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Drug photoallergy

机译:药物光过敏

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Drugs are one of the representative exogenous agents that cause photosensitive dermatitis. Both phototoxic and photoallergic mechanisms exist in photosensitivity to exogenous agents. While the phototoxic reaction is mediated mainly by reactive oxygen species, the photoallergic reaction is induced and elicited by immunological consequences. Two hypotheses have been put forward to explain the formation of photoallergen: prohapten and photohapten. The vast majority of clinically photoallergic drugs are photohapten rather than prohapten. Clinically, photocontact dermatitis and drug photosensitivity are the two major disorders caused by topical and systemic exogenous photosensitizers, respectively. The main cause of photocontact dermatitis is nonsteroidal anti‐inflammatory drugs. In drug photosensitivity, various causative agents have been reported and are recently represented by hydrochlorothiazide, quinolones, piroxicam, and flutamide. Orally administered drugs diffuse from the blood to the epidermis, and keratinocytes are photoderivatized with a given drug upon ultraviolet (UV) A irradiation, leading to photoantigen formation and cytokine production. In parallel, dendritic cells become photohapten‐bearing, T‐cell–sensitizing cells. Considering the mechanisms of photoallergy to chemicals, several in?vitro assessments have been proposed to detect the photoallergenicity. Finally, a recent observation with newly marketed drugs has demonstrated that drugs may function as immunomodulators and induce photosensitivity as typically seen in anti‐CCR4 antibody.
机译:药物是引起光敏性皮炎的代表性外源性​​药物之一。对外源剂的光敏性同时存在光毒性和光过敏机制。虽然光毒性反应主要由活性氧介导,但光过敏反应是由免疫学后果诱导和诱发的。提出了两个假设来解释光致敏原的形成:前肽和前肽。临床上大多数的光过敏药物是光半抗原而不是半抗原。在临床上,光接触性皮炎和药物光敏性分别是局部和全身性外源性光敏剂引起的两个主要疾病。光接触性皮炎的主要原因是非甾体类抗炎药。在药物的光敏性方面,已经报道了多种致病因素,最近以氢氯噻嗪,喹诺酮,吡罗昔康和氟他胺为代表。口服给药的药物从血液扩散到表皮,并且在紫外线(UV)A照射下,角质形成细胞被给定的药物光衍生,导致光抗原的形成和细胞因子的产生。同时,树突状细胞变成带有光半抗原的T细胞敏化细胞。考虑到光致化学物质的机理,已经提出了几种体外评估来检测光致过敏性。最后,最近对新上市药物的观察表明,药物可以起到免疫调节剂的作用,并诱导抗光敏性,如抗CCR4抗体中常见的那样。

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