Chen Wilbur H, Cohen Mitchell B, Kirkpatrick Beth D, Brady Rebecca C, Galloway David, Gurwith Marc, Hall Robert H, Kessler Robert A, Lock Michael, Haney Douglas, Lyon Caroline E, Pasetti Marcela F, Simon Jakub K, Szabo Flora, Tennant Sharon, Levine Myron M
Center for Vaccine Development, University of Maryland School of Medicine, Baltimore.
Cincinnati Children's Hospital Medical Center, Ohio.
Clin Infect Dis. 2016 Jun 1;62(11):1329-1335. doi: 10.1093/cid/ciw145. Epub 2016 Mar 21.
No licensed cholera vaccine is presently available in the United States. Cholera vaccines available in other countries require 2 spaced doses. A single-dose cholera vaccine that can rapidly protect short-notice travelers to high-risk areas and help control explosive outbreaks where logistics render 2-dose immunization regimens impractical would be a major advance.PXVX0200, based on live attenuated Vibrio cholerae O1 classical Inaba vaccine strain CVD 103-HgR, elicits seroconversion of vibriocidal antibodies (a correlate of protection) within 10 days of a single oral dose. We investigated the protection conferred by this vaccine in a human cholera challenge model.
Consenting healthy adult volunteers, 18-45 years old, were randomly allocated 1:1 to receive 1 oral dose of vaccine (approximately 5 × 10(8) colony-forming units [CFU]) or placebo in double-blind fashion. Volunteers ingested approximately 1 × 10(5) CFU of wild-type V. cholerae O1 El Tor Inaba strain N16961 10 days or 3 months after vaccination and were observed on an inpatient research ward for stool output measurement and management of hydration.
The vaccine was well tolerated, with no difference in adverse event frequency among 95 vaccinees vs 102 placebo recipients. The primary endpoint, moderate (≥3.0 L) to severe (≥5.0 L) diarrheal purge, occurred in 39 of 66 (59.1%) placebo controls but only 2 of 35 (5.7%) vaccinees at 10 days (vaccine efficacy, 90.3%; P < .0001) and 4 of 33 (12.1%) vaccinees at 3 months (vaccine efficacy, 79.5%; P < .0001).
The significant vaccine efficacy documented 10 days and 3 months after 1 oral dose of PXVX0200 supports further development as a single-dose cholera vaccine.
NCT01895855.
目前美国没有获得许可的霍乱疫苗。其他国家现有的霍乱疫苗需要分两剂接种。对于那些接到通知后短期内前往高风险地区的旅行者,一种能迅速提供保护的单剂量霍乱疫苗,以及在后勤条件使得两剂免疫方案不切实际的情况下有助于控制霍乱爆发的疫苗,将是一项重大进展。PXVX0200基于减毒活霍乱弧菌O1古典伊纳巴疫苗株CVD 103-HgR,单剂口服后10天内可引发杀弧菌抗体(一种保护相关指标)的血清转化。我们在人体霍乱攻毒模型中研究了该疫苗提供的保护作用。
年龄在18至45岁之间、同意参与的健康成年志愿者按1:1随机分配,以双盲方式接受1剂口服疫苗(约5×10⁸菌落形成单位[CFU])或安慰剂。志愿者在接种疫苗后10天或3个月摄入约1×10⁵CFU的野生型霍乱弧菌O1埃尔托伊纳巴菌株N16961,并在住院研究病房接受观察,以测量粪便排出量并进行补液管理。
疫苗耐受性良好,95名接种疫苗者与102名接受安慰剂者的不良事件发生率无差异。主要终点,即中度(≥3.0升)至重度(≥5.0升)腹泻,在66名安慰剂对照组中有39名(59.1%)出现,但在接种疫苗者中,10天时35名中有2名(5.7%)出现(疫苗效力,90.3%;P<0.0001),3个月时33名中有4名(12.1%)出现(疫苗效力,79.5%;P<0.0001)。
单剂口服PXVX0200后10天和3个月记录到的显著疫苗效力支持其作为单剂量霍乱疫苗进一步研发。
NCT01895855。