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1.
Allergol Immunopathol (Madr) ; 47(4): 378-385, 2019.
Article in English | MEDLINE | ID: mdl-30745246

ABSTRACT

INTRODUCTION AND OBJECTIVES: Allergic asthma is a chronic inflammatory disorder of the airways. Th1, Th2 and Th17 cells are the main cells involved in the pathophysiology of asthma. The function of these cells is affected by T-bet, GATA3 and RORγt transcription factors (respectively). Therefore, the aim of this study was to evaluate the effect of ginger (officinal Roscoe) extract on the expression of T-bet, GATA-3 and ROR-γ in peripheral blood mononuclear cells (PBMC) of asthmatic patients, in comparison with healthy volunteers as controls. MATERIALS AND METHODS: In this case-control study, a total of 50 individuals including 25 patients with severe, moderate and mild allergic asthma and 25 unrelated healthy controls were involved. The PBMCs were isolated and divided into four groups: negative control, two positive controls (Budesonide and PHA) and ginger-extract treated group. After cell treatment and incubation for 48h, PBMCs were isolated and cDNA was synthesized. Gene expressions of T-bet, GATA3 and ROR-γt were evaluated by Real-time PCR. RESULTS: According to the results of this study, hydroalcoholic extract of ginger could reduce the expression of GATA-3, ROR-γt, and T-bet in PBMCs of asthmatic patients in comparison with untreated PBMCs (P values=0.001, 0.001, and 0.002, respectively). It was also shown that the ginger extract could affect T-bet/GATA-3, T-bet/ROR-γt, and ROR-γt/GATA-3 expression ratios. CONCLUSIONS: This study showed that the use of ginger extract could control asthma and decrease the severity of this disease by affecting the main cells involving the symptoms of asthma in the airways.


Subject(s)
Anti-Asthmatic Agents/pharmacology , Asthma/drug therapy , GATA3 Transcription Factor/metabolism , Hypersensitivity/drug therapy , Leukocytes, Mononuclear/physiology , Nuclear Receptor Subfamily 1, Group F, Member 3/metabolism , Plant Extracts/pharmacology , T-Box Domain Proteins/metabolism , Adolescent , Adult , Case-Control Studies , Cells, Cultured , Child , GATA3 Transcription Factor/genetics , Gene Expression Regulation , Zingiber officinale/immunology , Humans , Nuclear Receptor Subfamily 1, Group F, Member 3/genetics , T-Box Domain Proteins/genetics , Young Adult
2.
Helminthologia ; 56(3): 196-201, 2019 Sep.
Article in English | MEDLINE | ID: mdl-31662691

ABSTRACT

Echinococosis is a zoonotic disease caused by the larval stages of Echinococcus spp. that occurs in most parts of the world. Herein, we aimed to evaluate the genotypes of isolated hydatid cysts from slaughtered animals in Shush county, southwestern Iran. Totally, 96 hydatid cysts were collected, including 11 buffaloes, 13 cattle, 12 goat and 60 sheep. The PCR was done by a primer pair (BDI and 4s) to amplify ITS1 fragment. Four restriction endonucleases including AluI, HpaII, RsaI, and TaqI were used for RFLP products and enzymatic reactions were electrophoresed. Finally, twenty PCR products were sent for sequencing and phylogenetic tree was drawn with MEGA6. Molecular identification of 96 hydatid cysts demonstrated a distinctive 1000 bp fragment in all samples from four animal hosts. RFLP analysis showed similar digestion patterns in all samples. AluI digestion yielded 800 bp and 200 bp fragments, HpaII digestion made 700 bp and 300 bp fragments and RsaI digestion entailed 655 and 345segments. Moreover, TaqI rendered no digestion pattern on rDNA-ITS1 region. Additionally, E. granulosus sensu stricto (G1-3 complex) was the prevailing genotype in all livestock samples, according to PCR-RFLP and sequencing analyses.

3.
Acta Virol ; 61(1): 97-104, 2017.
Article in English | MEDLINE | ID: mdl-28161964

ABSTRACT

Human cytomegalovirus (HCMV) establishes severe disease in fetus, newborn and immunocompromised individuals. Polytope DNA vaccine strategy allows us to choose conserved and immunodominant epitopes from different antigens that can stimulate cellular and humoral immune responses simultaneously. In this study, a synthetic chimeric gene fragment was subcloned in to DNA vaccine vector pcDNA3.1+. The recombinant vector was transferred in to suitable eukaryotic cell line HEK 293T and the expression level of polytope construct from HEK 293T-infected cells was determined by western blot. These results show that there was no mutantion in target segment and recombinant vector showed significant levels of expression. Base on these results, using a proper procedure for design can cause expression and stability of polytope peptide.


