Intro To Adaptive Immunity Flashcards

1
Q

What are the cell types in adaptive immunity?

A

B cells (secretes antibodies) and T cells (helper T cells and cytotoxic T cells which have different receptors)

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2
Q

What do B cells do?

A

Controls extracellular pathogens in peripheral tissues from hematopoietic stem cells -> lymphoid progenitor -> B-cell progenitor -> B cell

Has BCR (B-Cell RECEPTOR)

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3
Q

What do T cells do?

A

Control of intracellular pathogens

Helper T cells (Th cells) have cd4 molecule as receptor

Cytotoxic T cells (CTL) have cd8 molecule as receptor

Hematopoietic stem cell -> lymphoid progenitor -> T cell progenitor -> T helper cell or T cytotoxic cell (in thymus)

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4
Q

What is the different primary vs memory response?

A

Primary: first exposure to pathogens

Secondary/memory: subsequent exposure to same pathogen occurs larger and faster because memory b and T cells react at this response

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5
Q

What are the details of the primary immune response?

A
  1. Microorganism entry
  2. Establishment of infection
  3. Innate immune system starts inducing differentiation and clinal expansion from naive B and T cells
  4. Effector b and T cells control infection
  5. Effector B and T cells die through apoptosis
  6. Memory B and T cells remain in system for secondary response
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6
Q

What is the difference between effector and memory cells? How do they arise

A

Naive B/T cells differentiate into

Effector cells:
B cells -> plasma cells

helper T cells and cytotoxic t cells

Memory cells: remain after infection is resolved

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7
Q

What is the benefit of vaccination?

A

Primary immune response is skipped and adaptive response can work at real infection through immunological memory because more effector B and T cells produced

Memory of antibodies and cd8 and cd4 remain longer after infection

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8
Q

What are the primary and secondary lymphoid organs?

A

Primary: bone marrow and thymus (located above heart)

Secondary: lymph node

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9
Q

What is a general overview of what and where things occur in an immune response?

A
  1. Infection at barrier
  2. Innate immunity
  3. Lymphatic flow in to lymph node containing pathogen infected cell
  4. Lymphocyte development from bone marrow (B cell) and thymus (T cells) and movement through blood flow into lymph nOde
  5. Lymphocyte activation and different ion in lymph node to control pathogen
  6. Lymphatic flow out contains B and T cells to heart and out through blood
  7. B and T cells released to control other infected cells
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10
Q

What are the two types of lymphoid tissue? What occurs at each?

A

Primary lymphoid tissue: where lymphocytes are developed
- bone marrow (B cells and development of T cells)
- thymus (2nd development of T cells)

Secondary lymphoid tissue: where naive lymphocytes are further differentiated
- lymph nodes
- spleen
-mucosa-associated lymphatic tissue (MALT)

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11
Q

What is the lymphatic system?

A

network of tissues, vessels and organs that work in close proximity with the circulatory system

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12
Q

What is lymph?

A

interstitial tissue fluid that enters the lymphatic vessels to be transported by into the blood

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13
Q

What might the lymph carry?

A

pathogens or cellular waste and enter lymph nodes
- this is why surveils these entry points - lymph nodes and vessels

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14
Q

What is the connection between the lymphatic system and circulatory system?

A
  1. lymphatic capillaries run parallel to blood capillaries in all body tissues
  2. lymph leaves these tissues it carries waste products from tissues including dead cells, CO2, and pathogens
  3. lymph then passes and filters through lymph nodes
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15
Q

What is the significance of lymphatic vessels for injections?

A

injection into muscle where lymphatic vessel is to optimize immune response

(typically intramuscular on the arm where there is good blood flow)

injected vaccine components travel in the lymph to the nearest lymph nodes (arm pit)

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16
Q

How do T-cells develop?

A
  1. starts in bone marrow
  2. development continues in thymus lobule
  3. Double positive with both cd4 and CD8 receptors
  4. Differentiate into CD4+ (Th) and CD8+ (ctl) naive cells
17
Q

What are the parts of a lymph node?

