Abstract:Detection of plasma human herpesvirus (HHV)-8 DNA correlates with antibodies to lytic HHV-8 antigens, being predictive of Kaposi's sarcoma in HIV-infected patients. We show that the prevalence of plasma HHV-8 DNA was 10.6% for HIV infection through sexual contact and 7.1% for HIV infection through intravenous injection. In addition, the prevalence of plasma HHV-8 DNA was significantly associated with male gender (9.4%) and HIV viral load below 1000 copies mL(-1) (12.1%), but not age or CD4 cell count in HIV-in… Show more
“…Our finding correlated with the previous report in that no difference in the seropositive rate is associated with gender or age in patients with lymphoma, leukemia, autoimmune cytopenias and myeloproliferative disorders (Tsai et al , 2005). However, our finding was not in agreement with the association of male gender with prevalence of plasma HHV‐8 DNA in HIV‐infected patients (Lin et al , 2008). Moreover, higher prevalence of plasma HHV‐8 DNA in HIV‐infected patients was observed in those younger than 40 years (Lin et al , 2008).…”
Section: Positivity For Hhv‐8 Dna In Pbmcs According To Gender Age contrasting
confidence: 99%
“…However, our finding was not in agreement with the association of male gender with prevalence of plasma HHV‐8 DNA in HIV‐infected patients (Lin et al , 2008). Moreover, higher prevalence of plasma HHV‐8 DNA in HIV‐infected patients was observed in those younger than 40 years (Lin et al , 2008). The difference could be due to the risk of HHV‐8 transmission by sexual contact and intravenous injection routes in HIV patients.…”
Section: Positivity For Hhv‐8 Dna In Pbmcs According To Gender Age contrasting
confidence: 99%
“…Overall, 14 (10.29%) of the Taiwanese leukemia patients had HHV‐8 DNA detected in PBMCs, higher than the percentage (5.8%, 29/501) of plasma PCR‐positive HHV‐8 cases among malignant lymphoma patients in Spain (de Sanjosé et al , 2004). In this study, the percentage of HHV‐8 DNA in PBMCs of the relatives' cases (8.94%, 11/123) and leukemia patients (10.29%, 14/136) was similar to our previous research in that 8.9% of HIV‐infected Taiwanese patients had seropositivity of HHV‐8 DNA detected in plasma (Lin et al , 2008). Among the major leukemia subtypes, prevalence of HHV‐8 DNA in PBMCs was nonsignificantly associated with acute lymphoid leukemia (OR=0.84, 95% CI=0.32–2.18), acute myeloid leukemia (OR=1.05, 95% CI=0.28–3.98), chronic myeloid leukemia (OR=0.59, 95% CI=0.07–5.35), aplastic anemia (OR=0.88, 95% CI=0.10–7.46) and solid tumors (OR=0.39, 95% CI=0.04–3.83).…”
Section: Positivity For Hhv‐8 Dna In Pbmcs According To Gender Age supporting
confidence: 89%
“…Human herpesvirus 8 (HHV-8), also known as Kaposi's sarcoma (KS)-associated herpesvirus (KSHV), belongs to the gammaherpesvirus (Ablashi et al, 2002;Lin et al, 2008). HHV-8 causes KS, multicentric Castleman disease and primary effusion lymphoma (Ablashi et al, 2002;Haddad et al, 2008).…”
Human herpesvirus 8 (HHV-8) is associated with the development of Kaposi's sarcoma and several other human malignancies. The prevalence of HHV-8 DNA in peripheral blood mononuclear cells (PBMCs) in Taiwanese leukemia populations has not been investigated. In this study, HHV-8 DNA was extracted from PBMCs, and detected in 10.29% of the leukemia cases and 8.94% of the relatives' cases. In addition, the prevalence of HHV-8 DNA in PBMCs was nonsignificantly associated with gender, age and leukemia subtypes. The study examines the prevalence of HHV-8 DNA in PBMCs in Taiwanese leukemia and can be applied in further epidemiological studies.
