Literature DB >> 17074855

Immune response, ciprofloxacin activity, and gender differences after human experimental challenge by two strains of enterotoxigenic Escherichia coli.

T S Coster1, M K Wolf, E R Hall, F J Cassels, D N Taylor, C T Liu, F C Trespalacios, A DeLorimier, D R Angleberger, C E McQueen.   

Abstract

In order to test vaccines against enterotoxigenic Escherichia coli (ETEC)-induced diarrhea, challenge models are needed. In this study we compared clinical and immunological responses after North American volunteers were orally challenged by two ETEC strains. Groups of approximately eight volunteers received 10(9) or 10(10) CFU of E. coli B7A (LT+ ST+ CS6+) or 10(8) or 10(9) CFU of E. coli H10407 (LT+ ST+ CFA/I+). About 75% of the volunteers developed diarrhea after challenge with 10(10) CFU B7A or either dose of H10407. B7A had a shorter incubation period than H10407 (P = 0.001) and caused milder illness; the mean diarrheal output after H10407 challenge was nearly twice that after B7A challenge (P = 0.01). Females had more abdominal complaints, and males had a higher incidence of fever. Ciprofloxacin generally diminished or stopped symptoms and shedding by the second day of antibiotic treatment, but four subjects shed for one to four additional days. The immune responses to colonization factors CS6 and colonization factor antigen I (CFA/I) and to heat-labile toxin (LT) were measured. The responses to CFA/I were the most robust responses; all volunteers who received H10407 had serum immunoglobulin A (IgA) and IgG responses, and all but one volunteer had antibody-secreting cell (ASC) responses. One-half the volunteers who received B7A had an ASC response to CS6, and about one-third had serum IgA or IgG responses. Despite the differences in clinical illness and immune responses to colonization factors, the immune responses to LT were similar in all groups and were intermediate between the CFA/I and CS6 responses. These results provide standards for immune responses after ETEC vaccination.

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Year:  2006        PMID: 17074855      PMCID: PMC1828404          DOI: 10.1128/IAI.01131-06

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  59 in total

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Authors:  E R Hall; T F Wierzba; C Ahrén; M R Rao; S Bassily; W Francis; F Y Girgis; M Safwat; Y J Lee; A M Svennerholm; J D Clemens; S J Savarino
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5.  Identification and molecular characterization of EatA, an autotransporter protein of enterotoxigenic Escherichia coli.

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Review 6.  Chronic episodic disorders in women.

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Review 8.  The brain-gut axis in irritable bowel syndrome--clinical aspects.

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Authors:  David E Katz; Arthur J DeLorimier; Marcia K Wolf; Eric R Hall; Frederick J Cassels; John E van Hamont; Rhonda L Newcomer; Mitra A Davachi; David N Taylor; Charles E McQueen
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3.  A combination vaccine consisting of three live attenuated enterotoxigenic Escherichia coli strains expressing a range of colonization factors and heat-labile toxin subunit B is well tolerated and immunogenic in a placebo-controlled double-blind phase I trial in healthy adults.

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4.  Case series study of traveler's diarrhea in U.S. military personnel at Incirlik Air Base, Turkey.

Authors:  C K Porter; H El Mohammady; S Baqar; D M Rockabrand; S D Putnam; D R Tribble; M S Riddle; R W Frenck; P Rozmajzl; E Kilbane; A Fox; R Ruck; M Lim; Y J Johnston; E Murphy; J W Sanders
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5.  Establishment and Validation of Pathogenic CS17+ and CS19+ Enterotoxigenic Escherichia coli Challenge Models in the New World Primate Aotus nancymaae.

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6.  Refinement of a human challenge model for evaluation of enterotoxigenic Escherichia coli vaccines.

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7.  The oral, live attenuated enterotoxigenic Escherichia coli vaccine ACE527 reduces the incidence and severity of diarrhea in a human challenge model of diarrheal disease.

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9.  Enterotoxigenic Escherichia coli-blood group A interactions intensify diarrheal severity.

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10.  Genetic diversity of heat-labile toxin expressed by enterotoxigenic Escherichia coli strains isolated from humans.

Authors:  M A Lasaro; J F Rodrigues; C Mathias-Santos; B E C Guth; A Balan; M E Sbrogio-Almeida; L C S Ferreira
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