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Anatomy & Physiology

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Answer
immune system   protects from infectious agents & harmful substances (typically w/o awareness), composed of numerous cellular and molecular substances that function together to provide us with immunity, and its function is dependent on specific types of infectious agents  
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infectious agents   organisms that cause damage or death to host organism  
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pathogenic   a term used to describe infectious agents that cause harm  
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five major categories of infectious agents   bacteria, viruses, fungi, protozoans, and multicellular parasites  
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bacteria   single-celled organism, 1-2 micrometers, enclosed by cell wall, come in multiple shapes (spherical [cocci], rodlike [bacilli], coiled [spirilla]), and there are good and bad types  
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examples of diseases caused by bacteria   streptococcal infection (strep throat), tuberculosis, and Lyme disease  
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Viruses   acellular organisms that are composed of DNA or RNA within a protein shell, and they are smaller than bacteria (one-hundredth of a micrometer), and are obligate intracellular parasites  
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obligate intracellular parasites   must enter cell to reproduce, viral particles formed within infected cells, released from them to infect surrounding cells, and cell can be ultimately killed by virus or immune system  
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examples of diseases caused by a virus   depends partly on type of infected cell (i.e. chicken pox, HIV, common cold)  
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fungi   have cell wall external to plasma membrane, includes molds, yeasts, multicellular fungi, release proteolytic enxymes  
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proteolytic enzymes   induce inflammation causing redness and swelling  
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fungal diseases   in U.S. usually limited to superficial infections of skin, scalp, nails (i.e. ringworm and athlete's foot), others can infect mucosal linings or internal infection  
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protozoans   lack cell walls, are intracellular and extracellular parasites, and have the ability to move (with cilia)  
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protozoan disease examples   malaria, trichomoniasis  
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multicellular parasites   nonmicroscopic organisms that reside in host from which they take nourishment  
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example of parasitic diseases   parasitic worms such as tapeworms infect intestinal tract of humans and other mammals  
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leukocytes   formed in the red bone marrow, include three types of granulocytes, include monocytes, and include lymphocytes  
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types of granulocytes   neutrophils, eosinophils, and basophils  
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monocytes   become macrophages when take up residence in the tissues  
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lymphocytes   B-lymphocytes, T-lymphocytes, NK (natural killer) cells  
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structures that house immune system cells   most found not in the blood but in lymphatic tissue, select organs, epithelial and mucosal membranes, and connective tissue  
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lymphatic tissue   lymph nodes, spleen, tonsils, MALT, lymphatic nodules  
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lymphatic tissue   where many T- and B-lymphocytes, macrophages, NK cells are housed  
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select organs   macrophages also housed in other organs, some specifically named based on location (i.e. alveolar macrophages of lung, microglia of brain), may be permanent residents (fixed macrophages), and may migrate through tissues as wandering macrophages  
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epithelial layers of skin and mucosal membranes   dendritic cells here that derived from monocytes engulf pathogens in skin and mucosal membranes and migrate to lymph node through lymph vessels  
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connective tissue   mast cells located here, typically in close proximity to small blood vessels, abundant in dermis, and abundant in mucosa of respiratory, digestive, and urogenital tracts  
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two categories of the immune system   innate immunity and adaptive immunity  
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the two types of immune systems are...   organized based on type of immunity provided and work together to protect from harmful agents  
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how the two types of immune systems differ   cells involved, specificity of cell response, mechanisms of eliminating harmful substances, and amount of time for response  
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innate immunity   protects against numerous different substances, born with these defenses, does not require previous exposure to a foreign substance, and respond immediately to potentially harmful agent.  
