Romano A, Viola M, Bousquet P J, Gaeta F, Valluzzi R, Caruso C, Demoly P
Department of Internal Medicine and Geriatrics, UCSC-Allergy Unit, Complesso Integrato Columbus, Rome, Italy.
Allergy. 2007 Jan;62(1):53-8. doi: 10.1111/j.1398-9995.2006.01272.x.
Skin testing with penicilloyl polylysine (PPL) and minor determinant mixture (MDM) represents the first-line method for diagnosing beta-lactam hypersensitivity. However, in 2004, Allergopharma and Hollister-Stier announced their decision to stop the production of penicillin reagents (Allergopen and PrePen, respectively) within 1 year. Therefore, we decided to compare PPL and MDM from Allergopharma (Allergopen) with those from Diater (DAP).
We skin-tested 195 subjects with both Allergopen and DAP reagents, as well as with other beta-lactams; 74 (group A) had had immediate reactions to beta-lactams and 74 (group B) nonimmediate reactions, while 47 (group C) underwent prophylactic tests.
One hundred two patients (52.3%) had positive skin tests; 29 (14.9%) were positive to PPL and/or MDM. Of the 102 skin-test-positive patients, 44 belonged to group A, 57 to B and 1 to C; the last was positive only to Allergopen PPL (PPL-A) and tolerated the benzylpenicillin challenge. Minor determinant mixture reagents produced identical results in the 148 patients of groups A and B, 22 (14.9%) of which were positive. Both PPL reagents produced negative results in 139 of these 148 patients and positive ones in 5; one subject was positive to DAP PPL (PPL-D) and negative to PPL-A, while three patients were positive to PPL-A and negative to PPL-D; two of the latter tolerated benzylpenicillin challenges.
Minor determinant mixture reagents produced identical results in all 195 patients. Results of skin testing with PPL reagents were concordant in 190 (97.4%) of them. Therefore, DAP reagents are a reliable alternative to Allergopen ones.
用青霉噻唑聚赖氨酸(PPL)和次要决定簇混合物(MDM)进行皮肤试验是诊断β-内酰胺类药物超敏反应的一线方法。然而,2004年,Allergopharma公司和Hollister-Stier公司宣布决定在1年内停止生产青霉素试剂(分别为Allergopen和PrePen)。因此,我们决定比较Allergopharma公司(Allergopen)的PPL和MDM与Diater公司(DAP)的PPL和MDM。
我们用Allergopen试剂和DAP试剂以及其他β-内酰胺类药物对195名受试者进行了皮肤试验;74名(A组)受试者曾对β-内酰胺类药物有速发型反应,74名(B组)有迟发型反应,47名(C组)进行预防性试验。
102名患者(52.3%)皮肤试验呈阳性;29名(14.9%)对PPL和/或MDM呈阳性。在102名皮肤试验阳性的患者中,44名属于A组,57名属于B组,1名属于C组;最后一名仅对Allergopen PPL(PPL-A)呈阳性,且耐受苄青霉素激发试验。次要决定簇混合物试剂在A组和B组的148名患者中产生了相同的结果,其中22名(14.9%)呈阳性。在这148名患者中,两种PPL试剂在139名患者中产生阴性结果,5名患者产生阳性结果;1名受试者对DAP PPL(PPL-D)呈阳性,对PPL-A呈阴性,而3名患者对PPL-A呈阳性,对PPL-D呈阴性;后两名患者中有两名耐受苄青霉素激发试验。
次要决定簇混合物试剂在所有195名患者中产生了相同的结果。PPL试剂皮肤试验结果在其中190名(97.4%)患者中一致。因此,DAP试剂是Allergopen试剂的可靠替代品。