Immune system 2 Flashcards

1
Q

Primary lymphoid structures

A

thymus
bone marrow
site of formation, differentiation and maturation of lymphoid cells
no antigen contact

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2
Q

Secondary lymphoid structures

A

spleen
lymph nodes
tonsils & adenoids
Peyer’s patches
contains both T and B cells
Have contact with antigens
Allow initiation of adaptive immune response

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3
Q

Humoral immunity

A

through the blood/humors of the body
protection against extracellular microbes
B lymphocytes and antibodies secreted by B lymphocytes

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4
Q

Cell-mediated immunity

A

protection against intracellular microbes
T lymphocytes

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5
Q

Lymphocytes

A

very specific to antigens but are also very diverse
can migrate to sites of inflammation
lymphocyte classes do not interact with each other unless a stimulus is present (antigen, chemical messengers)

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6
Q

Naive cell

A

mature lymphocyte that has not encountered its specific antigen

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7
Q

Effector cell

A

differentiation of lymphocyte after antigen recognition, functions to eliminate microbes

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8
Q

Memory cell

A

differentiated lymphocyte after antigen recognition, in a state of heightened awareness to more effectively fight microbe if it returns

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9
Q

B lymphocytes

A

produced and mature in the bone marrow
provide humoral immunity
have membrane bound antibodies
once activated –> differentiate into memory B cells and effector cells
professional APC

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10
Q

effector B cell

A

come from plasma cells
produce circulating antibodies

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11
Q

If B cells are naive

A

must have T helper cells and chemical messengers to differentiate and multiply

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12
Q

Fab region on antibodies

A

antigen-binding fragment that contain recognition sites for antigen
contain variable regions that determine antigenc specificity

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13
Q

Fc region on antibody

A

crystalline fragment that is constant, responsible for activation of complement cascade and opsonization
Defines the class of the antibody (IgE, IgG, etc)

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14
Q

T lymphocytes

A

cell mediated immunity
mature in the thymus
once activated: differentiate
T cells cannot recognize antigens directly, T cells recognize antigen peptides presented on MHC

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15
Q

T helper cells (Th)

A

T helper effector cells: release cytokines and raise the alarm bells
have CD4 co-receptors –> bind to MHC 2
attracted to antigens presented that occurred from OUTSIDE of the cell (exogenous)
must be present to fully activate naive B cells (double check)

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16
Q

Cytotoxic T cells (Tc)

A

Tc effector cells: kill bad cells
have CD8 co-receptors –> bind to MHC 1
attracted to antigens presented that occurred from INSIDE the cell (endogenous)

17
Q

regulatory T cells (Treg)

A

subpopulation of Th cells – controls or limits the immune response, releases immunosuppressive cytokines, suppress antigen recognition

18
Q

Each B or T cells have only a

A

single receptor specificity and can only recognize one single antigen

19
Q

Generation of clonal diversity primarily occurs in

A

the fetus

20
Q

Clonal diversity is developed…

A

before any exposures to antigens occur
occurs primarily in lymphoid organs

21
Q

Where are T cells developed

A

liver in fetus
bone marrow in adults

22
Q

Central tolerance for T cells

A

the deletion of auto-reactive T cells within the thymus

23
Q

TCR that respond to self antigens are considered

A

auto reactive T cells

24
Q

Clonal deletion

A

a T cell undergoes apoptosis during maturation in the thymus

25
Q

Positive selection

A

process by which T cells are screened so that only those capable of binding to MHC are kept alive

26
Q

Negative selection

A

the process by which T cells are screened so that those with a high affinity for binding to self antigens (and potentially causing autoimmunity) are destroyed

27
Q

AIRE

A

autoimmune regulation = transcription factor
produced by medullary thymus epithelial cells and controls synthesis of self proteins found in periphery
allows expression of tissue-specific self antigens (TSAs) within the thymus medulla

28
Q

Peripheral tolerance in T cells

A

the deletion or anergy of lymphocytes that recognize self antigen in peripheral tissue

29
Q

Types of peripheral tolerance

A

Ignorance
Suppression
Anergy
Activation induced cell death

30
Q

Ignorance in T cells

A

T cell does not have opportunity to come in contact with antigen – held captive in lymph

31
Q

Suppression of T cells

A

t-regulatory cells is important in dampening the immune response

Ex: secretes cytokines IL-10 and TGF-beta

32
Q

Anergy of T cells

A

normal cell will not have co-stimulatory signal that an APC has

Ex: no B7 co-stimulation or Ag may not be presented within MHC

no cytokine activity from innate immune system

33
Q

Activation induced cell death

A

cell is activated repeatedly and induce apoptosis

Ex: reactivated cells induce Fas/FasL binding –> self apoptosis

This occurs mainly to cytotoxic T cells

34
Q

Central tolerance for B cells

A

in bone marrow

reactive B cells to self antigens undergo Ag receptor gene rearrangement

‘try again’ method

if this fails –> apoptosis

35
Q

Peripheral tolerance in B cells

A

anergy: B cells usually require TH activation

lack of this –> anergy or apoptosis

36
Q

Ignorance in B cells

A

B cells in lymph nodes will not see self ag

Will not meet appropriate Th cell with the same self ag binding