Lewis K E, Holdren M S, Maurer M F, Underwood S, Meengs B, Julien S H, Byrnes-Blake K A, Freeman J A, Bukowski T R, Wolf A C, Hamacher N B, Rixon M W, Dillon S R
Discovery Biology Group, ZymoGenetics Inc. (a Bristol-Myers Squibb Company), Seattle, WA, USA.
Preclinical Development Group, ZymoGenetics Inc. (a Bristol-Myers Squibb Company), Seattle, WA, USA.
J Eur Acad Dermatol Venereol. 2017 Jan;31(1):142-150. doi: 10.1111/jdv.13794. Epub 2016 Aug 8.
Overexpression or administration of interleukin 31 (IL-31) has been shown to induce a profound itch response in mice and dogs. The chronic pruritus observed in mouse IL-31 transgenic mice results in the development of skin lesions and alopecia through excoriation from excessive scratching, a condition similar to that observed in patients with atopic dermatitis (AD).
To test whether IL-31 induces pruritus in non-human primates and, if so, whether treatment with an anti-IL-31 neutralizing monoclonal antibody (mAb) can block the response.
A series of studies was conducted in cynomolgus monkeys to evaluate the itch response to recombinant cynomolgus IL-31 (cIL-31) administration. Three routes of cIL-31 administration (intravenous, intradermal, and subcutaneous) were evaluated. Subcutaneous treatment with a humanized anti-human IL-31 mAb cross-reactive to cIL-31 was subsequently tested for its ability to block the response to intradermal cIL-31 administration.
Each route of cIL-31 delivery elicited a scratching response immediately after cIL-31 administration and lasted at least 3 h. Treatment with the IL-31 mAb inhibited the cIL-31-mediated scratching response in a dose-dependent manner.
These results demonstrate that an IL-31 mAb can inhibit IL-31-mediated pruritus in vivo, and could be an effective therapy for pruritic skin conditions like AD where IL-31 upregulation may play a role.
白细胞介素31(IL-31)的过表达或给药已被证明可在小鼠和犬类中引发强烈的瘙痒反应。在小鼠IL-31转基因小鼠中观察到的慢性瘙痒会通过过度搔抓引起皮肤损伤和脱毛,这一情况与特应性皮炎(AD)患者中观察到的类似。
测试IL-31是否会在非人灵长类动物中诱发瘙痒,以及如果是这样,用抗IL-31中和单克隆抗体(mAb)进行治疗是否能阻断该反应。
在食蟹猴中进行了一系列研究,以评估对重组食蟹猴IL-31(cIL-31)给药的瘙痒反应。评估了cIL-31的三种给药途径(静脉内、皮内和皮下)。随后测试了与人源化抗人IL-31 mAb交叉反应的cIL-31皮下治疗阻断对皮内cIL-31给药反应的能力。
每种cIL-31给药途径在给药后立即引发搔抓反应,并持续至少3小时。用IL-31 mAb治疗以剂量依赖的方式抑制了cIL-31介导的搔抓反应。
这些结果表明,IL-31 mAb可在体内抑制IL-31介导的瘙痒,并且可能是治疗像AD这样的瘙痒性皮肤病的有效疗法,其中IL-31上调可能起作用。