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1.
Vox Sang ; 88(1): 10-6, 2005 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-15663717

RESUMO

BACKGROUND AND OBJECTIVES: The Japanese Red Cross screens seronegative blood donors by nucleic acid amplification testing (NAT) for hepatitis B, hepatitis C and human immunodeficiency virus-1 markers. NAT-positive donors thus identified seemed to have a different infectious background from serologically positive donors. The purpose of our study was to characterize this background in the hepatitis B virus (HBV) and hepatitis C virus (HCV) NAT-positive donors. MATERIALS AND METHODS: Some 328 HBV DNA-positive and 44 HCV RNA-positive donors were detected by NAT testing of seronegative blood donors. These were characterized regarding age, gender and genotype of HBV and HCV. RESULTS: Those who were HBV NAT-positive were mainly young, in particular teenage girls. In Japan, genotypes C and B have previously been dominant, but recently genotype A has increased, and genotype H was recently detected. In HBV NAT-positive donors, the rate of genotype A was high (12.2%) compared with patients in hospital (1.7-2%). Donors who were HCV NAT-positive were also young, but mostly men in their twenties. The ratio of genotype 1b to 2a or 1b to 2b in HCV NAT-positive donors differed from that of hospitalized patients in Japan. We did not find genotype 1a, which is dominant in the USA. CONCLUSIONS: The high-risk donors detected by NAT were mainly young, with a different distribution of genotypes from that of hospitalized patients, regarding both HBV and HCV. The rare HBV genotype H has been found for the first time in Japan. The findings reflect the present spread of hepatitis viruses B and C.


Assuntos
Doadores de Sangue , Hepatite B/epidemiologia , Hepatite C/epidemiologia , Técnicas de Amplificação de Ácido Nucleico , Adolescente , Adulto , Distribuição por Idade , Fatores Etários , Idoso , Epidemiologia , Feminino , Genótipo , Hepacivirus/genética , Hepacivirus/isolamento & purificação , Hepatite B/diagnóstico , Vírus da Hepatite B/genética , Vírus da Hepatite B/isolamento & purificação , Hepatite C/diagnóstico , Humanos , Japão/epidemiologia , Masculino , Pessoa de Meia-Idade , Fatores Sexuais
2.
Dev Biol (Basel) ; 108: 29-39, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12220140

RESUMO

The first nationwide nucleic acid amplification testing (NAT) for hepatitis B virus (HBV), hepatitis C virus (HCV), and human immunodeficiency virus type 1 (HIV-1) of voluntarily donated blood after serological pre-screening and before release of cellular components and plasma for fractionation was implemented by the Japanese Red Cross Blood Transfusion Services. The NAT screening assay using multiplex reagent is time-saving, cost effective, and labour-saving procedure for all blood and blood products including short-shelf life platelets. During the 50-mini-pool NAT screening of serologically negative donations (February 1, 2001-April 30, 2001), we were able to screen out 112 HBV-positive, 25 HCV-positive, and 4 HIV-1 positive units from blood and blood components.


Assuntos
Doadores de Sangue , Sangue/virologia , HIV-1/isolamento & purificação , Vírus de Hepatite/isolamento & purificação , Técnicas de Amplificação de Ácido Nucleico/métodos , Viremia , Transfusão de Sangue , DNA Viral , HIV-1/genética , Hepacivirus/genética , Hepacivirus/isolamento & purificação , Vírus da Hepatite B/genética , Vírus da Hepatite B/isolamento & purificação , Vírus de Hepatite/genética , Humanos , Japão , Programas de Rastreamento , RNA Viral/análise , Cruz Vermelha
3.
Vox Sang ; 76(3): 181-6, 1999.
Artigo em Inglês | MEDLINE | ID: mdl-10341335

RESUMO

BACKGROUND AND OBJECTIVES: The Japanese Red Cross Society recalled one lot of monoclonal-antibody-purified factor VIII (F VIII) and two lots of human serum albumin (HSA) 5 months after preparation of the final products, because of a procedural error that led to contamination by a unit of plasma positive for hepatitis B surface antigen (HBsAg). We evaluated the effectiveness of virus inactivation/removal in a large-scale process for manufacturing F VIII and HSA. MATERIALS AND METHODS: HBV DNA in the retained samples in process was measured by the polymerase chain reaction (PCR). The kinetics of virus inactivation by solvent-detergent (S/D) treatment was examined using model viruses. We also did a look-back survey of the patients who received corresponding products. RESULTS: Contaminated hepatitis B virus (HBV) DNA became undetectable beyond fraction S IV-I in the albumin process and immunoaffinity chromatography in the F VIII process, respectively. The model viruses were inactivated within 5 s by S/D treatment. There is no evidence that patients were infected by HBV after transfusion of these products. CONCLUSION: We conclude that virus inactivation/removal was effectively achieved in a large-scale manufacturing process for F VIII and HSA.


Assuntos
Fator VIII/isolamento & purificação , Setor de Assistência à Saúde , Vírus da Hepatite B/isolamento & purificação , Plasma/virologia , Albumina Sérica/isolamento & purificação , Humanos , Reprodutibilidade dos Testes , Estudos Retrospectivos
4.
Acta Paediatr ; 82(6-7): 620-3, 1993.
Artigo em Inglês | MEDLINE | ID: mdl-8339007

RESUMO

Growth hormone deficiency associated with hypogammaglobulinemia has been reported only in a few publications. Our patient was a male with recurrent episodes of infections. Serum immunoglobulin (Ig) G was extremely low although IgM concentration was much greater than the normal limit. Growth hormone responses to insulin, 1-Dopa and growth hormone-releasing hormone were low. The mean growth hormone concentration during sleep was less than the normal limit. These results are consistent with hyper-IgM immunodeficiency associated with growth hormone deficiency. The mode of transmission appears to be autosomal dominant. This combination has not been reported previously.


Assuntos
Transtornos do Crescimento/imunologia , Hormônio do Crescimento/deficiência , Hipergamaglobulinemia/complicações , Imunoglobulina M , Síndromes de Imunodeficiência/diagnóstico , Adolescente , Transtornos do Crescimento/complicações , Transtornos do Crescimento/genética , Humanos , Síndromes de Imunodeficiência/genética , Masculino , Linhagem
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