Author/Authors :
Hajilooi، Mehrdad نويسنده , , Abasi ، Mohammad نويسنده Department of Internal Medicine, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran , , Bazmani، Ahad نويسنده Research Center of Infectious Diseases and Tropical Medicine, Tabriz University of Medical Science, Tabriz, Iran . , , Ahmadi ، Alireza نويسنده Faculty of Medicine, Shahid Beheshti Hospital, Hamadan University of Medical Sciences, Hamadan, Iran , , Matini ، Mohammad نويسنده Department of Parasitology and Mycology, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran , , Solgi، Ghasem نويسنده Immunology Department, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran. , , Sardarian، Khosro نويسنده Department of Parasitology and Mycology, Hamadan University of Medical Sciences, Hamadan ,
Abstract :
Background: Interleukin (IL)-8 plays important roles in the recruitment and activation of immune cells during visceral leishmaniasis (VL). Genetic variations in IL-8 modulate the expression of IL-8 protein and may be associated with VL. This study aimed to evaluate polymorphisms at the IL-8 ?251 position in VL patients.
Methods: This cross-sectional study was performed on three groups: Leishmania-seropositive patients with clinical symptoms of VL (n=91), seropositive patients without clinical symptoms (n=104), and healthy controls (n=110). Polymorphisms at the IL-8?251 position were analyzed using allele-specific polymerase chain reaction (PCR). Anti-Leishmania antibody titers were assessed by immunofluorescence.
Results: IL-8?251 polymorphism was significantly associated with VL (P < 0.002). The IL-8?251 T/T genotype was significantly higher in group 1 than in groups 2 and 3 (P < 0.002). The validity of the data was analyzed using Hardy-Weinberg equilibrium and one-way analysis of variance (ANOVA), as well as x2 tests.
Conclusions: IL-8?251 polymorphism was significantly associated with impaired immune responses in VL and might be considered a risk factor for disease development.
