immune ii Flashcards

1
Q

Adaptive immune system

A
  • protects against infectious agents and abnormal body cells
  • amplifies inflammatory response
  • activates complement
  • must be primed by initial exposure to specific foreign substance
  • Specific, systemic, and has memory
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2
Q

humoral immunity

A
  • antibodies, produced by lymphocytes, circulating freely in body fluids
  • bind temporarily to target cells –> temporarily inactivate and mark for destruction by phagocytes or comlement
  • has extracellular tergets
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3
Q

Cellular immunity

A

lymphocytes act against target cell:

  • directly by killing infected cells
  • indirectly by releasing chems that enhance inflammatory response or activating other lymphocytes or macrophages
  • has cellular targets
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4
Q

Antigens

A
  • substances that can mobilize adaptive defenses and provoke an immune response
  • targets of all adaptive immune responses
  • most are big, complex molecules not normally found in body (non-self)
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5
Q

Complete antigens

A
  • Immunogenicity = ability to stimulate proliferation of specific lymphocytes
  • reactivity = ability to react with activated lymphocytes and antibodies released by immunogenic reactions

-e.g. foreign protein, polysaccharides, lipids, and necleic acids

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6
Q

Haptens (incomplete antigens)

A
  • small molecules, not immunogenic by themselves (peptides, nucleotides, some hormones)
  • may be immunogenic if attached to body proteins and combination is marked foreign
  • causes immune system to mount harmful attack

e.g. poison ivy, animal dander, detergents, and cosmetics

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7
Q

Antigenic determinants (epitopes

A
  • only certain parts (antigenic determinants) of entire antigen are immunogenic
  • antibodies and lymphocyte receptors bind to them as enzyme binds substrate
  • most naturally occuring antigens have numerous epitopes that mobilize several dif lymphocytes and form dif kinds of antibodies angainst them
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8
Q

MHC proteins (major histocompatibility complex)

A

Self antigens on surface of cells
MHC antigens
-MHC or human leukocyte antigens
-normal func to help T cells recognize foreign or self
-class I MHC = built into all body cells except RBCs
-Class II MHC = only on antigen presenting cells

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9
Q

Three cells of adaptive immune system

A
  1. B lymphocytes (humoral immunity)
  2. T lymphocytes (cellular immunity)
  3. Antigen presenting cells (APCs) (Don’t respond to specific antigens; play essential auxiliary role in immunity)
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10
Q

5 general steps of lymphocyte development

A
  1. Origin - all originate in red bone marrow
  2. Maturation - in thymus or bone marrow
  3. Seeding secondary lymphoid organs and circulating
  4. Antigen encounter and activation
  5. Proliferation and differentiation
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11
Q

Lymphocyte maturation

A
  • “educated” to become mature –> B cells in bone marrow, T cells in thymus
  • Immunocompetence: lymphocyte can recognize one specific antigen by binding to it –> B and T cells only have one type of antigen receptor
  • Self-tolerance = lymphocytes unresponsive to own antigens
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12
Q

B cell maturation

A

-mature in red bone marrow
-positively selected if successfully make antigen receptors
-those that are self-reactive are eliminated by apoptosis (clonal deletion
0

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13
Q

Seeding secondary lymphoid organs and circulation

A
  • immunocompetent B and T cells not yet exposed to antigen called naive
  • exported from primary lymphoid organs (bone marrow and thymus) to “seed” secondary lymphoid organs (lymph nodes, spleen, etc…) –> increases chances of encountering antigen
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14
Q

clonal selection

A
  • naive lymphocytes’ first encounter with antigen –> selected for further development
  • If correct signals present, lymphocyte will complete its differentiation
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15
Q

Antigen Receptor Diversity

A

-genes, not antigens, determine which foreign substances immune system will recognize –> immune cell receptors result of acquired knowledge of microbes likely in environment

Lymphocytes make up to a billion types of antigen receptors –> coded for by 25ooo genes –> gene segments are shuffled by somatic recombination

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16
Q

Antigen presenting cells (APCs)

A
  • engulf antigens
  • present fragments of antigens to T cells for recognition

Major types

  • dendritic cells in CT and epidermis
  • Macrophages in CT and lymphoid organs
  • B cells
17
Q

Dendritic cells (APC)

A
  • phagocytize pathogens
  • enter lymphatics to present antigens to T cells in lymph node
  • most effective antigen presenter
  • key link bt innate and adaptive immunity
18
Q

Macrophages (APC)

A
  • widespread in lymphoid organs and CT

- present antigens to T cells to activate themselves into voracious phagocytes that secrete bactericidal chemicals

19
Q

B lymphocytes (APC)

A
  • don’t activate naive T cells

- present antigens to activated helper T cells to assist own activation

20
Q

Exogenous antigens

A
  • present in fluid outside body cells

- APCs ingest antigen, process, and place next to MHC-II molecule in plasma membrane, and present to T cells

21
Q

Endogenous antigens

A
  • antigens inside body cells

- infected cell displays antigen next to MHC-I

22
Q

Antibody mediated immunity

A
  • During activation, antigen binds to B cell receptor
  • Can respond to unprocessed antigen
  • Response much more intense when B cell processes antigen –> antigen taken into B cell, combined with MHC-II, moved to plasma membrane–> helper T cell binds and delivers costimulation (interleukin 2 and other cytokines)

-B cell undergoes clonal selection: plasma cells secrete antibodies –> memory B cells don’t secrete antibodies, but wait for reappearance of antigen

23
Q

Immunological memory: primary immune response

A
  • cell proliferation and differentiation upon first antigen exposure
  • lag period: 3-6 days
  • peak levels of plasma antibody are reached in 10 days
  • antibody levels then decline
24
Q

Immunological memory: secondary immune response

A
  • re-exposure to same antigen gives faster, more prolonged, moreeffective response
  • sensitized memory cells respond within hours
  • antibody levels peak in 2-3 days at much higher levels
  • antibodies bind with greater affinity
  • antibody level can remain high for weeks to months
25
Q

Active humoral immunity

A

-when B cells encounter antigens and produce specific antibodies against them

2 types:

  • Naturally acquired = response to bacterial or viral infection
  • Artificially acquired = response to vaccine or dead/attenuated pathogens
26
Q

Vaccines

A
  • mostly dead or attenuated pathogens
  • spare us symptoms of primary response
  • provide antigentic determinants that are immunogenic and reactive
27
Q

Passive humoral immunity

A
  • readymade antibodies introduced into body
  • B cells aren’t challenged by antigens
  • immunological memory doesn’t occur
  • protection ends when antibodies degrade
28
Q

2 types of passive humoral immunity

A
  1. Naturally acquired = antibodies delivered to fetus via placenta or to infant through milk
  2. Artificailly acquired = injection of serum, like gamma globulin –> immediate protection, but ends when antibodies naturally degrade in body