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THE CELLULAR AND MOLECULAR ELEMENTS OF THE INTEGRATED IMMUNE RESPONSE
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Vaccination depends on the integrated specific immune response
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Table 36-2. Effector functions of antibodies.
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Effector functions of antibodies
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TypeFunctionsConcentration in peripheral blood
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IgGneutralisation5.0-16.0 g/L
Body_ID: T036002.150
 opsonization for neutrophils and macrophages 
Body_ID: T036002.200
 passive immunity for foetus via transplacental passage 
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 complement activation via classical pathway 
Body_ID: T036002.300
 antibody - dependent, cell - mediated cytotoxicity 
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 natural killer - cell killing of antibody bound cells 
Body_ID: T036002.400
 achieved by FcRs (receptors for the Fc portion) 
Body_ID: T036002.450
 major isotype used in a secondary antibody response 
Body_ID: T036002.500
IgAdefence of mucosal surfaces as the most0.5-4.0 g/L
Body_ID: T036002.550
 predominant immunoglobulin produced by MALT, 
Body_ID: T036002.600
 neutralisation 
Body_ID: T036002.650
IgMneutralisation0.5-2.0 g/L
Body_ID: T036002.700
 most effective classical complement pathway activator, 
Body_ID: T036002.750
 predominant isotype in primary antibody responses 
Body_ID: T036002.800
IgDpossible role in signal transduction and B cell maturation,0.03 g/L
Body_ID: T036002.850
 significance of circulating IgD is undefined 
Body_ID: T036002.900
IgEmajor role is defence of mucosal surfaces against multicellular microorganisms<120 kU/L
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Figure 36.10 Summary of the specific immune response. Interrelationships between cellular and humoral components of the specific immune response. APC, antigen presenting cell; Th, T-helper cell; Tc, cytotoxic T cell; MHC, major histocompatibility complex; TCR, T-cell receptor.
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Probably the single most beneficial application of the basic function of the immune response, as we have now described it, has been the vaccination. The process of vaccination illustrates well the interactions of the humoral and cellular arms of the specific immune response and the features that characterize it best - specificity and memory. On first encounter with antigen, the immune system and antigen interact to select lymphocytes with the receptors specific for that antigen. These undergo activation, proliferation and differentiation into effector memory cells, a process that may take up to 14 days to complete (Fig. 36.10). However, the process of memory cell generation, now leaves a body of cells semi-primed for that specific antigen. On subsequent exposure, the response is more rapid in view of the partly activated state of the memory cells, and more effective as a consequence of a degree of maturation of the response, due to the differentiation of the lymphocytes that has already taken place.
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With reference to antibody responses, the primary challenge elicits a predominantly IgM response. On subsequent challenge, the lymphocytes undergo further maturation and differentiation and isotype switching more rapidly to produce a predominantly IgG response. This provides additional effector functions to that obtained with just IgM. It is this heightened and more specific response that can reduce both the severity and the duration of any damage sustained by the offending antigen; this may be critical to the survival of the organism.
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