Antigenic stimulation refers to the activation of adaptive immune cells — T and B lymphocytes — in response to antigen exposure. This process initiates a specific immune response aimed at recognizing and eliminating foreign agents.
It underlies both naturally acquired immunity following infection and vaccine-induced immunity. The intensity and nature of the immune response depend on the antigen dose, route of entry, and the functional status of the host’s immune system.
The pathophysiological cascade unfolds through several key stages: Initially, the antigen is captured and processed by antigen-presenting cells (APCs), such as dendritic cells. APCs then present antigen fragments on their surface via major histocompatibility complex (MHC) molecules.
These MHC-antigen complexes are recognized by specific helper T cells, which become activated and subsequently stimulate B cells. Activated lymphocytes undergo clonal expansion and differentiate into effector cells (plasma cells that produce antibodies and cytotoxic T cells) as well as memory cells.
Understanding the mechanisms of antigenic stimulation is fundamental to clinical practice.
Antigenic stimulation, which activates adaptive (specific) immunity, must be differentiated from innate immune activation. Unlike the highly specific response induced by antigenic stimulation, innate immunity responds nonspecifically to common pathogen-associated structures and does not generate immunological memory.
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