2. Control of the Immune Response Flashcards

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1
Q

once an immune response is initiated, it can be rapidly expanded, therefore for an efficient immune response, __ __ must exist

A

regulatory mechanisms

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2
Q

regulation of immune responses: 2 regulations by antigen

A

immunity and tolerance

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3
Q

regulation of immune responses: 3 major regulators

A

antigen, antibody, cytokines

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4
Q

intrinsic properties and extrinsic factors affect the immunogenicity of proteins

A

size, dose, route, composition, form, similarity to self protein, adjuvants, interaction with host MHC
- amount of antigen affects immunogenicity response (intermediate dose will increase immunogenicity; high or low dose will decrease immunogenicity)

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5
Q

4 ways of regulation by antibody

A
  • antigen blocking
  • receptor cross-linking
  • passive regulation of antibody affinity
  • idiotypic regulation
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6
Q

antigen blocking

A
  • competition for antigen with antigen receptor on B cells
  • process is dependent on:
    • antibody concentration
    • antibody affinity
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7
Q

receptor cross-linking

A

antibody, when bound to antigen, can inhibit B cell differentiation by cross-linking antigen receptors with Fc receptors on B cells

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8
Q

passive regulation of Ab affinity

A
  • antibody in low concentrations cannot completely inhibit further antibody production but by sequestering some of the free antigen, it makes it scarce
  • only B cells with high affinity receptors for the antigen will bind it
    • these cells are the ones that will selectively differentiate and make antibodies of high affinity for the antigen
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9
Q

4 properties of cytokines

A
  • pleiotropism
  • redundancy
  • synergy
  • antagonism
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10
Q

cytokines in innate immune response

A
  • macrophages, dendritic cells, and NK cells are major producers of TNFalpha, IL-1, IL-6, IL-8, and many chemokines (these are all important intercellular communicators, inducing inflammation, and immune responses)
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11
Q

viruses and some bacteria induce IL-12 secretion by dendritic cells that can activate NK cells to produce IFNgamma, what happens next?

A

naive CD4 T cells, activated in the presence of IL-12 and IFNgamma, are committed to differentiate into Th1 cells

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12
Q

other pathogens (e.g. worms) may cause the synthesis and secretion of IL-4 by NKT cells, what happens next?

A

naive CD4 T cells activated in the presence of IL-4 are committed to differentiate into Th2 cells

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13
Q

cytokines in adaptive immune response

A
  • if an adaptive or cell-mediated response develops, T cells (especially CD4+) become a major producer of cytokines
  • their effects generally either promote or control further responses and they include IL-2, IL-4, IL-5, IL-10, IL-13, IL-17, IL-22, and TGFbeta (second wave of cytokines)
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14
Q

mechanisms of helper T cells mediated activation of B lymphocytes

A
  1. activated helper T cell expresses CD40L, secretes cytokines
  2. B cells are activated by CD40 engagement, cytokines
  3. B cell proliferation and differentiation
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15
Q

costimulatory signals

A

communicate between two cells

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16
Q

depending on the T cell costimulatory molecule and its ligand, you can have __ or __ stimulation

A

positive or negative

17
Q

idiotype

A

antigenic constitution of the variable region of an Ig molecule

18
Q

idiotopes

A

antigenic determinants of which the idiotype is made up

19
Q

paratope

A

part of the variable region which forms the antigen binding site

20
Q

anti-idiotype

A

antibody that recognizes idiotypic determinants of other antibodies (reacts to foreign-looking binding site of another Ab)
- anti-idiotypic Ab must have their own idiotypes, and Ab against those idiotypes must also exist (anti-anti-idiotypic Ab) and so on

21
Q

what does Jerne’s proposed idiotype network say about anti-idiotypic antibodies

A

anti-idiotypic antibodies do exist in circulation but Jerne’s network, while theoretically possible, proved not to play a major role in the regulation of Ab response (unlikely to cause major up/down regulation)

22
Q

major participants of cell network

A
  • macrophages
  • lymphocytes (particularly T lymphocytes)
    • helper T cells
    • regulatory T cells
    • B cells
23
Q

cellular networks control what?

A

up/down regulation

24
Q

regulatory T cells (Tregs)

A
  • aka suppressor T cells
  • subpopulation of T cells that modulate the immune system
  • maintain tolerance to self antigens and prevent autoimmune disease
  • immunosuppressive and downregulate the induction and activation of effector T cells
  • suppress the immune responses of other cells
  • “self-check” for the immune system to prevent excessive reactions
  • involved in shutting down responses after they have successfully eliminated invading organisms, and also in preventing autoimmunity
25
Q

T cell precursor cells within the thymus develop into cells with different effector functions

A
  • Tp (T cell precursor starts in thymus)
  • CD4+ and CD8+ (periphery)
26
Q

CD8+ cytotoxic T cell

A
  • kills infected target cell
  • participates in macrophage activation
  • releases perforin and granzymes
27
Q

CD4+ Th1 cell

A
  • produces IFNgamma
  • promotes cellular activity
  • participates in macrophage activation
28
Q

CD4+ Th2 cell

A
  • produces IL-4, IL-5, IL-13
  • promotes humoral immunity
  • promotes antiihelminth responses
29
Q

CD4+ Th17 cell

A
  • produces IL-17
  • involved in host defense and pathogenesis of autoimmune disease
30
Q

CD4+ Treg cell

A
  • modulates immune response