Literature DB >> 8605522

Safety and immunogenicity of oral killed whole cell recombinant B subunit cholera vaccine in Barranquilla, Colombia.

A Concha1, A Giraldo, E Castañeda, M Martínez, F de la Hoz, F Rivas, A Depetris, A M Svennerholm, D A Sack.   

Abstract

In January and February 1992, an assessment was conducted of the safety and immunogenicity of two doses of a new oral cholera vaccine prepared from the recombinant B subunit of the toxin and from killed whole cells (rBS/WC) in 1,165 individuals between the ages of 12 months and 64 years in Barranquilla, Colombia. This was a randomized, double-blind placebo-controlled study. Participants received two doses of either the vaccine or a placebo (killed Escherichia coli K12) over a two-week interval. Few symptoms were detected during the three days following administration of the initial dose and even fewer following the second. Sera obtained upon administration of the first dose and two weeks after administration of the second were tested for Vibrio cholerae 01 Inaba vibriocidal antibodies and antitoxins. Geometric mean titers (GMT) of vibriocidal antibodies were found to increase two-fold in subjects receiving the vaccine. In the paired samples taken from vaccinated subjects, two-fold or greater increases were observed in 44% and four-fold or greater increases were observed in 34%, as compared to similar increases in 9.2% and 2.2% of the sera taken from those receiving the placebo (P < 0.05). The GMTs of IgG and IgA antitoxins, as determined by ELISA, increased by factors of 4 and 3.2, respectively, in those receiving the vaccine, as compared to factors of 1.1 and 1.1 in those given the placebo (P < 0.001 for IgG, P < 0.01 for IgA). Approximately 80% of the paired samples from the vaccinated group showed an increase of both IgG and IgA antitoxins > or = 1.5, as compared to only about 20% of those in the placebo group (P < 0.000001). Belonging to the O blood group did not significantly affect the immune response. Children under age four tended to show a weaker vibriocidal antibody response and a stronger antitoxin response than older subjects. The two doses of oral vaccine were found to be safe and without attributable side-effects. The vibriocidal antibody and antitoxin responses were similar to those obtained previously with the conventional oral killed whole cell B subunit cholera vaccine.

Entities:  

Keywords:  Americas; Bacterial And Fungal Diseases; Biology; Cholera; Colombia; Developing Countries; Diseases; Double-blind Studies; Health; Hematological Effects; Hemic System; Immunity; Immunoglobulin Alterations; Immunological Effects; Infections; Latin America; Physiology; Public Health; Research Methodology; Research Report; Safety; South America; Studies; Vaccines--administraction and dosage; Vaccines--side effects

Mesh:

Substances:

Year:  1995        PMID: 8605522

Source DB:  PubMed          Journal:  Bull Pan Am Health Organ        ISSN: 0085-4638


  8 in total

1.  The WHO Global Programme for Vaccines and Immunization Vaccine Trial Registry.

Authors:  S E Robertson; M V Mayans; S Horsfall; P F Wright; J Clemens; B Ivanoff; P H Lambert
Journal:  Bull World Health Organ       Date:  1997       Impact factor: 9.408

Review 2.  Killed oral cholera vaccines: history, development and implementation challenges.

Authors:  Anna Lena Lopez; Maria Liza Antoinette Gonzales; Josephine G Aldaba; G Balakrish Nair
Journal:  Ther Adv Vaccines       Date:  2014-09

3.  Comparison of alternative buffers for use with a new live oral cholera vaccine, Peru-15, in outpatient volunteers.

Authors:  D A Sack; J Shimko; R B Sack; J G Gomes; K MacLeod; D O'Sullivan; D Spriggs
Journal:  Infect Immun       Date:  1997-06       Impact factor: 3.441

4.  Review of oral cholera vaccines: efficacy in young children.

Authors:  Cristina Masuet Aumatell; J M Ramon Torrell; Jane N Zuckerman
Journal:  Infect Drug Resist       Date:  2011-09-14       Impact factor: 4.003

Review 5.  Vaccines for the prevention of diarrhea due to cholera, shigella, ETEC and rotavirus.

Authors:  Jai K Das; Anjali Tripathi; Anum Ali; Amman Hassan; Chesarahima Dojosoeandy; Zulfiqar A Bhutta
Journal:  BMC Public Health       Date:  2013-09-17       Impact factor: 3.295

6.  Safety and immunogenicity of the killed bivalent (O1 and O139) whole-cell cholera vaccine in the Philippines.

Authors:  Maria Rosario Z Capeding; Maria Liza Antoinette M Gonzales; Mandeep Singh Dhingra; Naveena Aloysia D'Cor; Venkat Jayanth Midde; Badri Narayan Patnaik; Yaël Thollot; Eric Desauziers
Journal:  Hum Vaccin Immunother       Date:  2017-10-03       Impact factor: 3.452

7.  The Nontoxic Cholera B Subunit Is a Potent Adjuvant for Intradermal DC-Targeted Vaccination.

Authors:  Laura Antonio-Herrera; Oscar Badillo-Godinez; Oscar Medina-Contreras; Araceli Tepale-Segura; Alberto García-Lozano; Lourdes Gutierrez-Xicotencatl; Gloria Soldevila; Fernando R Esquivel-Guadarrama; Juliana Idoyaga; Laura C Bonifaz
Journal:  Front Immunol       Date:  2018-09-27       Impact factor: 7.561

8.  Bivalent oral cholera vaccine in participants aged 1 year and older in the Dominican Republic: A phase III, single-arm, safety and immunogenicity trial.

Authors:  Lina Cordero De Los Santos; Jesús Feris-Iglesias; Naveena Aloysia D'Cor; Venkata Jayanth Midde; Badri Narayan Patnaik; Yaël Thollot; Anvar Rasuli; Eric Desauziers
Journal:  Hum Vaccin Immunother       Date:  2018-02-22       Impact factor: 3.452

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.