PaxVax CVD 103-HgR single-dose live oral cholera vaccine

被引:52
|
作者
Levine, Myron M. [1 ]
Chen, Wilbur H. [1 ]
Kaper, James B. [2 ]
Lock, Michael [3 ]
Danzig, Lisa [3 ]
Gurwith, Marc [3 ]
机构
[1] Univ Maryland, Ctr Vaccine Dev, Sch Med, 685 W Baltimore St, Baltimore, MD 21201 USA
[2] Univ Maryland, Dept Microbiol & Immunol, Sch Med, 685 W Baltimore St, Baltimore, MD 21201 USA
[3] PaxVax Inc, Redwood City, CA USA
关键词
Cholera; cholera vaccines; live oral vaccine; travelers' vaccines; vaccine; DOUBLE-BLIND; STRAIN CVD-103-HGR; FIELD-TRIAL; HOUSEHOLD CONTACTS; ANTIBODY-RESPONSES; NORTH AMERICANS; UNITED-STATES; IMMUNOGENICITY; SAFETY; O1;
D O I
10.1080/14760584.2017.1291348
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction: Cholera remains a problem in developing countries and a risk for travelers. Hypochlorhydria, blood group O, cardiac and renal disease increase the risk of developing cholera gravis. Oral vaccines containing inactivated Vibrio cholerae and requiring two doses are available in some countries. No cholera vaccine had been available for U.S. travelers for decades until 2016 when CVD 103-HgR (VAXCHORA), an oral live attenuated vaccine, was licensed by the U.S. FDA.Areas covered: Enduring protection following wild-type cholera provided the rationale to develop a single-dose live oral vaccine. CVD 103-HgR is well-tolerated and protects against cholera caused by V. cholerae O1 of either serotype (Inaba, Ogawa) and biotype (El Tor, Classical). Since 90% vaccine efficacy is evident 10days post-ingestion of a single dose, CVD 103-HgR can rapidly protect travelers. Vibriocidal antibody seroconversion correlates with protection; >90% of U.S. adult (including elderly) vaccinees seroconvert. The U.S. Public Health Service's Advisory Committee on Immunization Practices recommends CVD 103-HgR for U.S. travelers to areas of ongoing cholera transmission.Expert commentary: Next steps include evaluations in children, post-licensure safety and effectiveness monitoring, diminishing cold chain constraints, optimizing a high-dose' formulation for developing countries, and diminishing/eliminating the need for water to administer a dose.
引用
收藏
页码:197 / 213
页数:17
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