Anatomy and Physiology of the Immune System Flashcards

1
Q
  1. Define: leukocytes, mononuclear cells, polymorphonuclear cells, granulocytes, mast cells, plasma and serum.
A

leukocytes:
– nucleated, white blood cells. They are in the buffy coat.
mononuclear cells:
– leukocytes whose nucleus has smooth outline –> become monocytes and lymphocytes.

polymorphonuclear cells:
– cells that have lobulated nuclei (aka granulocytes) –> basophils (related to mast cells), eosinophils, and neutrophils.
Granulocytes: -cells with granules in their cytoplasm, see above.

mast cells:
– basophils, kind of, but found in tissue instead of plasma. Involved with type I immunopathology (immediate hypersensitivity)

plasma and serum:
– plasma = blood without the actual cells; serum = plasma without clotting factors.

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2
Q
  1. Sketch schematically a neutrophil; eosinophil; basophil; small lymphocyte; lymphoblast; plasma cell; monocyte. Include the characteristic features which are used to distinguish each cell type.
A
  • Lymphocyte has round nucleus without much cytoplasm.
  • Lymphoblast has a big nucleus but with a bit more cytoplasm.
  • Plasma cells (differentiated B cells) have big nuclei with lots of protein product (ribosomes stain blue).
  • Neutrophils have lobulated nuclei with granules.
  • Eosinophils have lobular nuclei and orange granules.
  • Basophils have lobular nuclei (harder to see) and dark blue-black granules.
  • Monocytes have vacuoles, bigger nuclei, and lots of cytoplasm, some granules.
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3
Q
  1. List the normal adult white cell count and differential percentages. From these, calculate absolute counts for the different cell types (as cells of that type/uL).
A

-Total WBCs = 4,500-10,500 per microliter of blood (x109).

  • Neutrophils = 40-60% (1.8-8.8 x109).
  • Eosinophils = 1-4% ( 0-0.66 x109).
  • Basophils = 0.5-1% (0-0.22 x109) and monocytes = 2-8% (0.9-1.21 x109).

-Lymphocytes = 20-40% (0.8-5.5 x109). These counts may be higher in children.

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4
Q
  1. Name the major central and peripheral lymphoid organs.
A

Central organs:
-Where lymphocytes develop = bone marrow and thymus.

Peripheral organs:

  • Where lymphocytes do their job = lymph nodes, spleen, tonsils, adenoids, and Peyer’s patches in the small intestine.
  • Gut encounters so much foreign stuff, and patches line the intestine so they can rapidly decide if something is commensal or dangerous if they need to trigger an immune response.
  • Functional structure of Peyer’s patches include specialized mucosal M cells = gatekeepers that ingest proteins and transport them to the abluminal side where DC’s can take the antigens to the B cell follicles and T cell zones.

Spleen:

  • has red pulp contains lots of phagocytic cells and makes RBCs when necessary.
  • Also filters particulates and stores monocytes.
  • White pulp = cell islands.
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5
Q
  1. Describe the recirculation of lymphocytes from blood to lymph and back; include in your discussion the specialized features of lymph node blood vessel endothelium that permit recirculation.
A
  • Lymphocytes move in blood to get to destination faster.
  • Lymphatics dump into nodes that move towards heart, and culminate at thoracic duct that dumps into heart where lymph is added back into circulation.
  • Lymph nodes have a hilum through which blood enters and exits, where you get crossing over between blood and lymph.
  • Incoming lymph at the afferent lymph –> comes in at the periphery and percolates at the node, leaving via efferent lymph or in blood.
  • Cortex = outside of lymph node (has lymphoid follicles) and deeper = deep or paracortex, which is dense with lymphocytes so antigens get shown to as many cells possible.
  • Cells in cortex = B;
  • cells in paracortex = T.
  • Pattern of recirculation is when lymphocyte encounters cells lining postcapillary venules in the lymph nodes and the endothelial cells lining the venules are high and cuboidal –> have molecules on their surfaces that lymphocytes can interact with to leave blood and enter lymph.
  • This allows lymphocytes to get distributed throughout the body –> immunological memory happens via activated cells that spread out beyond the wound site.
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6
Q
  1. Define antigen, and compare it to immunogen. Define antigenic determinant and epitope.
A
  • Antigen is something that interacts with the immune response;
  • Immunogen is an antigen that can give rise to an immune response, actually creates it.
  • Tolerogen = form of antigen that would not provoke an immune response and would prevent development of a future immune response.
  • The part of an antigen that fits into the receptor on a B or T cell lymphocyte = the antigenic determinant/epitope.
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7
Q
  1. Discuss lymphocyte activation by antigen with respect to: receptor binding, proliferation, differentiation. Draw a graph showing relative time on one axis and relative lymphocyte numbers on the other, in response to antigen administration.
A

-Lymphocytes have receptors, each for a specific antigen.
-T cell receptors = alpha and beta chains;
-B cell receptors = antibodies.
-Bind the antigenic determinant/epitope –> if correctly binds, cell is activated and proliferates.
-Cells can also differentiate into effectors (B cells –> blasts and plasma cells; helper T –> cytokines, killer T –> kill targets) and memory cells.
-Can’t just have epitope binding though –> the right accessory interactions between T cell and dendritic cell have to happen, as well as a good fit.
-Then T cell gets activated.
-This is important because don’t want to rapidly divide the wrong kind of cell, so need other signals beyond just antigen-recognition.
(Graph would theoretically look exponential.)

Clones = amplified immune response.

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