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innate immunity includes   barriers of the skin and mucosal membranes, nonspecific cellular and molecular internal defenses  
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adaptive immunity   involves specific T-lymphocytes and B-lymphocytes, provides powerful means of eliminating foreign substances, and takes several days to be effective  
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T-lymphocytes and B-lymphocytes   respond differently to different foreign substances (i.e. particular lymphocytes responds to chickenpox virus  
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structures of innate immunity   prevent entry of potentially harmful substances, respond nonspecifically to wide range of harmful substances and include the first two lines of defense  
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first line of defense   skin and mucosal membrane  
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second line of defense   internal processes of innate immunity, activities of neutrophils, macrophages, NK cells, chemicals such as interferon and complement, and physiological processes such as inflammation and fever  
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physical barrier of skin   formed by epidermis and dermis, few microbes able to penetrate, has natural flora (nonpathogenic microorganisms residing here, help prevent growth of pathogenic microorganisms)  
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mucosal membrane barrier   membranes lining openings of the body, produce mucin (when hydrated, forms mucus), lined by harmless bacteria  
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barrier defenses   mechanisms usually successful, but infectious agents may enter if the barrier is compromised or there are too many microbes (this activates the innate immunity and adaptive immunity)  
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neutrophils and macrophages   cells of innate immunity  
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neutrophils   most prevalent leukocyte in blood, first to arrive during inflammatory response, and fights off bacteria  
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macrophages   reside in tissues throughout the body, arrive later and stay longer than the neutrophils, engulf unwanted substances through phagocytosis  
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basophils and mast cells   proinflammatory chemical-secreting cells that release substances to increase fluid movement from blood to injured tissue and are chemotactic  
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basophils   circulating in blood  
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mast cells   reside in connective tissue, mucosa, and internal organs  
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chemotactic   describes attracting immune cells as part of inflammatory response  
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granules released by basophils and mast cells during inflammatory response...   contain histamine and heparin  
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histamine   increases vasodilation and capillary permeability  
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heparin   anticoagulant  
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eicosanoids   released from the plasma membrane of basophils and mast cells and increase inflammation  
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natural killer cells   destroy wide variety of unwanted cells (i.e. virus/bacteria-infected cells, tumor cells, transplanted tissue cells), formed in bone marrow & circulate in blood, accumulate in secondary lymphatic structures, and patrol the body detecting unhealthy cells  
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immune surveillance   the patrolling of the body detecting unhealthy cells that is conducted by the natural killer cells  
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natural killer cells   destroy unhealthy cells by releasing cytotoxic chemicals (include perforin and granzymes)  
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perforin   forms transmembrane pore in unwanted cells  
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granzymes   initiate apoptosis  
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apoptosis   form of cellular death  
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eosinophils   target parasites, degranulation and release of enzymes and other substances, participate in immune response of allergy and asthma, and engage in phagocytosis of antigen-antibody complexes  
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inflammation   immediate, local, nonspecific response, occurs in vascularized tissue against variety of stimuli, major effector of innate immunity, and helps eliminate infectious agents from body  
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stimuli that ellicit inflammation   scratch of skin, bee sting, overuse of body structure  
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first event of inflammation   numerous chemicals are released from injured tissue, basophils, mast cells, and infectious organisms (including histamine, leukotrienes, prostaglandins, chemotactic factors)  
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second event of inflammation   released chemicals causing responses in local blood vessels, vasodilation (increased capillary permeability)  
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third event of inflammation   leukocytes recruited to the area  
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effects of inflammation   increased fluid, protein, immune cells leaving capillaries, delivers substances needed to eliminate pathogens and promote healing, raises hydrostatic pressure  
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effects of inflammation continued...   net movement of fluid from blood through infected area exudates additional fluid uptake by lymphatic capillaries, carries away infectious agents, dead cell, cellular debris, and lymph monitored as passes through lymph nodes  
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effects of inflammation within 72 hours (inflammatory response slowing down)   monocytes exit blood, become macrophages, & begin cleaning up affected area, bacteria, damaged host cells, dying neutrophils destroyed by macrophages, fibroblasts multiplying & synthesizing collagen, starts tissue repair, may lead to scar tissue formation  
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cardinal signs of inflammation   redness, heat, swelling, pain, and loss of function  
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redness results from...   increased blood flow  
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heat results from...   increased blood flow and increased metabolic activity within the area  
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swelling results from...   increase in fluid loss from capillaries to interstitial space  
