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Functions of Lymphatic System |
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Immunity Lipid absorption Fluid recovery (absorbs plasma proteins and fluid (2 to 4 L/day) from tissues and returns it to the bloodstream) |
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clear, colorless fluid, similar to plasma but much less protein |
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tethered to surrounding tissue by protein filaments endothelial cells loosely overlapped closed at one end creates valve-like flaps that open when interstitial fluid pressure is high, and close when it is low |
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course through many lymph nodes |
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drain major portions of body |
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receives lymph from R arm, R side of head and thorax; empties into R subclavian vein |
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larger and longer, begins as a prominent sac in abdomen called the cisterna chyli; receives lymph from below diaphragm, L arm, L side of head, neck and thorax; empties into L subclavian vein |
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Moved along by rhythmic contractions of lymphatic vessels flows at low pressure and speed aided by skeletal muscle pump Valves prevent backward flow flowing blood in subclavian veins, draws lymph into it |
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mature in thymus cell to cell interactions destroy pathogens throughout the body |
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activation causes proliferation and differentiation into plasma cells that produce antibodies |
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Natural killer (NK) cells |
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responsible for immune surveillance by destruction of foreign cells |
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macrophages (from monocytes) dendritic cells (in epidermis, mucous membranes and lymphatic organs) reticular cells (also contribute to stroma of lymph organs) |
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lymphocytes in mucous membranes and connective tissue (CT) of many organs Mucosa-Associated Lymphatic Tissue |
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Mucosa-Associated Lymphatic Tissue |
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MALT): prevalent in passages open to exterior |
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dense oval masses of lymphocytes, congregate in response to pathogens Peyer patches |
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more permanent congregation, clusters found at junction of small to large intestine |
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site where T and B cells become immunocompetent red bone marrow and thymus |
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site where T and B cells become immunocompetent red bone marrow and thymus |
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Secondary lymphatic organs |
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immunocompetent cells populate these tissues lymph nodes, tonsils, and spleen |
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- only organs that filter lymph the capsule arises trabeculae, which divides node into compartments containing stroma (reticular ) and parenchyma (lymphocytes and Antigen Presenting Cells) subdivided into cortex (lymphatic nodules) and medulla |
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swollen, painful node responding to foreign antigen |
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Reticular epithelial cells form blood thymus barrier in cortex isolates developing T lymphocytes from foreign antigens secretes hormones (thymopoietin, thymulin and thymosins) to promote development and action of T lymphocytes large in fetus |
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red pulp/white pulp functions: blood production in fetus blood reservoir RBC disposal immune reactions: filters blood, quick to detect antigens |
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sinuses filled with erythrocytes spleen |
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lymphocytes, macrophages; surrounds small branches of splenic artery spleen |
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Nonspecific defenses which are broadly effective, no prior exposure necessary
first line of defense external barriers
second line of defense phagocytic cells, antimicrobial proteins, inflammation and fever |
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Specific defenses which result from prior exposure, protects against only a particular pathogen third line of defense “the immune system” |
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First line of defense:skin |
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toughness of keratin dry and nutrient-poor defensins: peptides, from neutrophils attack microbes lactic acid (acid mantle) is a component of perspiration |
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First line of defense: mucous membranes |
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stickiness of mucus lysozyme: enzyme destroys bacterial cell walls |
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First line of defense: Subepithelial areolar tissue |
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tissue gel: viscous barrier of hyaluronic acid hyaluronidase: enzyme used by pathogens to spread |
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Phagocytize and kill bacteria degranulation lysosomes discharge into tissue fluid respiratory burst toxic chemicals are created (O2.-, H2O2, HClO) |
