Adaptive immunity occurs in vertebrates and involves specific recognition of pathogens.
It operates alongside the innate immune response simultaneously.
The two primary components of adaptive immunity are the humoral response (antibody-mediated defense) and cell-mediated response.
Pathogen Recognition: Antibodies provide pathogen-specific recognition, crucial for identifying harmful entities.
Lymphocytes: Key players include T cells and B cells, types of white blood cells that combat infections rather than red blood cells, which function mainly to carry oxygen.
T Cells: Mature in the thymus gland; involved in cell-mediated immunity.
B Cells: Responsible for antibody production; differentiate into plasma cells and memory B cells.
Definition: Antigens are substances that elicit an immune response; they can be proteins, polysaccharides, or even blood type mismatches.
Antigens stimulate the production of antibodies, creating an antibody-antigen complex in some cases, relevant for blood transfusions.
They are usually large molecules recognized by the immune system as foreign.
White blood cells have surface structures called antigen receptors manly involved in the binding of specific epitopes from antigens.
Epitopes: Small portions of antigens recognized by B cells and T cells, essential for the immune response.
B cell antigen receptors contain constant and variable regions; the variable regions are unique to each B cell.
Y-shaped proteins consisting of two heavy chains and two light chains.
Constant Region: Common to all B cell receptors, facilitating basic structure consistency.
Variable Region: Unique to each B cell, generated randomly; crucial for specificity in binding to antigens.
Upon binding to a matching epitope, B cells become activated and undergo clonal selection, producing numerous identical cells with the specific receptors for that antigen.
The antibodies produced are called immunoglobulins, which circulate in the bloodstream to bind to antigens.
Some activated B cells become memory B cells, which persist in the body for quicker responses during subsequent infections with the same pathogen.
Similar to B cells, T cells activate upon recognizing antigens presented by Major Histocompatibility Complex (MHC) molecules on infected cells.
Helper T Cells: Assist in activating other immune cells, including B cells, by secreting cytokines and promoting clonal expansion.
Cytotoxic T Cells: Target and kill infected cells; they release perforins to create holes in the target cell membranes and granzymes to induce apoptosis.
Primary Immune Response: Initial response upon first exposure to an antigen; slower response as B and T cells need time to activate and clone.
Secondary Immune Response: Faster response upon re-exposure to an antigen due to memory cells; produces more antibodies more quickly than the primary response.
Active Immunity: Developed through exposure to antigens; includes responses from natural infections or vaccinations.
Passive Immunity: Involves gaining pre-formed antibodies from another individual; occurs naturally through maternal antibodies or through treatments such as antivenom.
Understanding the mechanics of the immune response, including the roles of B and T cells and how immune memory is established, is critical for immunology and vaccine development.