The vaccine candidate Vibrio cholerae 638 is protective against cholera in healthy volunteers

被引:57
作者
García, L
Jidy, MD
García, H
Rodríguez, BL
Fernández, R
Año, G
Cedré, B
Valmaseda, T
Suzarte, E
Ramírez, M
Pino, Y
Campos, J
Menéndez, J
Valera, R
González, D
González, I
Pérez, O
Serrano, T
Lastre, M
Miralles, F
del Campo, J
Maestre, JL
Pérez, JL
Talavera, A
Pérez, A
Marrero, K
Ledón, T
Fando, R
机构
[1] Ctr Nacl Invest Cientif, Havana, Cuba
[2] Inst Finlay Sueros & Vacunas, Havana, Cuba
[3] Inst Med Trop Pedro Kouri, Havana, Cuba
关键词
D O I
10.1128/IAI.73.5.3018-3024.2005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Vibrio cholerae 638 is a living candidate cholera vaccine strain attenuated by deletion of the CTX Phi prophage from C7258 (O1, EI Tor Ogawa) and by insertion of the Clostridium thermocellum endoglucanase A gene into the hemagglutinin/protease coding sequence. This vaccine candidate was previously found to be well tolerated and immunogenic in volunteers. This article reports a randomized, double-blind, placebo-controlled trial conducted to test short-term protection conferred by 638 against subsequent V. cholerae infection and disease in volunteers in Cuba. A total of 45 subjects were enrolled and assigned to receive vaccine or placebo. The vaccine contained 10(9) CFU of freshly harvested 638 buffered with 1.3% NaHCO3, while the placebo was buffer alone. After vaccine but not after placebo intake, 96% of volunteers had at least a fourfold increase in vibriocidal antibody titers, and 50% showed a doubling of at least the lipopolysaccharide-specific immunoglobulin A titers in serum. At 1 month after vaccination, five volunteers from the vaccine group and five from the placebo group underwent an exploratory challenge study with 109 CFU of Delta CTX Phi attenuated mutant strain V. cholerae 81. Only two volunteers from the vaccine group shed strain 81 in their feces, but none of them experienced diarrhea; in the placebo group, all volunteers excreted the challenge strain, and three had reactogenic diarrhea. An additional 12 vaccinees and 9 placebo recipients underwent challenge with 7 x 10(5) CFU of virulent strain V. cholerae 3008 freshly harvested from a brain heart infusion agar plate and buffered with 1.3% NaHCO3. Three volunteers (25%) from the vaccine group and all from the placebo group shed the challenge agent in their feces. None of the 12 vaccinees but 7 volunteers from the placebo group had diarrhea, and 2 of the latter exhibited severe cholera (> 5,000 g of diarrheal stool). These results indicate that at 1 month after ingestion of a single oral dose (10(9) CFU) of strain 638, volunteers remained protected against cholera infection and disease provoked by the wild-type challenge agent V. cholerae 3008. We recommend that additional vaccine lots of 638 be prepared under good manufacturing practices for further evaluation.
引用
收藏
页码:3018 / 3024
页数:7
相关论文
共 27 条
[1]  
BENENSON AS, 1968, B WORLD HEALTH ORGAN, V38, P277
[2]  
Benitez JA, 1996, ARCH MED RES, V27, P275
[3]  
Benítez JA, 1999, INFECT IMMUN, V67, P539
[4]   Misleading negative findings in a field trial of killed, oral cholera vaccine in Peru [J].
Clemens, JD ;
Sack, DA ;
Ivanoff, B .
JOURNAL OF INFECTIOUS DISEASES, 2001, 183 (08) :1306-1308
[5]   Randomized, controlled human challenge study of the safety, immunogenicity, and protective efficacy of a single dose of Peru-15, a live attenuated oral cholera vaccine [J].
Cohen, MB ;
Giannella, RA ;
Bean, J ;
Taylor, DN ;
Parker, S ;
Hoeper, A ;
Wowk, S ;
Hawkins, J ;
Kochi, SK ;
Schiff, G ;
Killeen, KP .
INFECTION AND IMMUNITY, 2002, 70 (04) :1965-1970
[6]   A SOLID-PHASE ENZYME-LINKED IMMUNOSPOT (ELISPOT) ASSAY FOR ENUMERATION OF SPECIFIC ANTIBODY-SECRETING CELLS [J].
CZERKINSKY, CC ;
NILSSON, LA ;
NYGREN, H ;
OUCHTERLONY, O ;
TARKOWSKI, A .
JOURNAL OF IMMUNOLOGICAL METHODS, 1983, 65 (1-2) :109-121
[7]   Epidemiology, genetics, and ecology of toxigenic Vibrio cholerae [J].
Faruque, SM ;
Albert, MJ ;
Mekalanos, JJ .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 1998, 62 (04) :1301-+
[8]   VIBRIO-CHOLERAE HEMAGGLUTININ PROTEASE, COLONIAL VARIATION, VIRULENCE, AND DETACHMENT [J].
FINKELSTEIN, RA ;
BOESMANFINKELSTEIN, M ;
CHANG, Y ;
HASE, CC .
INFECTION AND IMMUNITY, 1992, 60 (02) :472-478
[9]  
Finkelstein Richard A., 1992, P155
[10]  
Imia LG, 1998, LAB ANIM SCI, V48, P538