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Immunology Exam 1

Zeynah Gomez Immunology English 191 cards

Candida Albicans

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  1. 1Nature of Pathogensany organism with the potential to cause disease.
    **Replication times favor the pathogen**
  2. 2Opportunistic Pathogenscause disease only if your body has a weakened defense (or it gets into a part of your body it isn't normally found)
  3. 3Four kinds of Pathogen that cause Human Disease**The immune system protects against 4 classes of pathogen**
  4. 4Four kinds of Pathogen 1st kind of Pathogen: Bacteria-Examples/Diseases:
    1. Salmonella enteritidis- Food poisoning
    2. Mycobacterium tuberculosis- Tuberculosis
  5. 5Four kinds of Pathogen 2nd kind of Pathogen: Viruses-Examples/Diseases:
    1. Variola- Small Pox
    2. Influenza- Flu
    3. HIV- AIDS
  6. 6Four kinds of Pathogen 3rd kind of Pathogen: FungiExamples/Diseases:
    1. Epidermophyton floccosum- Ringworm
    2. Candida albicans- Thrush
  7. 7Four kinds of Pathogen 4th kind of Pathogen: Parasites -protozoa -worms-Examples/Diseases:
    1. Trypanasoma brucei-
    Sleeping sickness
    2. Leishmania- Leishmaniasis
    3. Plasmodium falciparum- Malaria
  8. 8The Diversity of Human Pathogens*3 slides/cards regarding "The Diversity of Human Pathogens" next --->
  9. 9Candida Albicansnormal inhabitant of the human body, thrush and systemic infectionsCandida Albicans
  10. 10Staphylococcus AureusGram positive bacterium that colonizes human skin, pimples and boils (other strains = food poisoning)Staphylococcus Aureus
  11. 11Mycobacterium Tuberculosiscauses tuberculosisMycobacterium Tuberculosis
  12. 12The first line of external defense against infection of the body is _________?Answer: Skin (works as a tough inpenetrable barrier)
  13. 13Skin has what continuous " 3 things" with epithelia lining?Respiratory, Urogenital tracts, Gastrointestinal
  14. 14Impermeable skin gives way to specialized tissues that are more vulnerable to _______attack; known as __________ surfacesmicrobe; mucosal
  15. 15Mucosal surfaces are bathed in ______mucus (protective; has glycoproteins, proteoglycans and enzymes)
  16. 16Lysozymein tears and saliva- antibacterial
  17. 17___________ __________ is continously removed to clean unwanted materialRespiratory mucus
  18. 18Defensinspoke holes in the pathogen
  19. 19When skin and mucosal barriers are breached __________ ____________ responds.immune system
  20. 20Strong barriers to infections is?skin, hair and nailsStrong barriers to infections is?
  21. 21More vulnerable to infections are?Mucosal membranes like lungs, stomach and intestinesMore vulnerable to infections are?
  22. 22innate immune response leads to ______inflammation
  23. 23Complement (innate)proteins that tag the invader for uptake (phagocytosis) by other immune cells/or poking holes in the microbe by finishing the process of complement cascadeComplement (innate)
  24. 24inflammationinflammation
  25. 25Innate Immune System1st line of defense against infections, works quickly, rises to the acute inflammatory response, has a few specificity for microbes
  26. 26Adaptive Immune SystemTakes longer to develop (approx. 7 days). its highly specific to antigens, uses only one type of receptor to recognize pathogens, primary immune response: adaptive response is activated against a pathogen, seondary immune response: immune response is activated against a pathogne that's been exposed before
  27. 27Innate and Adaptive immune system work together through what?Direct cell contact, interactions with chemical mediators like Cytokines and Chemokines.
