Immunogenicity of New Primary Immunization Schedules With Inactivated Poliovirus Vaccine and Bivalent Oral Polio Vaccine for the Polio Endgame: A Review

被引:22
|
作者
Bandyopadhyay, Ananda S. [1 ]
Modlin, John F. [1 ]
Wenger, Jay [1 ]
Gast, Chris
机构
[1] Bill & Melinda Gates Fdn, 1432 Elliott Ave W, Seattle, WA 98119 USA
基金
比尔及梅琳达.盖茨基金会;
关键词
inactivated poliovirus vaccine; bivalent oral poliovirus vaccine; monovalent oral poliovirus vaccine; polio eradication; RANDOMIZED CONTROLLED-TRIAL; LATIN-AMERICAN INFANTS; OPEN-LABEL; INTESTINAL IMMUNITY; MUCOSAL IMMUNITY; SAFETY; CESSATION; RESPONSES; OPV; IPV;
D O I
10.1093/cid/ciy633
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In May 2016, countries using oral polio vaccine for routine immunization switched from trivalent oral poliovirus vaccine (tOPV) to bivalent type 1 and 3 OPV (bOPV). This was done in order to reduce risks from type 2 vaccine-derived polioviruses (VDPV2) and vaccine-associated paralytic poliomyelitis (VAPP) and to introduce >= 1 dose of inactivated poliovirus vaccine (IPV) to mitigate postswitch loss of type 2 immunity. We conducted a literature review of studies that assessed humoral and intestinal immunogenicity induced by the newly recommended schedules. Differences in seroconversion rates were closely associated with both timing of first IPV administration and number of doses administered. All studies demonstrated high levels of immunity for types 1 and 3 regardless of immunization schedule. When administered late in the primary series, a second dose of IPV closed the humoral immunity gap against polio type 2 associated with a single dose. IPV doses and administration schedules appear to have limited impact on type 2 excretion following challenge.
引用
收藏
页码:S35 / S41
页数:7
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