Regulation Tolerance Flashcards

1
Q

control of the immune response

A
  • response must be turned down when the antigen has been destroyed
  • failure may result in an AI
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2
Q

CTLA-4 competes with

A

CD28 for B7

-CTLA-4 causses an inhibitory response

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3
Q

PD-1

A

inhibitory receptor found on cytotoxic T cells
-it interacts with PD-L1 found on tumor cells and PD-L2 found on dendritic cells and macrophages thereby inhibiting the immune response

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4
Q

pembrolizumab and nivolumab

A

-anti-PD-1 checkpoint inhibitors

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5
Q

activation induced cell death

A

-activated T cells develop Fas Ligand that interacts with Fas normally presents on t cells results in apoptosis

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6
Q

T regulatory cells

A

-produce IL-10 and TGFbeta which supress T cells

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7
Q

IFN gama inhibits

A

TH2 cells

-produced by TH1

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8
Q

IL-4 inhibits

A
  • TH1

- produced by TH2

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9
Q

immunological tolerance

A
  • lack of response to a specific antigen

- failure to induce specific immunity to that antigen

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10
Q

self tolernce

A
  • unresponsiveness to self
  • occurs in the thymus (negative selection)
  • this is called a Central tolerance
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11
Q

peripheral tolerance

A

-cells that escape central olerance are dealt with by mechanisms of peripheral tolerance. This involves clonal deletion and clonal anergy

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12
Q

clonal deletion

-how is this mediated

A
  • continuous exposure to self antigens causes continuous stimulation of T cells causing apoptosis of autoreactive lymphocytes
  • this occurs by the process of activation-induced cell death (Fas-L)
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13
Q

clonal anergy

A

-absence of co-stimulatory signals especially B7-CD28

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14
Q

adult tolerance

A
  • difficult to induce
  • lack of co-stimulatory signals B7 and CD28 would fix but also would suppress the system overall
  • high dose of an antigen could cause tolerance under special circumstances but this is not useful in human situations
  • oral tolerance possible under special circumstances but this does not work in human trials
  • antigens without adjuvants may cause tolerance
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15
Q

autoimmune diseases

A
  • immunological response against self antigens due to loss of self tolerance
  • failure of negative selection in the thymus
  • failure of immunological control mechanisms
  • fundamental problem is an imbalance between immune activation and immune control
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16
Q

autoimmune hemolytic anemia

A
  • body creates antibodies against RBC’s

- blood film shows broken and fragmented red cells typical of hemolytic anemia

17
Q

immunological factors that could give rise to autoimmunity

A
  • exposure of hidden antigens (sympathetic opthalmia). damage to cell releases hidden antigen and immune response ensues
  • polyclonal lymphocyte activation: viruses (EBV) stimulate B cells nonspecifically or superantigens stimulate T cells
  • defective T cell regulation (TREGS and CTLA-4)
18
Q

super antigens

A
  • attaches to the outside of the T cell receptor and to the MHC class 2 molecule causing T cell activation
  • this happens nonspecifically
  • staphylococcal food poisoning and toxic shock syndrome
  • massive IL2 and IFN gama
19
Q

defective T cell regulation

A
  • T cell regulators (TREGS)

- CTLA-4: competes with CD28 for B7, if CTLA-4 is defective then there will be uncontrolled activation of the T cell

20
Q

genetic factors of autoimmunity

A
  • more common in family members.
  • increased incidence in twins
  • associated with many different MHC types
21
Q

microbial factors in AI

A
  • molecular mimicry
  • abnormal activation of lymphoid cells (EBV)
  • microbes may damage tissue leading to release of hidden antigens
  • microbes may function as adjuvants and stimulate immune responses
22
Q

Rheumatic fever

A

-caused by a strep infection that turns someones own immune system against them (molecular mimicry)

23
Q

hormonal factors of AI

A
  • most AI diseases are much more common in females
  • NZB/NZW mice
  • females die at 9 months
  • males die at 13 months
24
Q

damage to the tissues in AI may be mediated by

A
  • antibodies: autoimmune hemolytic anemia
  • T cells: crohns disease, IDDM, psoriasis, MS
  • both humoral and CMI: hasimotos thyroiditis or rheumatoid arthritis
25
Q

delayed sensitivity may cause

-these are t celll mediated AI diseases

A
  • insulin dependent diabetes mellitus
  • rheumatoid arthritis
  • multiple sclerosis
  • crohns disease
  • psoriasis
  • celiacs disease
  • these are primarily through t cell attack and may be followed by a secondary antibody production
26
Q

fetal tolerance

A

-fetuses are very easy to induce immunological tolerace in

27
Q

sympathetic opthalmia

A

-damage to one eye releases hidden antigens which will mount an immune response that could cause damage to the other eye

28
Q

polyclonal lymphocyte activation

A
  • this is an immunological factor contributing to AI
  • causes non-specific activation of lymphocytes
  • EBV (mono) stimulates B cells
  • superantigens stimulate T cells
29
Q

how could we treat t cell mediated AI diseases?

A
  • blocking the mhc-tcr interaction in the specific area which is being attacked
  • may be able to use antibodies to do so
30
Q

what is the most common AI disease in this country

A

-grave disease in women (hyperthyroidism)