  28. 28Adaptive- Lymphocyte selection and proliferationAdaptive- Lymphocyte selection and proliferation
  29. 29Recognition mechanisms of innate immunityrapid response (hours), fixed, limited number of specificites, constant during responseRecognition mechanisms of innate immunity
  30. 30recognition mechanisms of adaptive immunityslow response (days to weeks), numerous highly selective specificities, improve during responserecognition mechanisms of adaptive immunity
  31. 31Cells of the Immune System**4 slides coming up next about the cells in our immune system**
  32. 321. Lymphoid cells20-50% of white blood cells ; T cells, B cells and NK cells
  33. 332. Mononuclear PhagocytesMonocytes circulate blood, macrophages found in tissues
  34. 343. Granulocytic cells (Granulocytes)Neutrophils, Eosinophils, Basophils; based on morphology & cytoplasmic staining
  35. 35Dendritic cellsantigen to T cells; activation of T cells and serves initiation of adaptive immune response ;has high levels of MHC class IIDendritic cells
  36. 36Hematopoiesisgeneration of cellular elements of blood like both red and white blood cells, has megakaryocyte- Platelets
  37. 37Types of Hematopoietic CellsTypes of Hematopoietic Cells
  38. 38Abundance of Leukocytes in Bloodmost abundant leukocytes are neutrophils followed by lymphocytes
  39. 39Leukocytesgeneral for white blood cells
    ex: lymphocytes, granulocytes, monocytes
  40. 40Lymphocytesclass of white blood cells (has both large/small sizes of lymphocytes)
  41. 411st class of Lymphocytes1. Small lymphocyte (adaptive immunity cells)
    - B lymphocytes (B Cells)
    - T lymohocytes (T Cells)
    1st class of Lymphocytes
  42. 422nd class of lymphocytes2. Large granular lymphocytes
    -Natural killer (NK) cells
    -innate immunity
    2nd class of lymphocytes
  43. 43Natural Killer Cells (NK)found in tissues throughout the body but mainly in the circulation, has cytotoxic substances for protection against viruses/tumors, prevents viral replication, helps activate t cells
  44. 44Neutrophilseffectors of innate immunity, specialized in the capture, engulfment, and killing of microbes, oxygen dependent/independent pathway to destroy pathogens
  45. 45MonocyteMoncytes can turn into macrophages; circulate in the blood for abour 8 hours, then mature and migrate into tissuesMonocyte
  46. 46Mononuclear Phagocytesmoncyte progenitors in the bone marrow differentiate into pro-monocytes, which enter blood, where these differentiate into monocytes; fixed and free
  47. 47Mast Cellsfound in skin, connective tissue and mucosal epithelial tissue of both respiratory + digestive tracts; when activated they degranulate and release mediators that cause vasodilation, increase vascular permeability and attreact leukocytesMast Cells
  48. 48Follicular dendritic cells (FDC)hold intact antigens in specialized areas of lymphoid tissues
  49. 49Eosinophilsgranular leukocytes which stain with eosin, have phagocytic activity and responsible for extracellular killing of large parasites, usually binding to antibody-coated oarasite and degranulates into the parasites surfaceEosinophils
  50. 50Basophilstain w/basic dyes (blue), present in very low numbers in circulation, basophils and mast cells are similar in morphologyBasophil
  51. 51Megakaryocyteis a bone marrow cells, does production of blood platelets when cytoplasm becomes fragmented, these fragments are blood platelets, they can be 10 t0 15 times bigger than a red blood cells, function is determined by the number of cytokines including thrombopoietin
  52. 52Thromoboproteinis a glycoprotein hormone produced mainly by the liver and kidney which regulates production of platelets by bone marrow
  53. 53Erythrocytesbind to immune complexed composed of antigen and antibody, these are carried to the liver where its cleared by Kupffer cells; have an important immunological role clearing immune complexes from circulation in persistant infection and some autoimmune diseases
  54. 54Kupffer Cellsphagocytic cells of the liver that line the hepatic sinusoids
  55. 55Site of Hematopoiesis in Humans Changes During DevelopmentChanges with age; early embryo blood cells first produce the yolk sac and later in fetal liver. Within 3-7 months of fetal life the major site of hematopoiesis is the spleen. Bones develop 4-5 months then hematopoiesis shifts towards bone marrow. In adults hematopoiesis occurs mainly in the bone marrow.Site of Hematopoiesis in Humans Changes During Development