Subject(s)
Cytomegalovirus Infections/prevention & control , Cytomegalovirus Vaccines/immunology , Cloning, Molecular , DNA, Viral/immunology , HEK293 Cells , Humans , Plasmids , Vaccines, DNA/immunology
4.
Cell Mol Biol (Noisy-le-grand) ; 62(1): 30-3, 2016 Jan 11.
Article in English | MEDLINE | ID: mdl-26828983

ABSTRACT

Losartan is an angiotensin II receptor (AT-II-R) blocker that is widely used by human for blood pressure regulation. Also, it has antitumor property. In this study, we investigated the radiosensitizing effect of losartan on cellular toxicity induced by ionizing radiation on prostate cancer and non-malignant fibroblast cells. Human prostate cancer (DU-145) and human non-malignant fibroblast cells (HFFF2) were treated with losartan at different concentrations (0.5, 1, 10, 50 and 100 µM) and then these cells were exposed to ionizing radiation. The cell proliferation was determined using MTT assay. Our results showed that losartan exhibited antitumor effect on prostate cancer cells; it was reduced cell survival to 66% at concentration 1 µM. Losartan showed an additive killing effect in combination with ionizing radiation on prostate cancer cell. The cell proliferation was reduced to 54% in the prostate cancer cells treated with losartan at concentration 1 µM in combination with ionizing radiation. Losartan did not exhibit any toxicity on HFFF2 cell. This result shows a promising effect of losartan on enhancement of therapeutic effect of ionizing radiation in patients during therapy.


Subject(s)
Losartan/pharmacology , Prostatic Neoplasms/drug therapy , Prostatic Neoplasms/radiotherapy , Cell Line , Cell Line, Tumor , Cell Proliferation/drug effects , Cell Survival/drug effects , Humans , Male , Radiation, Ionizing
5.
Neuropsychobiology ; 67(2): 116-21, 2013.
Article in English | MEDLINE | ID: mdl-23406623

ABSTRACT

BACKGROUND/AIMS: Several lines of evidence point to the role of neurobiological mechanisms and genetic background in bipolar disorder (BD). The interleukin-1 receptor antagonist (IL-1Ra) is the principal regulator of IL-1α and IL-1ß bioactivities. This study aimed to investigate the potential role of the variable number of tandem repeats (VNTR) polymorphisms of the IL-1Ra gene (IL1RN) in conferring susceptibility to BD. METHODS: In total, 217 patients meeting DSM-IV-TR criteria for BD and 212 controls were recruited for the study. Genotyping of IL1RN was determined by polymerase chain reaction amplification of VNTR of 86 base pairs in intron 2 of IL1RN. RESULTS: The genotype distribution of IL1RN polymorphism was significantly different between BD patients and controls. The IL1RN*1/2 genotype was more prevalent in BD patients than in controls (44.2 vs. 30.2%, p = 0.003). Multiple logistic regression analysis demonstrated that IL1RN*1/2 heterozygotes had a significantly higher risk for BD (OR 1.83 and 95% CI 1.22-2.74, p = 0.003). Further stratification of the BD patients into IL1RN*2 allele carrier and noncarrier subgroups revealed a strong association between IL1RN*2 carriage and prolongation of the disease (p = 0.02). CONCLUSIONS: These findings suggest a positive association between VNTR polymorphism in IL1RN and BD. Additional studies, particularly with a prospective approach, are necessary to clarify the precise role of the VNTR polymorphism on the disease in different ethnic populations.


Subject(s)
Bipolar Disorder/genetics , Genetic Predisposition to Disease , Interleukin 1 Receptor Antagonist Protein/genetics , Introns/genetics , Minisatellite Repeats/genetics , Adult , Female , Gene Frequency , Genotype , Humans , Iran , Male , Middle Aged , Psychiatric Status Rating Scales , Young Adult
6.
J Helminthol ; 87(2): 240-4, 2013 Jun.
Article in English | MEDLINE | ID: mdl-22691442

ABSTRACT

Hydatidosis is an important public health problem in several parts of Iran. The aim of this molecular study is to investigate Echinococcus granulosus genotypes as the causative agents of hydatidosis in the south-west of Iran (Khuzestan province). In this study, isolates of 334 hydatid cysts were collected from the liver and lungs of 141 sheep, 104 cattle, 84 goats and 5 human cases. DNA was extracted and examined by nested polymerase chain reaction (PCR) of ribosomal DNA (rDNA) internal transcribed spacer 1 (ITS1) and restriction fragment length polymorphism (RFLP)-PCR. In addition, fragments of genes coding for ITS1 were sequenced. The results of RFLP-PCR analysis revealed the presence of the G1 genotype in all human, cattle, goat and sheep isolates. Furthermore, no camel strain (G6) was detected among all samples in the regions studied. The molecular findings indicate that the predominant genotype involved in E. granulosus transmission in south-west Iran is the common sheep strain (G1 genotype), which occurs in human, cattle, sheep and goat populations. In conclusion, these results may have important implications for hydatid disease control in the areas studied.


