Kott E, Hahn T, Huberman M, Levin S, Schattner A
Department of Neurology, Meir Hospital, Kfar Saba, Israel.
Q J Med. 1990 Sep;76(281):951-60.
The autoimmune response in myasthenia gravis is well characterized, but little is known about the mechanisms initiating it. We have studied the interferon system and natural killer cell activity in 25 patients with myasthenia gravis and compared them to 68 healthy subjects and 96 patients with acute viral infections. Forty-four per cent of patients had circulating interferon (greater than 16 mu/ml), and in a similar proportion their peripheral blood mononuclear cells were in an antiviral state, i.e., showed low levels of viral replication when infected by vesicular stomatitis virus. Spontaneous in vitro interferon production by patients' peripheral blood mononuclear cells was also common (greater than 10 mu/ml, 32 per cent), while the response to the alpha-interferon inducer poly I:C was lower than expected, possibly reflecting the already high state of activation of the interferon system. These results were essentially similar to those obtained in patients with viral illnesses and differed significantly from healthy controls. In many myasthenia gravis patients (16 of 22, 73 per cent), a markedly deficient natural killer cell activity was found, with a median cytotoxicity of 6.5 per cent compared to 29 per cent in healthy subjects (p less than 0.005). Thus, many patients with myasthenia gravis have evidence of an activated interferon system and defective natural killer cell activity, suggesting an occult viral infection or reflecting nonspecific stimulation which may nevertheless contribute to the pathogenesis of the autoimmune response.
重症肌无力的自身免疫反应已得到充分表征,但引发该反应的机制却知之甚少。我们研究了25例重症肌无力患者的干扰素系统和自然杀伤细胞活性,并将其与68名健康受试者和96例急性病毒感染患者进行了比较。44%的患者循环干扰素水平升高(大于16 μ/ml),外周血单个核细胞处于抗病毒状态的比例与之相似,即感染水疱性口炎病毒时病毒复制水平较低。患者外周血单个核细胞自发产生体外干扰素的情况也很常见(大于10 μ/ml,占32%),而对α干扰素诱导剂聚肌胞苷酸(poly I:C)的反应低于预期,这可能反映出干扰素系统已处于高度激活状态。这些结果与病毒感染患者的结果基本相似,与健康对照组有显著差异。在许多重症肌无力患者中(22例中有16例,占73%),发现自然杀伤细胞活性明显不足,细胞毒性中位数为6.5%,而健康受试者为29%(p<0.005)。因此,许多重症肌无力患者有干扰素系统激活和自然杀伤细胞活性缺陷的证据,提示存在隐匿性病毒感染,或反映了非特异性刺激,这可能在自身免疫反应的发病机制中起作用。