  56. 56Neutrophils are Mobilized from the Bone Marrow, and Target (home) to Infection SitesNeutrophils are Mobilized from the Bone Marrow, and Target (home) to Infection Sites
  57. 57Mononuclear Phagocyte SystemFound mainly in organs + tissues; monocytes are in the blood stream and settle in tissue macrophages
  58. 58Macrophage- like cells in the liverKupffer cells
  59. 59Macrophage- like cells in the brainMicroglia
  60. 60Process of PhagocytosisProcess of Phagocytosis
  61. 61Phagocytic Process Stages1.Phagocyte attraction to the site of infection
    2.Phagocyte contact with the microbe
    3. Ingestion (endocytosis)
    4. Killing of the ingested microbe by means of oxygen and oxygen-independent mechanisms
  62. 62OpsinizationMakes microbes more palatable to the phagocyte; molecules coat a microbe such as complement or antibody
  63. 63Macrophages are Key Players in the Innate and Adaptive Immune ResponseMacrophages are Key Players in the Innate and Adaptive Immune Response
  64. 64Macrophages Respond to Pathogens by Using Different Receptors to Stimulate Phagocytosis & Cytokine Secretion, what are they?(theres two) name one1. Bacterium (red) binds to cell -Phagocytic receptors of the macrophage (blue). Bacerium engulfs into a endocytic vesicle called a phagosomeMacrophages Respond to Pathogens by Using Different Receptors to Stimulate Phagocytosis & Cytokine Secretion, what are they?(theres two) ...
  65. 65Macrophages Respond to Pathogens by Using Different Receptors to Stimulate Phagocytosis & Cytokine Secretion, what are they?(theres two) name another one2. Fusion of Phagosome- w/lysosomes it forms an acidic vesicle called phagolysome; contains toxic molecules & hydroltic enzymes that kill bacteriumMacrophages Respond to Pathogens by Using Different Receptors to Stimulate Phagocytosis & Cytokine Secretion, what are they?(theres two) ...
  66. 66Macrophages Respond to Pathogens by Using Different Receptors to Stimulate Phagocytosis & Cytokine Secretion The cytokines are ______ and ________.Answer: synthesized and secretedMacrophages Respond to Pathogens by Using Different Receptors to Stimulate Phagocytosis & Cytokine Secretion The cytokines are ______ and...
  67. 67Name 2 mechanisms of protectionAnswer: Antigens and AntibodiesName 2 mechanisms of protection
  68. 68Antigensbound by a MHC molecules & presented to a "T" cells; can be proteins, lipids or sugars
  69. 69AntibodiesProteins molecules synthesized by cells of immune system-- part of humoral immunity
    -Humors= bodily fluids
    -That recognizes pathogens
  70. 70Adaptive Immunityinfection outruns innate immune response, innate immunity has restricted # of receptors to recognize pathogens; This activates the immune system, the adaptive immune response is mediated by lymphocytes; expands into effector cells & also persists memory; Diverse in immunoglobulins & T cell receptors;
  71. 71What are the primary organs of the immune system?Thymus(T cells mature thymus) and bone marrow(B cells mature bone marrow); (where maturation of lymphocytes takes place)
  72. 72What are the secondary organs of the immune system?Lymph nodes, spleen, peyer's patches and mucosal-associated tissues; trap antigen & promote lymphocyte activation
  73. 73Lymphocytesfound in lymphoid tissues, blood & lymph; activated in secondary lymphoid tissues; Arise from stem cells in bone marrow
  74. 74Lymphatic Systemsmall lymphocytes travel in both blood and lymph; antigens carried to lymph nodes as lymphocytes enabling interactions
  75. 75When an antigen is encountering the lymphocyte it will no longer_________.Answer: Recirculate
  76. 76Dendritic cells activated by infection also carry _________.antigens
  77. 77Lymphocytes leave______ and enter ______ -________ where they are activated by pathogens.Answer: blood; lymph-nodes
  78. 78___________ drain from site of infection (example:foot infection) to lymph nodesPathogens
  79. 79___________ _________ - _______ stay in lymph nodes and divide and differentiate into effector cells,while no-activated cells leave through efferent lymphaticsActivated; lymph-nodes
  80. 80Lymphocytes recirculate at a rate of ___X10^6 cells/min5
  81. 81Architecture of the Lymph NodeKidney shaped; packed w/lymphocytes & macrophages; Arriving at afferent lymph are pathogens & dendritic cells carrying pathogens; Pathogens degrade & stimulate lymphocytesArchitecture of the Lymph Node
  82. 82The spleenfilters blood & removes old/damaged cells = red pulp;blood bourne pathogens encounter lymphocytes( a secondary lymphoid organ)= white pulpThe spleen
