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HLA-DR B1共享基序的存在并不影响类风湿关节炎患者对环磷酰胺和甲氨蝶呤的细胞毒性。

The presence of HLA-DR B1 shared motif does not influence cyclophosphamide and methotrexate cytotoxicity in rheumatoid arthritis patients.

作者信息

Lacki J K, Wassmuth R, Korczowska I, Mackiewicz S, Muller W

机构信息

Department of Rheumatology and Clinical Immunology, Karol Marcinkowski University School of Medicine, Poznan, Poland.

出版信息

J Investig Allergol Clin Immunol. 2000 Jul-Aug;10(4):235-41.

Abstract

In the present study we investigated the relation between cyclophosphamide and methotrexate toxicity and the presence of HLA- DR B1 alleles in rheumatoid arthritis patients. Seventy-eight such patients (67 women and 11 men) were observed for 12 months. Eighteen were treated with intravenous cyclophosphamide, 28 with oral methotrexate, and 32 with intramuscular gold salts. The prevalence of this shared motif was higher in the study population than in the healthy controls. However, detailed observations did not demonstrate a relation between particular genotype and drug intolerance. Based on the obtained findings we concluded that HLA-DR B1 typing cannot affect cyclophosphamide or methotrexate tolerance in rheumatoid arthritis patients. However, taking into account the relatively small number of patients expressing single genotype, further studies are recommended.

摘要

在本研究中,我们调查了类风湿关节炎患者中,环磷酰胺和甲氨蝶呤毒性与HLA - DR B1等位基因存在情况之间的关系。观察了78例此类患者(67名女性和11名男性)12个月。18例接受静脉注射环磷酰胺治疗,28例接受口服甲氨蝶呤治疗,32例接受肌肉注射金盐治疗。该共享基序在研究人群中的患病率高于健康对照。然而,详细观察并未显示特定基因型与药物不耐受之间存在关联。基于所得结果,我们得出结论,HLA - DR B1分型不会影响类风湿关节炎患者对环磷酰胺或甲氨蝶呤的耐受性。然而,考虑到表达单一基因型的患者数量相对较少,建议进一步开展研究。

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