Immuno 2 (14.1/14.2) Flashcards
describe the path of lymphatic circulation
enters via afferent lymphatics
branches in subcapsular sinuses and trabecular sinuses
percolates thru the cortex and medullary cords
leaves via medullary sinus to efferent lymphatics
can lymphocytes entering via the systemic circulation leave the circulation? if so can they reenter?
yes they can leave
can’t reeenter systemic circulation so have to go through medullary cord and exit via efferent lymphatics
-so if leave systemic circulation in the medulla, then have to enter via lymphatics
describe the path of spleen circulation
-is this open or closed circulation
blood enters the splenic artery –> trabecular arteries –> central arteries –> radial arteries –> penicillar arteries –> sheathed capillaries –> splenic sinuses –> trabecular veins –> splenic vein
-closed circulation bc blood cells never leave an endothelial lined space
does spleen have systemic and/or lymphatic circulation
only systemic
what region do blood cells leave the endothelium ?
i.e. what portion of the spleen can blood enter into the CT space
marginal zone
bn red and white pulp
where do WBCs congregate
white pulp
white pulp surrounds the central arteries as a
PALS (peri-arterial lymphatic sheath)
what is the red pulp comprised of and hwat cells course through it
splenic cords and sinuses
-RBCs (erythrocytes) go through it
what’s the diff bn open and closed circulation
closed = blood cells never leave an endothelial lined space
-ex. splenic artery to splenic vein
open = blood cells come in, course through vessels, leaves vasculature, enters CT compartment of spleen
-ex. red pulp path through splenic cords and try to reenter the splenic sinus
what cells recognize and remove RBCs that lack functioning key surface proteins and erythrocytes that can no longer deform themselves
splenic macrophages
erythrocytes that cant deform themselves are mechanically prevented from entering the splenic sinuses by encircling what
reticular fibers
what is the difference bn how normal macrophages function vs macrophages that act on mycobacterium tuberculosis
normal -ingest bacteria in a phagosome and destroy it by binding the phagosome to a lysosome
TB - TB bacteria can modify the phagosome membrane to make it incapable of binding to the lysosome causing a battle bn incr immune system activation and hijacked macrophages
what do Th1 cells create
Th2?
Th1 create IgG antibodies
Th2 create IgE antibodies
IgE produces
-predominate in
allergic reactions
-in fetal life
theory as to why allergies arise
early exposure to environmental antigens is whe swtch that shifts its antibody production in favor of IgGs
without exposure, IgE predominates even in adult life
celiac disease is an autoimmune diease with problem in what target protein? major symptoms?
gluten of wheat
loss of villi in smal intestine –> means cant absorb nutrients from food
multiple sclerosis is an autoimmune diease with problem in what target protein? major symptoms?
autoimmunity to myelin
weakness (fatigue in muscles) & islands of white in white matter area where immune system destroyed the myelin
rheumatoid arthritis is an autoimmune diease with problem in what target protein? major symptoms?
targets proteins of cartilage (ex. type 2 collagen)
joint pain symptom
-wrong is there’s lots of immune cells (lymphocytes) and there’s bone fragments
diabetes is an autoimmune diease with problem in what target protein? major symptoms?
targets pancreatic islet B cells
glucose intolerance
-when t cell tolerance fails
how is HIV unique
can hide from the immune system (hides in Th cells)
low levels of the virus continue to be present creating the “chronic” phase of infection
in HIV, what cells are depleted
Th cells and CTL cells are gradually depleted
-depletion pass a critical amount leads to infections
name the technique
where individual cells are passed through a column and read one by one automatically by a machine
flow cytometry
what are the two types of flow cytometry mentioned that are based on physical properties and what do they relate to
forward scatter (i.e. transmittance) related to cell size side scatter related to cell granularity