Lecture 24: Immune/Lymphatic System I Flashcards
Innate Immunity
“Born with it”; lacks immune specificity and memory, inflammatory response
Acquired Immunity
Takes longer to develop and develops in response to antigens; more powerful than innate immunity and displays specificity and memory
Passive Immunity
Temporary immunity due to donated antibodies; ex: transplacental passing of maternal antibodies to fetus
Active immunity
Long lasting/permanent immunity due to self-exposure to antigen; results in memory T cells and B cells specific for antigens
Primary lymphoid organs
Thymus and Bone marrow: precursor cells mature into immunocompetent cells; each cell is programmed to recognize a specific antigen; lymphocytes originate here
Secondary lymphoid organs
Lymph nodes, spleen, tonsils; trapped antigens stimulate clonal expansions of mature T and B cells; lymphocytes reside here
Primary lymph follicle/nodule
Spherical, tightly packed accumulations of virgin B cells and dendritic reticular cells that have NOT been exposed to antigens
Secondary lymph follicle/nodule
Derived from PRIMARY follicles that HAVE been exposed to foreign antigens; these are not present at birth; Structurally: contain a corona (dark, peripheral region composed of densely packed B lymphocytes) and germinal center (central lighter stained region w/ B lymphocytes, memory B cells, plasma cells, dendritic reticular cells which function as antigen-presenting cells)
Diffuse vs. Aggregated Lymphatic Tissue
Diffuse=scattered clusters of cells located in the connective tissue stroma; ex: MALT/BALT/GALT
Aggregated=beneath and in contact with epithelium; ex: Peyer’s patches (ileum) and tonsils
Antibodies (Immunoglobulins)
5 classes: IgA, IgD, IgG, IgM, IgE; 2 heavy/2 light chains, Fab fragment responsible for diversity, Fc fragment determines class of antibody
Major Histocompatibility Complex (MHC)
Main function: Presentation of antigenic peptides to T-cells; 2 classes
MHC I
Expressed on surface of all cells EXCEPT trophoblast and RBCs; CD8+ T cells recognize peptide fragments of foreign proteins bound to MHC I
MHC II
Expressed on surface of B cells and antigen-presenting cells; CD4+ T cells recognize fragments of foreign protein fragments bound to MHC II
CD4+ T cells
Recognize antigens bound to MHC class II molecules; Helper cells: assist CD8+ cell differentiation and B cell differentiation
CD8+ T cells
Cytolytic T-cells: bind to antigen presenting cell and undergo mitosis; release perforins (punch holes in cell membranes) and Fas ligand (cause apoptosis)
Recognize antigens bound to MHC class I molecules, mediators of cellular immunity
CD16+ T cells
“Natural Killer” NK T cells: activated by tumor cell antigens and release cytokines: Interleukin-2, Interferon-gamma, macrophage activating factor, chemotactic factor, tumor necrosis factor
What is the most important opsonin in the complement cascade?
C3b = makes antigen attractive to macrophages
What are the results of the Complement cascade?
Activation of the membrane attack complex (MAC) on pathogen leading to perforations/lysis, production of opsonins (coatings that make antigens more palatable to phagocytes), release of chemokines which attract phagocytes to areas of infection/inflammation
Parenchyma
Consists of cells that typically pack areas of lymphoid organ (mostly lymphocytes)
Stroma
Consists mostly of reticular fibers and cells, including undifferentiated cells and fixed and free macrophages
Hilus of lymph node
Entry/exit point for vessels - sets up circulation pattern
Capsule of lymph node
dense collagen fibers, some elastic fibers and smooth muscle fibers
Cortex of lymph node
Outer area is bone marrow affiliated and contains lymph follicles; Follicles contain B cells, follicular dendritic cells, migrating dendritic cells, Secondary = mantle, germinal layer, Primary = lack mantle and germinal center
Deep area: contains T helper cells, macrophages, and HEVs
Medulla of lymph node
Irregular arrangement of loose medullary sinuses and dense medullary cords; sinuses lined with macrophages, cords consist of blood vessels/lymphoblasts/plasma cells; site of lymphocyte reentry into lymph stream; thymic-dependent areas in subcortical and deep medullary region