Differentiation/function of CD4+ & CD8+ Effector T cells Flashcards
what are the functions of CD4+ effector T cells?
- > recruit and activate phagocytes(macrophages/neutrophils) and other leukocytes that destroy intracellular and some extracellular microbes
- > help B lymphocytes produce antibodies
- > some can activate eosinophils to destroy particular types of microbes
what is cell-mediated immunity
the type of host defence that is mediated by T lymphocytes, and it serves as a defence mechanism against intracellular and phagocytosed microbes (cell-associated microbes)
how do CD4+ effector T cells activate phagocytes
via surface molecules, principally CD40 ligand and secreted cytokines
how are CD4+ T cells generated
by antigen recognition in secondary lymphoid organs
->but most of them leave these organs and migrate to peripheral sites of infection where they function in microbe elimination
what is delayed type hypersensitivity
T cell dependent injurious reaction where normal tissues are damaged from inflammation (leukocyte recruitment/activation) that accompanies many of the reactions of CD4+ T lymphocytes
-> TH1-mediated reaction that can cause significant tissue injury
what does the term hypersensitivity mean
tissue damage due to an immune response
how are the subsets of CD4+ effector T cells distinguished
by the type of cytokines they produce, the transcription factors they express and epigenetic changes in specific cytokine gene loci
->involved in host defence against different microbes
what are the signature cytokines produced by TH1, TH2 and TH17 CD4+ effector T cells
TH1 cells: IFN-Y
TH2 cells: IL-4, IL-5 and IL-13
TH17 cells: IL-17 and IL-22
what determines the the effector functions of T cells and their role in diseases?
the cytokines that they produce
what are some of the chemokine receptors that TH1, TH2 and TH17 CD4+ effector T cells express and what do they bind to?
TH1 cells: CSCR3, CCR5 (bind to chemokines elaborated in tissues during innate immune responsess), also express high levels of ligands for p and e selectin
TH2 cells: CCR3, CCR4, CCR8 (recognize chemokines that are highly expressed at sites of helminthic infection of allergic reactions)
TH17 cells: CCR6 (bind to chemokine CCL20)
what two things are required for the differentiation of CD4+ subsets??
involves transcriptional activation and epigenetic modification of cytokine genes
describe the three stages involved in the process of CD4+ T cell differentiation
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- induction: cytokines act on T cells stimulated by antigen and costimulators to induce the transcription of cytokine genes that are characteristic of each subset
- commitment: the subset’s cytokine genes become fixed in a transcriptionally active state (genes that encode cytokines not produced by that subset remain inactive) and the differentiating T cell becomes progressively committed to one specific pathway
- amplification: cytokines produced by any given subset promote the development of this subset and inhibit differentiation toward other CD4+ subpopulations. the net result is the accumulation of cells of one subset
what cells produce the cytokines that derive the development of CD4+ T cell subsets
produced by APCs (primarily dendritic cells and macrophages) and other immune cells present in the lymphoid organ where the immune response is initiated
- > DCs are activated to produce cytokines when they encounter microbes and may produce different cytokines depending on the microbe, influencing T cell subset development
- > DCs may selectively promote either TH1 or TH2 differentiation (without cytokine input)
how are the distinct cytokine profiles of differentiated cell populations controlled?
- by particular transcription factors that activate cytokine gene expression
- by chromatin modifications affecting accessibility to the promotors and regulatory elements of cytokine genes that these transcription factors bind to
(these epigenetic changes ensure that each subset can produce only its characteristic collection of cytokines
what particular leukocytes are recruited by the types of CD4+ effector T cells
T 1 activate macrophages
T 17 recruit mostly neutrophils but some macrophages
T 2 activate eosinophils
how derives the differentiation of TH1 cells
mainly the cytokines IL-12 and IFN-Y
- > occurs in response to microbes that activate DCs, macrophages and NK cells
- > stimulated by many intracellular bacteria and some parasites as well as viruses and administered protein antigens (all of which elicit innate immune reactions which produce cytokines that promote TH1 development)
what transcription factors do IFN-Y(produced by NK cells) and IL-12(produced by DCs/macrophages) activate to stimulate TH1 differentiation
T-bet, STAT1 and STAT4
IFN-Y activates STAT1 and T-bet which promotes IFN-Y production which sets up a positive amplification loop which derive TH1 differentiation
-> IL-12 binds to receptors and activates STAT1
what is the principle function of TH1 cells
To activate macrophages to ingest and destroy microbes
what is the principle macrophage-activating cytokine and what ligand does it work with to activate macrophages
IFN-Y acts with ligand CD40
what is classical macrophage activation
macrophage activation resulting in increased microbicidal activity (enhance macrophage killing)
why would TH1 produce IL-10
serves as a neg feedback loop to suppress TH1 activation by inhibiting DCs and macrophages