达利珠单抗
巴利昔单抗
医学
移植
钙调神经磷酸酶
器官移植
免疫毒素
不利影响
恶性肿瘤
肾移植
单克隆抗体
内科学
免疫学
他克莫司
抗体
作者
Jennifer L. Berard,R VELEZ,Richard B. Freeman,Shirley M. Tsunoda
标识
DOI:10.1592/phco.19.15.1127.30582
摘要
Daclizumab and basiliximab, engineered human IgG monoclonal antibodies to the interleukin‐2 (IL‐2) receptor α‐subunit, were approved to prevent acute rejection after rnal transplantation. Daclizumab was studied in adult and pediatric renal allograft recipients, liver allograft recipients, and calcineurin‐sparing protocols in renal transplant recipients. Basiliximab was studied in renal allograft recipients and subgroups of recipients of living‐related and cadaveric transplants, and in patients with diabetes mellitus. Both agents reduced acute rejection and were associated with few adverse effects. However, information regarding their long‐term effects on infection, malignancy, chronic rejection, and patient survival must be available before a final decision is made regarding their proper administration. We propose that a likely role the drugs will play in the field of solid organ transplantation is in new protocols that allow sparing of other more toxic immunosuppressive agents.
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