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necessity of adaptive immunity
- innate immune response is rapid and often effective but is not always sufficient to eliminate infection
- innate immunity has no memory
- another arm of the immune system is needed to clear more serious infections and respond to pathogens in a faster, better manner with memory
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steps of adaptive immunity
- initiated when circulating T lymphocytes recognize specific antigens on the surface of dendritic cells or other antigen presenting cells
- these T cells proliferate and differentiate into antigen specific effector cells
- T cells usually target intracellular pathogens
- B cells that recognize antigens differentiate into plasma cells and secrete anitgen-specific antibodies
- antibodies usually target extracellular microorganisms and their toxins
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Humoral immune response
- immature B cells in bone marrow, B cells mature in lymphoid tissue
- express IgM and IgD - antigens bind and activate B cells
- once activated undergo clonal expansion - differentiate into plasma cells that secrete antibodies
- some responses are T-cell independent
- usually directed at extracellular microorganisms and toxins
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antibody
a protein (immunoglobulin) produced by plasma cells (B cells) that recognize a target molecule (antigen) to be foreign
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IgG
protect against bacteria, viruses, enhance phagocytosis, neutralize toxins (crosses placental barrier)
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IgA
protects against infection on mucous membranes
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IgM
protects against early phase of infection; comprises anti-A and anti-B antibodies of ABO blood groups, can lyse microbes
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IgD
serves as receptors for activation of B cells
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IgE
invovled in allergic responses, triggers release of histamine
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primary response
- 5-10 days
- IgM>IgG
- limited affinity to antigen
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secondary response
- 1-3 days
- mostly IgG
- greater affinity for antigen
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combinatorial diversification
- variable regions are inherited as gene segments
- how an almost unlimited repertoire of antibodies get generated from a limited set of genes
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cell mediated immune response
- T lymphocytes mature in thymus, migrate to lymphoid tissues
- become activated when encountering antigen presented by antigen presenting cell
- once activated, multiply and differentiate - cytotoxic T cells and helper T cells
- once antigen cleared, most cells undergo apoptosis, others become memory cells
- usually directed at intracellular pathogens
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T cell diversity
- T helper cells (CD4):
- - Th1 cells = involved in control of intracellular pathogens, produce cytokines and chemokines to attract other T cells and marcrophages
- -Th2 cells = activates B cells into antibody producing plasma cells
- cytotoxic T cells (CD8): kill infected cells
- regulatory T cells: suppress activation of immune response, play a role in tolerating self-antigens
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antigen presentation
antigens are presented on the cellular surface in conjunction with major histocompatibility complex (MHC) molecule
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MHC class I
- present peptide fragments from proteins in the cytosol (intracellular)
- recognized by CD8 cytotoxic T cells
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MHC class II
- present peptides derived from phagosomes (extracellular)
- recognized by CD4 T helper cells
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