Lesson 13: The Adaptive Immune System
Lesson 13: The Adaptive Immune System
General Overview
Adaptive immunity involves specialized lymphocytes (B cells and T cells) that coordinate to eliminate or prevent pathogenic growth and tumor cells.
Enhanced response due to previous exposure to infectious pathogens.
Key Characteristics of Adaptive Immunity
Creates immunological memory after initial response to specific pathogens.
Allows for quick and specific recognition of pathogens, initiating a stronger and faster secondary immune response.
Immunological memory can last a lifetime.
Antigen Recognition
Molecular Recognition
The recognition mechanism in the adaptive immune system depends on diverse receptors.
Each receptor recognizes a specific feature of a pathogen known as an antigen, which triggers responses from B cells and/or T cells.
Antigen Binding
Antigen Recognition Process: A B cell or T cell binds to an antigen through a protein called an antigen receptor.
B cells and T cells produce millions of different antigen receptors, yet all receptors produced by a single B cell or T cell are identical (approximately 100,000).
The part of the antigen that binds is known as the epitope.
B Cells and Their Activation
Activation Mechanism
B cells become activated in lymph nodes or spleen when their antigen receptors (BCRs) bind to a specific antigen.
BCRs are Y-shaped structures made of four polypeptide chains (two heavy and two light chains) linked by disulfide bridges.
Structure of BCRs
Each chain contains a constant region (identical among B receptors) and a variable region (located at the tips of the Y, facilitating antigen binding).
Antigen Binding Characteristics
BCRs can bind to intact, undigested antigens; this can occur when antigens are free in lymph or part of a pathogen.
Sometimes, B cells are activated by antigen presenting cells (APCs), which is crucial for T cell activation.
T Cells and Their Activation
T Cell Structure
Upon maturation in the thymus, T cells possess a unique antigen receptor (TCR) composed of two different polypeptide chains (α and β chains) linked via a disulfide bridge.
The TCR binds to epitopes from antigen fragments only when presented by MHC molecules on host cells.
Antigen Presentation Process
Antigen Presentation: The combination of the antigen and an MHC protein is displayed on the surface of a host cell for T cell recognition.
Key antigen presenting cells include macrophages and dendritic cells that phagocytize pathogens, then present their fragments with MHC.
Types of T Cells
Helper T Cells (Th cells): Activated by macrophages and dendritic cells, releasing cytokines that stimulate immune responses, including B cell activation and cytotoxic T cell activation.
Cytotoxic T Cells (Tc cells): Activated by infected cells or cytokines from Th cells. These cells kill infected or damaged cells directly through granule secretion.
Mechanisms of Action of B Cells and Antibodies
B Cell Cloning and Differentiation
After recognizing an antigen, the specific B cell undergoes mitosis, creating numerous clones (clonal selection theory).
B cells differentiate into memory B cells (long-lived, responsible for quick responses upon reinfection) and plasma cells (short-lived, active in antibody production).
Antibody Function
Antibodies: Secreted form of activated BCRs, capable of neutralizing or marking pathogens for destruction.
Antibodies do not kill pathogens directly but interfere with their function or mark them for destruction by immune cells.
Mechanisms:
Opsonization: Marking pathogens for uptake by phagocytes.
Binding to toxins or pathogens, often leading to the formation of clumps that can be filtered out of blood.
Immunity Types
Active Immunity
Acquired through natural infection or artificially through vaccinations, which stimulate a primary immune response without causing the disease.
Passive Immunity
Transferred from one individual to another; can be natural (e.g., from mother to infant) or artificial (e.g., through medical treatment).
Additional Resources
Adaptive immune system articles from reliable sources (e.g., Boundless Anatomy and Physiology, Khan Academy).