Anti-cytokine autoantibodies: epiphenomenon or critical modulators of cytokine action.

P H van der Meide, H Schellekens
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引用次数: 31

Abstract

Low amounts of high-affinity autoantibodies to various cytokines have been detected in sera from healthy donors. Their levels, although highly variable, are increased in the circulation of patients subjected to cytokine therapy or suffering from a variety of immunoinflammatory diseases. It has been suggested that these autoantibodies play a regulatory role in the intensity and duration of an immune response. The antibodies may prevent the binding of a cytokine to its specific cell surface receptor thereby neutralizing its biological activity in vivo. They may also act as carrier proteins preventing the rapid elimination of a cytokine from the circulation and thus increase its bioactivity. Additionally or alternatively, autoantibodies may modulate cytokine-induced intracellular signal transduction pathways or trigger complement-mediated cytotoxicity towards cells carrying membrane-bound cytokines. The autoantibodies may exert their regulatory role in compliance with the other factors that control cytokine activity, including soluble cytokine receptors, cell surface decoy receptors, and receptor antagonists. Although not favored by many investigators, a less sophisticated role for naturally occurring anti-cytokine autoantibodies should be considered as well. Recent evidence has shown that autoantibodies are generated at a high frequency as part of a response to foreign antigens. These antibodies are produced by B cells arising from the process of somatic mutation. Thus anti-cytokine autoantibodies may be the result of a "leaky" B cell response triggered by immunoinflammatory processes. High-titered autoantibodies induced by cytokine therapy are of clinical concern since their occurrence is often associated with the loss of response to treatment. Moreover, they may also neutralize endogenously produced cytokines with possible pathological consequences. In this paper we have reviewed the available information on the biological and clinical significance of both naturally occurring and therapeutically induced anti-cytokine autoantibodies in animals and man with the emphasis on antibodies directed to interferons.

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抗细胞因子自身抗体:细胞因子作用的副现象或关键调节因子。
在健康供者的血清中检测到低量的各种细胞因子的高亲和力自身抗体。它们的水平虽然变化很大,但在接受细胞因子治疗或患有各种免疫炎性疾病的患者的循环中会增加。已有研究表明,这些自身抗体在免疫反应的强度和持续时间中起调节作用。所述抗体可阻止细胞因子与其特异性细胞表面受体的结合,从而在体内中和其生物活性。它们也可以作为载体蛋白,防止细胞因子从循环中迅速消除,从而增加其生物活性。此外,自身抗体可能调节细胞因子诱导的细胞内信号转导途径,或触发补体介导的对携带膜结合细胞因子的细胞的细胞毒性。自身抗体可能与其他控制细胞因子活性的因子(包括可溶性细胞因子受体、细胞表面诱饵受体和受体拮抗剂)一起发挥调节作用。尽管许多研究人员不赞成,但自然产生的抗细胞因子自身抗体也应考虑其较不复杂的作用。最近的证据表明,自身抗体的产生频率很高,是对外来抗原的反应的一部分。这些抗体是由B细胞在体细胞突变过程中产生的。因此,抗细胞因子自身抗体可能是由免疫炎症过程引发的“渗漏”B细胞反应的结果。细胞因子治疗诱导的高滴度自身抗体是临床关注的问题,因为它们的发生通常与治疗反应的丧失有关。此外,它们还可能中和内源性产生的细胞因子,从而产生可能的病理后果。在本文中,我们回顾了动物和人体内自然产生的和治疗诱导的抗细胞因子自身抗体的生物学和临床意义的现有信息,重点是针对干扰素的抗体。
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