  83. 83Topic: Spleen Blood is the only way in and out for_________ as well as __________.lymphocytes; pathogens
  84. 84Topic: Spleen Spleenic macrophages and _______ ________ in the spleen take-up antigen and stimulate "_" and "_" cellsdendritic cells;" T "," B "
  85. 85White pulp of the spleen has sheath of lymphocytes called _______ ________ _________.Periateriolar lymphoid sheath (PALS)
  86. 86PALS surrounds the ______ _______central arteriole (CA)
  87. 87T cells are the ______ to CA, while B cells are more ________, forming a B cell coronaclosest; peripheral
  88. 88Germinal centers form between the ___ and __ cell zones. The _______ zone contains differentiated B cells.Answer: T; B; marginalGerminal centers form between the ___ and __ cell zones. The _______ zone contains differentiated B cells.
  89. 89Mucosal-Associated Lymphoid Tissue (MALT)Mucosal surfaces lining digestive, respiratory and urogenital tracts are major sites of entry for pathogens which are defended by MALT;GALT and BALT are both apart of MALT;
  90. 90Tissues ______ from loosely organized _______ of lymphoid cells to well organized structures --tonsils, appendixRange;clusters
  91. 91The guy associated lymphoid tissues, GALT includes ______,______,_______ and Peyer's patches that line the gut.tonsils, adenoids, apendix
  92. 92B.A.L.T stands for what?Bronchial-associated lymphoid tissues
  93. 93Lymphocytes activated in the______ tend to stay in MALT and the________ cells serve the MALT in the future.MALT; memory
  94. 94A region of GALTA region of GALT
  95. 95Immunological MemoryLymphocytes that expand persist, providing long term memory;
    First time infection results in primary response leading to memory (T and B cells) of the pathogen;
    Subsequent infections with the same pathogen,same antigens, will elicit a secondary response that's much faster/stronger.
  96. 96Comparison of a Primary and Secondary Immune ResponseComparison of a Primary and Secondary Immune Response
  97. 97Immunodeficiency: Inherited or Infectious What do you know about this?Mutation in immune function genes leads to immunodeficiency -- different kinds….
    one aspect of immune response is affected then others show adaptive immunity being absent;
    Leads to devastating vulnerability towards all infections;
    Extreme example of immunodeficiency due to disease is the acquired immune deficiency syndrome, AIDS;
    Caused by infection with the human immunodeficiency virus, HIV
  98. 98Chapter 2: Innate immunityChapter 2
  99. 991st Defense CategoryPhysical barriers, Fixed or 'hard-wired' mechanisms (innate)
  100. 1002nd Defense CategoryInnate immune mechanisms called into action by initial innate immune response, take hours to days to work
  101. 1013rd Defense CategoryAdaptive immune response
    -“⬆️” vaccination
    -long-term protection
  102. 102ProtectionProtection
  103. 103Physical Barriers (Innate immunity)Outer epthelial
    -Physical barrier
    -Colonization by non pathogenic resident microorganisms
  104. 104Physical barriers: What if a pathogen does move in?The inate immune response quickly takes action to eliminate the bug
  105. 105Are the defenses of the innate immune response easy to assess?The innate immunity is very effective; inheritable immune mechanism defects leading to substantial protection reduction
  106. 106Aren’t most infections eliminated prior to development of symptoms?Maybe you don’t even have to see a doctor
    Conclusion = innate immunity is very effective
    After all we do have vast populations of resident microbes and most the time we are well
  107. 107Infectious diseases are caused by pathogens of diverse types that ____ and __________ in the human bodylive; replicate
  108. 1084 Human Pathogen TypesViruses, bacteria, fungi and parasites (unicelluar protozia and multi-celluar worms)
  109. 109Pathogens can _____ cells directly (intracellular) or live ______ of cells (extracellular).infect;outside
  110. 110Pathogens Can Live Inside or Outside of CellsPathogens Can Live Inside or Outside of Cells
  111. 111Different components of the immune system contribute to immunity against different types of _______ in different locationsmicrobes
  112. 112Extracellularsome pathogens, all stages are extracellular; accessible to soluble components of the immune systemExtracellular
  113. 113IntracelluarOthers, exploit intracellular sites to grow and replicate;
    not able to use soluble components.
