首页> 外文OA文献 >Dissection of antigenic and irritative effects of epicutaneously applied haptens in mice. Evidence that not the antigenic component but nonspecific proinflammatory effects of haptens determine the concentration-dependent elicitation of allergic contact dermatitis.
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Dissection of antigenic and irritative effects of epicutaneously applied haptens in mice. Evidence that not the antigenic component but nonspecific proinflammatory effects of haptens determine the concentration-dependent elicitation of allergic contact dermatitis.

机译:解剖表皮半抗原在小鼠中的抗原性和刺激性作用。半抗原的非抗原性成分而非非特异性促炎作用的证据决定了变应性接触性皮炎的浓度依赖性诱发。

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摘要

Allergic contact dermatitis differs from most other immune reactions by its strict dose dependence during the elicitation phase. Moreover, almost all known contact allergens can also induce dose-dependent irritative dermatitis and in general only elicit allergic contact dermatitis in sensitized individuals when applied within a narrow dose range. Therefore, we hypothesized that elicitation of contact hypersensitivity (CHS) may require two signals, antigen-specific effector cell activation and a non-antigen-specific proinflammatory signal, both of which are provided by application of a sufficient dose of hapten. To dissociate these putative two signals, oxazolone-sensitized mice were ear challenged with a dose of the specific hapten which was too low to elicit CHS. At the same time, an unrelated hapten was applied in a conventional concentration to the same skin site. Whereas neither treatment alone elicited a significant CHS response, application of both compounds together resulted in a strong CHS response that was indistinguishable from that elicited by the full dose of the specific hapten. Upon coadministration of the irrelevant hapten, allergic contact dermatitis could be elicited even when the dose of the specific hapten was further reduced by a factor of 10(3). In contrast, a dose reduction of the irrelevant hapten by a factor of two resulted in the loss of the CRS response. These data indicate that non-antigen-specific effects of epicutaneously applied haptens significantly contribute to the elicitation of CHS responses and that the capacity of the hapten to evoke this proinflammatory stimulus rather than its antigenicity is responsible for the strict concentration dependence.
机译:过敏性接触性皮炎与大多数其他免疫反应的不同之处在于其在诱导阶段的严格剂量依赖性。此外,几乎所有已知的接触性过敏原也可以诱发剂量依赖性的刺激性皮炎,并且通常仅在狭窄的剂量范围内使用时,才在致敏个体中引起过敏性接触性皮炎。因此,我们假设引起接触性超敏反应(CHS)可能需要两个信号,即抗原特异性效应细胞激活和非抗原特异性促炎信号,这两种信号均通过应用足够剂量的半抗原来提供。为了分离这两个推测的信号,对恶唑酮敏化的小鼠用特定剂量的半抗原进行耳声攻击,该剂量太低而不能引起CHS。同时,将不相关的半抗原以常规浓度应用于同一皮肤部位。尽管没有单独的治疗方法会引起显着的CHS反应,但将两种化合物一起使用会产生很强的CHS反应,这与特定剂量的半抗原所引起的反应没有区别。联合服用无关的半抗原后,即使将特定半抗原的剂量进一步减少了10(3),也可能引起过敏性接触性皮炎。相反,不相关的半抗原的剂量减少了两倍,导致了CRS反应的丧失。这些数据表明,经表皮施用的半抗原的非抗原特异性作用显着有助于引起CHS反应,并且半抗原激发这种促炎性刺激而不是其抗原性的能力是严格的浓度依赖性的原因。

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