(function(){ var content_array=["

关于Spesolimab<\/strong><\/p> \n

Spesolimab 是一款新型人源化选择性抗体,可阻断白介素 -36 受体 (IL-36R) 的激活。IL-36通路是免疫系统内的一种信号通路,已被证明与GPP等多种自身免疫性疾病的病因有关。[1],[4],[5] <\/span><\/sup>Spesolimab是首个专门靶向 IL-36 通路治疗 GPP急性发作的在研疗法,已在一项随机、安慰剂对照试验中获得了具有统计学意义的结果。目前,Spesolimab还在被开发用于预防GPP急性发作以及治疗其他嗜中性粒细胞性皮肤病,如掌跖脓疱病 (PPP) 和化脓性汗腺炎 (HS)。[6]<\/sup><\/sup>,[7]<\/sup><\/sup><\/span><\/p> \n

关于泛发性脓疱型银屑病<\/strong><\/p> \n

GPP 是一种罕见的、异质性的、危及生命的中性粒细胞性皮肤病,临床上与斑块型银屑病不同。 [1],[2]<\/span><\/sup>GPP 是由中性粒细胞(一种白细胞)在皮肤中积聚引起的,会导致疼痛性的无菌性脓疱。[2]<\/span><\/sup>GPP患者的临床病程各不相同,有些患者的疾病复发并伴有反复急性发作,而另一些患者的疾病持续存在且间歇性急性发作。[2]<\/span><\/sup>虽然 GPP急性发作的严重程度各不相同,但若不及时治疗,出现败血症和多系统器官衰竭等并发症,可能会危及生命。[5]<\/span><\/sup>这种慢性全身性疾病会对患者的生活质量产生重大影响,并带来医疗保健负担。GPP的患病率,在不同地理区域各不相同。[1],[8],[9],<\/span><\/sup>[10]<\/span><\/sup><\/p> \n

GPP的治疗<\/strong><\/p> \n

GPP患者急需获得能够快速解决急性发作的症状、防止疾病复发、且安全性可以接受的治疗方法。基于治疗斑块型银屑病患者的临床经验,免疫调节疗法(包括生物制剂)被用于治疗 GPP。然而,这些疗法治疗 GPP 的有效性和安全性的临床证据十分有限。<\/p> \n

勃林格殷格翰炎症领域:受患者启发的开创性科学<\/strong><\/p> \n

纤维化和炎症性疾病会极大地影响患者的情绪和身体。在我们重新定义治疗模式时,这些患者是我们的向导、合作伙伴和灵感来源。作为一家家族企业,我们可以进行长期规划。我们的目标是发现和开发同类首创的疗法。凭借对分子通路的深入了解,我们正在开创能够靶向、修复和预防多种纤维化和炎症疾病的科学突破。通过建立长期的外部合作,我们努力在最短的时间内为患者带来治疗上的突破。我们不会停下脚步,直到能让患者有机会过上他们想要的生活。<\/p> \n

勃林格殷格翰<\/strong><\/p> \n

勃林格殷格翰致力于研究突破性疗法,旨在改善人类和动物的健康。作为一家研发驱动的全球领先生物制药企业,公司在医疗需求高度未得到满足的领域通过创新展现价值。自1885年成立以来,勃林格殷格翰始终是一家独立的家族企业,从长远来看这一点将不会改变。在人用药品、动物保健和生物制药合同生产三大业务领域,全球有约5.2万名员工服务逾130个地区。更多详情,请访问:www.boehringer-ingelheim.com<\/a><\/p> \n

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References<\/span><\/p> \n

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[1] Crowley JJ, et al<\/em>. A brief guide to pustular psoriasis for primary care providers, Postgraduate Medicine. 2021;133(3):330-344.<\/span><\/p> <\/td> \n <\/tr> \n

[2] Navarini AA, et al<\/em>. European consensus statement on phenotypes of pustular psoriasis. JEADV<\/em>. 2017;31:1792-1799.<\/span><\/p> <\/td> \n <\/tr> \n

[3] Fujita H, et al<\/em>. Japanese guidelines for the management and treatment of generalized pustular psoriasis: The new pathogenesis and treatment of GPP. J Dermatol.<\/em> 2018;45(11):1235–1270.<\/span><\/p> <\/td> \n <\/tr> \n

[4] Furue K, et al<\/em>. Highlighting Interleukin-36 Signalling in Plaque Psoriasis and Pustular Psoriasis. Acta Derm Venereol.<\/em> 2018;98:5–13.<\/span><\/p> <\/td> \n <\/tr> \n

[5] Bachelez H, et al<\/em>. Inhibition of the Interleukin-36 Pathway for the Treatment of Generalized Pustular Psoriasis. N Engl J Med.<\/em> 2019; 380:981-983.<\/span><\/p> <\/td> \n <\/tr> \n

[6] ClinicalTrials.gov. A Study to Test Whether Spesolimab Helps People With a Skin Disease Called Hidradenitis Suppurativa. Available at: https:\/\/clinicaltrials.gov\/ct2\/show\/NCT04762277<\/a>. Accessed October 2021. <\/span><\/p> <\/td> \n <\/tr> \n

[7] ClinicalTrials.gov. A Study to Test Long-term Treatment With Spesolimab in People With Palmoplantar Pustulosis (PPP) Who Took Part in Previous Studies With Spesolimab. Available at https:\/\/clinicaltrials.gov\/ct2\/show\/NCT04493424<\/a>. Accessed: October 2021. <\/span><\/p> <\/td> \n <\/tr> \n

[8] Ohkawara A et al<\/em>. Generalized pustular psoriasis in Japan: two distinct groups formed by differences in symptoms and genetic background. Acta Derm Venereol<\/em>. 1996 Jan;76(1):68–71.<\/span><\/p> <\/td> \n <\/tr> \n

[9] Augey F, et al<\/em>. Generalized pustular psoriasis (Zumbusch): a French epidemiological survey. European Journal of Dermatology. 2006; 16(6):669-673.<\/span><\/p> <\/td> \n <\/tr> \n

[10] Jin H, et al.<\/em> Clinical features and course of generalized pustular psoriasis in Korea. The Journal of Dermatology. 2015; 42(7):674-678.<\/span><\/p> <\/td> \n <\/tr> \n <\/tbody> \n <\/table> \n<\/div> \n

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