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– no specific recognition of identity of foreign cell/matter • Same response regarless of stimuli • Prevention first |
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- liquid mixture of intersitial fluid, solutes, sometimes foreign material that is in the lymph vessels |
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lymphatic vessels and capillaries |
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• Contain 3 layers to it and have valves • Smaller than vessels are capillaries which are blind ended*- they just end without conncection to anything • Anchoring filaments hold their endothelial cells in place |
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• Lymphocytes packed in connective tissue • No capsule • Fount in CT under epithelium of respoiratory, digestive, urinary tracts • Eg. Tonsils, Peyer’s patches • GALT or MALT- mucosa associated lymphatic tissue o Group of these- tonsiles |
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• Bi lobed • A site for T cell maturation |
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• Located along the pathways of lymph vessels • Function is to filter antigens from lymph and initiate and immune response when needed • Fibrous capsuke; partitions o Trabeculae separate sections internallu • Afferent and efferent lymphatic vessels • Macrophages • 99% antigens removed, processed • dendritic cells- found in the lymphatic nodule and internalize antigens from lyph and present to other lymphatic cells |
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• Removes RBCs- phagocytes • Stores Iron • May initiate immune responses • Largest lymph organ in the body • Red pulp- RBC, platelt, macrophages, some plasma cells • White pul- clusters of t cells, b cells, and macrophages |
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• Body fluid homeostasis- returns interstitial fluid and solutes to blood stream • Immune system |
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• Inflammation • Phagocytosis |
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• Histamine • Heparin (both for inflmmation) |
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• Defend against parasitic worms |
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• Specific immunity (all except NK cells) • B eclls- specific immunity • T cells NK cells |
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• Cytotoxic • Helper • Suppressor |
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immune surveillance • Can kill a wide variety of infected cells • Bind directly and non specifically to virus infected cells and cancer cells to kill them |
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first line of defense (list) |
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skin and mucous membranes, ciliated mucosa of respiraotry system, friendly microorganisms, macrophages |
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skin and mucous membranes as 1st line of defense |
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physical barrier • Variety of protective chemicals • Acidity of skin • Gastric HCl, proteolytic enzymes • Lysozyme of salivia • Sticky mucous |
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inflammation may be set off by |
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o May be set off by- • Physical trauma • Intense heat • Irritating chemicals • Infection by pathogens |
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o 1. Entry of bacteria into issue or injury releases chemicals o 2.vasodilation of microcirulation in infected area, increased blood flow o 3. large increase in protein permeability of capillaries- resulting in filtration of this and fluid into intetsitial fluid o 4. chemotaxis- movement of leulocytes from venules into intersitial fluid to infected area o 5. Destruction bacteria o 6. tissue repair |
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• Neutrophils enter bloodstream • Margination (“pavementing”)- leukocytes cling to capillary walls • Diapedesis- leukocytes pass thry capillary walls • Chemotaxis- movement of leukocytes from the venules into the intersitial fluid of the infected area |
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(“pavementing”)- leukocytes cling to capillary walls |
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- leukocytes pass thry capillary walls |
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movement of leukocytes from the venules into the intersitial fluid of the infected area |
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• Released by mast cells • Vasodilation, increased capillary permeability |
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• Vasodilation, capillary permeability, also t=chemotaxis, stimulate neutorphils, induce pain |
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prostaglandins (eicosanoids) |
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• Senstitize blood vessels to effects of other mediators, pain |
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chemical factors that mediate inflammation (list |
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Definition
histmaines, kinins, prostaglandins, complement, cytokines |
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secreted by injured cells, monocytes, macrophages, neutrophils, lyphocytes, and several nonimmune cell types |
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o Major mechanism for destroying foreign substances • Over 20 plasma proteins • Activated via cascade |
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2 pathways for complement activaiton |
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Definition
• Classical- antigen antibody complex initiates “complement fixation” • Alternative- polysaccharides on cell surfaces of certain fungi and bacteria |
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once complement is actiavted |
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Definition
• Amplify all aspects of inflammation • Directly lyse target cells via “membrane attack complex” • Opsonication- to enhance phagocytosis (thru chemotaxis) |
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function of complement system |
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• Increase/enhance inflmmation • Kill bacteria, other cells • Mechanism for elimination of “tagged antigen (result of antibody mediated immune response) |
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o Defend against infection by microbes o Immune surveillance o Eliminate damaged cells o “Negative” aspect- allergies, autoimmune diseases, transplant rejection |
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phagocytosis (intracellular) |
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o Microbe enters by endocytosis o Phagosome formation with the microbe inside o Lysosome comes over and forms phagolysosome o This releases end products into or out o cell |
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o antimicrobial protein Protein family with antiviral effects o Host (not virus) specific o Interfere with viral replication, stimulate NK cells, stimulate macrophages |
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o Resetting of hypothalamic thermostat- pyrogens • Pyrogens- chemical released to induce fever- releases PGE2 which acts of hypothalamus |
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• Interferes with bacterial replication • Increased MR speeds up defensive reactions and repair |
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3 steps common to antibody and cell mediated immunity |
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Definition
o 1) antigen encounter and recognition by lymphocyte ( to activate need activated of special helpter T cells) o 2) lymphocyte activation and clonal expansion o 3) attack |
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o genetic, born with • Also used to refer to nonspecific defenses • Born immunocompetent (lyphocytes matured) |
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• Active- get disease, or get vaccie- your immune system activated • Passive- get antibodies from someone else • Ex) mom gives baby or shot to give antibodies |
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o effectors for cell mediated immunity o Attack infected/transformed cells o CD8 receptors |
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needed for both kinds of immunity o regulatory function in both cell mediated and antibody mediated o CD4 receptors |
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o Inhibit B and T cells o CD8 |
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• Mature (acquire receptors) in bone marrow • Give rise to antibody secreting plasma cells • Carry out antibody mediated immunity |
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• Two chained proteins which cannot bind (see) antigen unless Ag in complexed to MHC “self” proteins • Cytotoxic t cells – CD8 • Helper T cells – CD4 |
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• Immunoglobulin (Ig) attached to B cell • Ig is a copy of antibody that cell can produce |
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immunocompetence (maturation) |
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• Lymphocytes acquire ability ot recognize Ag when they acquire recepotrs specific to Ag • This process is genetically determined! • Confers specicity + versatility to specific immnune system |
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• Any foreign molecule that ca trigger specific immune reponse • Antigen determinants (epitopes)- antigenic sites- ca be multiple on one “bug” – need mutiple types of antobodies |
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• Specific defense protein secreted by specific B lymphocytes • Y chaped • Variable regions bind Ag- V of the Y- receptors here • Constant region involved in effector mechanism- stem of the Y • Finishes the job by activating complement system |
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• Cell chemicals that mediate immune respnse • Table 18.2V • Interferons, leukotries, CSFs • Interleukings |
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• IL-1, IL-2 and more • TNF • Lymphotoxins • perforins |
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typical Ab (80%), can cros placenta |
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first to appear after antigen |
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