Diagnostic value of IgG antibody and stool antigen tests for chronic Helicobacter pylori infections in Ibb Governorate, Yemen.

The stool antigen test (SAT) and the serum Helicobacter pylori (H. pylori) IgG antibody assays exhibit significant utility in the clinical diagnosis of H. pylori infection and in distinguishing between acute and chronic infections. The main objective of the current study was to identify the diagnostic value of serum H. pylori IgG antibody and SAT in the detection of H. pylori infections among chronic H. pylori-infected patients residing in Ibb Governorate, Yemen. 200 patients with H. pylori infection, confirmed through positive results in the serum immunochromatographic antibody test, were selected for H. pylori infection confirmation using serum H. pylori IgG antibodies and SAT across diverse hospitals, gastroenterology, and Hepatology clinics in Ibb Governorate. After the selection of patients, blood and stool specimens were obtained from all participants and underwent analysis via the Statistical Package for the Social Sciences (SPSS). The prevalence of H. pylori infection demonstrated variability based on the confirmatory tests, with rates of 54% for SAT and 78.5% for serum H. pylori IgG antibody, contrasting with a 100% prevalence observed in the screening serum immunochromatographic antibody test. Clinically, the study categorized H. pylori infections into four stages, whereby a significant proportion of patients (40.5%) exhibited positivity for both serum H. pylori IgG antibody and SAT, indicative of active chronic infections. The majority of positive cases only manifested serum H. pylori IgG antibody presence (chronic infections) at 38%, whereas 13.5% exclusively tested positive for SAT, corresponding to acute infections. Moreover, 88% of patients did not have either serum H. pylori IgG antibody or SAT (absence of infections) during confirmatory tests. Noteworthy is the study's approach employing multiple tests for H. pylori infection detection, focusing predominantly on chronic infections-prevailing types caused by H. pylori. The results revealed a significant association between serum levels of H. pylori IgG antibody and SAT results with the presence of diverse gastrointestinal symptoms among patients, which increased with long H. pylori infection durations.

A study of innate and adaptive immune responses in beta-thalassemic patients with chronic hepatitis C virus infection.

Thalassemia major is an inherited disorder particularly common in people of Mediterranean, African, and Southeast Asian ancestry. Hepatitis C virus (HCV) is responsible for 80 - 90% of post transfusion hepatitis in beta-Thalassemic patients. Marked liver iron overload, which is often inevitable in patients on regular blood transfusion, and HCV infection have been shown to have a potentiating effect on hepatic fibrogenesis in thalassemic patients. This study aimed at investigating the impact of combined chronic hepatitis C and beta-Thalassemia on innate and adaptive immune responses. The study was conducted on 60 patients and 15 apparently healthy controls. Patients were dived into three groups: group 1: 35 patients with combined beta-thalassemia and chronic hepatitis C (CHC) (betaTH/CHC), group II: 15 beta-thalassemia patients without HCV infection (betaTH), group III: 10 patients with chronic hepatitis C infection (CHC). Assessment of the number of CD3+, CD4+, CD8+ T cells, NK cells, and NKT cells was done by flowcytometry. Human IFN-delta and IL-15 levels were estimated by Enzyme -Linked Immunosorbent Assay (ELISA). betaTH/CHC patients had significantly reduced numbers of conventional T lymphocytes, NK, NKT, CD4+, and CD8+ T cells when compared to betaTH patients. Serum IFN-gamma levels were significantly reduced in betaTH/CHC patients (2.57 pg/ml) in comparison to CHC patients (6.89pg/ml) and normal controls (4.73 pg/ml). A significant elevation of serum IL-15 levels in betaTH/CHC patients (38.04pg/ml) was found when compared to betaTH patients (16.22 pg/ml). Splenectomized patients showed reduced numbers of NK cells, NK T cells and lower CD4:CD8 ratio in comparison to non-splenectomized ones among betaTH/CHC patients. In conclusion our data show an obvious defective cellular innate immunity (NK & NKT cells) and cellular adaptive immunity (CD4+ T cells, CD8+ T cells, & INF-gamma) in (betaTH/CHC) patients, in comparison to (betaTH) patients. This observation suggests a potentiating effect of both CHC and beta-thalassemia on depression of innate and adaptive immune status in these patients