- Immune response is initiated when the body encounters any
foreign molecules acting as exogenous or endogenous antigens).
- Various cytokines released from specific cells, like
interleukins (IL), tumor necrosis factor alpha (TNFα), activates
the production of mature phagocytic cells, like neutrophils,
macrophages and dendritic cells and induce their migration to the
site of infection or invasion.
- Phagocytic cells, engulf the foreign substances by phagocytosis
or endocytosis.
- The phagocytosed molecules processed and, then the peptide
fragments of antigens are expressed through membrane bound
glycoproteins called major histocompatibility complex (MHC).
- The antigenic polypeptide bound to MHC molecules further
induces B-lymphocytes (designated from Bursa of Fabricus in birds)
and T-lymphocytes (lymphocytes maturing in thymus), generating
humoral or cell mediated immune responses, as well as immunogenic
memory. Such specific activations lead to clonal selection, clonal
expansion and clonal deletion.
- Clonal deletion is the process by which immune cells (B-cells
or T-cells) that have receotors against self-antigens are
eliminated.
Activation of B-lymphocytes-
- B- cells may be activated, by direct interactions with TH
cells, and are called response to thymus-dependent (TD) antigens,
or may be activated without direct contacts with TH cells, by
thymus-independent antigens.
- Cytokines like IL3, IL-4. IL-5 activates TH2 cells.
- TH2 subtype in turn help in activation of B-cells
- These two types of signals may activate naïve B-cells
differentiates into memory B-cells and effector B cells (or plasma
cells).
- Plasma cells release antibodies. Antibodies, released to the
plasma, tissue fluid and lymph, contribute to humoral
immunity.