans, Peter W. M. .
VACCINE, 2006, 24 (26) :5434-5441
[5]   An inducible surface presentation system improves cellular immunity against human papillomavirus type 16 E7 antigen in mice after nasal administration with recombinant lactococci [J].
Bermúdez-Humarán, LG ;
Cortes-Perez, NG ;
Le Loir, Y ;
Alcocer-González, JM ;
Tamez-Guerra, RS ;
de Oca-Luna, RM ;
Langella, P .
JOURNAL OF MEDICAL MICROBIOLOGY, 2004, 53 (05) :427-433
[6]   Bronchus- and nasal-associated lymphoid tissues [J].
Bienenstock, J ;
McDermott, MR .
IMMUNOLOGICAL REVIEWS, 2005, 206 :22-31
[7]   Molecular epidemiology of pneumococcal colonization in response to pneumococcal conjugate vaccination in children with recurrent acute otitis media [J].
Bogaert, D ;
Veenhoven, RH ;
Sluijter, M ;
Wannet, WJW ;
Rijkers, GT ;
Mitchell, TJ ;
Clarke, SC ;
Goessens, WHF ;
Schilder, AG ;
Sanders, EAM ;
de Groot, R ;
Hermans, PWM .
JOURNAL OF CLINICAL MICROBIOLOGY, 2005, 43 (01) :74-83
[8]   Novel surface display system for proteins on non-genetically modified gram-positive bacteria [J].
Bosma, T ;
Kanninga, R ;
Neef, J ;
Audouy, SAL ;
van Roosmalen, ML ;
Steen, A ;
Buist, G ;
Kok, J ;
Kuipers, OP ;
Robillard, G ;
Leenhouts, K .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2006, 72 (01) :880-889
[9]   Intranasal immunization of mice with a mixture of the pneumococcal proteins PsaA and PspA is highly protective against nasopharyngeal carriage of Streptococcus pneumoniae [J].
Briles, DE ;
Ades, E ;
Paton, JC ;
Sampson, JS ;
Carlone, GM ;
Huebner, RC ;
Virolainen, A ;
Swiatlo, E ;
Hollingshead, SK .
INFECTION AND IMMUNITY, 2000, 68 (02) :796-800
[10]   Immunizations with pneumococcal surface protein A and pneumolysin are protective against pneumonia in a murine model of pulmonary infection with Streptococcus pneumoniae [J].
Briles, DE ;
Hollingshead, SK ;
Paton, JC ;
Ades, EW ;
Novak, L ;
van Ginkel, FW ;
Benjamin, WH .
JOURNAL OF INFECTIOUS DISEASES, 2003, 188 (03) :339-348