Clemmensen I, Jensen B A, Hølund B, Kappelgaard E, Neilsen H
Clin Exp Immunol. 1986 Jun;64(3):587-96.
A previously fit 66-years-old male primarily presented symptoms compatible with Henock-Schönlein's purpura, from which he seemingly recovered. Shortly hereafter he relapsed with an IgM lambda essential monoclonal cryoglobulinemia type I, presenting a systemic, necrotizing vasculitis, with low titer of circulating immune complexes and complement consumption. Glucocorticoid treatment and plasmapheresis did not prevent an ultimately lethal course. An indirect immunoperoxidase technique showed that the cryo-IgM bound to the interstitial connective tissue corresponding to the localization of collagen type I. In addition it bound to affinity purified human procollagen type I. These results indicate, that the IgM lambda of the proband was an autoantibody with collagen type I specificity.
一名既往健康的66岁男性最初出现了与过敏性紫癜相符的症状,随后似乎已康复。此后不久,他复发了I型IgM λ原发性单克隆冷球蛋白血症,表现为全身性坏死性血管炎,循环免疫复合物滴度低且补体消耗。糖皮质激素治疗和血浆置换未能阻止最终的致命病程。间接免疫过氧化物酶技术显示,冷球蛋白IgM与对应于I型胶原定位的间质结缔组织结合。此外,它还与亲和纯化的人I型前胶原结合。这些结果表明,该先证者的IgM λ是一种具有I型胶原特异性的自身抗体。