Gafvelin Guro, Thunberg Sarah, Kronqvist Marianne, Grönlund Hans, Grönneberg Reidar, Troye-Blomberg Marita, Akdis Mübeccel, Fiebig Helmut, Purohit Ashok, Horak Friedrich, Reisinger Jürgen, Niederberger Verena, Akdis Cezmi A, Cromwell Oliver, Pauli Gabrielle, Valenta Rudolf, van Hage Marianne
Clinical Immunology and Allergy Unit, Department of Medicine, Karolinska Institute and University Hospital, SE-171 76 Stockholm, Sweden.
Int Arch Allergy Immunol. 2005 Sep;138(1):59-66. doi: 10.1159/000087358. Epub 2005 Aug 11.
Recently, recombinant hypoallergenic derivatives of the major birch pollen allergen, Bet v 1, were used to treat birch-pollen-allergic patients in a double-blind, placebo-controlled, multi-centre immunotherapy study. The aim of this study was to evaluate the effects of vaccination with aluminium-hydroxide-adsorbed recombinant Bet v 1 derivatives versus placebo on T-cell, cytokine and antibody responses in a subgroup of patients.
Blood was drawn from patients of the Swedish centre (n = 27; rBet v 1 fragments: n = 10; rBet v 1 trimer: n = 8, and placebo-aluminium hydroxide: n = 9) before the start and after completion of the treatment. PBMC were stimulated with rBet v 1 and analysed for cytokine (IL-4, IL-5, IL-10, IL-12, IL-13 and IFN-gamma)-secreting cells by ELISpot. Bet v 1-specific antibody levels in serum (IgG(1-4), IgE and IgA) were measured by ELISA. Skin prick tests with defined Bet v 1 concentrations were performed before and 10-11 months after the beginning of the study.
Bet v 1-specific IgG levels, consisting of IgG(1), IgG(2) and IgG(4), were significantly increased after treatment with recombinant allergen derivatives. Treatment with rBet v 1 trimer led to a significant (p < 0.05) reduction of Bet v 1-reactive IL-5- and IL-13-producing cells, reflecting a reduced Th2 response. In addition, a decreased number of Bet v 1-reactive IL-4 producing (p = 0.07) and an increase of IL-12-producing (p = 0.06) cells was noted in the trimer-treated patients. In contrast to placebo, active treatment resulted in significantly reduced immediate-type skin reactions to Bet v 1 even 10-11 months after treatment.
Vaccination with recombinant hypoallergenic Bet v 1 derivatives induces a Bet v 1-specific IgG response and leads to reduced skin reactivity in allergic patients. A reduction of Bet v 1-specific Th2 responses was observed in trimer-treated patients, which may reflect the intrinsic property of this allergen derivative.
最近,主要桦树花粉过敏原Bet v 1的重组低变应原衍生物,在一项双盲、安慰剂对照、多中心免疫治疗研究中用于治疗桦树花粉过敏患者。本研究的目的是评估在一组患者中,接种氢氧化铝吸附的重组Bet v 1衍生物与接种安慰剂相比,对T细胞、细胞因子和抗体反应的影响。
在治疗开始前和结束后,从瑞典中心的患者(n = 27;rBet v 1片段组:n = 10;rBet v 1三聚体组:n = 8,以及安慰剂-氢氧化铝组:n = 9)采集血液样本。用rBet v 1刺激外周血单核细胞(PBMC),并通过酶联免疫斑点法(ELISpot)分析分泌细胞因子(IL-4、IL-5、IL-10、IL-12、IL-13和IFN-γ)的细胞。通过酶联免疫吸附测定法(ELISA)测量血清中Bet v 1特异性抗体水平(IgG(1 - 4)、IgE和IgA)。在研究开始前和开始后10 - 11个月,用规定浓度的Bet v 1进行皮肤点刺试验。
用重组变应原衍生物治疗后,由IgG(1)、IgG(2)和IgG(4)组成的Bet v 1特异性IgG水平显著升高。用rBet v 1三聚体治疗导致Bet v 1反应性IL-5和IL-13产生细胞显著减少(p < 0.05),这反映了Th2反应降低。此外,在三聚体治疗的患者中,观察到Bet v 1反应性IL-4产生细胞数量减少(p = 0.07),而IL-12产生细胞数量增加(p = 0.06)。与安慰剂相比,积极治疗即使在治疗后10 - 11个月,也能使对Bet v 1的速发型皮肤反应显著降低。
接种重组低变应原Bet v 1衍生物可诱导Bet v 1特异性IgG反应,并降低过敏患者的皮肤反应性。在三聚体治疗的患者中观察到Bet v 1特异性Th2反应降低,这可能反映了这种变应原衍生物的内在特性。