BIOL 250 - Chapter 16: Adaptive Immunity

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77 Terms

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adaptive immunity
the body's ability to recognize and defend against distinct species or strains of invaders; only present in vertebrates
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five attributes of adaptive immunity
specificity, inducibility, clonality, unresponsiveness to self, memory
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specificity
a particular response is specific to the "attacker"
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inducibility
the specific antigen-containing pathogen activates or induces cells of adaptive immunity
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clonality
once induced, cells of the adaptive immune system proliferate to form many generations of nearly identical cells
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unresponsiveness to self
adaptive immune cells do not attack normal body cells
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memory
adapts to respond faster and more effectively in subsequent encounters with a particular pathogen
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lymphocyte
main actor of the adaptive immune system; type of agranulocyte that originates in the red bone marrow and has nuclei that nearly fill the cell
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two types of lymphocytes
B lymphocytes (B cells) and T lymphocytes (T cells)
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B lymphocytes (B cells)
arises and matures in red bone marrow in adults; found in spleen, lymph nodes, red bone marrow and Peyer's patches of the intestines; secretes antibodies
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T lymphocytes
matures in the thymus and acts primarily against endogenous antigens
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antibodies
a protective protein secreted by descendants of a B cell that recognizes and strongly binds to the specific biochemical shape of the antigen
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two basic types of adaptive responses
humoral response and cell-mediated response
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humoral response (antibody immune response)
B lymphocytes attack extracellular pathogens; involves soluble proteins called antibodies
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cell-mediated response
T lymphocytes respond against intracellular pathogens
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lymphatic system
body system composed of lymphatic vessels and lymphoid tissues and organs
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lymphatic vessels
tubes that conduct lymph
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lymph
a colorless, watery liquid similar in composition to blood plasma
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antigen
molecule that triggers a specific immune response
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immunogenicity
the degree to which an antigen provokes an immune response; varies and depends on an antigen's biochemical features
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epitopes
the three-dimensional shape of a region of an antigen that is recognized by the immune system
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exogenous antigens
come from outside the body's cells and include toxins and other secretions and components of microbial cell walls, membranes, flagella and pili
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endogenous antigens
produced by protozoa, fungi, bacteria and viruses that reproduce inside a body's cells; only responded to when such cells incorporate antigens into their cytoplasmic membrane
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autoantigens
antigenic molecules derived from normal cellular processes
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major histocompatibility complex (MHC)
group of genes that code for proteins found on the surfaces of cells that help the immune system recognize foreign substances
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two classes of MHC proteins
class I MHC proteins and class II MHC proteins
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antigen-presenting cells (APCs)
dendritic cells, macrophages and B cells, which process antigens and activate cells of the immune system
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dendritic cells
cells of the epidermis and mucous membranes that devour pathogens
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processing endogenous antigens
1. each antigen is cut into smaller pieces (with their epitopes) and moved into the ER and bind to complementary antigen-binding grooves of MHC class I molecules in the ER
2. the ER membrane with lots of MHC class I proteins and epitopes is packaged to form vesicles
3. each vesicle fuses the the cytoplasmic membrane so that the vesicle's membrane becomes part of the cytoplasmic membrane
4. the cell displays the MHC I protein-epitope complex on the cell's surface
5. since each nucleated cell in the body makes class I MHCs, each cell displays epitopes from every endogenous antigen and every autoantigen inside that cell, allow for detection of all antigens inside cells
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processing exogenous antigens
1. a dendritic cell phagocytizes a pathogen and a lysosome with class II MHC molecules in its membrane fuses with the phagosome and clips antigens into epitopes within the phagolysosome
2. vesicle fuses with cytoplasmic membrane
3. MHC II-epitope complexes are left on cell's surface
4. empty MHC II molecules are degraded
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T cell receptor (TCR)
antigen receptor generated in the cytoplasmic membrane of T lymphocytes
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three types of T cells
cytotoxic, helper, regulatory
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cytotoxic T cell (Tc)
directly kill infected or abnormal cells (like cancer cells)
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helper T cells (Th)
help regulate the activities of B cells and Tc cells during immune responses by providing necessary signals and growth factors
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two types of Th cells
type 1 Th cells (Th1) and type 2 Th cells (Th2)
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type 1 helper T cells
assist Tc cells and stimulate and regulate innate immunity
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type 2 helper T cells
function in conjunction with B cells
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regulatory T cells (Tr)
activated by contact with other immune cells and secrete cytokines different from those secreted by helper T cells
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clonal deletion
process by which cells with receptors that respond to autoantigens are selectively killed via apoptosis
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apoptosis
programmed cell suicide
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B cell receptor (BCR)