Subject(s)
Echinococcosis/parasitology , Echinococcosis/veterinary , Echinococcus granulosus/classification , Echinococcus granulosus/genetics , Livestock/parasitology , Animals , Cattle , Cluster Analysis , DNA, Helminth/chemistry , DNA, Helminth/genetics , DNA, Ribosomal/chemistry , DNA, Ribosomal/genetics , DNA, Ribosomal Spacer/chemistry , DNA, Ribosomal Spacer/genetics , Echinococcosis/epidemiology , Echinococcosis/transmission , Echinococcus granulosus/isolation & purification , Genotype , Goats , Humans , Iran/epidemiology , Liver/parasitology , Lung/parasitology , Molecular Epidemiology , Molecular Sequence Data , Phylogeny , Polymerase Chain Reaction , Polymorphism, Restriction Fragment Length , RNA, Ribosomal, 28S/genetics , Sequence Analysis, DNA , Sheep
7.
J Helminthol ; 86(2): 241-4, 2012 Jun.
Article in English | MEDLINE | ID: mdl-21733275

ABSTRACT

Eosinophilia in human peripheral blood is caused by different agents, including toxocariasis. The present study aimed to evaluate the prevalence of toxocariasis in hypereosinophilic individuals in the city of Ahwaz, located in south-western Iran, using enzyme-linked immunosorbent assay and Western blot techniques. Serum samples were examined from 100 individuals with peripheral blood eosinophilia and also from another 100 individuals without eosinophilia as the control group. In hypereosinophilic individuals seroprevalence antibodies against Toxocara were found in 19 (19%), of whom 12 (63.15%) were female and 7 (36.85%) were male. Positive sera were subsequently confirmed by Western blot. All of the observed bands ranged from 24 to 100 kDa. Antibodies against Toxocara were found in 1% of the control group, but were not confirmed by Western blot. The results showed significant differences between the frequency of infection within age and gender (P < 0.05); the highest prevalence of infection was observed in adults. Differences between the hypereosinophilic and healthy individuals, in terms of Toxocara infection frequency, also proved significant (P < 0.05).The present study thus confirmed the significant prevalence of toxocariasis as a hygienic problem among hypereosinophilic individuals in this area. It is, therefore, necessary to examine these individuals for toxocariasis.


Subject(s)
Antibodies, Helminth/blood , Eosinophilia/etiology , Toxocara/immunology , Toxocariasis/epidemiology , Adolescent , Adult , Aged , Aged, 80 and over , Animals , Blotting, Western , Child , Child, Preschool , Enzyme-Linked Immunosorbent Assay , Female , Humans , Infant , Iran/epidemiology , Male , Middle Aged , Seroepidemiologic Studies , Young Adult
8.
Acta Trop ; 201: 105206, 2020 Jan.
Article in English | MEDLINE | ID: mdl-31586448

ABSTRACT

Albendazole is appropriate chemotherapy for treatment and prophylaxis of cystic echinococcosis (CE). The recent studies show Cytokine therapy could be useful for chronic and progressive diseases, therefore, the use of cytokine in prophylaxis and treatment of hydatidosis could be considerable. The aim of this study is to evaluate the efficacy of interleukin-12 + interferon-gamma, in combination with albendazole for prophylaxis and treatment of CE in Balb/c mice. Albendazole and cytokines were administrated for prophylaxis and treatment in CE. The efficacy of this agents were determined by measuring of size, weight, number of cysts, histology and lymphocyte response. Lymphocyte stimulation index and production of interleukin-12 and interferon-gamma were measured by MTT assay and ELISA respectively. Combination of albendazole and cytokines was very effective for prophylaxis and treatment in experimental CE.


