Adaptive (Acquired)Immunity (3rd line of defense)
Chapter 7
Adaptive/Acquired Immunity Antigens – Anything that cases a biological immune
response by this system of cells Specificity – Some antibodies are quite specific to an
antigen others are general to a “type” or “form” Memory – b-memory cells are formed and remain to
combat future exposures quickly (Active vs Passive immunity
Antibodies – the proteins formed by b-cells that combat antigens whether chemical or biological
Lymphocytes – cells involved in this response
Adaptive Immunity Clonal diversity
Production of T (Killer cell mediated response) and B lymphocytes (humoral/antibody response)
Antigen recognition – zone of attachment Lymphocyte specificity – Classes of Immunoglobulins
Clonal selection – CD cluster recognition table 7-2 Antigen processing – Recognition and binding depend on
size of molecule/cell/tissue/organism and class Cellular interaction
Active vs. Passive Immunity Active immunity
Antibodies or T cells produced after either a natural exposure to an antigen or after immunization
Passive immunity Preformed antibodies or T lymphocytes are
transferred from a donor to a recipient
Recognition and Response Required for a successful immune response Clusters of differentiation (CD)
Originally used to describe proteins found on the surface of lymphocytes
Now it is a labeling system used to identify a family of proteins on many cells
Antigens Immunogens vs. antigens Antigenic determinant (epitope) Self-antigen Tolerance
Central and peripheral tolerance Molecular size
Haptens Allergens
Antigen Presentation Antigen-presenting cells (APCs) Major histocompatibility complex (MHC)
Glycoproteins on the surface of all human cells (except RBCs)
Also referred to as human leukocyte antigens (HLAs) MHC class I molecules
A, B, and C MHC class II molecules
DR, DP, and DQ MHC class III molecules
Antigen Presentation
Transplantation Cells in transplanted tissue from one
individual will have a different set of MHC surface antigens than those of the recipient
Therefore, a recipient can mount an immune response against the foreign MHC molecules
Haplotype Combination of A, B, C, DR, DQ, and DP alleles
Transplantation
CD1 Antigen-presenting molecules Found on antigen-presenting and thymus cells Present lipid antigens
Antigen Recognition Antigen is directly recognized by circulating
antibody, antigen receptors on B cells (BCR), and T lymphocytes (TCR)
Antibodies Also called immunoglobulins Produced by plasma cells Classes of antibody
IgG, IgA, IgM, IgE, and IgD Characterized by antigenic, structural, and functional
differences
Antibodies
Antibodies
Immunoglobulin G (IgG) Most abundant class (80%-85%) Transported across the placenta Four classes
IgG1, IgG2, IgG3, and IgG4
Immunoglobulin A (IgA) Two classes
IgA1 molecules are found predominantly in the blood
IgA2 molecules are found predominantly in normal body secretions
IgAs found in body secretions are dimers anchored by a J chain and a “secretory” piece Secretory piece may function to protect IgAs
against enzyme degradation
Immunoglobulin M (IgM) Largest of the immunoglobulins Pentamer stabilized by a J chain First antibody produced during the primary
response to an antigen Synthesized during fetal life
Immunoglobulin D (IgD) Limited information on IgD function Low concentration in the blood Located primarily on the surface of
developing B lymphocytes Function as one type of B cell antigen
receptor
Immunoglobulin E (IgE) Least concentrated of the immunoglobulin
classes in the circulation Mediator of many common allergic responses Defender against parasites
Antibody Structure Antigen-binding fragment (Fab)
Recognition sites (receptors) for antigenic determinants
Crystalline fragment (Fc) Responsible for biological function
Polypeptide chains (4) Light chains (2) and heavy chains (2)
Antibody Structure Hinge region Constant and variable regions
Complementary determining regions (CDRs) Framework regions (FRs)
Antigen Binding Amino acid sequences of the variable regions of the
heavy and light chains Framework regions control antibody folding Lock and key
Noncovalent chemical interactions Antibody valence
IgG, IgD, and IgE—2 IgA—4 IgM—theoretically 10, likely 5
B Cell Receptor Complex Located on surface of B cells Consists of:
Antigen-recognition molecules Monomer IgM and IgD
Accessory intracellular-signaling molecules Ig-alpha and Ig-beta heterodimers
T Cell Receptor Complex Antibody-like transmembrane protein (TCR) Accessory proteins for intracellular signaling
Referred to as CD3
Generation of Clonal Diversity All necessary receptor specificities are
produced Takes place in the primary (central) lymphoid
organs Results in immature but immunocompetent T
and B cells Primarily occurs in the fetus
Clonal Selection Immunocompetent T and B cells migrate
from the primary lymphoid organs to the secondary lymphoid organs to await antigen
