immune response in peripheral lymphoid organs Flashcards

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1
Q

What happens to the B + T lympcytes after they mature and become immunocompetent in central Lymph organs

A

move to the peripheral or secondary lymphoid organs.
There, immune response is mounted and
carried out.

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2
Q

what is antigen dependant differentiation

A

Lymphocytes meet antigen and are
activated by it. They proliferate to clones
and differentiate to effector and memory
cells.

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3
Q

examples of peripheral lymphoid organs

A

lymph nodes, spleen, + mucosa-
associated lymphoid tissue (MALT).

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4
Q

what do lymph nodes do + why they swell with infection

A

Antigens penetrating tissues (esp.
after injury) will be drained by lymph and brought
to the nearest lymph node to be dealt with.

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5
Q

Structure of lymph node

A

covered in capsule of conn tissue

  • cortex - mostly a B-cell area. It contains cell
    aggregates called follicles.
  • paracortex - a T-cell area. There, T
    lymphocytes proliferate in cellular immune
    response.
  • medulla - rich in antibody-secreting plasma
    cells.
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6
Q

what are the follicles called if they are engaged in immune response and when they engaged in humoral response

A
  1. primary (small and dense)

2.secondary (enlarges + middle
forms area called germinal center. This is site of proliferation + antigen-dependent differentiation of B lymphocytes.)

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7
Q

What are HEV in lymph nodes

A

High Endothelial Venules

specialized blood vessels that deliver naïve lymphocytes from the bloodstream into the lymph nodes, where lymphocytes become matured by antigen-presenting cells
(e.g., dendritic cells).

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8
Q

how do lymphocytes exit into blood

A

through efferent lymph vessels and into thoracic duct

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9
Q

Steps of B cell differentiation in follicle

A
  1. Antigen recognition at
    the periphery of follicle.
  2. Stimulation by Тh (at the periphery).
  3. If B cells stay at PERIPHERY, they do not
    undergo class switch and
    hypermutations; differentiated into SHORT- lived plasms cells.

4 B clells that enter GERMINATIVE CENTER of follicle undergoes class switch + somatic hypermutations. differentiated into LONG lived plasma + memory cells

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10
Q

what does spleen do

A

reacts against blood borne antigens

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11
Q

structure of the spleen

A

RED pulp - formed by cords + vascular sinuses. function = blood storage

WHITE pulp - is lymphoid organ. concentrated around arterioles

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12
Q

page 9 for image of spleen. what is the periarteriolar. what is marginal zone

A
  1. lymphoid tissue closest to the arteriole (t cell area)
  2. peripheral white pulp bodering red (B cell area)
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13
Q

What does Musosa assoc lymphoid tissue (MALT) do

A

reacts against antigens encountered at mucosal surfaces of respiratory, gastro-intestinal and genito-urinary tract.

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14
Q

why is MALT also called non encapsulated lymphoid tissue. examle organs

A

its organs lack conn tissue capsules

tonsils, adenoids, peyers patches + appendix

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15
Q

what kind of Ig does mucosa assoc humoral immunity rely on comapered to humoral immune response

A

IgA
humoral response = IgG

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16
Q

what are MALT subcompartments

A

nasopharynx-associated lymphoid tissue,
bronchus-associated lymphoid tissue
gut-associated lymphoid tissue
genital tract-associated lymphoid tissue.

17
Q

does immune response occur in mammary glands

A

NO
but IgA antibodies are secreted to combat antigens in nasopharynx + gut

18
Q

Phases in immune response

A
  1. Antigen presentation + recognition.
  2. Lymphocyte activation.
  3. Lymphocyte proliferation (clonal expansion) and antigen-specific differentiation.
  4. Antigen elimination (effector phase).
  5. Contraction of the immune response.
  6. Memory.
19
Q

what a is the effector phase

A
  • elimination of antigen mediated by specific antibodies
    and T cells. carried out i peripheral lymph organs

-

20
Q

how are effectors made

A

interction btw T + B lymphocytes and antigen presenting cells

  • they interact by contact dependant and parcrine signalling (cytokines)
21
Q

what are t lymphocytes that haven’t participated in immune response called

A

naive , virgin, unprimed. in resting state

22
Q

how is a naive t cell activated

A

TCR needs to be engaged
co stimulatory signal needed ( delivered by membrane protein B7)

23
Q

what do dendritic cells express and where they found

A

MHC both classes+ B7

found under skin + mucosa (pathogens invade here)
in skin they called Langerhans cells)

24
Q

how does the dentritic cells activate t cells

A

After phagocytosing a particle, the dendritic cell migrates to nearest lymphoid organ to present its digested antigens.
There, it activates T cells, even if they are naïve.

25
Q

requiments for t helper cell activation

A

contact with MHCII + peptide and B7

26
Q

how are T killers activated

A

antigen presentation of MHC I + B7 AND TH1 helper recognizing same antigen

  • T killers and T helpers specific for the same antigen stay close but cant recognise eachother
  • they meet on the surface of antigen-presenting cell.
  • The activation signal from the T helper is a cytokine, most likely interleukin 2
27
Q

How do dendritic cells present peptides both by MHC-I and MHC-II (antigen cross presentation)

A

After phagocytosis in dendritic
cell, pathogen is processed
in lysosomes + presented by
MHC-II to be detected by T helper.

Some protein molecules of the same pathogen can be
transferred to proteasomes;
these will be presented by MHC-I
to be detected by Tc.

This allows DC to contact both
Th and Tc and to keep them
close to each other.

28
Q

what else can antigen cross presentation allow dendtritic cells do

A

present viral antigens without being
infected by the virus.

29
Q

Once activated, T cells start to divide, forming
clones. what happens after this

A

proliferation by interlukin 2.
they become effector cells

when activated t cell recognises antigen with appropriate MHC, its triggered to act

30
Q

Is there a need for co simulatory signals for activated t cells.

A

No doesnt need B7 or interleukin 1 to kill

31
Q

so how does activated TC kill

A

they activate T killers + macrophages, and activated Th2 cells activate B cells.
Activated T killers and Th1 helpers do not stay only
in lymphoid organs but disseminate to other organs
by circulation.

32
Q

B cells only hv IgM receptors (as from bone M) for immune response they need IgD too. where do they get

A

obtain it from the same genes by alternative RNA processing and coexpress IgM and IgD.

33
Q

activation of B cells

A
  1. do not need antigen presentation as T cells do. (can present antigen alone so acts like Ag presenting cell)
  2. Thymus independent antigens causes B cells recognising them to proliferate and differentiate to secrete IgM antibodies
34
Q

what is specific abt germline centre B cells

A

high affinity, class switched antibodies
requires somatic hypermutation to dvlp

they origin of best memory B cells

35
Q

whats specific abt short lived antibodies

A

quickly forms in secondary lymph organs but apoptosis few days after antibody secretion.

some survive and become part of long term humoral immunity

36
Q

Most antigens are T-dependent and cannot
activate naïve B cells by themselves. They
need a T helper of Th2 type.
how do these recognise eachtoher

A
  1. B cells internalize antigen bound to their
    receptors, process it + present it with class
    II MHC.
  2. allows B cells to be recognised by T helpers specific for same antigen
  3. T helper induces B cell to proliferate a + differentiate by cytokines
37
Q

Unlike IgD whch uses alternative splicing, how can B cell produce IGg, IgA, Igd?

A

site specific recombinsation

similar to VDJ