Subject(s)
Albendazole/therapeutic use , Anthelmintics/therapeutic use , Cytokines/therapeutic use , Echinococcosis/drug therapy , Immunotherapy/methods , Interferon-gamma/therapeutic use , Interleukin-12/therapeutic use , Animals , Disease Models, Animal , Echinococcus granulosus/drug effects , Mice , Mice, Inbred BALB C
9.
PLoS One ; 15(7): e0235965, 2020.
Article in English | MEDLINE | ID: mdl-32701960

ABSTRACT

Secondary lymphedema (SL)is a frequent and devastating complication of modern oncological therapy and filarial infections. A lack of a reliable preclinical model to investigate the underlying mechanism of clinical stage progression has limited the development of new therapeutic strategies. Current first line treatment has shown to be merely symptomatic and relies on lifetime use of compression garments and decongestive physiotherapy. In this study, we present the development of a secondary lymphedema model in 35 rats using pre- and intraoperative fluorescence-guided mapping of the lymphatics and microsurgical induction. In contrast to the few models reported so far, we decided to avoid the use of radiation for lymphedema induction. It turned out, that the model is nearly free of complications and capable of generating a statistically significant limb volume increase by water displacement measurements, sustained for at least 48 days. A translational, accurate lymphatic dysfunction was visualized by a novel VIS-NIR X-ray ICG-Clearance-Capacity imaging technology. For the first-time SL stage progression was validated by characteristic histological alterations, such as subdermal mast cell infiltration, adipose tissue deposition, and fibrosis by increased skin collagen content. Immunofluorescence confocal microscopy analysis suggested that stage progression is related to the presence of a characteristic α SMA+/HSP-47+/vimentin+ fibroblast subpopulation phenotype. These findings demonstrate that the in-vivo model is a reliable and clinically relevant SL model for the development of further secondary lymphedema therapeutic strategies and the analysis of the veiled molecular mechanisms of lymphatic dysfunction.


Subject(s)
Fluorescent Dyes/chemistry , Lymphedema/pathology , Microsurgery/adverse effects , Actins/metabolism , Animals , Collagen/metabolism , Disease Models, Animal , Disease Progression , Female , Fibroblasts/cytology , Fibroblasts/metabolism , Indocyanine Green/chemistry , Lymphedema/etiology , Microscopy, Fluorescence , Rats , Rats, Inbred Lew , Skin/pathology , Vimentin/metabolism
10.
Virus Res ; 290: 198197, 2020 12.
Article in English | MEDLINE | ID: mdl-33069815

ABSTRACT

The coronavirus disease-2019 (COVID-19) which caused by severe acute respiratory syndrome-related coronavirus (SARS-CoV-2), is a pandemic threat to global public health. It has a wide spectrum of clinical manifestations from mild to critical illness, the most serious of which is the complications of acute respiratory distress syndrome (ARDS). SARS-CoV-2 infection appears mild in infants and children, however, in adults, it can lead to serious consequences. In this review, we highlighted the differences between the immune responses of the lung in children and adults, immune dysregulation and their possible role in clinical manifestations in COVID-19. There is a reduction in population of immunocompetent cells during aging and subsequently induced ineffective inflammation in the faces of some infections. Dysregulation in the immune system can lead to an unappropriated local and systemic immune responses and subsequently the rapid spread of the virus, leading to severe COVID-19 disease. Therefore, recognizing the differences in the immune responses of various hosts as well as to improve the immune system disorder should always be part of research and treatment protocols.


Subject(s)
COVID-19/immunology , COVID-19/pathology , SARS-CoV-2/pathogenicity , Age Factors , Aging/immunology , COVID-19/virology , Host-Pathogen Interactions , Humans , Immunity , Inflammation , Lung/immunology , Lung/pathology , SARS-CoV-2/physiology , Sex Factors
11.
Arch Osteoporos ; 15(1): 103, 2020 07 10.
Article in English | MEDLINE | ID: mdl-32651719

