TMB lymphocytes play a major role in the specific immune response.
Understanding MHCs (Major Histocompatibility Complexes) is crucial for grasping this immune mechanism.
MHCs are akin to bulletin boards displaying antigens to the environment.
Two types of MHC:
MHC I: Expressed in all nucleated cells.
Allows communication with cytotoxic T cells (CD8+ T cells).
MHC II: Found only in immune system cells (macrophages, dendritic cells, B cells).
These are known as professional antigen presenting cells (APCs).
Nonprofessional antigen presenting cells express MHC I, whereas professional APCs express MHC II.
Each T or B lymphocyte can recognize specific antigens based on genetic determination.
The human body can recognize billions of different antigens and mount immune responses effectively.
The immune system avoids responding against self-antigens (self-tolerance).
T lymphocytes coordinate cell-mediated immunity, while B lymphocytes coordinate antibody-mediated immunity.
T lymphocytes primarily have two functions:
Destroy infected or damaged cells.
Support other immune cells.
T cells recognize specific parts of antigens, known as epitopes.
Various parts of an antigen (e.g., a component of a protein from bacteria) can be epitopes.
Each type of T cell responds to unique epitopes through their receptors.
Cytotoxic T Cells (CD8+):
Recognize antigens presented on MHC I and destroy infected cells.
Helper T Cells (CD4+):
Recognize antigens presented on MHC II and enhance the immune response by releasing cytokines.
TCRs are specific for certain epitopes.
Composed of alpha and beta chains on the plasma membrane, responsible for recognizing antigens.
Epitopes bind to regions on the alpha and beta chains.
Associated proteins known as Cluster Differentiation (CD) markers aid T cell function.
Cytotoxic T Cells (CD8+):
Interacts with MHC I through CD8 molecules.
Helper T Cells (CD4+):
Interacts with MHC II through CD4 molecules.
TCR diversity is achieved via VDJ recombination during T cell maturation:
Scrambling and rejoining of gene segments to create unique receptors.
Cytotoxic T Cells Activation:
Requires recognition of antigen via TCR and presentation on MHC I.
Requires co-stimulation (binding of CD28 on T cell to CD80 on APC).
Helper T Cells Activation:
Requires recognition of antigen via TCR and presentation on MHC II.
Also requires co-stimulation (binding of CD28 on T cell to CD80 on APC).
Co-stimulation is essential to prevent excessive immune responses that can lead to tissue damage.
Over-activation can cause autoimmune-like reactions (e.g., organ failure).
Cytotoxic T Cells:
Destroy infected cells by releasing perforins and initiating cell death.
Clone themselves for future immune responses.
Helper T Cells:
Release cytokines to enhance function of immune cells.
Clone themselves for ongoing immune support.
Helper T cells (CD4+) play a key role in linking T cells and B cells:
B cells can present antigens via MHC II to helper T cells.
Activation of B cells leads to antibody-mediated immunity (humoral immunity).