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Differential susceptibility between skin and vaginal mucosa in sensitization phase of allergic contact dermatitis in mice

机译:皮肤与阴道粘膜敏感阶段的差异敏感性,在小鼠中过敏性接触皮炎的敏化阶段

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Introduction Mechanisms underlying skin sensitization in allergic contact dermatitis have been actively studied using the murine contact hypersensitivity (CHS) model. However, much less is known about sensitization at the vaginal mucosa (VM). Methods We developed a CHS model with VM sensitization and epicutaneous elicitation at the ear. We then examined the proliferation activity of lymphocytes, the frequencies of T cells and the differentiation of hapten‐specific T cells in draining lymph nodes (dLNs) after sensitization. Results Hapten‐specific CHS responses to 2,4‐dinitrofluorobenzene (DNFB), 2,4,6‐trinitrochrolobenzene, and oxazolone assessed by ear swelling suggested that the VM would be an inductive site of CHS to haptens. In the comparisons of CHS responses to each of the three haptens examined, the lower responses in VM‐sensitized mice were observed than skin‐sensitized mice (e.g., DNFB‐induced responses, ?56%; p??.001, at 48?h?after challenge). Consistent with the CHS responses, the DNFB‐induced proliferation of cells in dLNs examined by 5‐bromo‐2?‐deoxyuridine assay was lower (?62%; p??.001) in VM‐sensitized mice than skin‐sensitized mice. On the other hand, between skin and VM sensitization, no significant differences were observed in the frequencies of interferon‐γ‐producing CD4+ and CD8+ effector, and regulatory T cells in dLNs after sensitization. We also observed no significant differences with respect to differentiation of hapten‐specific T cells based on the examination of cytokine production from dLN cells stimulated in vitro with 2,4‐dinitrobenzene sulfonate. Conclusion These findings suggested that the lower T cell proliferation after VM sensitization is important for the lower CHS responses with VM sensitization than skin sensitization.
机译:使用鼠接触超敏反应(CHS)模型,已经积极研究了皮肤致敏在过敏接触性皮炎中的引导机制。然而,关于阴道粘膜(VM)的敏化是较少的。方法我们开发了一种CHS模型,耳朵的VM敏化和外膜诱导。然后,我们检查了淋巴细胞的淋巴细胞,T细胞频率和分化在敏感后淋巴结的淋巴结(DLNS)的频率和分化。结果HAPTEN特异性CHS对2,4-二硝基氟苯(DNFB),2,4,6-三硝基罗洛洛尼苯和恶唑酮的反应表明,VM将是CHS的感应位点。在检查三个哈帕特的CHS反应的比较中,观察到VM致敏小鼠的较低响应而不是皮肤致敏的小鼠(例如,DNFB诱导的反应,Δ56%;p≤001,在48 ?H?挑战后)。与CHS响应一致,在5-溴-2-丁氧基脲测定中检测的DLN中的DNFB诱导的细胞增殖在VM敏化小鼠中较低(α62%;p≤001),而不是皮肤致敏的小鼠。另一方面,在皮肤和VM致敏之间,在敏化后,在干扰素-γ的CD4 +和CD8 +效应子的频率中没有观察到显着差异,并且在敏化后的DLN中的调节性T细胞。我们还观察到基于用2,4-二硝基苯磺酸盐刺激的DLN细胞的细胞因子产生的细胞因子产生的细胞因子产生没有显着差异。结论这些研究结果表明,VM致敏后的T细胞增殖较低对VM敏化性的低CHS反应而不是皮肤敏化。

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