TY - JOUR
T1 - Safety and immunogenicity of an oral, inactivated enterotoxigenic Escherichia coli plus cholera toxin B subunit vaccine in Bangladeshi adults and children
AU - Qadri, Firdausi
AU - Wennerås, Christine
AU - Ahmed, Firoz
AU - Asaduzzaman, Muhammad
AU - Saha, Debashish
AU - Albert, M. J.
AU - Sack, R. B.
AU - Svennerholm, Ann Mari
N1 - Funding Information:
This research was supported by the Swedish Agency for Research and Economic Cooperation (Sida-SAREC), the Swedish Medical Research Council and the International Centre for Diarrhoeal Disease Research, Bangladesh (ICDDR,B): Centre for Health and Population Research. The Centre is supported by agencies and countries which share its concern for the health problems of developing countries. This work was further supported by the Göteborg Medical Society stipend 94/275 and grant 93.270.
PY - 2000/6/1
Y1 - 2000/6/1
N2 - We have compared the B cell responses evoked in Bangladeshi, adults (n=11, median age 25 years) and children (n=21, median age 4.5 years), 7 days after intake of each of two doses of an oral, inactivated enterotoxigenic Escherichia coli (ETEC) vaccine composed of formalin-killed ETEC strains expressing the colonization factors, CFA/I, CFA/II and CFA/IV together with 1 mg of recombinant cholera toxin B-subunit (rCTB). The vaccine was well tolerated and only gave rise to negligible side effects. Peak antibody-secreting cell (ASC) response of the IgA isotype were seen 7 days after the first dose of the vaccine. The ASC responses to the different colonization factors (CFs) increased from a 29- to 46-fold (responder frequency 90-100%) in the adults and 13- to 24-fold (responder frequency 67-90%) in the children. The IgA-ASC response to rCTB also peaked after the first dose in the adults (426-fold, responder frequency 100%) and the children (46-fold, responder frequency 95%). Increased IgA antibody levels against CFA/I as well as IgA and IgG antibody levels to rCTB were seen in plasma after immunisation. About 86% of the children and 80% of the adults responded with faecal antibodies to rCTB, whereas about 67% of both groups responded to CFA/I.These results show that a single dose of the ETEC vaccine may elicit significant mucosal immune responses in both children and adults residing in an ETEC-endemic country such as Bangladesh. Copyright (C) 2000 Elsevier Science Ltd.
AB - We have compared the B cell responses evoked in Bangladeshi, adults (n=11, median age 25 years) and children (n=21, median age 4.5 years), 7 days after intake of each of two doses of an oral, inactivated enterotoxigenic Escherichia coli (ETEC) vaccine composed of formalin-killed ETEC strains expressing the colonization factors, CFA/I, CFA/II and CFA/IV together with 1 mg of recombinant cholera toxin B-subunit (rCTB). The vaccine was well tolerated and only gave rise to negligible side effects. Peak antibody-secreting cell (ASC) response of the IgA isotype were seen 7 days after the first dose of the vaccine. The ASC responses to the different colonization factors (CFs) increased from a 29- to 46-fold (responder frequency 90-100%) in the adults and 13- to 24-fold (responder frequency 67-90%) in the children. The IgA-ASC response to rCTB also peaked after the first dose in the adults (426-fold, responder frequency 100%) and the children (46-fold, responder frequency 95%). Increased IgA antibody levels against CFA/I as well as IgA and IgG antibody levels to rCTB were seen in plasma after immunisation. About 86% of the children and 80% of the adults responded with faecal antibodies to rCTB, whereas about 67% of both groups responded to CFA/I.These results show that a single dose of the ETEC vaccine may elicit significant mucosal immune responses in both children and adults residing in an ETEC-endemic country such as Bangladesh. Copyright (C) 2000 Elsevier Science Ltd.
KW - Antibody-secreting cells
KW - Eenterotoxigenic Escherichia coli
KW - Oral inactivated ETEC vaccine
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U2 - 10.1016/S0264-410X(00)00056-6
DO - 10.1016/S0264-410X(00)00056-6
M3 - Article
C2 - 10781858
AN - SCOPUS:0034213176
SN - 0264-410X
VL - 18
SP - 2704
EP - 2712
JO - Vaccine
JF - Vaccine
IS - 24
ER -