Immune System: Innate and Adaptive Flashcards

1
Q

What is the immune system

A

Provides resistance to disease

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2
Q

Is the immune system a functional system or organ system

A

a. A functional system

b. Innate and adaptive defenses are intertwined

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3
Q

Name and describe defenders of the two intrinsic systems

A

a. Innate (nonspecific) defense system
i. First line of defense: external body membranes (skin and mucose membrane)
ii. Second line of defense: antimicrobial proteins, phagocytes, and other cells inhibit spread of invaders; inflammation occurs
b. Adaptive (specific) defense system
i. Third line of defense: attacks particular foreign substances
ii. Takes longer to react than innate

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4
Q

What are pathogens?

A

Disease-causing microorganisms

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5
Q

What is the purpose of the innate (non-specific) immunity?

A

Use the first and/or second lines of defense to stop attacks by pathogens

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6
Q

Describe surface barriers (first line of defense)

A

a. Skin and mucous membranes, along with their secretions
b. Physical barrier to most microorganisms
c. Keratin is resistant to bacterial enzymes and toxins
d. Mucosae provide sticky mechanical barrier

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7
Q

What protective chemicals inhibit or destroy microorganisms?

A

a. Acid: acidity of skin and some mucous secretions inhibits growth
b. Enzymes: lysozyme of salvia, enzymes in stomach, and lacrimal fluid kills many microorganisms
c. Mucin, defensins, dermicidins (not important)

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8
Q

What is the respiratory system’s line of defense?

A

a. Mucus-coated hairs in nose trap inhalants

b. Cilia of upper respiratory tract sweep dust and bacteria-laden mucus toward mouth

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9
Q

Which cells and chemicals are necessary if microorganisms invade deeper in tissue (second line of defense)?

A

a. Phagocytes
b. Natural killer (NK) lymphocytes
c. Inflammatory response- macrophages, mast cells, WBCs, and inflammatory chemicals
d. Antimicrobial proteins- interferons and complement proteins
e. Fever

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10
Q

Describe phagocytosis

A

a. Adherence: starts when phagocyte adheres to pathogen’s carbohydrate ID tags
i. Opsonization: immune system uses antibodies or complement proteins as opsonins that coat pathogens- act as “handles” for phagocytes to grab onto
b. Ingestion and digestion: continues as cytoplasmic extensions (pseudopodia) bind to and engulf particle in phagosome – fuses with lysosome, forming phagolysosome, which is digested – indigestible and residual waste is exocytosed from phagocyte

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11
Q

When is inflammation triggered?

A

Whenever body tissues are injured (healing process)

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12
Q

What are benefits of inflammation?

A

a. Prevents spread of damaging agents
b. Disposes of cell debris and pathogens
c. Alerts adaptive immune system
d. Sets the stage for repair

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13
Q

What are four cardinal signs of acute inflammation?

A

a. Redness- rubor
b. Heat- calor
c. Swelling- tumor
d. Pain- dolor
e. Sometimes a 5th sign, impairment of function, is seen if movement or use of area is hampered

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14
Q

What are the stages of inflammation?

A

a. Inflammatory chemical release (inflammatory mediators)
b. Vasodilation and increased vascular permeability (large + leaky)
c. Phagocyte mobilization (chemotaxis)

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15
Q

Who are inflammatory mediators and what are their roles?

A

a. Kinins, prostaglandins (PGs), and complement (c3a and c5a)
b. All cause vasodilation of local arterioles
c. All make capillaries leaky
d. Many attract leukocytes to area
e. Some have other inflammatory roles, such as triggering pain receptors, or prompting release of more inflammatory chemicals

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16
Q

Vasodilation and permeability cause what?

A

a. Vasodilation and increased vascular permeability
b. Vasodilation causes hyperemia, which leads to redness and heat
c. Increased capillary permeability causes exudate to leak into tissue, leading to local swelling (edema) and pain

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17
Q

Describe phagocyte mobilization during inflammation

A

a. Leukocytosis: release of neutrophils from bone
marrow
b. Chemotaxis: inflammatory chemicals promote positive chemotaxis of neutrophils toward injured area
c. Margination: endothelial cells of capillaries in inflamed area project cell adhesion molecules
d. Diapedesis: neutrophils flatten and squeeze
between endothelial cells, moving into
interstitial spaces

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18
Q

What are abscess and pus?