antibody integral to the cytoplasmic membrane and expressed by B cells; a type of immunoglobulin made of six polypeptide chains
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parts of a BCR
heavy chains, light chains, disulfide bonds, transmembrane portion, variable region, antigen-binding sites
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antigen-binding sites
site formed by the variable regions of a heavy and light chain of an antibody; bind epitopes and account for the specificity of an antibody immune response
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plasma cells
B cells that are actively fighting against exogenous antigens and secreting antibodies
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five ways that antibodies function
activation of complement and inflammation, neutralization, opsonization, agglutination, and antibody-dependent cell-mediated cytotoxicity
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activation of complement and inflammation
antibodies trigger the complement cascade and stimulate the release of inflammatory mediators. IgE bound to antigen also attaches its stem to mast cells, eosinophils, and basophils, triggering the release of inflammatory chemicals
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neutralization
the action of a toxin or attachment of a pathogen is blocked; antibodies bind to a critical portion of the toxin so that it can no longer harm the body
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opsonization
antibodies act as opsonins, stimulating phagocytosis; changing the surface of an antigen so as to enhance phagocytosis
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agglutination
aggregation caused when antibodies bind to two antigens, hindering the activity of pathogenic microorganisms and increase probability of phagocytosis
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antibody-dependent cell-mediated cytotoxicity (ADCC)
process whereby NK cells lyse cells covered with antibodies; different from opsonization in that the target dies by apoptosis
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perforin-granzyme pathway (used in ADCC)
NK cell releases perforin and granzyme which triggers apoptosis
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perforins
makes pore complex in a virally infected cell
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granzyme
moves through pore and activates apoptosis enzymes
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five classes of antibodies
IgM, IgG, IgA, IgE, IgD
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immunoglobulin M (IgM)
the second most common antibody class and the predominant antibody produced first during a primary humoral immune response; most efficient at complement activation, which triggers inflammation. Can also be involved in agglutination and neutralization
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immunoglobulin G (IgG)
the predominant antibody class found in the bloodstream and the primary defender against invading bacteria; has many functions including roles in complement activation, opsonization, neutralization, and ADCC
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immunoglobulin A (IgA)
the antibody class most commonly associated with various body secretions, including tears and milk. IgA pairs with a secretory component to form secretory IgA
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secretory IgA
the combination of IgA and a secretory component, found in tears, mucous membrane secretions, and breast milk, where it agglutinates and neutralizes antigens
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immunoglobulin E (IgE)
signal antibody molecule that triggers the inflammatory response, particularly in allergic reactions and infections by parasitic worms
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immunoglobulin D (IgD)
a membrane-bound antibody molecule found in some animals as a B cell receptor
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cytokines
soluble regulatory proteins that act as intercellular signals to direct activities in immune responses
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five types of cytokines
interferons (IFNs), interleukins (ILs), growth factors, tumor necrosis factors (TNFs), and chemokines
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interleukins (ILs)
immune system cytokines that signal among leukocytes
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interferons (IFNs)
protein molecules that inhibit the spread of viral infections
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growth factors
organic chemical, such as a vitamin, required in very small amounts for metabolism. In immunology, an immune system cytokine that stimulates stem cells to divide, ensuring that the body is supplied with sufficient leukocytes of all types
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tumor necrosis factor (TNF)
an immune system cytokine secreted by macrophages and T cells to kill tumor cells and to regulate immune responses and inflammation
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chemokines
an immune system cytokine that signals leukocytes to rush to the site of inflammation or infection and activate other leukocytes
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four ways acquired immunity is categorized
natural or artificial and active or passive
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naturally acquired immunity
when the body mounts an immune response against antigens (ex. influenza viruses, food antigens) encountered in daily life
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artificially acquired immunity
the body's response to antigens introduced in vaccines, as occurs with immunization against tetanus and flu
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active immunity
the immune system responds actively to antigens via antibody or cell-mediated responses
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passive immunity
the body passively receives antibodies from another individual
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four types of acquired immunity
naturally acquired active immunity, naturally acquired passive immunity, artificially acquired active immunity, and artificially acquired passive immunity
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naturally acquired active immunity
type of immunity that occurs when the body responds to exposure to antigens by mounting specific immune responses
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naturally acquired passive immunity
type of immunity that occurs when a fetus, newborn, or child receives antibodies across the placenta or within breast milk
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artificially acquired active immunity
type of immunity that occurs when the body receives antigens by injection, as with vaccinations, and mounts a specific immune response
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artificially acquired passive immunotherapy
treatment in which patient receives via injection preformed antibodies in antitoxins or antisera, which can destroy fast-acting and potentially fatal antigens, such as rattlesnake venom