青霉素过敏单价特异性半抗原抑制剂ro6 -0787的临床研究。

A L De Weck, F Jeunet, K H Schulz, P Louis, J P Girard, J P Grilliat, D Moneret-Vautrin, H Storck, B Wuthrich, H Spengler, L Juhlin, F Scheiffarth, H Warnatz, F Wortmann, S R Virgaay
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引用次数: 0

摘要

来自欧洲9个不同研究小组的研究人员对90名青霉素过敏患者进行了第二次临床试验,该化合物Ro 6-0787是一种针对青霉素过敏反应的特异性单价青霉酰半抗原抑制剂。在大多数病例中,ro6 -0787-青霉素联合治疗的效果被认为是临床成功的,因为46例(91%)中有42例可以继续或恢复青霉素治疗而无过敏表现。单独使用ro6 -0787对中断青霉素治疗后急性过敏表现的影响更难评估,但26例患者中有17例(65%)被认为是满意的。在许多接受ro6 -0787-青霉素联合治疗的过敏患者中,对PPL和/或青霉素和青霉素衍生物的皮肤过敏反应的抑制有时持续数周或数月。在一些患者中,被动血凝检测的抗青霉素抗体滴度也表现出抑制作用。11例报告过敏表现抑制失败,其中部分可能是由于抑制半抗原剂量不足所致。过敏患者对Ro 6-0787的总体耐受性非常好。然而,目前广泛使用Ro 6-0787的主要障碍似乎是在大约5%的青霉素过敏患者中对该化合物出现阳性皮肤反应。目前尚不清楚对Ro 6-0787的偶发阳性皮肤反应和荨麻疹是否可能是由于该化合物的聚集或不完全溶解,或者是否反映了对另一种抗原决定因素的过敏。保留的是,皮肤试验对ro6 -0787呈阳性的患者暂时被排除在联合治疗之外,这种单价半抗原当然为明显对青霉素过敏的患者恢复和/或继续进行青霉素治疗提供了新的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical trial of Ro 6-0787, a monovalent specific hapten inhibitor of penicillin allergy.

A second clinical trial of the compound Ro 6-0787, which is a specific monovalent penicilloyl hapten inhibitor of allergic reactions to penicillin has been conducted by investigators from 9 different European groups in 90 patients allergic to penicillin. The effect of a combined Ro 6-0787-penicillin therapy was considered as clinically successful in the large majority of cases, since treatment with penicillin could be pursued or resumed without allergic manifestation in 42 from 46 cases (91 percent). The effect of Ro 6-0787 alone on acute allergic manifestations after interruption of penicillin therapy was more difficult to evaluate but was nevertheless considered satisfactory in 17 from 26 patients (65 percent). A depression of skin hypersensitivity to PPL and/or penicillin and penicillin derivatives sometimes persisting for weeks and months was obvious in numerous allergic patients submitted to combined Ro 6-0787-penicillin treatment. A depressing effect on antipenicillin antibody titers detected by passive hemaglutination was also manifest in some patients. Failure to suppress allergic manifestations was reported in 11 cases, among which some may have been due to insufficient dosage of inhibiting hapten. The overall tolerance of Ro 6-0787 in allergic patients has been very good. Nevertheless, the major obstacle to a wider general use of Ro 6-0787 at the present time appears to be the occurrence of positive skin reactions to that compound in approximately 5 percent of patients allergic to penicillin. It is not yet ascertained whether the occasional positive skin reactions and urticaria to Ro 6-0787 may have been due to aggregation, or incomplete dissolution of the compound or whether it reflects hypersensitivity to another antigenic determinant. With the reservation that patients with positive skin test to Ro 6-0787 have for the time being to be excluded from combined treatment, this monovalent hapten certainly offers a new possibility to resume and/or pursue penicillin therapy in patients demonstrably allergic to that drug.

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