人类最佳粘膜免疫应答的免疫途径和抗原递送系统。

Behring Institute Mitteilungen Pub Date : 1997-02-01
J Mestecky, S M Michalek, Z Moldoveanu, M W Russell
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引用次数: 0

摘要

在人类和动物身上进行的大量实验表明,刺激粘膜淋巴诱导部位(如肠Peyer's补丁)可导致平行免疫反应,其表现为远端腺体外分泌物中出现S-IgA抗体。然而,最近的实验表明,与上呼吸道、直肠和生殖道相关的诱导部位也可能作为淋巴样细胞的来源,以一定的选择性填充某些远端粘膜效应部位。此外,抗原特异性IgA抗体不仅可以通过在相应的粘膜组织(如阴道和直肠)附近的免疫,而且可以通过口服,特别是鼻内免疫在某些分泌物(如女性生殖道)中诱导产生。简单地将可溶性抗原递送到粘膜进行免疫是无效的,这刺激了对有效递送系统策略的广泛研究,这些策略将(a)增加抗原吸收,(b)防止其降解,以及(c)使免疫结果向预期目标倾斜(对传染病的保护性反应vs.耐受性;B细胞与T细胞反应;粘膜vs.全身)。通过使用合适的抗原递送系统,包括相关的细菌或病毒载体,表达微生物抗原的可食用转基因植物,将抗原掺入可生物降解的微球或脂质体中,以及将抗原与霍乱毒素B亚基联用或共同给药,可以在期望的粘膜部位诱导免疫反应。然而,只有少数广泛用于动物实验的抗原传递系统对其在人类中的有效性进行了评估。多种免疫途径的结合和使用合适的抗原递送系统可以完成一项重要的任务-在与给定病原体进入部位相关的部位诱导粘膜免疫反应。
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Routes of immunization and antigen delivery systems for optimal mucosal immune responses in humans.

Numerous experiments performed in humans and animals have revealed that stimulation of mucosal lymphoid inductive sites such as intestinal Peyer's patches results in parallel immune responses manifested by the appearance of S-IgA antibodies in the external secretions of remote glands. However, recent experiments suggest that inductive sites associated with the upper respiratory tract, rectum, and perhaps genital tract may also function as sources of lymphoid cells that populate, with some selectivity, certain remote mucosal effector sites. Furthermore, antigen-specific IgA antibodies can be induced in certain secretions (e.g., female genital tract) not only by immunization in the vicinity of corresponding mucosal tissues (e.g., vagina and rectum) but also by oral and especially intranasal immunization. The ineffectiveness of simple delivery of soluble antigens to mucosal membranes for immunization has stimulated extensive studies of strategies for effective delivery systems that would (a) increase the antigen absorption, (b) prevent its degradation, and (c) skew the outcome of immunization to a desired goal (protective response to infectious diseases vs. tolerance; B vs. T cell responses; mucosal vs. systemic). The induction of immune responses at a desired mucosal site can be accentuated with the use of a suitable antigen-delivery system including relevant bacterial or viral vectors, edible transgenic plants expressing microbial antigens, incorporation of antigens in biodegradable microspheres or liposomes, and linkage or coadministration of antigens with cholera toxin B subunit. However, only a few antigen-delivery systems extensively used in animal experimentation have been evaluated for their efficacy in humans. The combination of various immunization routes and the use of suitable antigen-delivery systems may accomplish an important task-the induction of mucosal immune responses at a location relevant to the site of entry of a given pathogen.

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