Volume 39, Issue 4 e12419
ORIGINAL ARTICLE

Evaluation of the immune response in BALB/c mice induced by a novel DNA vaccine expressing GRA14 against Toxoplasma gondii

E. Ahmadpour

E. Ahmadpour

Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran

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S. Sarvi

S. Sarvi

Toxoplasmosis Research Center, Mazandaran University of Medical Sciences, Sari, Iran

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M. B. Hashemi Soteh

M. B. Hashemi Soteh

Molecular and Cell Biology Research Center, Mazandaran University of Medical Sciences, Sari, Iran

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M. Sharif

M. Sharif

Toxoplasmosis Research Center, Mazandaran University of Medical Sciences, Sari, Iran

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M. T. Rahimi

M. T. Rahimi

School of Medicine, Shahroud University of Medical Sciences, Shahroud, Iran

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R. Valadan

R. Valadan

Molecular and Cell Biology Research Center, Mazandaran University of Medical Sciences, Sari, Iran

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M. Tehrani

M. Tehrani

Molecular and Cell Biology Research Center, Mazandaran University of Medical Sciences, Sari, Iran

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A. Khalilian

A. Khalilian

Biostatistics Department, Mazandaran University of Medical Sciences, Sari, Iran

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M. Montazeri

M. Montazeri

Toxoplasmosis Research Center, Mazandaran University of Medical Sciences, Sari, Iran

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A. Daryani

Corresponding Author

A. Daryani

Toxoplasmosis Research Center, Mazandaran University of Medical Sciences, Sari, Iran

Correspondence

Ahmad Daryani, Department of Parasitology and Mycology, Sari Medical School, Mazandaran University of Medical Sciences, Sari, Iran.

Email: [email protected]

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First published: 10 February 2017
Citations: 25

Summary

Toxoplasma gondii can cause severe and even fatal disease in human beings and animals. Effective vaccines may contribute to control toxoplasmosis. GRA14, a novel secreted dense granule protein of T. gondii, has been proposed as a vaccine candidate due to its intervacuolar transport and unique topology in the parasitophorous vacuole membrane. In this study, we constructed a DNA vaccine encoding GRA14 of T. gondii. BALB/c mice were immunized intramuscularly three times at 2 week intervals and challenged with T. gondii RH strain 5 weeks later. The immune responses were evaluated using lymphocyte proliferation assay, cytokine and antibody measurements. In addition, the survival times and parasite load of mice challenged with the virulent T. gondii RH strain were evaluated. The results showed that the mice immunized with pcGRA14 induced both enhanced specific humoral and Th1 cellular immune responses, and also mice immunized with the pcGRA14 showed an increased survival time and decreased parasite load compared with control groups (P<.05). The results indicated, for the first time, that the GRA14 is a potential DNA vaccine against toxoplasmosis.

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