Harvell C D
Section of Ecology and Systematics, Cornell University, Ithaca, N.Y. 14853.
Parasitology. 1990;100 Suppl:S53-61. doi: 10.1017/s0031182000073017.
Defences against parasites are characterized by inducible, amplifiable responses, often with a memory component. Inducible defences with similar properties are common in a variety of other types of interactions, for example many aquatic invertebrates produce inducible structural defences against their predators and competitors. Most inducible defences have the following properties: (1) a threshold of activation; (2) an amplification of response with increasing stimulus; (3) a memory component. Specificity, amplification and memory are the basis for defining a defence as 'immune' (Klein, 1982), and these properties are present in both the vertebrate and invertebrate internal defence responses to pathogens. Invertebrates differ in the absence of immunoglobulins and therefore in reduced specificity. Although the reduced specificity of invertebrate internal defence systems is often viewed as proof of their 'primitiveness', the differences in defence systems of vertebrates and invertebrates may be more related to their respective selection regimes than to phylogeny. The syngeneic recognition system of vertebrates functions to recognize small departures from self, such as would arise from neoplasia. Are vertebrates under more intense selection from neoplasia, perhaps due to a greater incidence of hormonal imbalance or hypersensitivity reactions? The invertebrate internal defence systems are all less discriminating than the vertebrate, but there are marked differences in degree of discrimination depending on whether the group is colonial or not. Even the phyla of colonial animals with quite simple body plans, the sponges and cnidarians, have a more discriminating recognition system than the phyla of solitary animals with more complex body plans, such as the molluscs and arthropods. The primary effectors of all invertebrate responses to parasites are encapsulation and phagocytosis, although in some phyla there are specific antibacterial proteins than can also be induced.(ABSTRACT TRUNCATED AT 250 WORDS)
对寄生虫的防御具有可诱导、可放大的反应特点,通常还带有记忆成分。具有类似特性的可诱导防御在多种其他类型的相互作用中很常见,例如许多水生无脊椎动物会针对其捕食者和竞争者产生可诱导的结构防御。大多数可诱导防御具有以下特性:(1)激活阈值;(2)随着刺激增加反应放大;(3)记忆成分。特异性、放大和记忆是将一种防御定义为“免疫”的基础(克莱因,1982年),这些特性在脊椎动物和无脊椎动物对病原体的内部防御反应中都存在。无脊椎动物缺乏免疫球蛋白,因此特异性较低。尽管无脊椎动物内部防御系统特异性较低常被视为其“原始性”的证据,但脊椎动物和无脊椎动物防御系统的差异可能更多地与其各自的选择机制有关,而非系统发育。脊椎动物的同基因识别系统功能是识别与自身的微小差异,例如肿瘤形成时出现的差异。脊椎动物是否因激素失衡或过敏反应发生率更高而受到来自肿瘤的更强烈选择?无脊椎动物的内部防御系统都比脊椎动物的辨别力差,但根据群体是否为群居,辨别程度存在显著差异。即使是身体结构相当简单的群居动物门类,海绵动物和刺胞动物,其识别系统也比身体结构更复杂的独居动物门类,如软体动物和节肢动物,更具辨别力。所有无脊椎动物对寄生虫反应的主要效应器是包囊化和吞噬作用,尽管在某些门类中也有可诱导的特定抗菌蛋白。(摘要截断于250字)