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Micro-Bio Chapter 21
Resistance and the Immune System 2
| Question | Answer |
|---|---|
| Immunological Memory | The ability to “remember” past pathogen exposures; specific; body fights any subsequent infections; directed against a specific antigen; anamnestic response |
| Antigens | Foreign molecules that provoke an immune response; composed of an epitope and carrier molecule |
| Properties of Antigens | Size Complexity Foreignness Degradability Molecule that makes best antigen |
| Epitopes | Unique antigenic determinants |
| Complete Antigen | Will both induce the body to produce antibodies and to combine to those antibodies |
| Hapten | An epitope without a carrier; will react with existing antibodies but cannot induce antibody production; if linked to proteins, it might provoke an allergic immune response |
| Immune Deficiency | Occurs if the body loses the ability to respond to antigens |
| Autoimmune Disease | Occurs when self-tolerance breaks down and the body starts attacking itself |
| B Lymphocytes (B cells) | Complementary response; involved in producing antibodies against epitopes (humoral immunity); formed in bone marrow |
| T Lymphocytes (T cells) | Complementary response; provide resistance through lysis of infected or abnormal cells (cell-mediated immunity); formed in the thymus |
| Humoral Immunity | Involves activation of B cells and production of antibodies against antigens |
| Cell-Mediated Immunity | Activated to eliminate “nonself” cells after microbes enter cells making antibodies useless; T cells regulate and control these activities |
| Clonal Selection | Activates B+T cells; B+T clones contain lymphocytes that develop into effector cells that target pathogens and memory cells that are capable of division on short notice |
| Antigen Exposure | Activates only B+T cells with receptors that recognize specific epitopes on the antigen |
| Origin of Immune System | Originates from stem cells; in fetus it originates from stem cells in the yolk sac and bone marrow |
| Myeloid Progenitors | Develop from stem cells; become red blood cells and most white blood cells |
| Lymphoid Prgenitors | Develop from stem cells; become lymphocytes |
| Natural Killer (NK) Cells | Type of lymphocytes |
| Immunoglobulins | Ig; antibodies; a class of proteins |
| Antibody Structure | 2 identical Light strands (short) and 2 identical Heavy strands (long) |
| Light Chain | Shorter strands of antibodies (2) |
| Heavy Chain | Longer strands of antibodies (2) |
| Constant Region | Part of chains of antibodies; determines the location and functional class of the antibody |
| Variable Region | Part of chains of antibodies; contains different amino acids for the many antibodies produced |
| Variability | Allows formation of specific antigen binding sites |
| Fab Fragment | Part of antibody; combines with the epitope |
| Fc Fragment | Part of antibody; has functions in opsonization, complement system activation, and allergic reactions |
| IgM | Class of immunoglobulin; the first, short-lived Ig; appears in circulation after B cell stimulation (pentameric) |
| IgG | Class of immunoglobulin; gamma globulin; the major circulating antibody; provides immunity to fetus and newborn |
| IgA | Class of immunoglobulin; provides resistance in respiratory and gastrointestinal tracts; mucosal immunity; found in colostrum and milk (dimeric) |
| IgE | Class of immunoglobulin; plays a role in allergic reactions; binds to basophils |
| IgD | Class of immunoglobulin; a cell surface receptor on B cells and activates them |
| Primary Antibody Response | Occurs the first time the body encounters a pathogen |
| Secondary Antibody Response | Occurs with a subsequent infection by the same pathogen; more powerful and sustained response; anamnestic response |
| Antigen-Antibody Complex | Antibodies mediate antigen disposal; these complexes cause antigen to be inactivated, die, or increase its susceptibility |
| Complement | Activated by Antigen-Antibody Complexes leading to cell lysis and other activities such as chemotaxis, opsonization, or inflammation |
| Cellular Immunity | Relies on T cell receptors and recognition for cell-mediated immunity |
| Cytotoxic T Cells | Have TCRs and CD8 coreceptor proteins; recognize and bind to MHC-1/peptide complexes on infected cells, then release toxins like perforin and granzymes that cause cell death; recognize and kill tumor cells |
| Helper T Cells | Have TCRs and CD4 coreceptor proteins |
| CD4 Cells | T cell coreceptor proteins that can help with both humoral and cell-mediated immunity |
| T Cell Receptors (TCRs) | Allow T cells to recognize and bind to the major histocompatibility complex (MHC) |
| MHC Proteins | Unique for nearly all individuals; mark the body’s cells as “self” cells |
| Class II MHC Proteins | On the surface of immune cells that present antigen fragments to CD4 T cells; called antigen-presenting cells (APCs) |
| Class I MHC Proteins | Found on the surface of nearly all the body’s cells |
| Virus-Infected Host Cells | Can degrade viral antigens and present peptide fragments with MHC-1 proteins on cell surface |