4.4 Article

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

期刊

EXPERT REVIEW OF VACCINES
卷 16, 期 3, 页码 197-213

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1080/14760584.2017.1291348

关键词

Cholera; cholera vaccines; live oral vaccine; travelers' vaccines; vaccine

资金

  1. NIH from the National Institute of Allergy and Infectious Diseases, NIH [AI19716]
  2. NIH [N01 42553, N01 45251]
  3. US Army Medical Research and Development Command [DAMA17-78-C-8011]
  4. National Institute of Allergy and Infectious Diseases, NIH [N01 AI 12666, N01 AI 45251, N01 62528, U01 35948, AI 15096]
  5. Consultative Group on Vaccine Development of the National Vaccine Program, USA
  6. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI019716] Funding Source: NIH RePORTER

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据