    Intracelluar
  114. 114Extracellular vs. intracellular infections can be further subdividedWhile elimating pathogens differnt sites affect the type of immune mechanism; Extracelluar form aren't accesible to soluble immune system molecules; Intracelluar forms aren't accessible to soluble immune system molecules
  115. 115Most pathogens infect only a few related ______ - _______.Host-species
  116. 116How does the pathogen's ability to persist outside of the body vary?It determines the ease, of it which a particular disease is spread.
    Examples:
    1. Anthrax= spores= resistant to heat/desiccation
    2. HIV sensitive to environment change; requires intimate contact/exchange of infected body fluids
  117. 117Parasites may require an intermediate passage through distantly related organism WHY?to complete it's life cycle
  118. 118Complement, why does it do?Tags pathogens and extracelluar molecules for destruction by phagocytic cells like macrophages.
  119. 119How can complement destroy pathogens directly?by poking holes in the outer membrane or cell wall with membrane attack complex (MAC)
  120. 120What are the 3 complement pathways?Alternative, Lectin,and classical
  121. 121Figure 2.5 : The 3 PathwaysFigure 2.5 : The 3 Pathways
  122. 122Complement Fixation Figure 2.3:Complement Fixation Figure 2.3:
  123. 123Complement activation by the alternative pathway tags microorganisms for _______.destruction
  124. 1241st immune system components to be activated = complement How?1. its ubiquitous in blood and lymph
    2. Soluable proteases that circulate from an inactivate form called zymogens
    3. A molecular defense that can be ultilized immediately
  125. 125The Thioester BondThe Thioester Bond
  126. 1261st Step in the _________ __________ involves spontaneous hydrolysis and activation of complement component C3alternative pathway
  127. 127What is iC3?is the product of C3 hydrolysis but there is no cleavage of C3
  128. 128Alternative Pathway – Slide 1 of 2Alternative Pathway – Slide 1 of 2
  129. 129Alternative Pathway – Slide 2 of 2Alternative Pathway – Slide 2 of 2
  130. 130C3 convertase of the alternative pathway, How? Where do we start?-Factor B binds to C3b fragments & is drived by factor D, then a C3bBb is formed on the pathogen's surface, this ='s C3 convertase of the alternative pathway!
  131. 131C3b Tags Pathogens for _________.Phagocytosis
  132. 132Opsonina protein bound to the surface of a pathogen that facilitates its phagocytosis.
  133. 133CR1 (complement receptor 1)Recognizes C3b;
    binds to C3b deposited on microbial surfaces --> phagocytosis
    ;Also plays a protective role on human cell surfaces by disrupting C3 convertase.
  134. 134Figure 2.10:Figure 2.10:
  135. 135How is the sequence of complement-activating reactions continued?Binding C3b to existing C3bBb complexes at pathogens surface forms the alternative C5 convertase =C3b2Bb
    (C4b2a3b in classical pathway
  136. 136What happens when C5 is activated?goes to terminal components of complements
    (C6-C9)
    Pores--> transmembrane-
    channels -->Pathogen lysis
    What happens when C5 is activated?
