Cholera vaccines

Citation
Et. Ryan et Sb. Calderwood, Cholera vaccines, CLIN INF D, 31(2), 2000, pp. 561-565
Citations number
36
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Immunology
Journal title
CLINICAL INFECTIOUS DISEASES
ISSN journal
10584838 → ACNP
Volume
31
Issue
2
Year of publication
2000
Pages
561 - 565
Database
ISI
SICI code
1058-4838(200008)31:2<561:CV>2.0.ZU;2-G
Abstract
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, paren terally administered, phenol-inactivated vaccine is available. Outside the United States, 2 additional vaccines are commercially available: an oral ki lled whole cell-cholera toxin recombinant B subunit vaccine (WC-rBS) and an oral live attenuated Vibrio cholerae vaccine (CVD 103-HgR), These oral vac cines are well tolerated. In field trials, WC-rBS provides 80%-85% protecti on front cholera caused by V. cholerae serogroup O1 for at least 6 months. In volunteer studies, CVD 103-HgR provides 62%-100% protection against chol era caused by V. cholerae for at least 6 months. No commercially available cholera vaccine protects against disease caused by V. cholerae serogroup O1 39. New cholera vaccines are being developed.