Cholera vaccines

被引:60
作者
Ryan, ET
Calderwood, SB
机构
[1] Massachusetts Gen Hosp, Div Infect Dis, Trop & Geog Med Ctr, Travelers Advice & Immunizat Ctr, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
[3] Harvard Univ, Sch Med, Dept Microbiol & Mol Genet, Boston, MA 02115 USA
关键词
D O I
10.1086/313951
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cholera causes significant morbidity and mortality worldwide. For travelers, the risk of developing cholera per month of stay in a developing country is similar to 0.001%-0.01%, and cholera may present as traveler's diarrhea. In the United States, only a poorly tolerated, marginally effective, parenterally administered, phenol-inactivated vaccine is available. Outside the United States, 2 additional vaccines are commercially available: an oral killed whole cell-cholera toxin recombinant B subunit vaccine (WC-rBS) and an oral live attenuated Vibrio cholerae vaccine (CVD 103-HgR), These oral vaccines are well tolerated. In field trials, WC-rBS provides 80%-85% protection front cholera caused by V. cholerae serogroup O1 for at least 6 months. In volunteer studies, CVD 103-HgR provides 62%-100% protection against cholera caused by V. cholerae for at least 6 months. No commercially available cholera vaccine protects against disease caused by V. cholerae serogroup O139. New cholera vaccines are being developed.
引用
收藏
页码:561 / 565
页数:5
相关论文
共 36 条
[1]  
[Anonymous], 1992, MMWR-MORBID MORTAL W, V41, P134
[2]   IMMUNOGENICITY IN PERUVIAN VOLUNTEERS OF A BOOSTER DOSE OF ORAL CHOLERA VACCINE CONSISTING OF WHOLE CELLS PLUS RECOMBINANT-B-SUBUNIT [J].
BEGUE, RE ;
CASTELLARES, G ;
CABEZAS, C ;
SANCHEZ, JL ;
MEZA, R ;
WATTS, DM ;
TAYLOR, DN .
INFECTION AND IMMUNITY, 1995, 63 (09) :3726-3728
[3]  
CLEMENS JD, 1986, LANCET, V2, P124
[4]   FIELD TRIAL OF ORAL CHOLERA VACCINES IN BANGLADESH - RESULTS FROM 3-YEAR FOLLOW-UP [J].
CLEMENS, JD ;
SACK, DA ;
HARRIS, JR ;
VANLOON, F ;
CHAKRABORTY, J ;
AHMED, F ;
RAO, MR ;
KHAN, MR ;
YUNUS, M ;
HUDA, N ;
STANTON, BF ;
KAY, BA ;
WALTER, S ;
EECKELS, R ;
SVENNERHOLM, AM ;
HOLMGREN, J .
LANCET, 1990, 335 (8684) :270-273
[5]   CROSS-PROTECTION BY B-SUBUNIT WHOLE CELL CHOLERA VACCINE AGAINST DIARRHEA ASSOCIATED WITH HEAT-LABILE TOXIN PRODUCING ENTERO-TOXIGENIC ESCHERICHIA-COLI - RESULTS OF A LARGE-SCALE FIELD TRIAL [J].
CLEMENS, JD ;
SACK, DA ;
HARRIS, JR ;
CHAKRABORTY, J ;
NEOGY, PK ;
STANTON, B ;
HUDA, N ;
KHAN, MU ;
KAY, BA ;
KHAN, MR ;
ANSARUZZAMAN, M ;
YUNUS, M ;
RAO, MR ;
SVENNERHOLM, AM ;
HOLMGREN, J .
JOURNAL OF INFECTIOUS DISEASES, 1988, 158 (02) :372-377
[6]  
CLEMENS JD, 1988, LANCET, V1, P1375
[7]  
COSTER TS, 1995, LANCET, V345, P949, DOI 10.1016/S0140-6736(95)90698-3
[8]   SAFETY AND IMMUNOGENICITY OF A BOOSTER DOSE OF VIBRIO-CHOLERAE CVD-103-HGR LIVE ORAL CHOLERA VACCINE IN SWISS ADULTS [J].
CRYZ, SJ ;
LEVINE, MM ;
LOSONSKY, G ;
KAPER, JB ;
ALTHAUS, B .
INFECTION AND IMMUNITY, 1992, 60 (09) :3916-3917
[9]   Phase 1 evaluation of Vibrio cholerae O1, serotype Inaba, polysaccharide-cholera toxin conjugates in adult volunteers [J].
Gupta, RK ;
Taylor, DN ;
Bryla, DA ;
Robbins, JB ;
Szu, SSC .
INFECTION AND IMMUNITY, 1998, 66 (07) :3095-3099
[10]  
Holmgren J., 1994, P415