abdolghader tane

 Hepatitis B Virus (HBV) is a universal health challenge all around the world. Several factors like viral load, genetic characteristics, age, sex, and immune status contribute to variable clinical outcomes of HBV infection. The sequels of HBV infection vary remarkably among persons ranging from the spontaneous deletion of infection to persistent infection.

 The present study aimed to evaluate the association of single nucleotide polymorphisms IL10-1082 with HBV clearance.

 Sixty subjects with Chronic Hepatitis B (CHB) infection and 60 subjects who spontaneously recovered HBV were enrolled in the study. The IL-10-1082 polymorphisms were determined by Polymerase Chain Reaction with Restriction Fragment Length Polymorphism (PCR–RFLP).

 The clearance of HBV infection demonstrated a significant association with IL-10-1082 polymorphisms in the GG genotype (P = 0.03), while there was no association with other genotypes. Reduced risk of chronic hepatitis B infection was associated with IL-10-1082 GG (OR: 2.33, 95% CI: 1.07 - 5.09). Besides, IL-10-1082 A/G alleles did not differ clearly between the two study groups (P = 0.07)

 The IL-10-1082 polymorphisms may be associated with a reduced risk of CHB infection and recovery after HBV infection.
 

Maternal immunity to Toxoplasma gondii is critical during pregnancy. Non-immunized women may be at the risk of toxoplasmosis during pregnancy. This parasite can pass through the placenta to the fetus and causes severe complications in the fetus. This study aimed to investigate the seroepidemiology of Toxoplasma infection in pregnant women of Gonabad.

Three hundred blood samples were collected from pregnant women and abortive women of 18-40 years old who referred to the health centers and hospitals of Gonabad. The immunoglobulin G (IgG) and immunoglobulin M (IgM) antibody titers were measured by the enzyme-linked immunosorbent assay.

The samples were taken from 252 (84.0%) pregnant women and 48 (16.0%) women with abortion. The average age of these women was 29.23 ± 6.24 years. Among these subjects, 56 (22.2%) pregnant women and 15 (31.3%) women with a history of abortion had anti-Toxoplasma IgG antibodies while 196 (77.8%) pregnant women and 33 (68.7%) women with abortion history did not have this specific antibody. Based on the results, 3 (1.2%) pregnant women had IgM antibodies while this antibody was not observed in any woman with a history of abortion. Finally, the prevalence of toxoplasmosis was 23.6%.

According to the results, 76.33% of pregnant and abortive women in Gonabad have no history of Toxoplasma infection. Therefore, they are prone to toxoplasmosis infection during their pregnancies. In this regard, it is necessary to establish public health and preventive actions, as well as a rapid diagnosis to eliminate risk factors during pregnancy

Chronic Hepatitis B virus infection is a multifactorial disease with a variety of clinical outcomes. Since interferon-gamma (IFN-γ) is a significant immune factor in antiviral defense, this case-control study aimed to investigate the potential relationship between single nucleotide polymorphism of rs2430561 and hepatitis B infection outcome in a population of Birjand city, eastern Iran. Blood samples were collected from 60 chronically HBV- infected patients and 60 healthy subjects with the history of HBV infection. Genomic DNA was extracted from whole blood by the salting-out method. The first intron of IFN-γ with a length of 264 bp was amplified by Amplification Refractory Mutation System Polymerase Chain Reaction (ARMS-PCR) followed by sequencing. Our results exhibited a statistically significant difference between patients and control individuals (p-value<0.001). The frequency of the allele A was 73.3% in HBV- infected patients, whereas in controls (individuals with a history of HBV infection) it was 46.7%. A statistically significant relationship was found between the IFN-γ (+874T/A, rs2430561) single nucleotide polymorphism (SNP) and chronic HBV infec tion in the studied population. The obtained results showed that HBV infected individuals with T allele have less risk of progressing to chronic HBV infection. It also suggests that the homozygous carriers of the A allele are more vulnerable to chronic HBV infection.