ABSTRACT

Musculoskeletal diseases (MSDs) are the leading cause of disability and facing them demands updated reports on their burden for efficient policymaking. We showed Iran had the highest female-to-male ratio and highest increase in the burden of musculoskeletal diseases, in the past three decades, worldwide. We further confirmed the role of population aging as the main cause. PURPOSE: MSDs comprise most of the top causes of years lived with disability (YLDs) worldwide and are rapidly increasing in lower- and middle-income countries. Here, we present disability and mortality due to MSDs in Iran at the national level from 1990 to 2017. METHODS: We used Global Burden of Disease (GBD) 2017 Study data and standard methodology and presented the burden of MSDs in rates of years of life lost (YLLs), YLDs, and disability-adjusted life years (DALYs) during 1990-2017, for population aged ≥ 5 years old. We further explored attributable risk factors and decomposed the changing trend in DALYs to assess underlying causes. RESULTS: In Iran, MSDs were responsible for 1.82 million (95%uncertainty interval [UI] 1.3-2.4) DALYs, in 2017. During the past 28 years, with 1.75% annualized percentage change (APC), Iran had the highest percentage increase in the all-ages MSD DALYs rate worldwide, while the age-standardized DALYs APC was negligible. Low back pain was the greatest contributor to DALYs and caused 4.5% of total DALYs. The female population is experiencing considerably higher burden of MSDs, with 115% and 48% higher all-ages YLLs and YLDs rates per 100,000, respectively (YLLs 28.7; YLDs 2629.1), than males (YLLs 13.2; YLDs 1766.1). However, due to wide UIs, difference was not significant. Only 17.6% of MSD YLDs are attributable to assessed risk factors. CONCLUSION: Despite that MSDs are rising as an important cause of disability in Iran, these conditions are not sufficiently addressed in health policies. There is urgent need for cross-sectoral engagement, especially addressing the MSDs in females.


Subject(s)
Global Burden of Disease , Musculoskeletal Diseases , Female , Global Health , Humans , Iran/epidemiology , Life Expectancy , Male , Musculoskeletal Diseases/epidemiology , Quality-Adjusted Life Years
12.
J Periodontal Res ; 44(1): 88-93, 2009 Feb.
Article in English | MEDLINE | ID: mdl-18973547

ABSTRACT

BACKGROUND AND OBJECTIVE: Periodontitis is a multifactorial disease in which environmental and genetic determinant factors contribute to individual subjects susceptibility. A DNA polymorphism in the regulating region of adhesion molecule genes is suggested to modulate the molecules physiological effects. The aim of this study was to investigate the genetic association between the E-selectin Ser128Arg and L-selectin Phe206Leu polymorphisms and periodontitis. MATERIAL AND METHODS: DNA was isolated from the whole blood of 88 patients with periodontitis and 139 healthy individuals. All samples were genotyped for the E-selectin Ser128Arg and L-selectin Phe206Leu polymorphisms using the polymerase chain reaction with sequence specific primers. RESULTS: Our findings revealed a significant difference in the Ser128Arg polymorphism of E-selectin, but not in the L-selectin polymorphism, between periodontal patients and controls. The 128Arg allele was present more frequently in patients than in healthy individuals (31.25% vs. 12.2%, p < 0.0001). In addition, there was an association between the presence of the 128Arg allele and periodontitis (odds ratio 2.9; 95% confidence interval: 1.75-4.4, p < 0.0001). No significant association was found between the polymorphisms tested and the subgroups of periodontal disease (i.e. chronic periodontitis and aggressive periodontitis). CONCLUSION: The findings of this study showed that the Ser128Arg polymorphism of E-selectin might contribute to the susceptibility of Iranian individuals to periodontitis.


Subject(s)
E-Selectin/genetics , L-Selectin/genetics , Periodontitis/genetics , Polymorphism, Genetic/genetics , Adenine , Adolescent , Adult , Aggressive Periodontitis/genetics , Alleles , Arginine/genetics , Chronic Periodontitis/genetics , Cytosine , Dental Plaque/classification , Female , Genetic Predisposition to Disease/genetics , Gingival Hemorrhage/classification , Humans , Leucine/genetics , Male , Middle Aged , Periodontal Attachment Loss/classification , Periodontal Pocket/classification , Periodontitis/classification , Phenylalanine/genetics , Serine/genetics , Socioeconomic Factors , Thymine , Young Adult
13.
J Ethnopharmacol ; 242: 111929, 2019 Oct 05.
Article in English | MEDLINE | ID: mdl-31054317

