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青霉素酰多聚赖氨酸和次要决定簇混合物皮试在评估青霉素类非即刻反应中的作用非常有限。

The very limited usefulness of skin testing with penicilloyl-polylysine and the minor determinant mixture in evaluating nonimmediate reactions to penicillins.

机构信息

Allergy Unit, Complesso Integrato Columbus, Rome, Italy.

出版信息

Allergy. 2010 Sep;65(9):1104-7. doi: 10.1111/j.1398-9995.2009.02318.x. Epub 2010 Jan 28.

Abstract

BACKGROUND

The contribution of skin testing with penicilloyl-polylysine (PPL) and the minor determinant mixture (MDM) to the diagnosis of hypersensitivity reactions to penicillins differs greatly according to the type of reaction: immediate (occurring within 1 h after the last drug administration) or nonimmediate (occurring more than 1 h after the last drug administration).

OBJECTIVE

To assess the contribution of skin testing with PPL and MDM to the diagnosis of nonimmediate reactions to penicillins.

METHODS

We evaluated 162 adults who had had 232 nonimmediate reactions to penicillins, mostly aminopenicillins, and presented positive skin and/or patch tests to one or more penicillin reagents: PPL, MDM, benzylpenicillin, ampicillin, and amoxicillin, as well as any responsible penicillins.

RESULTS

A total of 157 subjects (96.9%) displayed patch-test and/or delayed-reading intradermal-test positivity to penicillin reagents, which indicates a cell-mediated hypersensitivity; six of them also presented immediate-reading skin-test positivities. All 157 patients with a cell-mediated hypersensitivity were positive to the responsible penicillins (parent drugs); 16 of them also displayed delayed-reading intradermal-test positivity to MDM. Five (3.1%) of the 162 patients displayed only immediate-reading skin-test positivity (four to PPL and one to amoxicillin). Overall, 158 subjects (97.5%) presented positive responses to the responsible penicillins, while only 9 (5.5%) and 17 (10.5%) were positive to PPL and MDM, respectively.

CONCLUSIONS

The contribution of skin testing with PPL and MDM in diagnosing nonimmediate hypersensitivity reactions to penicillins, especially cell-mediated ones, is very limited. This finding could be useful at a time when PPL and MDM are not available in all countries.

摘要

背景

皮试青霉素酰基多聚赖氨酸(PPL)和次要决定簇混合物(MDM)对青霉素类药物过敏反应的诊断贡献差异很大,具体取决于反应类型:即刻(末次用药后 1 小时内发生)或非即刻(末次用药后 1 小时后发生)。

目的

评估 PPL 和 MDM 皮肤试验对青霉素类药物非即刻反应的诊断价值。

方法

我们评估了 162 名成人,他们对青霉素类药物(主要为氨基青霉素类)发生了 232 次非即刻反应,对一种或多种青霉素试剂(PPL、MDM、苄青霉素、氨苄青霉素和阿莫西林)的皮肤和/或斑贴试验呈阳性,以及任何相关的青霉素类药物。

结果

共有 157 名受试者(96.9%)的青霉素试剂斑贴试验和/或迟发型皮内试验呈阳性,提示细胞介导的超敏反应;其中 6 名受试者还存在即刻型皮肤试验阳性。所有 157 名细胞介导超敏反应患者对相关青霉素类药物(母药)均呈阳性;其中 16 名患者对 MDM 的迟发型皮内试验也呈阳性。162 名患者中,有 5 名(3.1%)仅表现为即刻型皮肤试验阳性(4 名对 PPL 阳性,1 名对阿莫西林阳性)。总的来说,158 名患者(97.5%)对相关青霉素类药物呈阳性反应,而仅 9 名(5.5%)和 17 名(10.5%)患者对 PPL 和 MDM 呈阳性反应。

结论

PPL 和 MDM 皮肤试验在诊断青霉素类药物非即刻超敏反应,特别是细胞介导的超敏反应中的作用非常有限。在并非所有国家都能获得 PPL 和 MDM 的情况下,这一发现可能具有一定的实用价值。

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