Each T cell is also committed to a given
antigen and recognizes it by one of two
TCRs. They may have TCR2s composed of
gamma (γ) and delta (δ) chains or TCR2s
composed of another heterodimer of alpha
(α) and beta (β) chains. These TCR2s are
associated with a group of transmembrance
proteins on the CD3 molecule,
which takes the antigen recognition signal
inside the cell. Signal transduction via
the CD3 complex is regulated by a series
of kinases, which are associated with the
tails of the CD3–TCR complex and regulate
phosphorylation. Defi ciencies or blocks
in the T-cell signaling pathways either at the cell-surface complex or at the level of
the kinases may result in various forms of
immunodefi ciency. Two other important
antigens present on TCR2 cells recognize
histocompatibility antigens and will be
discussed later. The genes for TCR chains
are on different chromosomes with the β
and α molecules on chromosome 7, while
the α and δ are on chromosome 14. As seen
in Figure 1.5, the four chains are made up
of a variable region and a constant region
similar to those observed with the immunoglobulins.
The variable regions are also
numerous and joined at D and J regions
by RAG1 and RAG2. This permits a diversity
of antigen recognition similar to that
observed with immunoglobulin, but additional
somatic mutation is not involved in
T cells. These similarities have led to the
concept that genes for antigen-specifi c T
cells evolved in the same manner as immunoglobulin
from a parent gene, and both
are members of a superantigen family.
The TCR complex recognizes small
peptides presented to it by the MHC class
I and II and depends on the type of T cell. Helper T cells (CD4) recognize class II antigens
while suppressor cytotoxic T cells
(CD8) recognize class I antigens. Because
of the rather low affi nity of the reactions,
recognition of processed antigen alone is
not suffi cient to activate T cells. Soluble
interleukins are needed to complete the
picture and are generated during the antigen
processing.
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