Immune Responses of Mice Immunized with Active Recombinant Shiga Toxin and Its Derivatives

Bacterial protein toxins have been exploited as therapeutic agents and as vaccines. An issue of deserving interest is development of new generations of vaccines and immune adjuvants. In this study an active assembled recombinant Shiga toxin of Escherichia coli (rStx1) and its derivatives, recombi...

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Main Authors: Mana Oloomi, Saeid Bouzari, Soheila Ajdary
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2008-06-01
Series:Iranian Journal of Allergy, Asthma and Immunology
Subjects:
Online Access:https://ijaai.tums.ac.ir/index.php/ijaai/article/view/200
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spelling doaj-50e7f995b7484fca8750303465bfe5b32020-11-25T04:12:30ZengTehran University of Medical SciencesIranian Journal of Allergy, Asthma and Immunology1735-15021735-52492008-06-0172200Immune Responses of Mice Immunized with Active Recombinant Shiga Toxin and Its Derivatives Mana Oloomi0 Saeid Bouzari1 Soheila Ajdary2 Bacterial protein toxins have been exploited as therapeutic agents and as vaccines. An issue of deserving interest is development of new generations of vaccines and immune adjuvants. In this study an active assembled recombinant Shiga toxin of Escherichia coli (rStx1) and its derivatives, recombinant A and B subunits (Stx1-A and Stx1-B), were used to immunize mice. The elicited antibody responses were compared with and without using adjuvant.  Protection against intraperitoneal lethal dose of rStx challenge was observed by immunization with sublethal dose of rStx1, rStx-A and rStx-B subunits. The immunological studies on toxin subunits can be used for immunization against systemic shiga toxin mediated disease and also subunits as a vector for antigen presentation in immunotherapeutic approaches. In our experiment, while stimulation of the immune system by A and B subunits were different, both subunits produced neutralizing antibodies. Regarding B subunit the amount of specific IgG1/IgG2a antibody ratio was higher than A subunit. In addition B subunit stimulated proliferation of immune cells with IFNg production the same as rStx1, suggesting that B subunit can be used as an immunomodulator to stimulate the immune response in conjunction with other recombinant proteins. https://ijaai.tums.ac.ir/index.php/ijaai/article/view/200A and B subunitsImmunomodulationShiga toxin
collection DOAJ
language English
format Article
sources DOAJ
author Mana Oloomi
Saeid Bouzari
Soheila Ajdary
spellingShingle Mana Oloomi
Saeid Bouzari
Soheila Ajdary
Immune Responses of Mice Immunized with Active Recombinant Shiga Toxin and Its Derivatives
Iranian Journal of Allergy, Asthma and Immunology
A and B subunits
Immunomodulation
Shiga toxin
author_facet Mana Oloomi
Saeid Bouzari
Soheila Ajdary
author_sort Mana Oloomi
title Immune Responses of Mice Immunized with Active Recombinant Shiga Toxin and Its Derivatives
title_short Immune Responses of Mice Immunized with Active Recombinant Shiga Toxin and Its Derivatives
title_full Immune Responses of Mice Immunized with Active Recombinant Shiga Toxin and Its Derivatives
title_fullStr Immune Responses of Mice Immunized with Active Recombinant Shiga Toxin and Its Derivatives
title_full_unstemmed Immune Responses of Mice Immunized with Active Recombinant Shiga Toxin and Its Derivatives
title_sort immune responses of mice immunized with active recombinant shiga toxin and its derivatives
publisher Tehran University of Medical Sciences
series Iranian Journal of Allergy, Asthma and Immunology
issn 1735-1502
1735-5249
publishDate 2008-06-01
description Bacterial protein toxins have been exploited as therapeutic agents and as vaccines. An issue of deserving interest is development of new generations of vaccines and immune adjuvants. In this study an active assembled recombinant Shiga toxin of Escherichia coli (rStx1) and its derivatives, recombinant A and B subunits (Stx1-A and Stx1-B), were used to immunize mice. The elicited antibody responses were compared with and without using adjuvant.  Protection against intraperitoneal lethal dose of rStx challenge was observed by immunization with sublethal dose of rStx1, rStx-A and rStx-B subunits. The immunological studies on toxin subunits can be used for immunization against systemic shiga toxin mediated disease and also subunits as a vector for antigen presentation in immunotherapeutic approaches. In our experiment, while stimulation of the immune system by A and B subunits were different, both subunits produced neutralizing antibodies. Regarding B subunit the amount of specific IgG1/IgG2a antibody ratio was higher than A subunit. In addition B subunit stimulated proliferation of immune cells with IFNg production the same as rStx1, suggesting that B subunit can be used as an immunomodulator to stimulate the immune response in conjunction with other recombinant proteins.
topic A and B subunits
Immunomodulation
Shiga toxin
url https://ijaai.tums.ac.ir/index.php/ijaai/article/view/200
work_keys_str_mv AT manaoloomi immuneresponsesofmiceimmunizedwithactiverecombinantshigatoxinanditsderivatives
AT saeidbouzari immuneresponsesofmiceimmunizedwithactiverecombinantshigatoxinanditsderivatives
AT soheilaajdary immuneresponsesofmiceimmunizedwithactiverecombinantshigatoxinanditsderivatives
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