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Immunization of C57BL/6 Mice with GRA2 Combined with MPL Conferred Partial Immune Protection against Toxoplasma gondii
BACKGROUND: We have previously reported that immunization with GRA2 antigen of Toxoplasma gondii induces protective immunity in CBA/J (H2k) and BALB/c mice (H2d). We aimed to examine whether immunization of a distinct strain of rodent with recombinant dense granule antigens (GRA2) combined with mono...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Pasteur Institute
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5712381/ https://www.ncbi.nlm.nih.gov/pubmed/28646827 http://dx.doi.org/10.22034/ibj.22.1.22 |
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author | Babaie, Jalal Amiri, Samira Homayoun, Robab Azimi, Ebrahim Mohabati, Reyhaneh Berizi, Mahboobe Sadaie, M. Reza Golkar, Majid |
author_facet | Babaie, Jalal Amiri, Samira Homayoun, Robab Azimi, Ebrahim Mohabati, Reyhaneh Berizi, Mahboobe Sadaie, M. Reza Golkar, Majid |
author_sort | Babaie, Jalal |
collection | PubMed |
description | BACKGROUND: We have previously reported that immunization with GRA2 antigen of Toxoplasma gondii induces protective immunity in CBA/J (H2k) and BALB/c mice (H2d). We aimed to examine whether immunization of a distinct strain of rodent with recombinant dense granule antigens (GRA2) combined with monophosphorryl lipid A (MPL) adjuvant elicits protective immune response against T. gondii. METHODS: C57BL/6 (H2b haplotype) mice were immunized with GRA2, formulated in MPL adjuvant. RESULTS: Strong humoral response, predominantly of IgG1 subclass and cellular response, IFN-γ, was detected at three weeks post immunization. Mice immunized with GRA2 had significantly (p < 0.01) fewer brain cysts than those in the adjuvant group, upon challenge infection. Despite the production of a strong antibody response, IFN-γ production and brain cyst reduction were not significant when the immunized mice were infected four months after the immunization. CONCLUSIONS: We can conclude that GRA2 immunization partially protects against T. gondii infection in C57BL/6 mice, though the potency and longevity of this antigen as a standalone vaccine may vary in distinct genetic backgrounds. This observation further emphasizes the utility of GRA2 for incorporation into a multi-antigenic vaccine against T. gondii. |
format | Online Article Text |
id | pubmed-5712381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Pasteur Institute |
record_format | MEDLINE/PubMed |
spelling | pubmed-57123812018-01-01 Immunization of C57BL/6 Mice with GRA2 Combined with MPL Conferred Partial Immune Protection against Toxoplasma gondii Babaie, Jalal Amiri, Samira Homayoun, Robab Azimi, Ebrahim Mohabati, Reyhaneh Berizi, Mahboobe Sadaie, M. Reza Golkar, Majid Iran Biomed J Full Length BACKGROUND: We have previously reported that immunization with GRA2 antigen of Toxoplasma gondii induces protective immunity in CBA/J (H2k) and BALB/c mice (H2d). We aimed to examine whether immunization of a distinct strain of rodent with recombinant dense granule antigens (GRA2) combined with monophosphorryl lipid A (MPL) adjuvant elicits protective immune response against T. gondii. METHODS: C57BL/6 (H2b haplotype) mice were immunized with GRA2, formulated in MPL adjuvant. RESULTS: Strong humoral response, predominantly of IgG1 subclass and cellular response, IFN-γ, was detected at three weeks post immunization. Mice immunized with GRA2 had significantly (p < 0.01) fewer brain cysts than those in the adjuvant group, upon challenge infection. Despite the production of a strong antibody response, IFN-γ production and brain cyst reduction were not significant when the immunized mice were infected four months after the immunization. CONCLUSIONS: We can conclude that GRA2 immunization partially protects against T. gondii infection in C57BL/6 mice, though the potency and longevity of this antigen as a standalone vaccine may vary in distinct genetic backgrounds. This observation further emphasizes the utility of GRA2 for incorporation into a multi-antigenic vaccine against T. gondii. Pasteur Institute 2018-01 /pmc/articles/PMC5712381/ /pubmed/28646827 http://dx.doi.org/10.22034/ibj.22.1.22 Text en Copyright: © Iranian Biomedical Journal http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Length Babaie, Jalal Amiri, Samira Homayoun, Robab Azimi, Ebrahim Mohabati, Reyhaneh Berizi, Mahboobe Sadaie, M. Reza Golkar, Majid Immunization of C57BL/6 Mice with GRA2 Combined with MPL Conferred Partial Immune Protection against Toxoplasma gondii |
title | Immunization of C57BL/6 Mice with GRA2 Combined with MPL Conferred Partial Immune Protection against Toxoplasma gondii |
title_full | Immunization of C57BL/6 Mice with GRA2 Combined with MPL Conferred Partial Immune Protection against Toxoplasma gondii |
title_fullStr | Immunization of C57BL/6 Mice with GRA2 Combined with MPL Conferred Partial Immune Protection against Toxoplasma gondii |
title_full_unstemmed | Immunization of C57BL/6 Mice with GRA2 Combined with MPL Conferred Partial Immune Protection against Toxoplasma gondii |
title_short | Immunization of C57BL/6 Mice with GRA2 Combined with MPL Conferred Partial Immune Protection against Toxoplasma gondii |
title_sort | immunization of c57bl/6 mice with gra2 combined with mpl conferred partial immune protection against toxoplasma gondii |
topic | Full Length |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5712381/ https://www.ncbi.nlm.nih.gov/pubmed/28646827 http://dx.doi.org/10.22034/ibj.22.1.22 |
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