ABSTRACT

ETHNOPHARMACOLOGICAL RELEVANCE: .Colorectal cancer (CRC) is now one the fourth cause of mortality and morbidity due to cancer throughout the globe. Cachexia is more prevalent in patients with this cancer and has a negative effect on response to chemotherapy and radiotherapy. Inflammatory cytokines such as TNF-α, IL-1ß, and IL-6 could play a key role in cachexia. Moreover strong chemotherapy medications such as doxorubicin have complications such as toxicity and cachexia. Citrus unshiu Peel have been used as traditional herbal drugs for the treatment of cancer in traditional oriental medicine (TOM). Since its main components have anti-inflammatory effects, we evaluated the anti-cachexia activity in order to support the traditional usage of Citrus unshiu peel. Aim of the study; We aimed to assess the preventive or therapeutic effect of Citrus unshiu Peel Extract (CUPE) on cachexia by reducing of inflammatory cytokines in mice bearing C26 tumor. Also the contribution role of CUPE has evaluated on improvement of chemotherapy through reducing of inflammatory cytokines. Materials and Methods; The CUPE was prepared by Soxhlet extractor and quantitative and qualitative analysis of aqua extract was performed by high performance liquid chromatography (HPLC). C26 tumor bearing BALB/c male mice were immunized with different formulation of oral Prophylactic-therapeutic CUPE and/or intraperitoneal doxorubicin and then were monitored for weight gain, food intake and tumor size throughout the study. On the 32nd day after tumor injection, inflammatory cytokines levels, IL6, TNF-α and IL-1ß were evaluated by Enzyme-linked Immunosorbent Assay (ELISA) and Malondialdehyde- Thiobarbituric acid (MDA) levels were measured by standard method. Results; Oral administration of CUPE in both prophylactic and therapeutic formulation to C26 adenocarcinoma bearing mice reduced the weight loss, tumor volume, and serum MDA levels compared with untreated tumor-bearing mice and Doxorubicin (Dox) groups. Also, the combination therapy of (CUPE + Dox) leads to reducing the levels of serum IL-6, TNF-α, IL-1ß and tumor volume compared with untreated tumor-bearing mice and Dox groups. Serum MDA levels were considerably reduced by combination therapy of (CUPE + Dox) compared with Dox groups. Conclusions; These findings confirm the safety and efficacy of CUPE on C26 adenocarcinoma bearing mice as pure and adjuvant therapy, the results of which might be used in further human studies as a valuable natural anticancer agent alone or in combination with chemotherapy. Also the results showed that simultaneous application of CUPE and Dox leads to significant reduction of cachexia from the Dox chemotherapy.


Subject(s)
Adenocarcinoma/drug therapy , Antibiotics, Antineoplastic/adverse effects , Cachexia/drug therapy , Citrus , Colonic Neoplasms/drug therapy , Doxorubicin/adverse effects , Plant Extracts/therapeutic use , Adenocarcinoma/blood , Adenocarcinoma/pathology , Animals , Cachexia/chemically induced , Cell Line , Colonic Neoplasms/blood , Colonic Neoplasms/pathology , Cytokines/blood , Male , Mice, Inbred BALB C , Tumor Burden/drug effects
14.
J Periodontal Res ; 43(1): 111-5, 2008 Feb.
Article in English | MEDLINE | ID: mdl-18230112

ABSTRACT

BACKGROUND AND OBJECTIVE: Periodontitis is a multifactorial disease and immunologic and genetic factors have an important role in its pathogenesis. Mutation in the promoter regions of the interleukin-4 and interferon-gamma genes has been reported to modify the protein expression. The objective of this study was to evaluate the possible role of interleukin-4 (C-590T) and interferon-gamma (G5644A) polymorphisms in the susceptibility to periodontitis. MATERIAL AND METHODS: In this case-control study, 53 patients (36 women and 17 men), comprising 27 patients with aggressive periodontitis and 26 patients with chronic periodontitis, and 56 healthy volunteers, were enrolled. DNA was isolated from all subjects, and the polymerase chain reaction-sequence specific primer method was used to study the interleukin-4 (C-590T) and interferon-gamma (G5644A) gene polymorphisms. RESULTS: Our results showed no significant difference in the allele and genotype frequencies of interleukin-4 (C-590T) and interferon-gamma (G5644A) gene polymorphisms between patients with periodontal disease and controls. CONCLUSION: The results suggest that the interleukin-4 (C-590T) and interferon-gamma (G5644A) gene polymorphisms may not be associated with the susceptibility of Iranian individuals to periodontitis.


Subject(s)
Interferon-gamma/genetics , Interleukin-4/genetics , Periodontitis/genetics , Polymorphism, Genetic/genetics , Adolescent , Adult , Alleles , Chronic Disease , Epidemiologic Methods , Female , Genotype , Humans , Interferon-gamma/blood , Interleukin-4/blood , Iran , Male , Middle Aged , Periodontitis/blood
15.
Trop Biomed ; 35(1): 32-40, 2018 Mar 01.
Article in English | MEDLINE | ID: mdl-33601774

