Cells of the Adaptive Immune System Flashcards
Dendritic Cells
have long cytoplasmic projections (dendrites) that enable them to trap antigens. They increase the cell surface area, increasing the efficiency of antigen trapping. Located in lymphoid organs and under epithelial surfaces. 100x more effective than macrophages.
Only antigen processing ells that can activate naive T cells
dendritic cells
Types of Dendritic Cell
Plasmacytoid, classical type I, classical type II, follicular, Langherhans cells
What do Lymphoid Organs Do?
- regulate the production of lymphocytes
- provide an environment for trapping foreign antigens, processing them
- Maximize the opportunity for lymphocytes to encounter and interact with these foreign antigens
Types of Lymphoid Organs
primary and seecondary
Primary Lymphoid Organs
where lymphocytes mature and self-reactive cells are eliminated. Thymus, bursa, peyer’s patches, bone marrow
Secondary Lymphoid Organs
where lymphocytes encounter and respond to antigens. Tonsils, spleen, lymph nodes, Peyer’s Patches, bone marrow
Sources of lymphocytes
yolk sac- fetal liver- bone marrow
Where do T cells mature?
thymus
Where do B cells mature?
birds- bursa of Fabricius
primates and rodents- bone marrow
rabbits and ruminants- intestinal lymphoid tissues
Thymus
source of T cells, eliminate self-reactive cells (negative selection) and stimulate the remaining T cells (positive selection)
Negative Selection
thymocytes with receptors that bind self-antigens strongly and that could therefore cause autoimmunity are killed by apoptosis. Thymocytes with no receptor and thus cant react to any processed antigen are also killed
Peyer’s Patches
primary lymphoid organ in some species (ruminants and pigs). secondary in all other species
Lymph Nodes
filter lymphatic fluid. Major site of antigen-lymphocyte interaction. Cortex is major site of B cell responses. Paracortex inhabited by T cells. Medulla rich in antigen-processing cells, DC, and macrophages
Germinal Centers
major site of B cell somatic mutation and selection. B cells dividing and mutating in dark zone. B cells responding to antigen presentation in light zone. Low-affinity B cells undergo apoptosis. High-affinity B cells continue to multiply.