Gaspard I, Guinnepain M T, Laurent J, Bachot N, Kerdine S, Bertoglio J, Pallardy M, Lebrec H
INSERM U461, Faculté de Pharmacie, Châtenay-Malabry, France.
J Clin Immunol. 2000 Mar;20(2):107-16. doi: 10.1023/a:1006682413834.
Beta-lactam antibiotics elicit CD4+ and CD8+ T-cell-mediated immune responses that play a central role in allergic reactions. However, the involvement of a type 1- (Th1 or Tc1) or a type 2-like (Th2 or Tc2) differentiation in drug allergy remains unclear. We investigated the expression of interleukin 4 (IL-4) and interferon gamma (IFN-gamma) mRNA by quantitative reverse transcription and polymerase chain reaction (RT-PCR) in patient-derived peripheral blood lymphocytes following specific in vitro stimulation. Samples were collected from a total of 19 patients who had developed immediate or delayed clinical manifestations of hypersensitivity to beta-lactam and from 11 control subjects. Peripheral blood mononuclear cells (PBMCs) were stimulated with either free antibiotics or antibiotic-human serum albumin (HSA) conjugates. Specific induction of IFN-gamma mRNA expression was observed in 11 of 11 allergic patients with immediate reactions, in 6 of 8 patients with delayed reactions, and in 4 of 11 control subjects. IL-4 mRNA expression was induced in 5 of 11 allergic individuals with immediate reactions but in none of the 8 patients with delayed responses and none of the 11 control subjects. IL-4 mRNA expression was only induced following activation with free drugs, while IFN-gamma mRNA expression was predominantly induced in CD4+ T cells following stimulation with HSA-conjugated drugs. Immediate-type hypersensitivity to beta-lactams was not associated with a pure type 2-like response when PBMCs were specifically stimulated in vitro: Some patients with well-documented history of beta-lactam-induced immediate allergic reaction showed a high IFN-gamma response. Contact dermatitis involved Tc1 and Th1 cells and other delayed hypersensitivity reactions to beta-lactams were restricted to Th1 responses.
β-内酰胺类抗生素引发CD4+和CD8+ T细胞介导的免疫反应,这些反应在过敏反应中起核心作用。然而,1型(Th1或Tc1)或2型样(Th2或Tc2)分化在药物过敏中的参与情况仍不清楚。我们通过定量逆转录聚合酶链反应(RT-PCR)研究了患者来源的外周血淋巴细胞在特定体外刺激后白细胞介素4(IL-4)和干扰素γ(IFN-γ)mRNA的表达。样本共采集自19名对β-内酰胺类药物出现速发型或迟发型过敏临床表现的患者以及11名对照受试者。外周血单个核细胞(PBMCs)用游离抗生素或抗生素-人血清白蛋白(HSA)偶联物进行刺激。在11名有速发型反应的过敏患者中的11名、8名有迟发型反应的患者中的6名以及11名对照受试者中的4名中观察到IFN-γ mRNA表达的特异性诱导。11名有速发型反应的过敏个体中有5名诱导出IL-4 mRNA表达,但8名有迟发型反应的患者和11名对照受试者中均未诱导出。IL-4 mRNA表达仅在用游离药物激活后诱导,而IFN-γ mRNA表达在用HSA偶联药物刺激后主要在CD4+ T细胞中诱导。当PBMCs在体外被特异性刺激时,对β-内酰胺类药物的速发型过敏与单纯的2型样反应无关:一些有充分记录的β-内酰胺类药物诱导的速发型过敏反应病史的患者表现出高IFN-γ反应。接触性皮炎涉及Tc1和Th1细胞,对β-内酰胺类药物的其他迟发型过敏反应仅限于Th1反应。