Christiansen Stephen P, Peterson Daniel, To Thu, Youle Richard, McLoon Linda
Department of Ophthalmology, University of Minnesota, 2001 6th Street SE, Minneapolis, MN 55455, USA.
Invest Ophthalmol Vis Sci. 2002 Mar;43(3):679-85.
PURPOSE: The immunotoxin, ricin-mAb 35, composed of ricin conjugated to a monoclonal antibody against the nicotinic acetylcholine receptor of skeletal muscle, has been proposed as a potential new agent for treatment of focal muscle dystonias. It has been demonstrated that direct injection of ricin-mAb 35 into rabbit extraocular muscle (EOM) results in significant muscle loss within 1 week. In this study, the long-term myopathic effects of ricin-mAb 35 on extraocular muscle were investigated. METHODS: Rabbit superior rectus muscles were injected with ricin-mAb 35 at a dose of 0.2 microg/kg, with the contralateral superior rectus muscle serving as the control. After 56 days, 105 days, and 1 year, the superior rectus muscles were removed and prepared for light or electron microscopy. Postinjection changes in muscle fiber morphometry and ultrastructure were examined. Immunohistochemical markers were used to identify inflammatory cellular infiltrate and myosin heavy chain (MHC) isoform expression. RESULTS: Despite evidence of ongoing regeneration, treated muscles continued to show a decrease in both myofiber number and in total cross-sectional area 56 and 105 days after injection. Individual myofiber cross-sectional areas were markedly heterogeneous at 56 days. Myofiber number and muscle cross-sectional area returned to normal 1 year after injection, but pronounced heterogeneity of myofiber size remained. The most significant changes in myosin heavy chain (MHC) isoform expression occurred in the orbital layer, where, at 56 and 105 days, there were increased numbers of fast and neonatal myofibers and decreased numbers of slow myofibers. In the global layer, after both 105 days and 1 year, there was a decrease in myofibers that were positive for slow, neonatal, and developmental MHC expression. CONCLUSIONS: EOM injection with ricin-mAb 35 results in a sustained decrease in muscle mass at 105 days after injection, with subtler morphometric changes persisting even to 1 year. Changes in muscle force development as a result of ricin-mAb 35 injection are currently under investigation. This novel immunotoxin may be useful in the treatment of strabismus if these studies show sustained weakness in treated muscles.
目的:免疫毒素蓖麻毒素 - 单克隆抗体35(ricin - mAb 35)由蓖麻毒素与抗骨骼肌烟碱型乙酰胆碱受体的单克隆抗体偶联而成,已被提议作为治疗局灶性肌肉肌张力障碍的一种潜在新药。已证明将ricin - mAb 35直接注射到兔眼外肌(EOM)中会在1周内导致明显的肌肉损失。在本研究中,调查了ricin - mAb 35对眼外肌的长期肌病效应。 方法:以0.2微克/千克的剂量将ricin - mAb 35注射到兔上直肌中,对侧上直肌作为对照。在56天、105天和1年后,取出上直肌并制备用于光镜或电镜检查。检查注射后肌纤维形态计量学和超微结构的变化。使用免疫组织化学标记物来识别炎性细胞浸润和肌球蛋白重链(MHC)同工型表达。 结果:尽管有持续再生的证据,但在注射后56天和105天,处理过的肌肉的肌纤维数量和总横截面积仍持续减少。在56天时,单个肌纤维横截面积明显不均一。注射1年后,肌纤维数量和肌肉横截面积恢复正常,但肌纤维大小仍存在明显的不均一性。肌球蛋白重链(MHC)同工型表达的最显著变化发生在眶层,在56天和105天时,快肌纤维和新生肌纤维数量增加,慢肌纤维数量减少。在整体层,在105天和1年后,慢肌、新生肌和发育型MHC表达阳性的肌纤维数量均减少。 结论:注射ricin - mAb 35到眼外肌中会导致注射后105天时肌肉质量持续下降,甚至到1年时仍存在更细微的形态计量学变化。目前正在研究注射ricin - mAb 35导致的肌肉力量发展变化。如果这些研究表明处理过的肌肉持续无力,这种新型免疫毒素可能对斜视治疗有用。
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