  137. 137What does C5a do?recruits neutrophils to infection site
    *Most potent anaphylatoxin*
  138. 138The terminal complement components that form the membrane-attack complexThe terminal complement components that form the membrane-attack complex
  139. 139The terminal complement components that form the membrane-attack complex: Protein C5 (concentration in serum:85) What's its function?initiates assembly of the membrane-attack complex in solution
  140. 140The terminal complement components that form the membrane-attack complex: Protein C6 (concentration in serum:60) What's its function?Binds to ans stabilizes C5b. Forms a binding site for C7
  141. 141The terminal complement components that form the membrane-attack complex: Protein C7 (concentration in serum:55) What's its function?Binds to C5b6 and exposes a hydrophobic region that permits attachment to the cell membrane
  142. 142The terminal complement components that form the membrane-attack complex: Protein C8 (concentration in serum:55) What's its function?Binds to C5b67 and exposes a hydrophobic region that inserts into the cell membrane
  143. 143The terminal complement components that form the membrane-attack complex: Protein C9 (concentration in serum:60) What's its function?Polymerization on the C5b678 complex to form a membrane-spanning channel that disrupts the cells's integrity & results to cell death
  144. 144Protection on Human Cells Against MACProtection on Human Cells Against MAC
  145. 145Complement Receptors (CR)Complement Receptors (CR)
  146. 146CR 1 recognizes _____Answer: C3b
  147. 147What is the soluable C3 convertase and how it is formed?Answer: iC3Bb
  148. 148CR2 is a __-cell co-receptor and recognizes _______.Answer: B ; C3b
  149. 149CR3 & CR4 recognize ______.Answer: iC3b
    ** iC3b can be recognized
    by phagocytic cells
  150. 150What is the classical C3 convertase? What is the alternative C3 convertase? **(Hint: Both questions share the same answer)**Answer to both questions is:
    C4b2a
  151. 151“a” (anaphylatoxins) Fragments Help Lead to Inflammation, C3a and C5a contribute to ______ - ________.Acute inflammation
  152. 152What exactly do they( "a" fragments) do?bind mast cells, phagocytes and endothelial cells
    -->release of histamine from mast cells
    Histamine increases blood vessel permeability & blood flow
    Activate endothelial cells ---> direct phagocytes to site of infection
  153. 153What does C5a do?Increases adherence of monocytes and neutrophils to blood vessel walls and acts as a powerful chemotactic factor
  154. 154C5a is able to attract ______to areas where _______has been fixed.phagocytes;complement
  155. 155What about protecting the host cell, in regulatory proteins?-Proteins controls complement activation
    -Ensures C3b is close-set in place on microbial surfaces; not on the surfaces of human cells
    - Plasma protein = properdin (factor P)
  156. 156Factor P binds to C3 convertase (C3bBb) on microbial surfaces and protects it from inhibition by factor ____. (Hint: one letter answer)Answer: "H"
  157. 157What is factor "H"?Factor H plasma protein reduces complement reactions by making C3b susceptible to cleavage by factor I creating a iC3b fragment that is incapable of forming a C3 convertase
  158. 158On human cells the complement pathway is stopped by human ___-_______ _______ decay-accelerating factor (DAF) and membrane co-factor protein (MCP).Answer: Cell-factor protein
  159. 159DAF and MCP control proteins destroy C3 convertase activity by binding to ____.Answer: C3b
  160. 160CR-1 also plays a protective role on ______ cells.Answer: Human
  161. 161When C3bBb is formed on a human cell surface it is rapidly disrupted by the action of one of the regulatory membrane proteins: ______ ______ ________ (D.A.F) or _______ ________ _______ (MCP).Answer: decay accelerating factor (DAF) or membrane cofactor protein (MCP)
  162. 162Complement activation limits bacterial infections…but some bacteria mimic human cells to evade the actions of complement. (Give two examples that relate to this statement)Example 1:
    Streptococcus pyogenes
    Example 2:
    Staphylococcus aureus
  163. 163Several classes of plasma protein limit the spread of ________.Answer: Infection
  164. 164—
  165. 165What does this symbol mean?Answer: AlphaWhat does this symbol mean?
