Tacket C O, Cohen M B, Wasserman S S, Losonsky G, Livio S, Kotloff K, Edelman R, Kaper J B, Cryz S J, Giannella R A, Schiff G, Levine M M
Center for Vaccine Development, University of Maryland School of Medicine, Baltimore, Maryland 21201, USA.
Infect Immun. 1999 Dec;67(12):6341-5. doi: 10.1128/IAI.67.12.6341-6345.1999.
CVD 103-HgR is a live oral cholera vaccine strain constructed by deleting 94% of the gene for the enzymatically active A subunit of cholera toxin from classical Inaba Vibrio cholerae O1 569B; the strain also contains a mercury resistance gene as an identifying marker. This vaccine was well tolerated and immunogenic in double-blind, controlled studies and was protective in open-label studies of volunteers challenged with V. cholerae O1. A randomized, double-blind, placebo-controlled, multicenter study of vaccine efficacy was designed to test longer-term protection of CVD 103-HgR against moderate and severe El Tor cholera in U.S. volunteers. A total of 85 volunteers (50 at the University of Maryland and 35 at Children's Hospital Medical Center/University of Cincinnati) were recruited for vaccination and challenge with wild-type V. cholerae El Tor Inaba. Volunteers were randomized in a double-blind manner to receive, with buffer, a single oral dose of either CVD 103-HgR (2 x 10(8) to 8 x 10(8) CFU) or placebo (killed E. coli K-12). About 3 months after immunization, 51 of these volunteers were orally challenged with 10(5) CFU of virulent V. cholerae O1 El Tor Inaba strain N16961, prepared from a standardized frozen inoculum. Ninety-one percent of the vaccinees had a >/=4-fold rise in serum vibriocidal antibodies after vaccination. After challenge, 9 (39%) of the 23 placebo recipients and 1 (4%) of the 28 vaccinees had moderate or severe diarrhea (>/=3-liter diarrheal stool) (P < 0.01; protective efficacy, 91%). A total of 21 (91%) of 23 placebo recipients and 5 (18%) of 28 vaccinees had any diarrhea (P < 0.001; protective efficacy, 80%). Peak stool V. cholerae excretion among placebo recipients was 1.1 x 10(7) CFU/g and among vaccinees was 4.9 x 10(2) CFU/g (P < 0.001). This vaccine could therefore be a safe and effective tool to prevent cholera in travelers.
CVD 103-HgR是一种口服霍乱活疫苗株,通过从经典稻叶型霍乱弧菌O1 569B中删除94%的霍乱毒素酶活性A亚基基因构建而成;该菌株还含有一个汞抗性基因作为识别标记。在双盲对照研究中,这种疫苗耐受性良好且具有免疫原性,在对受霍乱弧菌O1攻击的志愿者进行的开放标签研究中具有保护作用。一项关于疫苗效力的随机、双盲、安慰剂对照、多中心研究旨在测试CVD 103-HgR对美国志愿者中、重度埃尔托型霍乱的长期保护作用。总共招募了85名志愿者(马里兰大学50名,辛辛那提儿童医院医学中心/辛辛那提大学35名)进行疫苗接种并接受野生型霍乱弧菌埃尔托型稻叶株的攻击。志愿者以双盲方式随机接受,用缓冲液口服单剂量的CVD 103-HgR(2×10⁸至8×10⁸CFU)或安慰剂(灭活大肠杆菌K-12)。免疫后约3个月,其中51名志愿者口服10⁵CFU的强毒霍乱弧菌O1埃尔托型稻叶株N16961,该菌株由标准化冷冻接种物制备。91%的疫苗接种者接种疫苗后血清杀弧菌抗体升高≥4倍。攻击后,23名安慰剂接受者中有9名(39%)和28名疫苗接种者中有1名(4%)出现中度或重度腹泻(腹泻粪便≥3升)(P<0.01;保护效力为91%)。23名安慰剂接受者中有21名(91%)和28名疫苗接种者中有5名(18%)出现任何腹泻(P<0.001;保护效力为80%)。安慰剂接受者粪便中霍乱弧菌排泄峰值为1.1×10⁷CFU/g,疫苗接种者为4.9×10²CFU/g(P<0.001)。因此,这种疫苗可能是预防旅行者霍乱的一种安全有效的工具。