Author/Authors :
Bavand, Anahita Dept. of Clinical Research- Pasteur Institute of Iran, Tehran , Aghakhani, Arezoo Anatomical & Clinical Pathologist- Dept. of Clinical Research- Pasteur Institute of Iran, Tehran , Mohraz, Minoo Infectious Diseases Specialist- Iranian Research Center for HIV/AIDS, Tehran , Banifazl, Mohammad Iranian Society for Support of Patients with Infectious Disease, Tehran , Karami, Afsaneh Infectious Diseases Specialist- Zanjan University of Medical Sciences, Zanjan , Golkar, Majid Molecular Parasitology Laboratory- Dept. of Parasitology- Pasteur Institute of Iran, Tehran , Babaie, Jalal Molecular Parasitology Laboratory- Dept. of Parasitology- Pasteur Institute of Iran, Tehran , Saleh, Parviz Infectious Diseases Specialist- Kidney Research Center- Tabriz University of Medical Sciences, Tabriz , Mamishi, Setareh Pediatric Infectious Disease Research Center- Tehran University of Medical Sciences, Tehran , Ramezani, Amitis Infectious Diseases Specialist- Dept. of Clinical Research- Pasteur Institute of Iran, Tehran
Abstract :
Background & Objective: Toxoplasma gondii infection has public health importance
and can lead to serious diseases in immunosuppressed patients, such as HIV cases.
Appropriate control of T. gondii infection in HIV patients requires information about
the prevalence of T. gondii antibodies and DNA in different population. In this study,
we aimed to determine the prevalence of Toxoplasma gondii antibodies and DNA in
HIV patients in Tehran, Iran.
Methods: A total of 149 HIV patients from the Iranian Research Center for HIV/
AIDS, Tehran, Iran were enrolled in the study. Anti-Toxoplasma IgG and IgM were
detected by ELISA and T. gondii DNA was evaluated by PCR and quantitative realtime
PCR. IgG positive samples were also assessed for their avidity.
Results: Anti-Toxoplasma IgG and IgM were positive in 46.3% and 2.7% of cases
respectively. 92.7% of our patients showed past infection and 4.3% revealed recently
acquired toxoplasmosis based on their IgG avidity test. T. gondii DNA was not detected
by PCR but real-time PCR results showed DNA in 4.7% of total patients and
13.1% of the IgG seropositive cases.
Conclusion: Our findings indicated that latent toxoplasmosis was relatively prevalent
in our study population, but new T. gondii infection had low prevalence. Almost
half of our patients were IgG negative and at risk of acquiring toxoplasma infection.
Low copy numbers of DNA were detected in 4.7% of the cases without any clinical
manifestation. Therefore, detection and monitoring of anti-Toxoplasma antibodies
and DNA in HIV patients is substantial to estimate the risk of reactivation and new
infection.
Keywords :
Reactive Inhibition Antibodies , Human Immunodeficiency Virus (HIV) , IgG , Toxoplasma gondii , IgM