T cells (both CD4 "helper" and CD8 "cytotoxic" cells) are activated by antigen presenting cells (i.e. dendritic cells). This involves 3 different signals from the dendritic cell:
1. Major Histocompatibility Complex (MHC) presents an antigen (foreign peptide) to the T cell
2. A co-stimulatory signal (checking that it is a "professional" antigen presenting cell) which is a B7 molecule binding to a CD28 on the T cell
3. Cytokines (signalling molecule)
It is this 3rd type of signal, the cytokines which is important in the creation of the different T cells (CD8, or cytotoxic T cells and CD4, helper T cells).
Dendritic cells are able to release different cytokines, which cause T cell differentiation.
CD4 cells are presented antigen by MHC class II, whereas CD8 cells are presented antigen by MHC I.
Antigen-presenting cells (APCs) such as dendritic cells bind with antigens and present them to B cells, T cells, and macrophages, leading to their activation. This process is crucial for initiating immune responses against pathogens and foreign substances in the body.
The first step in the activation of naive B cells is the binding of an antigen to the B cell receptor (BCR) on the surface of the B cell. This interaction leads to receptor clustering and internalization of the antigen-BCR complex, initiating a signaling cascade that promotes B cell activation. Additionally, for optimal activation, naive B cells often require help from T helper cells, which provide necessary co-stimulatory signals and cytokines.
T cell priming refers to the process by which naive T cells encounter antigen-presenting cells, receive signals, and become activated to mount an immune response against specific antigens. This activation is essential for T cells to differentiate into effector T cells capable of carrying out their immune functions.
Yes. The first signal that a T cell receives from an antigen presenting cell (dendritic cell) is MHC presenting an antigen (foreign peptide). This gives the T cell specificity to this antigen.
Antigen presentation is essential for the activation and clonal selection of T cells, particularly CD4+ helper T cells and CD8+ cytotoxic T cells. Antigen-presenting cells (APCs), such as dendritic cells, macrophages, and B cells, process and present antigens on their surface using major histocompatibility complex (MHC) molecules. This interaction, along with co-stimulatory signals, initiates T cell activation, leading to proliferation and differentiation into effector cells. This process is crucial for the adaptive immune response against pathogens.
The surface immunoglotulin that serves as the B-Cell antigen receptor (BCR) has two roles in B-cell activation. First, like the antigen receptor on T cells, it transmits signals directly to the cell's interior when it binds antigen. Second, the B-Cell antigen receptor delivers the antigen to intracellular sites where it is degraded and returned to the B-cell surface as peptides bound to MHC class II molecules.
The Treg cell that inhibits the activity of B and T lymphocytes is called the CD4+ regulatory T cell, specifically the FOXP3+ subset. These cells play a crucial role in maintaining immune tolerance and preventing autoimmune responses by suppressing the activation and proliferation of other immune cells, including B and T lymphocytes. They achieve this through various mechanisms, including the secretion of inhibitory cytokines and direct cell-to-cell contact.
Antigen presentation: Antigen-presenting cells (APCs) process and present antigens to T cells. T cell activation: APCs activate T cells by binding to their T cell receptors and providing co-stimulatory signals. T cell proliferation and differentiation: Activated T cells undergo clonal expansion and differentiate into effector T cells, such as cytotoxic T cells and helper T cells. Target cell destruction: Effector T cells recognize and kill infected or abnormal cells through various mechanisms, such as releasing cytotoxic molecules or activating other immune cells.
t cell lymphoma
The first signal required to activate a T cell is MHC(Major Histocompatibility Complex) presenting an antigen(foreign peptide) to the T cell receptor.
T cells are activated by antigens presented on the surface of antigen-presenting cells, such as dendritic cells. B cells are activated primarily by recognizing antigens with their B cell receptor, although they may also require T cell help for full activation.
Antigen-presenting cells (APCs), primarily dendritic cells, macrophages, and B cells, introduce epitopes to T cells. They process and present peptide fragments of antigens on their surface using major histocompatibility complex (MHC) molecules. This interaction is crucial for T cell activation, allowing them to recognize and respond to specific pathogens or infected cells. Dendritic cells are particularly effective at initiating T cell responses due to their ability to capture and present antigens in lymphoid tissues.