Alleviation of severe chronic arthritic pain using polyvalent immunoglobulins (KMP01): Two case reports.

IF 0.9 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Barry G Woodcock, Peter Braun, Martin Gasser, Laura Sly, Reinhard Lissner
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引用次数: 0

Abstract

Background: Treatment of arthritis is carried out using corticosteroids, methotrexate, sulfasalazine-like agents, and TNF-α-blocking agents such as infliximab and adalimumab. The disadvantages of these agents are high-cost, severe side effects including leucopenia, and in some cases the necessity of administration by injection. Polyvalent immunoglobulin formulations derived from bovine colostrum and marketed as a standardized formulation for oral application, are reported to be efficacious in chronic pain syndromes but are rarely, if ever, used as an alternative medication in such patients.

Aims: To treat arthritis in a real-world setting using polyvalent immunoglobulins in 2 patients, in one case where no alternative treatment modality was available and in another patient in whom the use of polyvalent immunoglobulins appeared to be a suitable option.

Materials and methods: Two male subjects aged 46 and 82 years with confirmed diagnosis but not well-controlled arthritis/polyarthritis receiving either high-dose NSAIDS, corticosteroids, methotrexate injections, with previous use of, or recommendations for treatment with monoclonal antibodies (etanercept and adalimumab) were treated with oral polyvalent immunoglobulins (KMP01; dose range 10 - 20 g daily) in real-world settings, in one case during a field excursion in Peru.

Results: The treatment produced a rapid alleviation of pain in both patients, in one patient where the symptoms were severe and debilitating. In the second patient methotrexate SC injections could be discontinued, and there was a progressive reversal of leucopenia (leucocyte count 3.9 × 103/µL) over a period of ~ 3 months.

Discussion: Polyvalent immunoglobulins have been shown previously to reduce the expression of interleukin-6 and C-reactive protein in peripheral blood monocytes, events attributed to the neutralization of gut-derived endotoxin ligands lipopolysaccharides (LPS) driving the basal immune response. The mode of action of KMP01 on cytokine expression is therefore similar to the TNF-α-blocking agents etanercept and adalimumab.

Conclusion: Findings from two case reports support the rationale for using polyvalent immunoglobulins as an effective and safe alternative in arthritis patients receiving standard treatments, in particular, methotrexate and TNF-α-blocking agents.

使用多价免疫球蛋白(KMP01)缓解严重的慢性关节炎疼痛:两个病例报告。
背景:治疗关节炎的方法包括使用皮质类固醇、甲氨蝶呤、磺胺嘧啶类药物和 TNF-α 阻断剂(如英夫利昔单抗和阿达木单抗)。这些药物的缺点是成本高、副作用大(包括白细胞减少症),而且在某些情况下必须注射给药。据报道,从牛初乳中提取的多价免疫球蛋白制剂作为口服用药的标准化制剂上市,对慢性疼痛综合征具有疗效,但很少被用作此类患者的替代药物,甚至从未被用作替代药物:两名年龄分别为46岁和82岁的男性受试者确诊为关节炎/多关节炎,但未得到很好的控制,他们正在接受大剂量非甾体类抗炎药、皮质类固醇激素、甲氨蝶呤注射,曾使用或被建议使用单克隆抗体(依那西普和阿达木单抗)治疗,他们在实际环境中接受了口服多价免疫球蛋白(KMP01;剂量范围为每天10-20克)治疗,其中一名受试者是在秘鲁野外考察期间接受治疗的:结果:治疗使两名患者的疼痛迅速缓解,其中一名患者的症状严重,身体虚弱。第二名患者可以停止甲氨蝶呤(SC)注射,白细胞减少症(白细胞计数为 3.9 × 103/µL)在约 3 个月的时间内逐渐逆转:讨论:多价免疫球蛋白以前曾被证明能降低外周血单核细胞中白细胞介素-6和C反应蛋白的表达,这些事件归因于中和驱动基础免疫反应的肠源性内毒素配体脂多糖(LPS)。因此,KMP01对细胞因子表达的作用模式与TNF-α阻断剂依那西普(etanercept)和阿达木单抗(adalimumab)相似:两份病例报告的研究结果支持将多价免疫球蛋白作为接受标准治疗(尤其是甲氨蝶呤和 TNF-α 阻断剂)的关节炎患者的一种有效而安全的替代疗法。
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来源期刊
CiteScore
1.70
自引率
12.50%
发文量
116
审稿时长
4-8 weeks
期刊介绍: The International Journal of Clinical Pharmacology and Therapeutics appears monthly and publishes manuscripts containing original material with emphasis on the following topics: Clinical trials, Pharmacoepidemiology - Pharmacovigilance, Pharmacodynamics, Drug disposition and Pharmacokinetics, Quality assurance, Pharmacogenetics, Biotechnological drugs such as cytokines and recombinant antibiotics. Case reports on adverse reactions are also of interest.
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