Describe the sequence of events that occurs during a primary immune response with reference to the roles of: • macrophages • B-lymphocytes, including plasma cells • T-lymphocytes, limited to T-helper cells and T-killer cells
Describe the sequence of events that occurs during a primary immune response with reference to the roles of: • macrophages • B-lymphocytes, including plasma cells • T-lymphocytes, limited to T-helper cells and T-killer cells
Answer
The primary immune response is the body’s initial response to a specific pathogen after it is encountered for the first time. This response involves a complex interplay of various immune cells, including macrophages, B-lymphocytes (B-cells), and T-lymphocytes (T-cells). Here’s a detailed sequence of events that occur during a primary immune response:
1. Antigen Recognition and Phagocytosis
- Macrophages:
- When a pathogen enters the body, macrophages act as antigen-presenting cells (APCs). They engulf (phagocytize) the pathogen through a process called phagocytosis.
- After ingesting the pathogen, macrophages break it down into smaller pieces (antigens) and present these antigens on their surface using Major Histocompatibility Complex (MHC) class II molecules.
2. Activation of T-Lymphocytes
- T-helper Cells (CD4+ T-cells):
- The antigen-presenting macrophages travel to the lymph nodes, where they interact with naive T-helper cells. The binding of the T-cell receptor (TCR) on T-helper cells to the antigen-MHC complex activates these T-cells.
- Activated T-helper cells proliferate (multiply) and secrete cytokines, which play crucial roles in orchestrating the immune response by stimulating other immune cells, including B-cells and T-killer cells.
3. Activation of B-Lymphocytes
- B-Lymphocytes (B-cells):
- Naive B-cells can also encounter the same antigen directly. When they bind to the antigen through their B-cell receptors (BCR), they become activated.
- T-helper cells provide additional signals (via cytokines) that promote B-cell activation and differentiation.
4. Differentiation of B-Lymphocytes
- Activated B-cells undergo clonal expansion, where they proliferate and differentiate into two main types of cells:
- Plasma Cells: These cells produce and secrete large amounts of antibodies (immunoglobulins) specific to the antigen. The antibodies circulate in the bloodstream and help neutralize or mark the pathogen for destruction.
- Memory B-Cells: Some B-cells differentiate into memory B-cells, which remain in the body long-term and provide a quicker and stronger response if the same antigen is encountered again in the future.
5. Activation of T-Killer Cells
- T-Killer Cells (Cytotoxic T-Lymphocytes, CD8+ T-cells):
- Some of the activated T-helper cells also stimulate naive T-killer cells. These cells recognize and bind to infected cells that present the specific antigen on MHC class I molecules.
- Upon activation, T-killer cells proliferate and differentiate, seeking out and destroying infected cells by inducing apoptosis (programmed cell death).
6. Response and Resolution
- As the immune response progresses, antibodies produced by plasma cells help neutralize pathogens, while T-killer cells eliminate infected cells.
- Once the pathogen is cleared, the immune response begins to wind down. Memory B-cells and T-cells remain in circulation, providing long-lasting immunity.
Summary of Roles:
- Macrophages: Engulf pathogens, present antigens to T-cells, and secrete cytokines to recruit other immune cells.
- B-Lymphocytes: Produce antibodies to neutralize pathogens, differentiate into plasma cells (for immediate response) and memory B-cells (for long-term immunity).
- T-Lymphocytes:
- T-Helper Cells: Activate and support B-cells and T-killer cells through cytokine secretion.
- T-Killer Cells: Directly kill infected cells displaying the specific antigen.