Oral delivery of nanoparticle-based vaccines

被引:121
作者
Marasini, Nirmal [1 ]
Skwarczynski, Mariusz [1 ]
Toth, Istvan [1 ,2 ]
机构
[1] Univ Queensland, Sch Chem & Mol Biosci, St Lucia, Qld 4072, Australia
[2] Univ Queensland, Sch Pharm, Woolloongabba, Qld 4102, Australia
基金
英国医学研究理事会;
关键词
adjuvant; bilosomes; liposomes; M-cells; mucosal vaccine; nanoparticle-based vaccine; oral vaccine; virus-like particle; VIRUS-LIKE PARTICLES; SYSTEMIC IMMUNE-RESPONSES; ANTHRAX PROTECTIVE ANTIGEN; IN-VITRO CHARACTERIZATION; M-CELLS; STIMULATING COMPLEXES; GOLD NANOPARTICLES; CHITOSAN NANOPARTICLES; MUCOSAL IMMUNIZATION; ENHANCED MUCOSAL;
D O I
10.1586/14760584.2014.936852
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Most infectious diseases are caused by pathogenic infiltrations from the mucosal tract. Therefore, vaccines delivered to the mucosal tissues can mimic natural infections and provide protection at the first site of infection. Thus, mucosal, especially, oral delivery is becoming the most preferred mode of vaccination. However, oral vaccines have to overcome several barriers such as the extremely low pH of the stomach, the presence of proteolytic enzymes and bile salts as well as low permeability in the intestine. Several formulations based on nanoparticle strategies are currently being explored to prepare stable oral vaccine formulations. This review briefly discusses several molecular mechanisms involved in intestinal immune cell activation and various aspects of oral nanoparticle-based vaccine design that should be considered for improved mucosal and systemic immune responses.
引用
收藏
页码:1361 / 1376
页数:16
相关论文
共 127 条
[1]  
Anonymous, 2010, Morbidity and Mortality Weekly Report, V59, P626
[2]   Imaging of size-dependent uptake and identification of novel pathways in mouse Peyer's patches using fluorescent organosilica particles [J].
Awaad, Aziz ;
Nakamura, Michihiro ;
Ishimura, Kazunori .
NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2012, 8 (05) :627-636
[3]   Enhancing Oral Vaccine Potency by Targeting Intestinal M Cells [J].
Azizi, Ali ;
Kumar, Ashok ;
Diaz-Mitoma, Francisco ;
Mestecky, Jiri .
PLOS PATHOGENS, 2010, 6 (11)
[4]  
Azmi Fazren, 2014, Hum Vaccin Immunother, V10, P778
[5]   Micro/nanoparticle adjuvants for antileishmanial vaccines: Present and future trends [J].
Badiee, Ali ;
Shargh, Vahid Heravi ;
Khamesipour, Ali ;
Jaafari, Mahmoud Reza .
VACCINE, 2013, 31 (05) :735-749
[6]   Quillaja saponaria extract as mucosal adjuvant with chitosan functionalized gold nanoparticles for mucosal vaccine delivery: Stability and immunoefficiency studies [J].
Barhate, Ganesh ;
Gautam, Manish ;
Gairola, Sunil ;
Jadhav, Suresh ;
Pokharkar, Varsha .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2013, 441 (1-2) :636-642
[7]   Re-utilization of germinal centers in multiple Peyer's patches results in highly synchronized, oligoclonal, and affinity-matured gut IgA responses [J].
Bergqvist, P. ;
Stensson, A. ;
Hazanov, L. ;
Holmberg, A. ;
Mattsson, J. ;
Mehr, R. ;
Bemark, M. ;
Lycke, N. Y. .
MUCOSAL IMMUNOLOGY, 2013, 6 (01) :122-135
[8]   Evaluation of immune responses to an oral typhoid vaccine, Ty21a, in children from 2 to 5 years of age in Bangladesh [J].
Bhuiyan, Taufiqur R. ;
Choudhury, Feroza K. ;
Khanam, Farhana ;
Saha, Amit ;
Abu Sayeed, Md. ;
Salma, Umme ;
Lundgren, Anna ;
Sack, David A. ;
Svennerholm, Ann-Mari ;
Qadri, Firdausi .
VACCINE, 2014, 32 (09) :1055-1060
[9]   Mucosal immunization with a novel nanoemulsion-based recombinant anthrax protective antigen vaccine protects against Bacillus anthracis spore challenge [J].
Bielinska, Anna U. ;
Janczak, Katarzyna W. ;
Landers, Jeffrey J. ;
Makidon, Paul ;
Sower, Laurie E. ;
Peterson, Johnny W. ;
Baker, James R., Jr. .
INFECTION AND IMMUNITY, 2007, 75 (08) :4020-4029
[10]  
Bolhassani A, 2013, HUM VACC IMMUNOTHER, V10, P2013