Lecture 18 Flashcards
Distinguish between passive and active immunity.
Passive Immunity: temporary immunity due to donated antibodies (this occurs early in life when maternal antibodies are transferred to the fetus)
Active Immunity: Long-lasting/ permanent immunity due to self exposure to antigens resulting in memory T cells and B cells specific for those antigens
differentiate between primary and secondary immune tissue/organs. List the organs for each and explain the process of each.
Primary immune organs: Thymus and bone marrow
Precursor cells mature into immunocompetent cells and each cell is programmed to recognize a specific antigen.
Secondary immune organs: lymph nodes, spleen, tonsils
Trapped antigens stimulate clonal expansions of mature T and B cells
Describe distinguishing characteristics of a primary lymph follicle and compare with a secondary lymph follicle.
Primary lymph follicle: spherical, tightly packed accumulations of virgin B cells and dendritic reticular cells that have not been exposed to antigens
Secondary lymph follicle: Are not present at birth and are derived from primary follicles that have been exposed to nonself antigens
Describe the function of the MHC (Major histocompatibility complex) and compare the two subdivisions of the MHC.
The main function of MHC gene products is the presentation of antigenic peptides to T cells
Subdivisions
MHC I: expressed on the surface of all cells except trophoblast and RBCs
MHC II: expressed on the surface of B cells and antigen-presenting cells
describe CD4+ T cells and their functions
CD4+ T cells: helper cells that recognize antigens bound to MHC class II molecules
Assist CD8+ T cell and B cell differentiation
Describe CD8+ T cells and their functions
CD8+ T cells: Cytolytic T cells that bind to an antigen presenting cell (they only recognize antigens bound to MHC class I molecules) and release perforins (perforates cell membranes in order to destroy them) and Fas Ligand
Undergo mitosis
They are mediators of cellular immunity
Describe CD16+ T cells and their function. be sure to explain what the following cytokines do when CD16+ T cells release them: Interleukin0-2, Interferon-gamma, MAF, and Chemotactic factor.
CD16+ T cells: Natural Killer (NK) cells that release cytokines when activated by tumor cell antigens
Interleukin-2: stimulates proliferation of NK cells
Interferon-gamma: activates NK cells
Macrophage activating factor (MAF): activates macrophages
Chemotactic factor
Tumor necrosis factor (TNF-beta): kills tumor cells directly
Outline the interplay among T-helper cells, macrophages, B cells, and the MHC complex in the immune response.
Macrophages phagocytize foreign material and breaks them down into fragments, some of which have “epitopes” (antigenic properties)
These epitopes are then expressed on the surface of macrophage-bound to MHC-II
This MHC-II/antigen complex is then presented to activated helper T cells
The activated T cells then undergoes mitosis where some daughter cells become memory cells and some daughter cells secrete interleukins
This T cell activity attracts B cells, which have access to free antigens
B cells then undergo mitosis where some daughter cells become memory cells and some daughter cells become plasma cells (which secrete appropriate antibodies)
Describe the differences between B and T cells when they undergo mitosis while participating in an immune response
The activated T cells then undergoes mitosis where some daughter cells become memory cells and some daughter cells secrete interleukins
B cells then undergo mitosis where some daughter cells become memory cells and some daughter cells become plasma cells (which secrete appropriate antibodies)
Describe the components of C1, and their functions that aid in the conduction of the complement cascade
C1 is the first component of the complement cascade and it consists of 3 components (C1q, C1r, and C1s)
C1q: binds to the Fg region of the Ig
C1r: is activated by C1q binding and in turn activates C1s
C1s: is a serine protease
C1s has 2 functions:
cleaves complement protein C4 into C4a and C4b (binds to the pathogen)
Cleaves C2 into C2a and C2b (binds to C4b)
Beginning with the function of C1s, describe the complement cascade, ending with the fate of the pathogen
After C1s cleavages occur, C4b, the pathogen it is bound to, and C2b bind to one another to form a complex (this complex is called C3 convertase)
Multiple C3b’s will bind to C3 convertase in order to form C5 convertase (C4b-C2b-C3b complex)
C5 convertase activates C5, which makes it split into C5a and C5b
C5b joins the C5 convertase complex to form the Final opsinization complex
Once the final opsinization complex is formed, C6, C7, C8, and C9 are added to the complex, forming pores in the membrane of the pathogen to kill it.
Name the most important opsonin.
C3b is the most important opsonin
List the results of the complement cascade.
Activation of the MAC (membrane attack complex) on the pathogen leading to perforations and lysis
Production of opsonins, which are coatings that make the antigens more palatable to phagocytes
Release of chemotactic agents (chemokines) which attract phagocytes (they move via chemotaxis) to the ares of infection or inflammation
Distinguish between stroma and parenchyma.
Stroma: consists of mostly reticular fibers and cells including undifferentiated cells and fixed and free macrophages
Parenchyma: consists of cells, mostly lymphocytes, that pack the areas of the lymphoid organ
When it comes to lymph nodes, what is the site of lymphocyte entry into the the lymph system?
the medulla of the lymph node is where this occurs