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pain results from...   stimulation of pain receptors from compression from interstitial fluid  
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loss of function results from...   may occur in severe cases  
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fever   abnormal elevation of body temperature (at least 1 degree Celsius from normal 37 degrees Celsius), may accompany inflammatory response, requires increased fluid intake to prevent dehydration (due to excess fluid loss)  
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events of fever   onset, stadium, and defervescence  
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onset   period during which temperature begins to rise, hypothalamus stimulating dermis blood vessels to vasoconstrict, may occur with chills and shivering  
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stadium   period when elevated temperature maintained, increased metabolic rate, promotes physiologic processes involved in eliminating harmful substance  
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defervescence   period when temperature returning to normal set point, hypothalamus stimulating mechanisms to release heat (i.e. increased vasodialtion of skin blood vessels, sweating  
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benefits of fever   inhibits reproduction of bacteria and viruses, increases activity of adaptive immunity, accelerates tissue repair, and recommended to leave a low fever untreated  
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risks of high fever   high fevers are potentially dangerous, change in metabolic pathways and denaturation of proteins, possible seizures, irreversible brain damage if over 106 F and death likely if over 109 F  
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adaptive immunity   initiated upon entry of foreign substance, takes longer to respond than innate immunity, contact with antigen (causes lymphocyte to proliferate and form specialized "army"), lymphocytes and products released, considered third line of body's defense  
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immune response   lymphocytes and products released with adaptive immunity  
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two branches of immunity   cell-mediated immunity and humoral immunity  
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cell-mediated immunity   immune response involving T-lymphocytes  
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humoral immunity   immune response involving B-lymphocytes, develop into plasma cells to release antibodies  
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foreign antigens   different in structure from human body's molecules and bind body's immune components  
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self-antigens   body's molecules, typically do not bind immune components  
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immune system is generally able to distinguish between   foreign and self-antigens  
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autoimmune disorder   when the body reacts to self-antigens as if foreign  
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T- and B-lymphocytes   have unique receptor complexes, about 100,000 per cell, each complex binding specific antigen  
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B-lymphocytes   make direct contact with antigen  
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T-lymphocytes   must have antigen processed, antigen presented in plasma membrane of another cell type, and have additional receptor molecules (coreceptors)  
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coreceptors   facilitate T-lymphocyte interaction with cell presenting antigen  
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two types of T-lymphocytes   helper T-lymphocytes and cytotoxic T-lymphocytes  
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Helper T-lymphocytes   help activate B-lymphocytes and other immune cells, contain CD4 in plasma membrane, and classified as CD4 cells and bind to MHC II complex  
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cytotoxic T-lymphocytes   release chemicals toxic to cells, contain CD8 in plasma membrane, classified as CD8 cells that bind to MHC I complex  
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antigen presentation   display of an antigen on a cell's plasma membrane, process performed by other cells (help T-lymphocytes "see" the antigen), and two types of cells presenting antigen to T-lymphocytes  
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two types of cells presenting T-lymphocytes   all nucleated cells of the body and antigen-presenting cells (APCs)  
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antigen-presenting cells   any immune cell communicating antigen presence to T-lymphocytes (dendritic cells, macrophages, and B-lymphocytes  
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antigen presentation   requires physical attachment of antigen to transmembrane protein (termed major histocompatibility complex [MHC] and a group of genes codes for MHC molecules in plasma membrane)  
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two major MHC groups   MHC I and MHC II  
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MHC I   found in all nucleated cells  
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MHC II   found in APCs (in addition to MCH I)  
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three events in life of lymphocytes   formation and maturation, activation of lymphocytes, and effector response  
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formation and maturation of lymphocytes   occurs within primary lymphatic structures (red bone marrow and thymus), become able to recognize one specific foreign antigen  
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activation of lymphocytes   migrate to secondary lymphatic structures, usually where they are first exposed to antigen they bind, and become activated and replicate to form identical lymphocytes  
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effector response   action of T-lymphocytes and B-lymphocytes to eliminate antigen (T-lymphocytes migrate to site of infection and B-lymphocytes remain within secondary lymphatic structures)  
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B-lymphoctyes remaining within secondary lymphatic structures   synthesize and release large quantities of antibodies against antigen, enter blood and lymph and are transported to infection site  
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mechanisms activated lymphocytes use to help eliminate antigen   Helper T-lymphocytes (release IL-2 and other cytokines, regulate cells of adaptive and innate immunity), cytotoxic T-lymphocytes (destroy unhealthy cells by apoptosis), and plasma cells (produce antibodies)  
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