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过敏的功能:针对毒素的免疫防御。

The function of allergy: immunological defense against toxins.

作者信息

Profet M

机构信息

Division of Biochemistry & Molecular Biology, University of California, Berkely 94720.

出版信息

Q Rev Biol. 1991 Mar;66(1):23-62. doi: 10.1086/417049.

DOI:10.1086/417049
PMID:2052671
Abstract

This paper proposes that the mammalian immune response known as "allergy" evolved as a last line of defense against the extensive array of toxic substances that exist in the environment in the form of secondary plant compounds and venoms. Whereas nonimmunological defenses typically can target only classes of toxins, the immune system is uniquely capable of the fine-tuning required to target selectively the specific molecular configurations of individual toxins. Toxic substances are commonly allergenic. The pharmacological chemicals released by the body's mast cells during an IgE antibody-mediated allergic response typically cause vomiting diarrhea, coughing, tearing, sneezing, or scratching, which help to expel from the body the toxic substance that triggered the response; individuals frequently develop aversions to substances that have triggered such responses. A strong allergic response often includes a decrease in blood pressure, which slows the rate at which toxins circulate to target organs. The immune system identifies as toxic the following kinds of substances: (1) those low-molecular-weight substances that bind covalently to serum proteins (e.g., many plant toxins); (2) nontoxic proteins that act as carriers of toxins with low molecular weights (e.g., plant proteins associated with plant toxins); (3) specific substances of high molecular weight that harmed individuals in ancestral mammalian populations for a span of time that was significant from the standpoint of natural selection (e.g., the toxic proteins of bee venom. Substances that bind covalently to serum proteins generally are acutely toxic, and because many of these substances also bind covalently to the DNA of target cells, they are potentially mutagenic and carcinogenic as well. Thus, by protecting against acute toxicity, allergy may also defend against mutagens and carcinogens. The toxic hypothesis explains the main phenomena of allergy; why IgE-mediated allergies usually occur within minutes of exposure to an allergen and why they are often so severe; why the manifestations of allergy include vomiting, diarrhea, coughing, sneezing, scratching, tearing, and a drop in blood pressure; why covalent binding of low-molecular-weight substances to serum proteins frequently causes allergy; why allergies occur to many foods, pollens, venoms, metals, and drugs; why allergic cross-reactivity occurs to foods and pollen from unrelated botanical families; why allergy appears to be so capricious and variable; and why allergy is more prevalent in industrial societies than it is in foraging societies. This hypothesis also has implications for the diagnosis, prevention, and treatment of allergy.

摘要

本文提出,被称为“过敏”的哺乳动物免疫反应是作为抵御环境中以次生植物化合物和毒液形式存在的大量有毒物质的最后一道防线而进化出来的。非免疫防御通常只能针对特定种类的毒素,而免疫系统却独特地具备针对个体毒素的特定分子构型进行选择性微调的能力。有毒物质通常具有致敏性。在IgE抗体介导的过敏反应过程中,机体肥大细胞释放的药理化学物质通常会引发呕吐、腹泻、咳嗽、流泪、打喷嚏或瘙痒,这有助于将引发反应的有毒物质排出体外;个体通常会对引发此类反应的物质产生厌恶。强烈的过敏反应通常还包括血压下降,这会减缓毒素循环至靶器官的速度。免疫系统将以下几类物质识别为有毒物质:(1)那些与血清蛋白共价结合的低分子量物质(例如,许多植物毒素);(2)作为低分子量毒素载体的无毒蛋白质(例如,与植物毒素相关的植物蛋白);(3)在祖先哺乳动物群体中,在从自然选择角度来看具有重要意义的一段时间内对个体造成伤害的特定高分子量物质(例如,蜂毒的有毒蛋白质)。与血清蛋白共价结合的物质通常具有急性毒性,而且由于其中许多物质还会与靶细胞的DNA共价结合,它们还可能具有致突变性和致癌性。因此,通过预防急性毒性,过敏反应也可能抵御诱变剂和致癌物。毒性假说解释了过敏的主要现象;为什么IgE介导的过敏通常在接触过敏原后几分钟内就会发生,以及为什么它们往往如此严重;为什么过敏的表现包括呕吐、腹泻、咳嗽、打喷嚏、瘙痒、流泪和血压下降;为什么低分子量物质与血清蛋白的共价结合经常会引发过敏;为什么对许多食物、花粉、毒液、金属和药物会发生过敏;为什么对来自不相关植物科的食物和花粉会出现过敏交叉反应;为什么过敏似乎如此多变无常;以及为什么过敏在工业社会比在觅食社会更为普遍。这一假说对过敏的诊断、预防和治疗也具有启示意义。

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