Speerstra F, Reekers P, van de Putte L B, Vandenbroucke J P
Tissue Antigens. 1985 Jul;26(1):35-40. doi: 10.1111/j.1399-0039.1985.tb00932.x.
HLA phenotype frequencies were studied in 21 rheumatoid arthritis (RA) patients with haematotoxic reactions to aurothioglucose (AuTG) or D-penicillamine (DP), 65 matched RA controls and 277 healthy controls. Antigens B8 and DR3 were significantly increased in the toxic RA patient group as compared to both RA controls and healthy controls. These contrasts were strongest in the patients with AuTG-induced thrombocytopenia or leucopenia: all patients developing either reaction to this drug were B8- and/or DR3-positive (p less than 0.001), 7 (78%) being positive for both antigens. In the patient group with DP-induced reactions these antigens were also increased but these differences were not significant. In the latter group the prevalence of antigen DR4 was high, especially in the patient group with DP-induced thrombocytopenia, all 12 patients with this type of reaction being DR4 positive. Our data suggest that haematotoxic reactions to AuTG and DP develop primarily (or even exclusively) in genetically predisposed RA patients. Furthermore, the HLA phenotype contributing to an increased risk seems not to be the same for the two anti-rheumatic drugs studied.
对21例对金硫葡萄糖(AuTG)或青霉胺(DP)有血液毒性反应的类风湿关节炎(RA)患者、65例匹配的RA对照以及277例健康对照进行了HLA表型频率研究。与RA对照和健康对照相比,毒性RA患者组中的抗原B8和DR3显著增加。这些差异在AuTG诱导的血小板减少或白细胞减少患者中最为明显:所有对该药物产生任何一种反应的患者均为B8和/或DR3阳性(p<0.001),7例(78%)两种抗原均为阳性。在DP诱导反应的患者组中,这些抗原也有所增加,但差异不显著。在后一组中,抗原DR4的患病率较高,尤其是在DP诱导的血小板减少患者组中,所有12例此类反应患者均为DR4阳性。我们的数据表明,对AuTG和DP的血液毒性反应主要(甚至完全)发生在具有遗传易感性的RA患者中。此外,对于所研究的两种抗风湿药物,导致风险增加的HLA表型似乎并不相同。