The clonal selection theory is a fundamental concept in immunology that explains how the adaptive immune system responds to specific antigens. Each B and T cell in the body possesses unique B cell receptors (BCRs) or T cell receptors (TCRs) that allow them to recognize and respond to particular antigens. When an infection occurs, the immune system must identify and activate only those B and T cells that can effectively respond to the invading antigen.
According to the clonal selection theory, when a specific antigen is detected, only the B and T cells that can bind to that antigen are selected for activation. This selection process leads to the proliferation of these specific cells, creating a large number of identical clones that can effectively combat the infection. The cells that do not recognize the antigen remain inactive and do not proliferate.
To illustrate this process, consider a mixed population of B cells. Each B cell has identical BCRs that respond to the same antigen, but different B cells have different BCRs that respond to various antigens. For example, if a red antigen is present, only the B cell with the appropriate BCR to bind to this antigen will be activated. This selected B cell will then undergo activation and proliferation, resulting in an army of clones capable of targeting the specific antigen.
Following proliferation, the activated B cells differentiate into two main types: plasma cells and memory B cells. Plasma cells are responsible for secreting antibodies that specifically target the antigen, aiding in its elimination. Memory B cells, on the other hand, remain in the body to provide a faster and more robust response if the same antigen is encountered again in the future.
In summary, the clonal selection theory emphasizes the importance of specificity in the immune response, ensuring that only the B and T cells that can effectively recognize and respond to a particular antigen are activated and proliferated. This mechanism is crucial for the adaptive immune system's ability to remember and respond to previously encountered pathogens.