A

a. Pus: creamy yellow mixture of dead neutrophils, tissue/cells, and living/dead pathogens
b. Abscess: collagen fibers are laid down, walling off sac of pus; may need to be surgically drained

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19
Q

Describe antimicrobial proteins (INFs)

A

a. Interferons (IFNs)
b. Cells infected with viruses can secrete IFNs that enter neighboring cells, stimulating production of antiviral proteins AVPs that block viral reproduction

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20
Q

Briefly describe the complement system

A

a. The Complement system consists of ~20 blood proteins that circulate in blood in inactive form
b. Includes major proteins C1–C9, and other regulatory proteins
c. Provides major mechanism for destroying foreign substances by enhancing inflammation and immunity

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21
Q

Describe the complement system pathways

A

a. Complement system can be activated by different pathways:
b. Classical pathway
i. Antibodies first bind to invading organisms and then bind to complement components, activating them (C1, C2, C4…C3)
ii. Once initial complement proteins are activated,
an activation cascade is triggered
iii. C3 can lead to increased inflammation, opsinization, or cytolysis
c. Alternative pathway
i. Complement cascade is activated spontaneously when certain complement factors bind directly to foreign invader

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22
Q

Describe the general nature of the complement system pathways

A

a. Each pathway involves activation of proteins in an orderly sequence:
b. Each step catalyzes the next, in cascade fashion
c. Each pathway converges on C3, which cleaves into C3a and C3b
d. Splitting C3 initiates other pathways that enhance inflammation, promotes phagocytosis, and causes cell lysis

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23
Q

Describe complement (cytolysis)

A

C3b binds to target cell, triggering insertion of complement proteins C5-C9 called membrane attack complex (MAC)
MAC forms and stabilizes hole in membrane of microbe, causing influx of water and lysis of microbe

24
Q

Describe complement (opsonization)

A

C3b (alone) can cause opsonization

25
Q

Describe pyrogeny

A

a. Fever
b. Abnormally high body temperature that is systemic response to invading microorganisms
c. Leukocytes exposed to foreign substances secrete pyrogens
d. Pyrogens act on body’s thermostat in hypothalamus, raising body temperature

26
Q

Describe the adaptive immune system

A

a. Adaptive immune system is a specific defensive system that eliminates almost any pathogen or abnormal cell in body
b. Amplifies inflammatory response
c. Activates complement
d. Priming by initial exposure to specific foreign substance takes time

27
Q

What is the duality of the adaptive system

A

a. The duality of the adaptive system
b. Humoral (antibody-mediated) immunity (B cells- antibodies)
c. Cellular (cell-mediated) immunity (T cells- cell mediation)

28
Q

Describe humoral immunity

A

a. Humoral immunity
b. Antibodies, produced by lymphocytes, circulate freely in body fluids
c. Bind temporarily to target cell and mark them for destruction by phagocytes or complement
d. Humoral immunity has extracellular targets

29
Q

Describe cellular immunity

A

a. Cellular Immunity (cell mediation) (T cells)
b. Lymphocytes act against target cell
c. Directly—by killing infected cells
d. Indirectly—by releasing chemicals that enhance inflammatory response; or activating other lymphocytes or macrophages

30
Q

Define and describe antigens

A

a. Antigens: substances that can mobilize adaptive defenses and provoke an immune response
b. Most are large molecules not normally found in body
c. An antigen can be a complete antigen or hapten (incomplete)

31
Q

Name and describe the three crucial cell types of the adaptive immune system

A

a. Adaptive immune system involves three crucial types of cells
i. Two types of lymphocytes
ii. B lymphocytes (B cells)—humoral immunity
iii. T lymphocytes (T cells)—cellular immunity
b. Antigen-presenting cells (APCs)
i. Specialized macrophages

32
Q

Describe lymphocyte development, maturation, and activation

A

a. Origin: both lymphocytes originate in red bone
marrow
b. Maturation - Lymphocytes are “educated” as they mature – Immunocompetent lymphocytes can recognize only one specific antigen
c. Antigen encounter and activation- Naive lymphocyte’s first encounter with antigen. It is selected to differentiate into active cell by clonal selection

33
Q

Describe clonal selection of lymphocytes

A

a. Proliferation and differentiation
b. Once selected and activated, lymphocyte proliferates
c. Forms army of clones
d. Most clones become effector cells that fight infections
e. A few remain as memory cells and are able to respond to same antigen more quickly second time it is encountered

34
Q

Describe antigen-presenting cells (APCs)

A

Macrophages engulf antigens and present fragments of antigens to T cells for recognition (Th cells)

35
Q

Describe humoral immune response

A

a. When B cell encounters target antigen, it provokes humoral immune response
b. Antibodies specific for that particular antigen are then produced and secreted

36
Q

What happens to clone cells that do not become plasma cells?

