Madhok R, Pullar T, Capell H A, Dawood F, Sturrock R D, Dick H M
Ann Rheum Dis. 1985 Sep;44(9):589-91. doi: 10.1136/ard.44.9.589.
In a study of the clinical and immunogenetic profiles of 17 patients with rheumatoid arthritis and thrombocytopenia (platelet count less than 150 000/mm3 (150 x 10(9)/l)) due to gold therapy two clinical patterns were distinguished without knowledge of HLA type: group I, an early precipitous thrombocytopenia (10 patients), and group II, a less dramatic fluctuant fall (seven patients). In group I patients the clinical and laboratory features suggested an immune mediated, peripheral destruction of platelets, and all patients in this group were found to be HLA-DR3 positive. Two patients subsequently received penicillamine without toxicity. In group II the basis of thrombocytopenia appeared to be different, and only two patients in this group were HLA-DR3 positive. All group II patients had received penicillamine; four developed a thrombocytopenia. Mechanisms of toxicity in both groups are discussed. It would appear that HLA typing in unlikely to help in predicting all those patients at risk of toxicity during chrysotherapy.
在一项针对17例因金制剂治疗导致类风湿性关节炎和血小板减少症(血小板计数低于150 000/mm³(150×10⁹/L))患者的临床和免疫遗传学特征研究中,在不了解HLA类型的情况下区分出两种临床模式:第一组,早期急剧血小板减少症(10例患者),第二组,血小板减少程度较轻且呈波动下降(7例患者)。在第一组患者中,临床和实验室特征提示血小板的免疫介导性外周破坏,且该组所有患者均被发现HLA - DR3阳性。随后两名患者接受青霉胺治疗且未出现毒性反应。在第二组中,血小板减少症的病因似乎不同,该组只有两名患者HLA - DR3阳性。第二组所有患者均接受过青霉胺治疗;其中四名患者出现了血小板减少症。文中讨论了两组中毒性反应的机制。看来HLA分型不太可能有助于预测所有在金疗法期间有中毒风险的患者。