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Phagocytize antigen-antibody complexes Antiparasitic effects (tapeworms, roundworms) Promote action of basophils, mast cells Enzymes block excess inflammation, limit action of histamine (allergic responses) |
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Aid mobility and action of WBC’s by secretion of two chemicals histamine+heparin |
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(vasodilator) increases blood flow to infected tissue which delivers leukocytes to the area EOSINOPHILS |
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(anticoagulant) prevents immobilization of phagocytes |
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Natural Killer (NK) Cells |
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Large Granular Lymphocytes (LGL’s) not lymphocytes though Release Perforins which form a hole in target cell and release cytotoxic granules called Granzymes into the cell and kills it |
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Secreted by certain cells invaded by viruses diffuse to neighboring cells and stimulate them to produce antiviral proteins activate natural killer cells, T cells and macrophages |
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enhanced inflammation phagocytosis promoted by opsonization cytolysis membrane attack complex forms on target cell immune clearance RBCs carry Ag-Ab complexes to macrophages in liver and spleen |
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classical pathway (complment system) |
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requires antibody; specific immunity |
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alternate pathway (complement system) |
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lectin pathway (complement system) |
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Complement proteins form ring in plasma membrane of target cell causing cytolysis |
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DNA is degraded and packaged and cell dies also known as “programmed cell death” or “cellular suicide” |
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limits spread of pathogens, then destroys them removes debris initiates tissue repair |
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small proteins regulate inflammation and immunity; include interferons, interleukins, tumor necrosis factor, and chemotactic factors |
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redness (erythema) caused by hyperemia ( blood flow) swelling (edema) caused by capillary permeability and filtration heat caused by hyperemia pain caused by inflammatory chemicals (bradykinin, prostaglandins) secreted by damaged cells, pressure on nerves |
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margination (leukocyte deployment) |
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selectins cause leukocytes to adhere to blood vessel walls |
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diapedesis (emigration) (leukocyte deployment) |
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leukocytes squeeze between endothelial cells into tissue space |
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promotes interferon activity accelerating metabolic rate and tissue repair inhibiting pathogen reproduction 105F may cause delirium, 111F- 115F, coma-death |
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cytokine pyrogen secreted by macrophages, stimulates anterior hypothalamus to secrete PGE which resets body thermostat higher |
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Specificity Memory Cellular immunity Humoral defense |
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(cell-mediated) via T-Cells. Attack fungi, parasites, viruses, cancer cells and foreign tissue. |
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(antibody-mediated) with B-cells. B-cells become plasma cells, leave the nodes and produce antibodies (Ig’s). Attack bacteria and viruses. |
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(produces memory cells) production of one’s own antibodies or T cells as a result of infection or natural exposure to antigen |
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Artificial active immunity |
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(produces memory cells) production of one’s own antibodies or T cells as a result of a vaccination |
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(through placenta, milk) temporary, fetus acquires antibodies from mother |
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Artificial passive immunity |
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(snakebite, rabies, tetanus) temporary, injection of immune serum (antibodies) |
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Trigger an immune response proteins, polysaccharides, glycoproteins, glycolipids Epitopes |
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(antigenic determinants) stimulate immune responses |
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too small, host macromolecule must bind to them to stimulate initial immune response |
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depends on activities of two general classes of lymphocytes B-Cells T-Cells |
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Arise from stem cells in red bone marrow Mature in thymus naïve T cells colonize lymphatic tissue and organs |
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stimulate maturing T cells to produce antigen receptors |
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T-Cell Maturation in Thymus |
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thymic hormone secreted by reticular epithelial (RE) cells stimulate them to develop surface antigen receptors.