Primarily after birth Clonal selection is initiated by antigen Final products
Plasma cells that produce antibody, effector cells that help Th, Tc, or Treg, and memory B and T cells
T Cell Maturation The thymus is the central lymphoid organ of T cell
development T cells move from the thymic cortex to the medulla Changes
Development of the T cell receptors and expression of surface molecules
T cells are released into the blood and take up residence in the secondary lymph organs
Antigen Processing and Presentation Antigens require processing and presentation
by antigen-presenting cells (APCs) Dendritic cells, macrophages, and B lymphocytes
For processing and presentation to occur, the antigen must be of the appropriate type, the lymphocytes must be prepared to recognize the presented antigen, and the antigen must be presented appropriately
Antigen Processing and Presentation
Antigen Processing and Presentation
Helper T Lymphocytes “Help” the antigen-driven maturation of B and T
cells Facilitate and magnify the interaction between APCs
and immunocompetent lymphocytes Steps
Th interacts through antigen-specific and antigen-independent mechanisms
Undergoes differentiation Mature Th interacts with plasma or T-effector cells
Antigen Processing and Presentation
Helper T Lymphocytes Subsets
Th1 cells provide help in developing cell-mediated immunity
Th2 cells provide help in developing humoral immunity
Differences based on cytokine production
B Cell Activation When an immunocompetent B cell encounters
an antigen for the first time, B cells with specific BCRs are stimulated to differentiate and proliferate
A differentiated B cell becomes a plasma cell A plasma cell is a factory for antibody
production Single class or subclass of antibody
Primary and Secondary Responses Primary response
Initial exposure Latent period or lag phase
B cell differentiation is occurring
After 5 to 7 days, an IgM antibody for a specific antigen is detected
An IgG response equal or slightly less follows the IgM response
Primary and Secondary Responses Secondary response
More rapid Larger amounts of antibody are produced Rapidity is due to the presence of memory cells
that do not have to differentiate IgM is produced in similar quantities to the
primary response, but IgG is produced in considerably greater numbers
Class Switch Immunocompetent B cells use IgM and IgD
as receptors During clonal selection, B cells have the
option of changing the class of the antibody One of four IgGs, one of two IgAs, IgE, or an
IgM in a pentamer form DNA rearrangement
B Cell Clonal Selection
T Cell Activation Binding antigen to specific T cell receptors Allows:
Direct killing of foreign or abnormal cells Assistance or activation of other cells
T regulatory cells (Treg) Regulate the immune response to avoid attacking
“self” Memory T cells
T Cell Activation
Superantigens (SAGs) Bind the variable portion of the TCR and the
MHC class II molecules outside of their antigen-presentation sites
Activates a large population of T lymphocytes regardless of antigen specificity
SAGs induce an excessive production of cytokines Causes fever, low blood pressure, fever, and
potentially shock
Antibody Function Direct
Neutralization Agglutination Precipitation
Indirect Opsonization
Degree of antibody protection is assessed by an antibody titer
Secretory (Mucosal) Immune System Lymphoid tissues that protect the external
surfaces of the body Antibodies present in tears, sweat, saliva,
mucus, and breast milk IgA is the dominant immunoglobulin
Small numbers of IgG and IgM are present
Secretory (Mucosal) Immune System
IgE Function Provides protection from large parasites
Initiates an inflammatory reaction to attract eosinophils
When produced against innocuous environmental antigens, they are a common cause of allergies Fc portions of IgEs are bound to mast cells
IgE Function
Cell-Killing Mechanisms Cytotoxic T lymphocytes
Destroy cancer cells or cells infected with virus Perforin, granzymes, or direct receptor
interactions
Cell-Killing Mechanisms
Other Cells Natural killer (NK) cells
Complement Tc cell mechanisms Regulatory T cells (Treg)
Provide peripheral tolerance Affect recognition of antigen and suppress
proliferative steps of antigen recognition
Fetal and Neonatal Immunity Antibody function is deficient
Capable of primary IgM response; unable to produce an IgG challenge
Immunity provided by maternal antibody Trophoblastic cells transport maternal IgG across
the placenta Newborn IgG levels are near adult levels
Fetal and Neonatal Immunity
Aging and Immune Function Decreased T cell activity
Thymic size is 15% of its maximum size Decreased production of specific antibodies Increase in circulating antigen-antibody
complexes Increase in circulating autoantibodies Decrease in circulating memory B cells
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