Activated slower than the innate immune system but lasts longer.
Involves lymphocytes (B and T cells).
Main function: produce and secrete antibodies.
B cells turn into plasma cells (antibody-secreting cells).
Become effector T cells.
Two main types:
Helper T cells: Help activate other immune cells.
Cytotoxic T cells: Kill infected cells.
Raises an immune response against pathogens that evade the innate immune system.
Needed to completely clear an infection when innate immunity isn't enough.
Key feature differentiating it from the innate immune system.
Adaptive immune system adapts and remembers pathogens.
Repeat exposures lead to a faster, larger, and more effective response.
First exposure: Takes about 10 days for antibody levels to increase.
Second exposure: Antibody levels increase much earlier (around day three), and the response is faster and larger.
Lymphocytes remember the pathogen.
Vaccinations: Expose you to an antigen, priming your immune response, leading to memory against that antigen.
B and T cells are pre-exposed in a non-infectious state.
When encountering the actual pathogen, the adaptive immune system recognizes it and mounts a quick response.
B and T cells express antigen-binding receptors on their surface.
Each B and T cell has approximately 1000 receptors, all specific to a single antigen.
A single B or T cell can only recognize one type of antigen from one type of pathogen (e.g., one B cell specific to COVID, another to influenza A).
Different B and T cells have different antigen-binding receptors to detect different antigens, providing diversity.
Adaptive immune system generally doesn't attack the body's own cells.
Failure of this leads to autoimmune diseases.
Two subdivisions of the adaptive immune system, differing by the type of lymphocyte involved (B cells or T cells).
Involves B cells producing antibodies.
Antibodies prevent extracellular pathogens from entering and infecting cells.
Eliminates pathogens before they enter cells.
Involves T cells.
Focused on intracellular microbes.
Important when pathogens have already entered cells and are actively infecting them.
Helper T cells: Activate phagocytes to destroy pathogens and activate B cells to produce antibodies.
Cytotoxic T cells: Kill infected cells.
Humoral immunity (B cells) prevents pathogens from entering cells (extracellular response).
Cell-mediated immunity (T cells) acts on pathogens that have already entered cells.
Involves B cells secreting antibodies.
Naive B cells: B cells that haven't encountered an antigen yet, express antigen-binding receptors (immunoglobulins) on their plasma membrane.
When an antigen binds to the specific B cell receptor, the B cell is activated and undergoes clonal expansion (proliferation).
Helper T cells assist in activating B cells.
After clonal expansion, B cells differentiate into:
Plasma cells: Synthesize and secrete antibodies specific to the antigen. Short-lived (4-7 days) but produce many antibodies (approximately 2,000 antibody molecules every second).
Memory B cells: Long-lived cells responsible for the faster response upon re-encountering the antigen; they circulate and monitor for future infections.
Five different classes of antibodies, each with different features and functions:
IgM: Most common class produced in response to an antigen.
IgG: Can cross the placenta during pregnancy, providing immunity to the fetus.
IgE: Responsible for allergies (e.g., hay fever).
Controlled by T cells.
T cells recognize intracellular antigens.
Antigen must be presented to the T cell by an antigen-presenting cell (APC) using a major histocompatibility complex (MHC) molecule.
APCs: Macrophages and dendritic cells.
Infected cells present the antigen to the T cell via the MHC molecule.
Antigen binds to the MHC molecule, and the complex is transported to the cell surface.
T cells only detect intracellular antigens presented by APCs.
Two classes of MHC molecules:
MHC class one: Expressed on all nucleated cells (not specific to immune cells).
MHC class two: Expressed only by APCs (dendritic cells, macrophages, and B cells).
APCs are found scattered throughout the body, especially in areas where pathogens can easily enter (skin, GI tract, respiratory tract).
They reside in tissues, waiting for an antigen.
Upon detecting an antigen, they are activated and migrate to the spleen or lymph nodes.
In the lymph nodes, they present the antigen to T cells, activating them.
Pathogen enters through a cut.
Langerhans cells (macrophages) in the epidermis pick up the antigen.
Langerhans cells migrate to the dermis and present the antigen to dendritic cells.
Dendritic cells are activated and migrate to the lymph nodes.
In the lymph node, dendritic cells mature and increase MHC expression.
They present the antigen to naive T cells, activating them.
MHC class one activates cytotoxic T cells to kill infected cells.
MHC class two activates helper T cells to help other immune cells.
Macrophages presenting antigen via MHC class two activate helper T cells, which then activate the macrophage to destroy the pathogen.
B cells can also activate T cells by presenting an antigen via MHC class two; the activated helper T cell then helps activate the B cell to produce more antibodies.
Naive T cells: T cells that haven't encountered an antigen.
When an APC presents an antigen to a T cell, a sequence of events occurs, and the T cell is activated and undergoes clonal expansion.
T cells differentiate into:
Effector T cells: Respond to clear the infection.
Memory T cells: Reside in the tissue at the site of infection and act as a surveillance mechanism for long-lived immunity.
Memory B and T cells (lasting months or years) help activate humoral and cell-mediated immunity upon re-encountering a pathogen.