Once naive T cells encounter antigen, they become primed effector cell
s. The scope of effector functions mediated by these cells defines the
efferent arm of the immune response. The change from naive to primed
effector cell is known as adaptive immunity and takes 2 forms: cell me
diated, in which T cells mediate effector function, and humoral, in wh
ich antibodies are the effector molecules. There are 3 types of effect
or T cells: inflammatory CD4 T cells, which activate macrophages; help
er CD4 T cells, which help B lymphocytes produce antibody; and cytotox
ic CDS T cells, which kill their target cells. The interaction of prim
ed effector cells with their targets results in phenotypic changes in
the cells and the secretion of cytokines. These cytokines may be secre
ted by the primed effector T cell, the target cell, or both. Cytokines
function in either autocrine (secreted and used by the same cell) or
paracrine (secreted by 1 cell and used by a different cell) circuits a
nd have marked regulatory effects on cells in both the immune and skel
etal systems. Many of these cytokines, which were once thought to be p
roducts exclusively of immune cells, are now known to be produced by c
ells of the skeletal system. Both the specific and nonspecific compone
nts of the immune response have profound effects on remodeling of the
musculoskeletal system during normal and pathologic states.