  166. 166What does this symbol mean?Answer: BetaWhat does this symbol mean?
  167. 167Antimicrobial Peptides - Defensins: What are the two types of defensins?1st : Alpha -defensins
    2nd : Beta -defensins.
  168. 168Alpha Defensins?Produced mainly by neutrophils and Paneth cells (specialized epithelial cells of the small intestine)
  169. 169Beta Defensins?Expressed mainly by epithelial cells of the respiratory tract the urogenital tract and the skin.
  170. 170Amphipathic (both ________ and _________) regions.Answer: hydrophobic and hydropholic
  171. 171Human B1-Defensin (Figure 2.17)Human B1-Defensin (Figure 2.17)
  172. 172Alpha Defensins: Class, Name, Site of Synthesis, Tissues defended, Regulation of Synthesis Figure 2.19:Alpha Defensins: Class, Name, Site of Synthesis, Tissues defended, Regulation of Synthesis Figure 2.19:
  173. 173Beta Defensins: Class, Name, Site of Synthesis, Tissues defended, Regulation of Synthesis Figure 2.19:Beta Defensins: Class, Name, Site of Synthesis, Tissues defended, Regulation of Synthesis Figure 2.19:
  174. 174What are the secondary lymphatic organs?Lymph nodes, spleen and mucosal-associated tissues
  175. 175What happens in secondary lymphatic organs?Trap antigen and promote lymphocyte activation
  176. 176Are pathogens found on human cells or pathogen cells?Answer: on pathogen cells
  177. 177What are the primary lymphatic organs? What happens in the primary lymphatic organs?Answer to Q1: Thymus and bone marrow
    Answer to Q2: Maturation of lymphocytes
  178. 178Chapter 3: Information in Test 1Chapter 3
  179. 179C- Reactive ProteinActivates classical complement cascade.
  180. 180What can bind to C1q to initiate a classical pathway of complement fixation in absence of Abs and also acts as an opsonin?C-reactive protein
  181. 181Mannose-binding lectin (MBL)-Activates the Lectin complement cascade
    -Enhances complement fixation to pathogen surfaces
    -Binds mannose-containing carbohydrates of bacteria and yeast
  182. 182Acute-Phase Responseincreases the supply of the recognition molecules of innate immunity
  183. 183Besides showcases the acute phase response, what else does this picture showcase?It shows opsonization of pathogen by MBL and CRPBesides showcases the acute phase response, what else does this picture showcase?
  184. 184MBL activates a proteolytic enzyme complex: MBL-associated serine protease = MASP. How does it initiate complement activation?-lectin pathway of complement activation;
    -MBl serves as an opsonin to faciliate bacteria uptale by monocytes in the blood.
  185. 185C-reactive protein and MBL are present at low levels in plasma: What phase occurs when these levels increase during acute-phase response?- C-reactive and MbL both bind structures that are common to pathogens but absent in human cells
    -Fixation by a apthway alsomost identical to classical pathway used by Abs.
  186. 186C4 and C3 are similar in ______, ________and the _______ bond and C2 and factor B are similar.Answer: function; structure and thioester bond
  187. 187What are the two C3 convertases?Alternative- C3b2a
    Classical- C4b2a
    What are the two C3 convertases?
  188. 188Classical Pathway Initiated by what?Answer: AbsClassical Pathway Initiated by what?
  189. 189Initiation of the Classical PathwayC1 binds to C-reaactive protein on the pathogen surface activates the classical pathway of complement fixation.
  190. 190MASP and C1 – Similar Structure and FunctionBoth have binding portions
    and protease action
    MASP and C1 – Similar Structure and Function
  191. 191Close structural relationships between components of the alternative, lectin-mediated & classical pathways of complement activationClose structural relationships between components of the alternative, lectin-mediated & classical pathways of complement activation

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Professor: Gregory Weigel Chapters 1,2 & part of Chapter 3
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Zeynah Gomez
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