“…Our finding correlated with the previous report in that no difference in the seropositive rate is associated with gender or age in patients with lymphoma, leukemia, autoimmune cytopenias and myeloproliferative disorders (Tsai et al , 2005). However, our finding was not in agreement with the association of male gender with prevalence of plasma HHV‐8 DNA in HIV‐infected patients (Lin et al , 2008). Moreover, higher prevalence of plasma HHV‐8 DNA in HIV‐infected patients was observed in those younger than 40 years (Lin et al , 2008).…”
Section: Positivity For Hhv‐8 Dna In Pbmcs According To Gender Age contrasting
confidence: 99%
“…However, our finding was not in agreement with the association of male gender with prevalence of plasma HHV‐8 DNA in HIV‐infected patients (Lin et al , 2008). Moreover, higher prevalence of plasma HHV‐8 DNA in HIV‐infected patients was observed in those younger than 40 years (Lin et al , 2008). The difference could be due to the risk of HHV‐8 transmission by sexual contact and intravenous injection routes in HIV patients.…”
Section: Positivity For Hhv‐8 Dna In Pbmcs According To Gender Age contrasting
confidence: 99%
“…Overall, 14 (10.29%) of the Taiwanese leukemia patients had HHV‐8 DNA detected in PBMCs, higher than the percentage (5.8%, 29/501) of plasma PCR‐positive HHV‐8 cases among malignant lymphoma patients in Spain (de Sanjosé et al , 2004). In this study, the percentage of HHV‐8 DNA in PBMCs of the relatives' cases (8.94%, 11/123) and leukemia patients (10.29%, 14/136) was similar to our previous research in that 8.9% of HIV‐infected Taiwanese patients had seropositivity of HHV‐8 DNA detected in plasma (Lin et al , 2008). Among the major leukemia subtypes, prevalence of HHV‐8 DNA in PBMCs was nonsignificantly associated with acute lymphoid leukemia (OR=0.84, 95% CI=0.32–2.18), acute myeloid leukemia (OR=1.05, 95% CI=0.28–3.98), chronic myeloid leukemia (OR=0.59, 95% CI=0.07–5.35), aplastic anemia (OR=0.88, 95% CI=0.10–7.46) and solid tumors (OR=0.39, 95% CI=0.04–3.83).…”
Section: Positivity For Hhv‐8 Dna In Pbmcs According To Gender Age supporting
confidence: 89%
“…Human herpesvirus 8 (HHV-8), also known as Kaposi's sarcoma (KS)-associated herpesvirus (KSHV), belongs to the gammaherpesvirus (Ablashi et al, 2002;Lin et al, 2008). HHV-8 causes KS, multicentric Castleman disease and primary effusion lymphoma (Ablashi et al, 2002;Haddad et al, 2008).…”
Human herpesvirus 8 (HHV-8) is associated with the development of Kaposi's sarcoma and several other human malignancies. The prevalence of HHV-8 DNA in peripheral blood mononuclear cells (PBMCs) in Taiwanese leukemia populations has not been investigated. In this study, HHV-8 DNA was extracted from PBMCs, and detected in 10.29% of the leukemia cases and 8.94% of the relatives' cases. In addition, the prevalence of HHV-8 DNA in PBMCs was nonsignificantly associated with gender, age and leukemia subtypes. The study examines the prevalence of HHV-8 DNA in PBMCs in Taiwanese leukemia and can be applied in further epidemiological studies.
“…Sensitivity and specificity of ORF66 and ORF-K12-based western blot strip assay and ELISA Twelve serum samples from the plasma HHV-8 DNApositive patients that were analysed in our previous report (Lin et al 2008) were used to determine the sensitivity of the recombinant protein-based Western blot strip assay (Fig. 2).…”
Section: Generation Of Recombinant Orf66 and Orfk12 Fusion Proteinsmentioning
Human herpesvirus 8 (HHV-8), also known as Kaposi's sarcoma (KS)-associated herpesvirus (KSHV), is not routinely isolated in cell cultures, and thus detection of HHV-8-specific antibodies is usually performed. In this study, we performed recombinant antigens ORF66- and ORFK12-based Western blot strip assays and ELISA, and surveyed the seroprevalence of HHV-8 antibodies in HIV-positive and -negative patients. In serum samples from patients with positive plasma HHV-8 DNA, the sensitivity of the Western blot strip assay was 100% for the anti-ORF66 antibodies and 83.3% for the anti-ORFK12 antibodies. In addition, ORF66-based ELISA showed higher levels of specificity (87.3%) and sensitivity (84.8%) than ORFK12-based ELISA. Moreover, the area under the receiver-operating characteristics curves (AUROC) was 0.76 for ORF66-based ELISA and 0.66 for ORFK12-based ELISA. The seroprevalence of HHV-8 antibodies to ORF66 and/or ORFK12 in the HIV-infected patients (55%, 97/176) was significantly higher than in the DM patients (45%, 135/301) (P = 0.03) and the HIV-/DM-negative group (11%, 11/100) (P < 0.01). In the HIV-infected patients, the seropositivity of the HHV-8-specific antibody was 30% to both antigens, 19% to ORFK12 and 5.7% to ORF66. Importantly, HHV-8 seropositivity in the HIV-infected patients was significantly associated with the transmission method of intravenous injection and high levels of HIV RNA loading (P < 0.01), but not with gender, CD4 cell numbers or AIDS symptoms. This study assessed the sensitivity and specificity of ORF66 and ORFK12 for the detection of HHV-8 antibodies, providing novel antigens for the diagnosis of HHV-8 infection and epidemiology of HHV-8 seroprevalence.
To evaluate the pathogenic mechanisms and transmission routes involved in KSHV infection in 22 Cuban individuals who maintained close contact with epidemic KS patients, real-time PCR was used to quantify KSHV-DNA in clinical samples of plasma, saliva and peripheral blood mononuclear cells (PBMC). KSHV-DNA was detected in 72.7% (16/22) of the contacts. The highest levels of KSHV load were detected in saliva, followed by PBMC (average log copies/100 ng DNA = 1.28 and 1.12), while significantly lower levels were detected in plasma (average log copies/ml = 0.37). Two of three intra-domiciliary and two serodiscordant sexual contacts of AIDS-KS patients were infected with KSHV. The rate of KSHV-DNA detection in saliva and PBMC samples in men who have sex with men (MSM) was significantly higher than in heterosexuals (HT) (p = 0.014). MSM were more likely to harbor KSHV-DNA in saliva when compared with HT individuals (OR 4.33; 95% CI 1.117-16.8). These results emphasize that, in Cuba, KSHV horizontal transmission through saliva may occur, although homosexual behavior may predispose an individual to KSHV acquisition. Even in the absence of disease, KSHV could cause an asymptomatic systemic infection in individuals who maintain close contact with AIDS-KS patients.
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