Immunology Immune Cells and Organs Flashcards

1
Q

How does the lymphatic system operate?

A

Fluid drained from between tissue cells absorbed into lymph
- 2 to 3 litres of lymph are returned to the blood each day (via superior vena cava)
- In the process of draining, lymph can “capture” pathogens
- Fluid passes through lymph nodes which survey for pathogens

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2
Q

What is the whole process of function of lymph nodes? Movement of lymph, shape of lymph nodes, entering and exiting, names of junctions,

A

LYMPH NODES
- Kidney shaped organs > 1cm
- During immune response, swell in size
- Fluid enters through AFFERENT vessel
- Fluid leaves via EFFERENT vessel
- Lymph perculates through all lymphocytes before
leaving the node
- Usually a SUMMATIVE junction, i.e. there are many
afferent vessels but one efferent vessel
- Rich blood supply lets lymphocytes into the lymph
nodes via the HIGH ENDOLTHELIAL VENUES
- T-cell zone: parafollicular cortex
- B-cell zone: lymphoid follicle- mostly on the periphery of the lymph node
- During immune response, there is a massive proliferation of B cells, which leads to the formation of a
GERMINAL CENTRE
- Specific chemokines target their respective lymphocytes to their specific areas, e.g. T-cells to the
parafollicular cortex
- The lymph entering lymph nodes may also contain cells such as dendritic cells and macrophages

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3
Q

What is the spleen used for? Process? Structure?

A

Spleen
- Filter for antigens in the blood
- Large organ in the abdomen
- Separated into
white pulp: lymphoid cells around blood vessels, full of lymphocytes
red pulp: contains old damaged RBC
- Any diseases involving RBC, i.e. sickle-cell, often results in an enlargement of the spleen

  • T cell area: peri-arteriolar lymphatic sheath (PALS)
  • B cell area is located further away from blood vessels
  • Not a vital organ: Individuals who do not have a spleen are highly susceptible to infections with encapsulated bacteria
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4
Q

What does the mucosal associated tissue do?

A

Mucosal Associated Lymphoid Tissue (MALT)
• Epithelium is the first line of defence
• mucosae and skin form a physical barrier
• very large surface area, in large part a single layer of cells
• heavily defended by the immune system in case it breaks

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5
Q

Secondary Lymphoid Organs

Gut Associated Lymphoid Tissue - Structure, Function?

A
  • Many villi, plus smoother regions
  • Involved in the mesenteric lymphatic drainage system to mesenteric lymph nodes, including intraepithelial lymphocytes
  • PEYER’S PATCH: non-capsulated aggregation
    of lymphoid tissue- predominantly B lymphocytes and contain germinal centres during immune responses
  • M-CELLS: sample contents of the intestine, surveying for pathogens which they can then deliver to immune cells
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6
Q

What is the function of the cutaneous immune system?

A

Cutaneous Immune System
- I.e. the skin
- Epidermis contains keratinocytes, Langerhans cells
and intraepidermal lymphocytes
- The dermis heavily guards the epidermis with
immune cells, e.g. macrophages, T lymphocytes etc
- The demis also consists of venules and lymphatic
vessels, providing entry to the blood circulation and drainage to regional lymph node

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7
Q

What are the primary lymphoid organs? And elaborate on them.

Hint: Where the process happens, Shape,

A

Bone Marrow
- Site of haematopoesis, i.e. generation of blood cells
- In an embryo, this happens in amniotic sac
- In foetus, occurs in all bones, liver and spleen. Marrow is also very
cellular
- In adults, this occurs mostly in flat bones, vertebrae, Iliac bones, Ribs
and the ends of long limbs

Thymus
- Where maturity of T-cells occurs
- Bi- lobed
- Medulla and cortex regions
- No change during immune response to antigens, continuous development of T cells
- Hassalls’ corpuscle secretes soluble factors, and is important in regulatory T cells

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8
Q

What is the problem of lymphocytes meeting antigen?

A

Large number of T cells with different specificities
Large number of B cells with different specificities
BUT limited amounts of antigen
How does the body ensure that the antigen meets lymphocyte with specific receptor?

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9
Q

What is lymphocyte recirculation?

A
  • Pathogen on mucosal surface
  • Naive lymphocytes leave BM and Thymus and enter the bloodstream
  • Recirculate through peripheral lymphoid tissue
  • Recognition of antigen would result in massive B cell proliferation in secondary lymphoid tissue (lymphocyte activation)
  • Otherwise the lymphocytes die
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10
Q

Describe process of extravasion of naive T cells into lymph nodes

A

Extravasion of naive T cells into the lymph nodes (occurs during immune response)
- The naive T cell “rolls” along the
epithelium
- These are then stopped and
activated by specific chemokines at a particular place on the epithelium. This “right place” is determined by SELECTINS
-INTEGRINS then increase adhesion of the T cell to the epithelium, leading to arrest of the cell Transendothelial migration of the T cell from the bloodstream into the lymph node then occurs
Antigens also enter the lymph nodes via the draining lymphatics
Naive lymphocytes recirculate approx once per day – enter lymph node—high endothelial venue – lymphocyte is activated by antigen – stops recirculatng – massive proliferation of B lymphocytes – reenter the blood via the superior vena cava (via the efferent vessel) – target invading microbes/pathogen

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11
Q

What are CD markers?

A

CD Markers
Found in T and B lymphocytes with agranular cytoplasm
• an internationally recognised systematic nomenclature for cell surface molecules
• used to discriminate between cells of the haematopoietic system
• more than 300 CD markers
• clinical importance e.g. CD4 in HIV

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12
Q

Compare and Contrast phenotypic characteristics of B and T cells.

A

T Lymphocytes
• all express CD3- antigen specific receptor (TCR)
• gamma sigma TCR, about 10% in blood
• alpha sigma TCR, about 90% in blood: ~2/3 express CD4, ~1/3 express CD8. All mature T cells express one or the other
 CD4+ = T helper cells, regulatory T cells- Secrete cytokines
 CD8+ = cytotoxic T cells- Lyse infected cells, secrete cytokines
• Thymic output of naive T cells declines with age, and the thymus atrophies. Therefore older people have a
reduced ability to respond to new infections. However the total number of T cells does not change, there are just more memory cells.
ANTIGEN RECOGNITION
• only recognise processed antigen presented at the surface of another cell using T cell receptor
• antigen is presented by an MHC molecule

B lymphocytes
• Produced by and develop in bone marrow
• Surface antigen receptor (B cell receptor) : immunoglobulin like molecule
• Express CD markers CD19 & CD20 (not CD3, CD4 or CD8)
• Express MHC Class II (can present antigen to helper T cells)
• Effector function is to produce antibodies
ANTIGEN RECOGNITION
• recognise intact antigen free in body fluids (so not presented by another molecule)
• Use B cell receptor, a membrane anchored form of antibody linked to signalling subunits

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13
Q

Give examples of antigen presenting cells (APCs) and their locations

A

Antigen presenting cells (APC)
cells that can present processed antigen (peptides) to T lymphocytes to initiate an acquired (adaptive) immune response:

Dendritic cells (DC)
- Location: Widely spread e.g. Skin & mucosal tissue
- Presents to T cells

B lymphocytes
- Location: lymphoid tissue
- Presents to T cells

Macrophages (activated)
- Location: lymphoid tissue
- Presents to T cells

Follicular dendritic cells
- Location: lymph node follicles
- Presents whole antigens to B cells

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