ABSTRACT

Echinococcosis and toxocariasis are considered two important zoonotic diseases worldwide. The aim of the study was to evaluate the seroprevalence of cystic echinococcosis and toxocariasis and identify the role of variable factors such as age, gender, occupation, level of education, and having contact with domestic dogs and cats in the transmission of the parasites in rural inhabitants of Khuzestan Province, located in the southwest of Iran. A total of 410 rural inhabitants, who had contact with domestic dogs and cats, were randomly enrolled in the current study. Antigen B (AgB) was purified from the hydatid cyst fluid, and the ELISA test was performed for seropositive detection of cystic echinococcosis. Toxocara IgG was evaluated by ELISA DRG kit, and the positive samples were examined by Western blotting IgG LDBIO kit to confirm and validate the results of ELISA. Of the 410 sera examined, 20 (4.9%) samples were positive for cystic echinococcosis by ELISA test. A significant association was observed on the different type of occupations and seropositivity (p<0.05), but no significant differences were observed between age groups, gender, and educational levels for cystic echinococcosis. Eight (2.0%) cases were found to be positive for toxocariasis by ELISA, but none of the positive cases was confirmed by the Western blotting test. Our study showed that factors such as education, raising awareness, and health improvement in Khuzestan Province may have influenced the prevalence of echinococcosis and toxocariasis in recent years. Local health and sanitary authorities should pay more attention to the health problems in the rural areas.

16.
J Mycol Med ; 28(2): 269-273, 2018 Jun.
Article in English | MEDLINE | ID: mdl-29545123

ABSTRACT

Mucormycosis is a devastating infection caused by Mucoralean fungi (Mucormycotina, Mucorales). Data concerning the global epidemiology of mucormycosis are scarce and little is known about the characteristics of mucormycosis in Iran. In this study, we aimed to understand the distribution of this infection in Iran retrospectively and to ascertain whether the patterns of infection are associated with specific host factors or not. A total of 208 cases were included in this study occurring during 2008-2014 and were validated according to (EORTC/MSG) criteria. A rising trend as significant increase from 9.7% in 2008 to 23.7% in 2014 was observed. The majority of patients were female (51.4%) with median age of 50 and the infections were seen mostly in autumn season (39.4%). Diabetes mellitus (75.4%) was the most common underlying condition and sinus involvement (86%) was the mostly affected site of infection. Amphotericin B (AmB) was the drug of choice for the majority of cases. Sixty four isolates did not show any growth in the lab and only 21 cases were evaluated by ITS sequencing, among them; Rhizopus arrhizus var. arrhizus was the dominant species. Considering the high mortality rate of mucormycosis, early and accurate diagnosis, with the aid of molecular methods may provide accurate treatments and improve the survival rate. Therefore, increased monitoring and awareness of this life-threatening disease is critical.


Subject(s)
Mucorales/isolation & purification , Mucormycosis/epidemiology , Adult , Aged , Amphotericin B/therapeutic use , Antifungal Agents/therapeutic use , DNA, Ribosomal Spacer/genetics , Diabetes Complications/microbiology , Diabetes Mellitus/microbiology , Female , Host-Pathogen Interactions , Humans , Iran/epidemiology , Male , Middle Aged , Mucorales/drug effects , Mucormycosis/diagnosis , Mucormycosis/mortality , Paranasal Sinuses/microbiology , Retrospective Studies , Rhizopus/drug effects , Rhizopus/isolation & purification , Seasons
17.
Clin Microbiol Infect ; 13(1): 97-100, 2007 Jan.
Article in English | MEDLINE | ID: mdl-17184296

ABSTRACT

This study examined the association between transforming growth factor (TGF)-beta1 polymorphisms and brucellosis. The TGF-beta1 genotypes at codons 10 and 25 were determined by an amplification refractory mutation system-PCR among 425 brucellosis patients and 213 healthy volunteers. The frequencies of TGF-beta1 codons 10 C and 25 G were significantly higher among patients than among controls, as was that of TGF-beta1 codon 10 C/C. The high-producer haplotype (CG/TG) was more frequent among patients than among controls. The findings suggest that genetic polymorphism in codons 10 and 25 of the TGF-beta1 gene might contribute to the development of brucellosis.


Subject(s)
Brucellosis/genetics , Codon/genetics , Polymorphism, Genetic , Transforming Growth Factor beta1/genetics , Female , Genotype , Haplotypes/genetics , Humans , Male , Risk Factors
18.
Vet J ; 174(2): 422-4, 2007 Sep.
Article in English | MEDLINE | ID: mdl-16919980

ABSTRACT

Serum samples from 290 cattle, 400 goats and 588 sheep slaughtered for food in various areas of the Mazandaran province, Iran were tested for antibodies to Toxoplasma gondii by the indirect immunofluorescence antibody test (IFAT), from December 2004 to April 2005. Antibodies to T. gondii were found in 30% (120/400) goats and 35% (206/588) sheep and 0% (0/290) cattle, at a dilution of 1:16 or more for goats and sheep and 1:128 or more for cattle. The highest titres observed in cattle, goats and sheep were 1:64 (0.7%), 1:128 (1%), 1:64 (2%), respectively. These results indicate that T. gondii antibodies are widespread in the animal populations and suggest that toxoplasmosis is a widely spread zoonotic infection in northern Iran.


