活生物治疗产品在过敏性疾病中的潜力:当前发现与未来方向

Isabel Tarrant, B. B. Finlay
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摘要

随着全球过敏性疾病发病率以惊人的速度持续上升,对有效、安全的治疗方法的需求已成为当务之急。鉴于生命早期微生物群对免疫发育的关键作用,新的研究表明,活生物治疗产品(LBP)可用于预防和治疗儿童过敏症。然而,研究结果有限且不一致。因此,本综述对枸杞多糖在过敏症中的治疗价值、枸杞多糖可能介导过敏易感性的潜在免疫学机制、当前研究需要解决的局限性以及未来的研究方向等方面的现有动物和人类数据进行了批判性评估。据此,枸杞多糖可通过生命早期的几种免疫和生理机制预防过敏性疾病,包括调节 Th1/Th2 平衡、SCFA 诱导的 GPR41/43 激活和 HDAC 抑制以及上皮屏障完整性的成熟。综上所述,目前的研究结果表明枸杞多糖对过敏性免疫反应具有强大的免疫调节作用,枸杞多糖有望成为治疗儿童过敏症的新型治疗工具。然而,枸杞多糖对过敏症的疗效非常复杂,受到许多人群和方法因素的影响,导致治疗效果各不相同。虽然迄今为止的研究主要集中在传统的益生菌菌株上,但对从非过敏性婴儿微生物群中挑选出来的微生物联合体进行更深入的研究,可能更有希望成为治疗过敏性疾病的工具。在将研究结果转化为临床应用以治疗儿童过敏性疾病之前,有必要开展进一步的研究,尤其是对长期疗效、菌株特异性效应、最佳补充方案以及多菌株联合体的使用等方面的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The potential of live biotherapeutic products in allergic disease: current findings and future directions
With the global prevalence of allergic disease continuing to rise at an alarming rate, the need for effective and safe therapeutics is paramount. Given the critical role of the early-life microbiota on immune development, emerging research suggests the potential use of live biotherapeutic products (LBP) for the prevention and treatment of childhood allergy. However, findings are limited and inconsistent. Therefore, the present review critically evaluates the current animal and human data on the therapeutic value of LBPs in allergy, the underlying immunological mechanisms by which LBPs may mediate allergy susceptibility, limitations of the current research that need to be addressed, and future research directions. Accordingly, LBPs may protect against allergic disease through several immunological and physiological mechanisms during early-life, including regulation of Th1/Th2 balance, SCFA-induced activation of GPR41/43 and HDAC inhibition, and maturation of epithelial barrier integrity. Taken together, current findings indicate powerful immunomodulatory properties of LBPs on allergic immune response, with LBPs offering exciting potential as a novel therapeutic tool for childhood allergy. However, the efficacy of LBPs in allergy is complex and influenced by many population and methodological factors, resulting in varied therapeutic benefits. While research thus far has focused on traditional probiotic strains, greater investigation into microbial consortiums selected from the microbiota of non-allergic infants may provide greater promise as a therapeutic tool for allergic disease. Further investigation, particularly into long-term efficacy, strain-specific effects, optimal supplementation regimes, and use of multi-strain consortiums, is necessary before findings can be translated into clinical applications to tackle childhood allergic disease.
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