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特异性过敏疫苗接种诱导产生的阻断性抗体,通过抑制血清IgE促进的过敏原呈递,来阻止CD4+T细胞的激活。

Blocking antibodies induced by specific allergy vaccination prevent the activation of CD4+ T cells by inhibiting serum-IgE-facilitated allergen presentation.

作者信息

van Neerven R J, Wikborg T, Lund G, Jacobsen B, Brinch-Nielsen A, Arnved J, Ipsen H

机构信息

ALK-Abelló, Horsholm, Denmark; and Lung and Allergy Clinic, Copenhagen, Denmark.

出版信息

J Immunol. 1999 Sep 1;163(5):2944-52.

Abstract

Allergen-specific CD4+ T lymphocytes are activated at extremely low allergen concentrations in vivo as a result of serum-facilitated allergen presentation (S-FAP). It is not clear at present if specific allergy vaccination (SAV) has an effect on this mechanism. Here we show that birch allergen-specific serum-IgE facilitates the presentation of Bet v 1, the major birch pollen allergen, to Bet v 1-specific CD4+ T lymphocytes by a factor of >100. This process is CD23 mediated, could be detected in sera from the majority of birch-allergic patients, and was clearly dose dependent. S-FAP of Bet v 1 was inhibited in patients undergoing long-term birch SAV, but not by sera from patients undergoing grass SAV, indicating that birch-specific Abs are involved. This resulted in decreased proliferation and IL-4, IL-5, IL-10, and IFN-gamma production of Bet v 1-specific T cells. The inhibition was already noted after 3-9 mo of SAV and could not be solely explained by increased serum levels of birch-specific IgG4. When IgG- and IgA/IgM-containing fractions of long-term SAV sera were used to inhibit S-FAP, only IgG-containing fractions were shown to inhibit S-FAP. These results indicate that blocking IgG Abs induced by SAV inhibits the occurrence of S-FAP at very low allergen concentrations, resulting in significantly higher allergen threshold levels to obtain T cell proliferation and cytokine production and thus allergen-induced late-phase responses.

摘要

由于血清促进过敏原呈递(S-FAP),过敏原特异性CD4+ T淋巴细胞在体内极低的过敏原浓度下即可被激活。目前尚不清楚特异性变应原疫苗接种(SAV)是否对该机制有影响。在此我们表明,桦树过敏原特异性血清IgE可使主要桦树花粉过敏原Bet v 1向Bet v 1特异性CD4+ T淋巴细胞的呈递增强100倍以上。这一过程由CD23介导,在大多数桦树过敏患者的血清中均可检测到,且明显呈剂量依赖性。长期接受桦树SAV治疗的患者中,Bet v 1的S-FAP受到抑制,但接受草SAV治疗患者的血清则无此作用,表明桦树特异性抗体参与其中。这导致Bet v 1特异性T细胞的增殖以及IL-4、IL-5、IL-10和IFN-γ的产生减少。在SAV治疗3 - 9个月后即已观察到这种抑制作用,且不能仅用桦树特异性IgG4血清水平升高来解释。当使用长期SAV血清中含IgG和含IgA/IgM的组分来抑制S-FAP时,只有含IgG的组分显示出抑制S-FAP的作用。这些结果表明,SAV诱导产生的阻断性IgG抗体可抑制极低过敏原浓度下S-FAP的发生,从而使获得T细胞增殖和细胞因子产生以及过敏原诱导的迟发反应所需的过敏原阈值水平显著升高。

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