3 research outputs found
Prevalence and 9-year incidence of hepatitis E virus infection among north italian blood donors: Estimated transfusion risk
Recent European guidelines recommend that screening policiesfor Hepatitis E virus (HEV) in blood donors should be based on local risk assessments. We determined the prevalence of current and past HEV infection in donors from Lombardy, the Italian region providing 24% of the Italian blood supply. We also calculated the incidence of infection over a period of 10 years, and estimated the risk of transfusion-related transmission. The study was conducted within the framework of BOTIA, an EU-funded project. HEV RNA was detected by individual donation testing, and the prevalence and incidence of anti-HEV antibodies were determined in two subgroups. The risk of receiving an infected blood unit was estimated on the basis of HEV RNA yields and serology. RESULTS: One of the 9726 donors was truly viremic. The prevalence of confirmed anti-HEV IgG reactivity was 52/767 (6.8%; 95%CI 5.1-8.8%). The incidence of HEV infection was 7.6/10000 per year (95%CI 2.1-2.5 per year). The estimated transfusion-related risk of infection was 1/10000 blood donations on the basis of HEV RNA yield (upper limit of the 95%CI 1:1666), and 1/16666 donations on the basis of the incidence data (95%CI 1:435-1:57000).In conclusion, The frequency of current and past HEV infection in blood donors living in Northern Italy is among the lowest so far reported in Europe. The estimated transfusion-related risk of infection was similar regardless of whether it was calculated on the basis of HEV RNA yield or serological incidence, thus suggesting stable infection pressure over the last ten years
Naïve/Effector CD4 T cell ratio as a useful predictive marker of immune reconstitution in late presenter HIV patients: A multicenter study
A significant proportion of HIV-infected patients experiencing a late diagnosis highlights the need to define immunological protocols able to help the clinicians in identifying patients at higher risk for immunological failure. The aim of the study was to evaluate the feasibility of easy cytometric tests in defining the effect of antiretroviral treatment (cART) on immunological homeostasis and in identifying predictive markers of early immune recovery. Chronic HIV infected patients (n = 202) were enrolled in a prospective multicentric study, and their immunological profile was studied before (w0) and after 24 weeks (w24) of antiretroviral treatment (cART) using a standardized flow cytometric panel. Based on CD4 T cell count before treatment, patients were divided in late (LP: CD4 <350/mmc), intermediate (IP: 350/mmc<500/mmc) and early (EP: CD4 >500/mmc) presenters. In all groups, cART introduction increased CD4 and CD4/CD8 T cell ratio, naïve T cell (CD4 and CD8) and CD127-expressing CD4 T cells. In parallel, cART significantly reduced effector memory T cells (CD4 and CD8) and T cell activation (CD38+CD8 and CD95+CD4 T cells). Moreover, the frequency of Naïve and Effector CD4 T cells before treatment correlated with several immune parameters key associated with the pathogenesis of HIV, thus mirroring the health of immune system. Interestingly, we identified the Naïve/Effector CD4 T cell ratio (N/EM) at w0 as a marker able to predict early immune recovery. Specifically, in LP, N/EM ratio was significantly higher in immunological responder patients (CD4>500/mmc at w24) when compared to immunological non responder (CD4 T cells <500/mmc at w24). Finally, a multivariate analysis indicates that after 24w patients with N/EM ratio higher than 1.86 at w0 recovered 96 CD4 T cells more than those with N/EM ratio lower than 0.46. Altogether, our data define an easy protocol able to define reliable immunological markers useful for the characterization of immune profile in viremic HIV patients and identify the naïve/effector CD4 T cell ratio as a new tool able to predict an early immune reconstitution potential