A
  • artery vein (circulatory system)
  • efferent & afferent lymphatic vessel (lymphatic system)
  • germinal centre
  • T cell zone
  • B cell zone

T cells and B cells colocatized at the follicular border allowing for interaction

18
Q

What is the purpose of mucosa-associated lymphoid tissue?

A

Site where B and T cells meet pathogens in mucosal area

Contains m cells (micro fold) which helps transport antigens into the tissue

19
Q

Where is MALT found?

A

oral-pharyngeal cavity and gastrointestinal, respiratory, and urogenital tracts

(Tonsils, lungs, colon, appendix)

20
Q

What is the role of the spleen?

A

Filters blood so blood flows in and out

shows B and T cell meeting blood-borne pathogens which is why immune system surveils here

Similar organization to to lymph nodes

21
Q

How are tonsils protected by the immune system?

A

Mucosa tissue located for inhaled and ingested pathogens

Nasopharynx (monitors respiratory tract)
Oropharynx (monitor the gastrointestinal tract)

22
Q

How are pathogens recognized?

A

Surface receptors:

T-cell receptors (TCR)
B cell receptors (BCR)

23
Q

What do naive T cells and B cells do once developed from thymus and bone marrow?

A

Enters circulation and migrate to SLTs to look for pathogens

24
Q

What do B cell receptors look like?

A
  • variable region contains light and heavy region
  • constant region is mainly heavy chain and some variable chain
  • v shaped antigen binding site
  • transmembrane region
  • cytoplasmic tail
25
What do T cell receptors look like?
- variable region contain alpha and beta segments - constant region - transmembrane region - cytoplasmic tail -antigen-binding site on variable region
26
What are antigens?
(anti body generators) - any substance that the variable region of a BCR/TCR can bind to - a microbe expresses many copies of its own unique antigen
27
Where can antigens be found?
- microbes - our cells (blood type has A,B, and Rh factor) - pathogens
28
What is the interaction between antigens and epitope?
antigens many contain several EPITOPE that are recognized by immune cells. the EPITOPE on the surface of the antigen is recognized by BCR/TCR based on shape and size
29
What is the difference between an antigen and PAMPs?
antigens are generally unique to a specific antigen receptor (BCR/TCR) and is used in adaptive response PAMPs are expressed by a wide variety of pathogens and is recognized by PRRs and is used in innate response
30
How does antigen recognition occur?
- shape and size of antigen determines specificity of recognition by antigen binding site of the receptor - antibodies can recognize linear (exposed) or conformational determinants in folded proteins
31
What is the difference between a B cell receptor (BCR) and an antibody?
- BCR is the membrane bound form that has a hydrophobic segment - antibody is the secreted form that has a hydrophilic segment THEY HAVE THE SAME ANTIGEN SPECIFICITY CAN BOTH BIND TO PATHOGEN DIRECTLY
32
What is a key difference between b and T cell receptors?
T cell receptors need the antigen to be presented to them by a molecule
33
How are B and T cell receptors diverse?
1. BCRs and TCRs have 2 variable regions 2. BCR: variable regions are heavy-chain and light-chain TCR: alpha and beta regions 3. variable regions have UNIQUE coding sequence through cell division and are not passed through germ line B and T cells express many exact copies of a receptor with a unique antigen binding site - adaptive immunity specificity is based on this
34
How is adaptive specificity achieved?
each b and T cell expresses a bar with a variable region specific for 1 unique peptide but have multiple copies of the same variable region around the cell to which the epitope on the antigen can bind
35
What is the process of deletion in primary lymphoid organs?
some clones of T and B cells that came from naive t and B cells are eliminated to get rid of self-recognizing receptors
36
What is clonal expansion?
an effector cell that encounter a pathogenic antigen use this process to proliferate more cells with the SAME SPECIFICITY