Rotavirus vaccines Opportunities and challenges

被引:45
作者
Grimwood, Keith [1 ,2 ]
Lambert, Stephen B. [1 ,3 ]
机构
[1] Royal Childrens Hosp, Sir Albert Sakzewski Virus Res Ctr, Queensland Paediat Infect Dis Lab, Herston, Qld 4029, Australia
[2] Univ Queensland, Discipline Pediat & Child Hlth, Brisbane, Qld, Australia
[3] Univ Queensland, Clin Med Virol Ctr, Brisbane, Qld, Australia
来源
HUMAN VACCINES | 2009年 / 5卷 / 02期
关键词
rotavirus; gastroenteritis; diarrhea; vaccine; immunisation; 1ST; 2; YEARS; UNITED-STATES; ANTIBODY-RESPONSES; ACUTE GASTROENTERITIS; SERUM ANTIBODY; YOUNG-CHILDREN; DOUBLE-BLIND; RISK-FACTORS; INFECTION; INFANTS;
D O I
10.4161/hv.5.2.6924
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Each year rotavirus gastroenteritis episodes in young children cause more than 500,000 deaths and 2.4 million hospital admissions worldwide. Vaccine development became a priority when improved personal hygiene and living standards failed to significantly reduce this disease burden. Rotavirus vaccines were developed mimicking natural immunity by protecting against severe gastroenteritis in young children, which would otherwise lead to health-care attendance, hospitalization or even death. Licensed rotavirus vaccines appear safe and are well-tolerated. In high and middle-income countries they provide 80-100% protection against severe disease and 70-80% protection against rotavirus gastroenteritis of any severity, depending upon the population studied. However, rotavirus vaccines remain to be fully evaluated in low-income countries where reduced immunogenicity of oral vaccines, greater strain diversity and difficulties reaching target populations might decrease immunization program performance. Nevertheless, if these challenges are met, rotavirus vaccines should help reduce the 5% of all childhood deaths attributable to rotavirus gastroenteritis.
引用
收藏
页码:57 / 69
页数:13
相关论文
共 151 条
[1]   Timeliness of vaccination and its effects on fraction of vaccinated population [J].
Akmatov, Manas K. ;
Kretzschmar, Mirjam ;
Kraemer, Alexander ;
Mikolajczyk, Rafael T. .
VACCINE, 2008, 26 (31) :3805-3811
[2]   Rotavirus infection in adults [J].
Anderson, EJ ;
Weber, SG .
LANCET INFECTIOUS DISEASES, 2004, 4 (02) :91-99
[3]  
ANSARI SA, 1991, REV INFECT DIS, V13, P448
[4]   Excretion of serotype G1 rotavirus strains by asymptomatic staff: A possible source of nosocomial infection [J].
Barnes, GL ;
Callaghan, SL ;
Kirkwood, CD ;
Bogdanovic-Sakran, N ;
Johnston, LJ ;
Bishop, RF .
JOURNAL OF PEDIATRICS, 2003, 142 (06) :722-725
[5]   Early phase II trial of human rotavirus vaccine candidate RV3 [J].
Barnes, GL ;
Lund, JS ;
Mitchell, SV ;
De Bruyn, L ;
Piggford, L ;
Smith, AL ;
Furmedge, J ;
Masendycz, PJ ;
Bugg, HC ;
Bogdanovic-Sakran, N ;
Carlin, JB ;
Bishop, RF .
VACCINE, 2002, 20 (23-24) :2950-2956
[7]   PROTECTION CONFERRED BY NEONATAL ROTAVIRUS INFECTION AGAINST SUBSEQUENT ROTAVIRUS DIARRHEA [J].
BHAN, MK ;
LEW, JF ;
SAZAWAL, S ;
DAS, BK ;
GENTSCH, JR ;
GLASS, RI .
JOURNAL OF INFECTIOUS DISEASES, 1993, 168 (02) :282-287
[8]   Safety and immunogenicity of two live attenuated human rotavirus vaccine candidates, 116E and I321, in infants: Results of a randomised controlled trial [J].
Bhandari, Nita ;
Sharma, Pooja ;
Glass, Roger I. ;
Ray, Pratima ;
Greenberg, Harry ;
Taneja, Sunita ;
Saksena, Manju ;
Rao, C. Durga ;
Gentsch, Jon R. ;
Parashar, Umesh ;
Maldonado, Yvonne ;
Ward, Richard L. ;
Bhan, M. K. .
VACCINE, 2006, 24 (31-32) :5817-5823
[9]   CLINICAL IMMUNITY AFTER NEONATAL ROTAVIRUS INFECTION - A PROSPECTIVE LONGITUDINAL-STUDY IN YOUNG-CHILDREN [J].
BISHOP, RF ;
BARNES, GL ;
CIPRIANI, E ;
LUND, JS .
NEW ENGLAND JOURNAL OF MEDICINE, 1983, 309 (02) :72-76
[10]   VIRUS-PARTICLES IN EPITHELIAL-CELLS OF DUODENAL MUCOSA FROM CHILDREN WITH ACUTE NON-BACTERIAL GASTROENTERITIS [J].
BISHOP, RF ;
DAVIDSON, GP .
LANCET, 1973, 2 (7841) :1281-1283