Adjuvants and inactivated polio vaccine: A systematic review

被引:34
|
作者
Hawken, Jennifer [1 ]
Troy, Stephanie B. [1 ]
机构
[1] Eastern Virginia Med Sch, Off Student Affairs, Norfolk, VA 23501 USA
关键词
Adjuvant; Inactivated polio vaccine (IPV); Immunogenicity; MINERAL OIL ADJUVANT; IMMUNE-RESPONSE; IMMUNOGENIC ACTIVITY; CALCIUM-PHOSPHATE; STEARYL TYROSINE; MACACA MULATTA; CLINICAL-TRIAL; CPG DNA; SAFETY; CHITOSAN;
D O I
10.1016/j.vaccine.2012.09.059
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Poliomyelitis is nearing universal eradication; in 2011, there were 650 cases reported globally. When wild polio is eradicated, global oral polio vaccine (OPV) cessation followed by use of universal inactivated polio vaccine (IPV) is believed to be the safest vaccination strategy as IPV does not mutate or run the risk of vaccine derived outbreaks that OPV does. However, IPV is significantly more expensive than OPV. One strategy to make IPV more affordable is to reduce the dose by adding adjuvants, compounds that augment the immune response to the vaccine. No adjuvants are currently utilized in stand-alone IPV; however, several have been explored over the past six decades. From aluminum, used in many licensed vaccines, to newer and more experimental adjuvants such as synthetic DNA, a diverse group of compounds has been assessed with varying strengths and weaknesses. This review summarizes the studies to date evaluating the efficacy and safety of adjuvants used with IPV. (c) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6971 / 6979
页数:9
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