Immunization of C57BL/6 Mice with GRA2 Combined with MPL Conferred Partial Immune Protection against Toxoplasma gondii

نویسندگان

  • Ebrahim Azimi Molecular Parasitology Lab., Department of Parasitology, Pasteur Institute of Iran, Tehran, Iran
  • Jalal Babaie Molecular Parasitology Lab., Department of Parasitology, Pasteur Institute of Iran, Tehran, Iran
  • M. Reza Sadaie NovoMed Consulting, Silver Spring, Maryland, USA
  • Mahboobe Berizi Molecular Parasitology Lab., Department of Parasitology, Pasteur Institute of Iran, Tehran, Iran
  • Majid Golkar Molecular Parasitology Lab., Department of Parasitology, Pasteur Institute of Iran, Tehran, Iran
  • Reyhaneh Mohabati Molecular Parasitology Lab., Department of Parasitology, Pasteur Institute of Iran, Tehran, Iran
  • Robab Homayoun Molecular Parasitology Lab., Department of Parasitology, Pasteur Institute of Iran, Tehran, Iran
  • Samira Amiri Molecular Parasitology Lab., Department of Parasitology, Pasteur Institute of Iran, Tehran, Iran
چکیده مقاله:

BBackground: We have previously reported that immunization with GRA 2 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 GRA 2, formulated in MPL adjuvant. Results: Strong humoral response, predominantly of IgG1 subclass and cellular response, IFN-&gamma;, was detected at three weeks post immunization. Mice immunized with GRA 2 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-&gamma; 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 GRA 2 for incorporation into a multi-antigenic vaccine against T. gondii.

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عنوان ژورنال

دوره 22  شماره 1

صفحات  22- 32

تاریخ انتشار 2018-01

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