Menghini V V, Savcenko V, Olson L J, Tazelaar H D, Dec G W, Kao A, Cooper L T
Department of Internal Medicine, Mayo Clinic Rochester, Minn 55905, USA.
Mayo Clin Proc. 1999 Dec;74(12):1221-6. doi: 10.4065/74.12.1221.
Giant cell myocarditis (GCM) is a rare and frequently fatal disorder with no proven treatment. Case reports and data from a rat model of GCM suggest that immunosuppressive therapy directed against T lymphocytes may have clinical benefit. We describe a 47-year-old man with severe acute heart failure due to GCM in whom the left ventricular ejection fraction normalized and the myocardial inflammatory infiltrate resolved rapidly after treatment with muromonab-CD3, cyclosporine, azathioprine, and corticosteroids. Three previously published cases with less impressive responses to treatment including muromonab-CD3 and a critical review of the published data on immunosuppressive therapy are included in this report. The response to immunosuppressive therapy is highly variable, and direct comparisons between immunosuppressive regimens do not exist. Therefore, despite individual reports of dramatic improvement after immunosuppressive treatment, firm conclusions cannot be made about the benefit of immunosuppression for GCM. The benefits of immunosuppressive therapy must be confirmed in a prospective, randomized trial.
巨细胞性心肌炎(GCM)是一种罕见且常致命的疾病,尚无经证实有效的治疗方法。病例报告及来自GCM大鼠模型的数据表明,针对T淋巴细胞的免疫抑制疗法可能具有临床益处。我们描述了一名47岁因GCM导致严重急性心力衰竭的男性患者,在用莫罗单抗-CD3、环孢素、硫唑嘌呤和皮质类固醇治疗后,其左心室射血分数恢复正常,心肌炎性浸润迅速消退。本报告纳入了3例先前发表的对包括莫罗单抗-CD3在内的治疗反应欠佳的病例,以及对已发表的免疫抑制疗法数据的批判性综述。免疫抑制疗法的反应差异很大,且不存在免疫抑制方案之间的直接比较。因此,尽管有个别报告称免疫抑制治疗后有显著改善,但对于免疫抑制对GCM的益处仍无法得出确凿结论。免疫抑制疗法的益处必须在前瞻性随机试验中得到证实。