“tested” to see if they recognize self antigens and MHC antigens |
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T-cells that recognize either self or MHC antigens are eliminated
clonal deletion (destruction) or anergy (they remain alive but are non responsive). |
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T-cells that have “passed” (only 2% graduate!) the test now move to the thymic medulla
and form clones of T-cells with varying antigenic specificity. |
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development (Bone marrow) other fetal stem cells remain in bone marrow B cells should not react to self antigens or suffer clonal deletion or anergy |
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Antigen-Presenting Cells (APCs) |
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B cells, macrophages, reticular cells and dendritic cells (special type of macrophage) function as APC’s and display antigens which are combined with MHC proteins on their surface to T cells
When an APC encounters an antigen, it internalizes it by endocytosis, digests it into molecular fragments and displays the relevant fragments (epitopes) in the grooves of the MHC proteins. This is called ‘Antigen Processing” |
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major histocompatability complex |
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proteins which are expressed on antigen presenting cells (APC’s
MHC proteins are structurally unique to every person and act as cell “ID” tags |
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Chemical messengers between leukocytes Used by lymphocytes and APCs to communicate |
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T cells attack diseased host tissues or cells invaded by microbes and can “remember” these antigens and prevent from future attack. |
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(TC cells) carry out attack |
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(TH cells): help promote TC cell and B cell action and nonspecific defense mechanisms |
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provide immunity from future exposure to antigen |
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MHC-I proteins found on nearly all nucleated body cells display peptides produced by host cells |
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binding of cytotoxic T cells (CD8 cells) to abnormal peptides on MHC-I and costimulation via a cytokine triggers clonal selection: clone of identical T cells against cells with same epitope |
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role of MHC-II proteins found only on antigen presenting cells display only foreign antigens stimulate helper T cells (CD4 cells) |
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Attack Phase: Role of Helper T Cells |
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Secretes interleukins attract neutrophils, NK cells, macrophages stimulate phagocytosis stimulate T and B cell mitosis and maturation |
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Attack Phase: Cytotoxic T Cells |
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Only T cells directly attack enemy cells docks on cell with antigen-MHC-I protein complex releases perforin, granzymes - kills target cell interferons - decrease viral replication and activates macrophages tumor necrosis factor: kills cancer cells |
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Humoral Immunity(B-Cells) |
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B cell receptors bind antigen, take in and digest antigen then display epitopes on its MHC-II protein After costimulation by TH cell, divide repeatedly, differentiate into plasma cells, produce antibodies specific to that antigen ‘tag it’ for destruction some B cells differentiate into memory cells |
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DNA segments shuffled and form new combinations of base sequences to produce antibody genes |
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B cells in lymph nodules rapidly mutate creating new sequences |
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: monomer in plasma; dimer in mucus, saliva, tears, milk, intestinal secretions, prevents adherence to epithelia |
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monomer; B cell membrane antigen receptor |
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monomer; on mast cells; stimulates release of histamines, attracts eosinophils; immediate hypersensitivity reactions |
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monomer; 80% circulating, crosses placenta to fetus, 2 immune response, complement fixation |
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: pentamer, 10% in plasma, 1 immune response, agglutination, complement fixation |
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Neutralization (humural immunity) |
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antibodies mask pathogenic region of antigen |
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Complement fixation (humural immunity) |
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antigen binds to IgM or IgG, antibody changes shape, initiates complement binding; primary defense against foreign cells, bacteria |
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antibody has 2-10 binding sites; binds to multiple enemy cells immobilizing them |
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Precipitation (humoral immunity) |
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antibody binds antigen molecules (not cells); creates antigen-antibody complex that precipitates, phagocytized by eosinophil |
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Type I (acute reaction) hypdersensitivity |
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Antibody mediated (IgE), (food allergies, asthma, anaphylaxis) |
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Type II (antibody-dependent cytotoxic)hypersensitivity |
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Antibody mediated (IgG, IgM), subacute (blood transfusion reactions, some drug reactions) binds to antigens on cells; complement activation and lyses or opsonization may bind to cell surface receptors and either interferes with function or over-stimulate cell |
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Type III (immune complex) hypersensitivity |
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Antibody mediated (IgG, IgM), subacute (autoimmune acute glomerulonephritis and lupus
IgG or IgM form widespread antigen-antibody complexes Complexes precipitate and trigger intense inflammation involved in acute glomerulonephritis and in systemic lupus erythematosus |
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Type IV (delayed) cell mediated, delayed (12 to 72 hr), hypersensitivity |
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), (allergies to haptens in cosmetics, poision ivy, graft rejection, tuberculosis skin test, insulin-dependent diabetes)
APC’s in lymph nodes display antigens to helper T cells, which secrete interferon and cytokines that activate cytotoxic T cells and macrophages Cosmetic and poison ivy allergies - haptens TB skin test |
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occurs in sensitized people allergen caps IgE on mast cells, basophils release inflammatory chemicals |
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most common chronic illness in children inhaled allergens, histamines, bronchiole constriction |
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bronchiole constriction, dyspnea, vasodilation, shock, death; treatment- epinephrine |
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invades helper T cells, macrophages and dendritic cells by “tricking” them to internalize viruses by receptor mediated endocytosis
reverse transcriptase (retrovirus), uses viral RNA as template to synthesize DNA, new DNA inserted into host cell DNA, may be dormant for months to years |
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