EFFECTOR MECHANISMS OF CELL
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Transcript EFFECTOR MECHANISMS OF CELL
Chapter 10
Cell-mediated immunity (CMI) is the type of host defense that is mediated by T
lymphocytes, and it serves as a defense mechanism against intracellular and
phagocytosed microbes
Reactions of CD4+ T cells in cell-mediated immunity
Cell-mediated immunity to Listeria
monocytogenes
In
CMI
responses
against
phagocytosed microbes, T cells
specifically
recognize
microbial
antigens but phagocytes actually
destroy the pathogens
Inflammation, consisting of leukocyte
recruitment
and
activation,
accompanies many of the reactions of
CD4+ T lymphocytes and may
damage normal tissues. This T cell–
dependent injurious reaction is called
delayed-type hypersensitivity (DTH)
SUBSETS OF CD4+ EFFECTOR T CELLS
The Th1 Subset
The TH1 subset is induced by microbes that are ingested by and activate
phagocytes, and is the major effector T cell population in phagocyte-mediated
host defense, the central reaction of cell-mediated immunity
TH1 differentiation is driven mainly by the cytokines IL-12 and IFN-γ and
occurs in response to microbes that activate dendritic cells, macrophages, and
NK cells
Development of TH1 cells
Functions of TH1 cells
Interferon-γ
IFN-γ is the principal macrophage-activating cytokine and serves critical
functions in immunity against intracellular microbes
IFN-γ activates macrophages to kill phagocytosed microbes
IFN-γ acts on B cells to promote switching to certain IgG subclasses, notably
IgG2a or IgG2c (in mice), and to inhibit switching to IL-4–dependent isotypes,
such as IgE
IFN-γ promotes the differentiation of CD4+ T cells to the TH1 subset and inhibits
the development of TH2 and TH17 cells
IFN-γ stimulates expression of several different proteins that contribute to
enhanced MHC-associated antigen presentation and the initiation and
amplification of T cell–dependent immune responses
Other TH1 Cytokines
In addition to IFN-γ, TH1 cells produce TNF and various chemokines, which contribute
to the recruitment of leukocytes and enhanced inflammation. Somewhat surprisingly,
TH1 cells are also important sources of IL-10, which functions mainly to inhibit dendritic
cells and macrophages and thus to suppress TH1 activation. This is an example of a
negative feedback loop in T cell responses.
Macrophage activation by TH1 cells
Classical and alternative macrophage activation
THE TH2 SUBSET
Functions of TH2 cells
Cytokines Produced by TH2 Cells
Interleukin-4 (IL-4)
IL-4 is the major stimulus for the production of IgE antibodies and for the development
of TH2 cells from naïve CD4+ helper T cells
IL-4 stimulates B cell Ig heavy chain class switching to the IgE isotype
IL-4 stimulates the development of TH2 cells and functions as an autocrine growth factor
for differentiated TH2 cells
IL-4, together with IL-13, contributes to an alternative of macrophage activation
IL-4 (and IL-13) stimulate peristalsis in the gastrointestinal tract, and IL-13 increases
mucus secretion from airway and gut epithelial cells
IL-4 and IL-13 stimulate the recruitment of leukocytes
Interleukin-13
IL-13 is structurally and functionally similar to IL-4 and also plays a key role in defense
against helminths and in allergic diseases
IL-13 is produced mainly by the TH2 subset, but basophils, eosinophils, and NKT cells
The receptor is expressed on a wide variety of cells, including B cells, mononuclear
phagocytes, dendritic cells, eosinophils, basophils, fibroblasts, endothelial cells, and
bronchial epithelial cells. T cells do not express the IL-13 receptor
IL-13 works together with IL-4 in producing biologic effects associated with allergic
inflammation
Interleukin-5
IL-5 is an activator of eosinophils and serves as the principal link between T cell
activation and eosinophilic inflammation
The principal actions of IL-5 are to activate mature eosinophils and to stimulate the
growth and differentiation of eosinophils
THE TH17 SUBSET
TH17 cells secrete cytokines that recruit leukocytes, mainly neutrophils, to sites of
infection
Most of the inflammatory actions of these cells are mediated by IL-17, but other
cytokines produced by this subset may also contribute
Development of TH17 cells
Functions of TH17 cells
Interleukin-17
IL-17 is an unusual cytokine because neither it nor its receptor is homologous to any
other known cytokine receptor pair
The IL-17 family includes six structurally related proteins, of which IL-17A and IL-17F
are the most similar, and the immunologic activities seem to be mediated primarily by IL17A. IL-17A and IL-17F are produced mainly by TH17 cells
IL-17 is an important link between T cell–mediated adaptive immunity and the innate
immune system, especially the inflammatory component of innate responses
IL-17 induces neutrophil-rich inflammatory reaction
IL-17 stimulates the production of antimicrobial substances, including defensins, from
numerous cell types
Other TH17 Cytokines
IL-22 is a member of the IL-10 cytokine family. It is produced by activated T cells,
particularly TH17 cells, and by NK cells. The actions of IL-22 appear contradictory.
Some studies indicate that it contributes to inflammation and tissue injury, but the bulk
of the available data suggests that it is produced in epithelial tissues, especially of the skin
and gastrointestinal tract, and serves to maintain epithelial integrity, mainly by
promoting the barrier function of epithelia and by stimulating repair reactions
IL-21 is produced by activated CD4+ T cells, including TH17 cells, which has a wide
variety of effects on B and T cells and NK cells. An important function of IL-21 is in
antibody responses, especially the reactions that occur in germinal centers. IL-21 is
required for the generation of follicular helper T cells and is also produced by follicular
helper cells and stimulates B cells in germinal centers
FUNCTIONS OF OTHER T CELL SUBSETS
γδ T Cells
Less than 5% of all T cells express this form of TCR
The limited diversity of the γδ TCRs in many tissues suggests that the ligands for these
receptors may be invariant and conserved
More than 50% of lymphocytes in the small bowel mucosa of mice and chickens, called
intraepithelial lymphocytes, are γδ T cells. In mouse skin, most of the intraepidermal T
cells express the γδ receptor
Only about 10% of human intestinal intraepithelial T cells express the γδ TCR
γδ T cells do not recognize MHC-associated peptide antigens and are not MHC restricted
Some γδ T cell clones recognize small phosphorylated molecules, alkylamines, or lipids
that are commonly found in mycobacteria and other microbes and that may be presented
by “non-classical” class I MHC–like molecules
Many γδ T cells are triggered by microbial heat shock proteins
A number of biologic activities have been ascribed to γδ T cells, including secretion of
cytokines and killing of infected cells, but the function of these cells remains poorly
understood
NKT Cells
A small population of T cells also expresses markers that are found on NK cells, such as
CD56; these are called NKT cells
Because of this limited diversity, these cells are also called invariant NKT (iNKT) cells
All NKT cell TCRs recognize lipids that are bound to class I MHC–like molecules called
CD1 molecules
NKT cells are capable of rapidly producing cytokines such as IL-4 and IFN-γ after
activation, and they may help marginal zone B cells to produce antibodies against lipid
antigens