Læknablaðið : fylgirit - 01.10.1980, Blaðsíða 23

Læknablaðið : fylgirit - 01.10.1980, Blaðsíða 23
17 identical to different types of pathogene- tic mechanism. The specifically altered reactivity depends either on antigen inter- action with specific extracellular immuno- globulin, which is present in the blood or other body fluids, or it depends upon anti- gen interaction with specifically reacting T-effector lymphocytes with consequent re- lease of lymphokines, biologically active substances that can cause inflammatory changes and tissue damage. Table I. Immunological tissue damage. Illustration of etiology and pathogenesis. 1. Identification of antigen self not self cell component microbial cell product other macromolecular not-self hapten 2. Identification of antibody and/or specifically reactive T-effector lymphocytes Specific ensured Ig class type of lymphocyte 3. Location of antigen on external/internal surface cell membrane bound in circulation in AgAb complexes in tissue target 4. Location of antibody on mast cell membrane on macrophage/monocyte in circulation in complexes in tissue target 5. Location of specifically reactive T-effector lymphocytes in circulation in tissue target in lymphoid organs All these points and questions should be enlightened as far as possible. The immunological specificity must always be ensuded. To illustrate, classify and pathogeneti- cally describe a disease process associated with inflammation, it is therefore necessary to find the answers to a series of questions, represented in table I. Firstly, are immuno- logical factors involved at all in the in- flammatory reaction? Can an association be demonstrated between the inflamma- tory reaction and an anti'gen and/or a specific antibody or specifically reactive lymphocytes? In a elinical disease process: Can a similar association be found in other cases of the same disorder? Investigations should endeavour to detect antigen in the surroundings to trace the route by which the antigen has penetrated the body sur- face into the tissues, to trace where anti- gen is located in relation to the inflamma- tory process. The antigen could be of pro- tein or of polysaccaride nature, or perhaps cojugated to a large molecule. The chemi- cal nature of the antigen/hapten should be defined as far as possible. The antigen may also be totally or in part a component be- longing to the organism itself, an autoanti- gen, either belonging to tissue structures and cell structures or be a non structural self product. If the antigen has been de- fined along these line as far as possible, the antibody or the specifically reactive lymphocytes should be traced with equal thoroughness: Class and subclass of immu- noglobulin, class and subclass of lympho- cytes and location and concentration of these immunologically active products in TYPE I 4 4 * MEDIATOREFFECT Figure 1.

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