Response to immunosuppressive therapy and an HLA-DRB1 allele in patients with aplastic anaemia: HLA-DRB1*1501 does not predict response to antithymocyte globulin

被引:20
作者
Nakao, S [1 ]
Takami, A [1 ]
Sugimori, N [1 ]
Ueda, M [1 ]
Shiobara, S [1 ]
Matsuda, T [1 ]
Mizoguchi, H [1 ]
机构
[1] TOKYO WOMENS MED COLL,DEPT HAEMATOL,TOKYO 162,JAPAN
关键词
aplastic anaemia; antithymocyte globulin; cyclosporine; HLA-DRB1; HLA-DR2;
D O I
10.1046/j.1365-2141.1996.293825.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
HLA-DRB1*1501, a subtype of HLA-DR2, has been shown to be closely associated with a good response to cyclosporine (CyA) therapy in patients with aplastic anaemia (AA). To determine whether this DRB1 allele can also predict a response to antithymocyte globulin (ATG) therapy in AA patients, we analysed the results of HLA-DRB1 typing in 59 Japanese patients who received ATG within 2 years after diagnosis of AA and also in 52 patients treated with CyA. All patients were divided into three groups: those with DRB1*1501, those with DRB1*1502, and those without either of these two alleles (DR2(-)). The response rate to ATG in DRB1*1501(+) patients (56%) was not significantly higher than that in DRB1*1502(+) patients (47%) and in the other DR2(-) patients (54%). In contrast, the response rate to CyA therapy in DRB1*1501(+) patients (92%) was significantly higher than that in the DRB1*1502(+) (41%) and in DR2(-) patients (57%). Multi-variate analysis revealed that possessing DRB1*1501 was an independent factor significantly predictive of a good response to CyA. These results indicate that although identifying the DRB1*1501 allele in AA patients prior to therapy is predictive of a good response to CyA therapy, it does not have a predictive value for ATG therapy.
引用
收藏
页码:155 / 158
页数:4
相关论文
共 16 条
[1]   INCREASED FREQUENCY OF DR2 IN PATIENTS WITH APLASTIC-ANEMIA AND INCREASED DR SHARING IN THEIR PARENTS [J].
CHAPUIS, B ;
VONFLIEDNER, VE ;
JEANNET, M ;
MERICA, H ;
VUAGNAT, P ;
GRATWOHL, A ;
NISSEN, C ;
SPECK, B .
BRITISH JOURNAL OF HAEMATOLOGY, 1986, 63 (01) :51-57
[2]   TREATMENT OF APLASTIC-ANEMIA WITH ANTILYMPHOCYTE GLOBULIN AND METHYLPREDNISOLONE WITH OR WITHOUT CYCLOSPORINE [J].
FRICKHOFEN, N ;
KALTWASSER, JP ;
SCHREZENMEIER, H ;
RAGHAVACHAR, A ;
VOGT, HG ;
HERRMANN, F ;
FREUND, M ;
MEUSERS, P ;
SALAMA, A ;
HEIMPEL, H .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (19) :1297-1304
[3]  
GLUCKMAN E, 1992, BLOOD, V79, P2540
[4]   GENE-FREQUENCIES AND HAPLOTYPIC ASSOCIATIONS WITHIN THE HLA REGION IN 916 UNRELATED JAPANESE INDIVIDUALS [J].
HASHIMOTO, M ;
KINOSHITA, T ;
YAMASAKI, M ;
TANAKA, H ;
IMANISHI, T ;
IHARA, H ;
ICHIKAWA, Y ;
FUKUNISHI, T .
TISSUE ANTIGENS, 1994, 44 (03) :166-173
[5]  
Imanishi T., 1992, HLA 1991, P1065
[6]   INVITRO INTERFERON-GAMMA PRODUCTION BY CULTURED T-CELLS IN SEVERE APLASTIC-ANEMIA - CORRELATION WITH GRANULOMONOPOIETIC INHIBITION IN PATIENTS WHO RESPOND TO ANTI-THYMOCYTE GLOBULIN [J].
LAVER, J ;
CASTROMALASPINA, H ;
KERNAN, NA ;
LEVICK, J ;
EVANS, RL ;
OREILLY, RJ ;
MOORE, MAS .
BRITISH JOURNAL OF HAEMATOLOGY, 1988, 69 (04) :545-550
[7]   CYCLOSPORINE THERAPY OF APLASTIC-ANEMIA, CONGENITAL AND ACQUIRED RED-CELL APLASIA [J].
LEONARD, EM ;
RAEFSKY, E ;
GRIFFITH, P ;
KIMBALL, J ;
NIENHUIS, AW ;
YOUNG, NS .
BRITISH JOURNAL OF HAEMATOLOGY, 1989, 72 (02) :278-284
[8]  
MANIATIS T, 1992, MOL CLONING LABORATO, P280
[9]   IDENTIFICATION OF A SPECIFIC HLA CLASS-II HAPLOTYPE STRONGLY ASSOCIATED WITH SUSCEPTIBILITY TO CYCLOSPORINE-DEPENDENT APLASTIC-ANEMIA [J].
NAKAO, S ;
TAKAMATSU, H ;
CHUHJO, T ;
UEDA, M ;
SHIOBARA, S ;
MATSUDA, T ;
KANESHIGE, T ;
MIZOGUCHI, H .
BLOOD, 1994, 84 (12) :4257-4261
[10]   HLA-DR2 PREDICTS A FAVORABLE RESPONSE TO CYCLOSPORINE THERAPY IN PATIENTS WITH BONE-MARROW FAILURE [J].
NAKAO, S ;
YAMAGUCHI, M ;
SAITO, M ;
YASUE, S ;
SHIOBARA, S ;
MATSUDA, T ;
NITTA, M ;
SASAKI, M .
AMERICAN JOURNAL OF HEMATOLOGY, 1992, 40 (03) :239-240