Subject(s)
Abattoirs , Antibodies, Protozoan/blood , Cattle Diseases/epidemiology , Goat Diseases/epidemiology , Sheep Diseases/epidemiology , Toxoplasma/immunology , Toxoplasmosis, Animal/epidemiology , Animals , Cattle , Female , Fluorescent Antibody Technique, Indirect/veterinary , Goats , Iran/epidemiology , Male , Seroepidemiologic Studies , Sheep
19.
East Mediterr Health J ; 13(1): 41-8, 2007.
Article in English | MEDLINE | ID: mdl-17546904

ABSTRACT

We investigated the prevalence of human CE among nomadic communities in 4 areas of Khuzestan province: Behbahan, Shoush, Masjed Soleiman and Izeh. Blood samples from 3446 individuals from 700 randomly selected families were examined for detection of antibody against Echinococcus granuIosus. Family members were interviewed to assess possible risk factors for infection such as age, sex, dog ownership. The prevalence of CE was 13.8%: 1.9% in Behbahan, 12.4% in Shoush, 17.3% in Masjed Soleiman and 18.2% in Izeh. These differences were statistically significant. There was no significant association between CE seropositivity and age, sex and dog ownership.


Subject(s)
Echinococcosis/epidemiology , Endemic Diseases/statistics & numerical data , Transients and Migrants/statistics & numerical data , Adolescent , Adult , Age Distribution , Animals , Animals, Domestic/parasitology , Antibodies, Helminth/blood , Child , Child, Preschool , Dogs/parasitology , Echinococcosis/blood , Echinococcosis/immunology , Echinococcosis/prevention & control , Echinococcus granulosus/immunology , Endemic Diseases/prevention & control , Female , Humans , Infant , Iran/epidemiology , Male , Middle Aged , Population Surveillance , Prevalence , Risk Factors , Seroepidemiologic Studies , Sex Distribution , Surveys and Questionnaires , Urban Health/statistics & numerical data
20.
Vet Parasitol ; 142(1-2): 91-4, 2006 Nov 30.
Article in English | MEDLINE | ID: mdl-16959429

ABSTRACT

Immunodiagnostic confirmation of cystic human hydatidosis is frequently required before surgical intervention or of chemotherapy. However, it remains inadequate to detect specific antibodies or antigens in some confirmed cases of echinococcosis. This study was carried out to investigate the accuracy of three different immunodiagnostic tests for detection of specific circulating antigens or antibodies in the serum and urine of 13 experimentally infected sheep. For this purpose, Echinococcus granulosus were collected from small intestine of experimentally infected dogs, and 2000 taenid eggs were orally administered to each of the 13 sheep. There were six other sheep, which were kept as the control group. Biweekly serum and urine samples were collected from all the sheep for 4 months after infection. The sera were subjected to indirect hemagglutination test and the concentrated urine samples were subjected to coagglutination and counter immunoelectrophoresis tests. The results revealed that the sensitivity of these tests in detecting the hydatid antigens in the urine or antihydatid antibodies in the serum of the infected sheep reached their maximum in 12th and 13th week after infection; then it decreased in the following weeks. Examination of the non-infected sheep samples throughout the experiment showed that the aforesaid findings were specific only to the infected sheep. It seems that the appearance of specific hydatid antigen in urine and its antibodies in the serum were simultaneous. Although these tests are highly specific, false negative outcomes were encountered in their detection of cystic echinococcosis. In general, it seems rational to establish some series of diagnostic procedures in order to reveal antibodies and antigen of metacestode in serum and urine of the patients.


Subject(s)
Antibodies, Helminth/blood , Antibodies, Helminth/urine , Echinococcosis/veterinary , Echinococcus granulosus/immunology , Sheep Diseases/diagnosis , Animals , Antigens, Helminth/immunology , Diagnosis, Differential , Echinococcosis/blood , Echinococcosis/diagnosis , Echinococcosis/urine , False Negative Reactions , Female , Sensitivity and Specificity , Sheep , Sheep Diseases/blood , Sheep Diseases/urine , Time Factors
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