New approaches in oral rotavirus vaccines

被引:6
作者
Defo, Zenas Kuate [1 ]
Lee, Byong [1 ,2 ]
机构
[1] McGill Univ, Dept Microbiol & Immunol, Duff Med Bldg,3775 Univ St,Room 511, Montreal, PQ H3A 2B4, Canada
[2] Jiangnan Univ, Sch Biotechnol, Wuxi, Peoples R China
关键词
Biodegradable polymers; combination therapy; lactic acid bacteria; rotaviral dehydrating diarrhea; virus-like particle; VIRUS-LIKE PARTICLES; INTUSSUSCEPTION RISK; INDUCED DIARRHEA; IMMUNE-RESPONSE; VACCINATION PROGRAMS; ANTIBODY FRAGMENTS; GNOTOBIOTIC PIGS; CONTROLLED-TRIAL; DOUBLE-BLIND; IMMUNOGENICITY;
D O I
10.3109/1040841X.2014.962479
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Rotavirus is the leading cause of severe dehydrating diarrhea worldwide, and affects primarily developing nations, in large part because of the inaccessibility of vaccines and high rates of mortality present therein. At present, there exist two oral rotaviral vaccines, Rotarix and RotaTeq. These vaccines are generally effective in their actions: however, associated costs often stymie their effectiveness, and they continue to be associated with a slight risk of intussusception. While different programs are being implemented worldwide to enhance vaccine distribution and monitor vaccine administration for possible intussusception in light of recent WHO recommendation, another major problem persists: that of the reduced efficacy of the existing rotaviral vaccines in developing countries over time. The development of new oral rotavirus vaccine classes - live-attenuated vaccines, virus-like particles, lactic acid bacteria-containing vaccines, combination therapy with immunoglobulins, and biodegradable polymer-encapsulated vaccines - could potentially circumvent these problems.
引用
收藏
页码:495 / 505
页数:11
相关论文
共 101 条
[51]   VP6-sequence-based cutoff values as a criterion for rotavirus species demarcation [J].
Matthijnssens, Jelle ;
Otto, Peter H. ;
Ciarlet, Max ;
Desselberger, Ulrich ;
Van Ranst, Marc ;
Johne, Reimar .
ARCHIVES OF VIROLOGY, 2012, 157 (06) :1177-1182
[52]   Uniformity of rotavirus strain nomenclature proposed by the Rotavirus Classification Working Group (RCWG) [J].
Matthijnssens, Jelle ;
Ciarlet, Max ;
McDonald, Sarah M. ;
Attoui, Houssam ;
Banyai, Krisztian ;
Brister, J. Rodney ;
Buesa, Javier ;
Esona, Mathew D. ;
Estes, Mary K. ;
Gentsch, Jon R. ;
Iturriza-Gomara, Miren ;
Johne, Reimar ;
Kirkwood, Carl D. ;
Martella, Vito ;
Mertens, Peter P. C. ;
Nakagomi, Osamu ;
Parreno, Viviana ;
Rahman, Mustafizur ;
Ruggeri, Franco M. ;
Saif, Linda J. ;
Santos, Norma ;
Steyer, Andrej ;
Taniguchi, Koki ;
Patton, John T. ;
Desselberger, Ulrich ;
Van Ranst, Marc .
ARCHIVES OF VIROLOGY, 2011, 156 (08) :1397-1413
[53]   A calculated risk: the Salk polio vaccine field trials of 1954 [J].
Meldrum, M .
BRITISH MEDICAL JOURNAL, 1998, 317 (7167) :1233-1236
[54]  
Mullooly J, 1999, AM J EPIDEMIOL, V149, P186
[55]   Reappraisal of the association of intussusception with the licensed live rotavirus vaccine challenges initial conclusions [J].
Murphy, BR ;
Morens, DM ;
Simonsen, L ;
Chanock, RM ;
La Montagne, JR ;
Kapikian, AZ .
JOURNAL OF INFECTIOUS DISEASES, 2003, 187 (08) :1301-1308
[56]   Improved Immunogenicity of Biodegradable Polymer Particles Entrapped Rotavirus Vaccine [J].
Nayak, Bismita ;
Ray, Alok R. ;
Panda, Amulya K. ;
Ray, Pratima .
JOURNAL OF BIOMATERIALS APPLICATIONS, 2011, 25 (05) :469-496
[57]  
Nayak B, 2009, J MICROENCAPSUL, V26, P154, DOI [10.1080/02652040802211709 , 10.1080/02652040802211709]
[58]   Poly(lactide-co-glycolide) microparticles for the development of single-dose controlled-release vaccines [J].
O'Hagan, DT ;
Singh, M ;
Gupta, RK .
ADVANCED DRUG DELIVERY REVIEWS, 1998, 32 (03) :225-246
[59]   Rotarix™ (RIX4414):: an oral human rotavirus vaccine [J].
O'Ryan, Miguel .
EXPERT REVIEW OF VACCINES, 2007, 6 (01) :11-19
[60]   Update on Rotarix™: an oral human rotavirus vaccine [J].
O'Ryan, Miguel ;
Linhares, Alexandre C. .
EXPERT REVIEW OF VACCINES, 2009, 8 (12) :1627-1641