A

a. Clone cells that do not become plasma cells become memory cells
b. Provide immunological memory
c. Mount an immediate response to future exposures to same antigen

37
Q

Describe active humoral immunity and two ways you can acquire it

A

a. Active immunity occurs when B cells actively produce specific antibodies
i. Naturally acquired: formed in response to
actual bacterial or viral infection
ii. Artificially acquired: formed in response to
vaccine of dead or attenuated pathogens

38
Q

Describe passive humoral immunity and two ways you can acquire it

A

a. Passive immunity occurs when ready-made antibodies are introduced into body (given to you)
i. Naturally acquired: antibodies delivered to fetus
via placenta or to infant through milk
ii. Artificially acquired: injection of serum, such as
gamma globulin
iii. Immunological memory does not occur
iv. Protection ends when antibodies degrade

39
Q

What are antibodies?

What are they also known as?

A

Antibodies—also called Immunoglobulins (Igs)—are proteins secreted by plasma cells and can be grouped into one of five Ig classes

40
Q

Describe the basic antibody structure

A

a. Y-shaped antibody monomer consists of four polypeptide chains linked by disulfide bonds
b. Four chains consist of:
c. Two identical heavy (H) chains
d. Two identical light (L) chains
e. Variable (V) regions at one end of each arm combine to form two identical antigen-binding sites
f. Stems makeup constant (C) regions that determines antibody class

41
Q

What are the major classes of antibodies (names, no details)

A

a. Five major classes: IgM, IgA, IgD, IgG, and IgE

42
Q

Describe antibody targets and functions

A

a. Antibodies do not destroy antigens; they inactivate and tag them forming antigen-antibody complexes
b. Defensive mechanisms caused by antibodies:
i. Neutralization
ii. Agglutination
iii. Precipitation
iv. Complement fixation

43
Q

Describe neutralization

A

Antibodies block specific sites on viruses or bacterial exotoxins or prevent antigens from binding to receptors on tissue cells

44
Q

Describe agglutination

A

a. Allows for antigen-antibody complexes to become cross-linked into large lattice-like clumps
b. Process referred to as agglutination
i. Example: clumping of mismatched blood cells

45
Q

Describe complement fixation and activation

A

When several antibodies are bound close together on same antigen, complement-binding sites on their stem regions are aligned

46
Q

Which cell is more complex than B cells in classification and function?

A

T cells

47
Q

Name two populations of T cells

A

a. CD4 cells usually become helper T cells (TH) that can activate B cells, other T cells, and macrophages
b. CD8 cells become cytotoxic T cells (TC) that are capable of destroying cells harboring foreign antigens

48
Q

Once primed by APC presentation of antigen, helper T cells:

A

a. Help activate B cells and other T cells
b. Induce T and B cell proliferation
c. Secrete cytokines that recruit other immune cells

49
Q

Without TH, there is no _______

A

Immune response

50
Q

Describe Cytotoxic T (T3) cells (CD8)

A

a. Directly attack and kill other cells using a lethal hit using two mechanisms:
b. Perforins create pores through which granzymes enter target cell and stimulate apoptosis

51
Q

Describe complement (inflammation)

A

c. C3a and C5a cleavage products amplify inflammation by:
d. Stimulating mast cells and basophils to release histamine
e. Attracting neutrophils and other inflammatory cells

52
Q

Describe IgM

A

b. IgM
i. Pentamer (larger than others); first antibody released
ii. Readily activates complement

53
Q

Describe IgA

A

c. IgA (secretory IgA)
i. Monomer or dimer; found in mucus and other secretions
ii. Helps prevent entry of pathogens

54
Q

Describe IgD

A

d. IgD

i. Monomer attached to surface of B cells

55
Q

Describe IgG

A

e. IgG
i. Monomer; 75–85% of antibodies in plasma
ii. Crosses placental barrier

56
Q

Describe IgE

A

f. IgE
i. Monomer causes basophils to release histamine
ii. Active in some allergies and parasitic infections