A Clinical And Epidemiologic-Study Of Human-Leukocyte Antigen-Dpb Alleles In Hodgkins-Disease

Am Oza,S Tonks, J Lim,Ma Fleetwood,Ta Lister,Jg Bodmer, Wm Howell, S Devereux,Gm Taylor, D Gokale,C Loeliger, P Kuehnl,G Pellegris, K Takacs, G Petranyi, E Gazit, T Klein, E Dutoit,R Martell,Mg Hammond, Sv Vantonder,R Liang, T Wong,V Chan, W Klitz,A Begovich,G Woodfield, M Roberts,Jd Bignon, A Mikata, T Takenouchi,D Cunningham, E Robinson, N Haim, Pm Chen, E Ferreira,Jma Whitehouse,J Sweetenham,Gm Mead,D Crowther,P Woll,W Zeller,Dk Hossfeld, W Kuse, G Bonadonna, Z Molnar, S Eckhardt, I Benbassat,P Jacobs, C Johnson, Dj Kenoyer,D Todd,Tk Chan,S Horning, S Rosenberg,V Harvey, P Thompson,P Browett, Jl Harousseau

CANCER RESEARCH(1994)

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摘要
An international study to investigate the role of human leukocyte antigen (HLA)-DPB alleles in Hodgkin's disease was conducted with 17 participating centers in 12 countries. A total of 741 patients and 686 controls were typed using polymerase chain reaction amplification of HLA-DPB alleles and subsequent sequence specific oligonucleotide hybridization. The frequency of HLA-DPB1*0301 was found to be significantly increased in white patients, compared with ethnically matched controls. In this population group, the DPB1*0301 allele is associated with a relative risk of 1.95 (P < 0.01). There was also a significant reduction in the frequency of HLA-DPB1*0401 in patients from Japan and Taiwan (relative risk, 0.15; P < 0.01). Clinical analysis from data on 551 patients demonstrated a significantly inferior remission duration in patients with HLA-DPBI*0901, overall (P < 0.05), and in the Japanese and Taiwanese populations (P = 0.02), where this allele is most prevalent. This analysis suggests an epidemiological as well as a possible prognostic association between HLA-DPB alleles and Hodgkin's disease.
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