Author/Authors :
Aurora Jurado، نويسنده , , Blanca C?rdaba، نويسنده , , Paloma Jara، نويسنده , , Pilar Cuadrado، نويسنده , , Loreto Hierro، نويسنده , , Belén de Andrés، نويسنده , , Victoria del Pozo، نويسنده , , M Isabel Cortegano، نويسنده , , Soledad Gallardo، نويسنده , , Carmen Camarena، نويسنده , , Rafael Barcena، نويسنده , , José L. Casta?er، نويسنده , , Rita Alvarez، نويسنده , , Carlos Lahoz، نويسنده , , Pilar Palomino، نويسنده ,
Abstract :
Background/Aims: Markers for hepatitis C virus are often detectable in patients suffering chronic hepatitis with liver-kidney microsomal type 1 antibodies. Several authors have suggested that two subsets of those patients can be defined: a) hepatitis C virus negative and b) hepatitis C virus positive. The aim of this work was to further analyze the possible genetic association, HLA class I and II, in these two groups of patients.
Methods: HLA was analyzed in 49 patients. Class I was studied using a standard lymphocytotoxicity test and in class II a reverse hybridization-based test for DRB1 typing and PCR-SSO for DQB1 typing were used. Sixty healthy Spanish subject and 39 chronic hepatitis C subjects without anti-LKM1 antibodies were used as control groups for the “a” and “b” subsets, respectively.
Results: No significant association was found with class I specificities in either group. DQB1 typing showed a very significant increase of DQ2 in the “a” group (93.3% vs. 48%; RR=15; pc=0.0025), and DRB1 typing from the “b” group reversed a high association with DR7 (82.3% vs. 43.6%; RR=6; pc=0.0086).
Conclusions: Our stuides revealed a strong association with DQ2 for the “a” group and for the first time an extremely high association with DR7 antigen for the “b” subset. Hence it is possible to establish a different genetic profile in these two patient groups.
Keywords :
amino acids , hepatitis C virus , Liver kidney microsomal antibodies. , Humanleukocyte antigens