The stimulation of transcription of acute-phase protein (APP) genes in
the liver is incorporated in the complex interchange of cytokines, gr
owth factors and glucocorticoid hormones that are released during the
systemic defence reaction in response to trauma, Through the broad spe
ctrum of their activities, this heterogenous group of circulating prot
eins assists the injured organism in restoring homeostasis by assuming
a protective role, APPs accomplish this by inactivating vasoactive, p
roteolytic and cytotoxic molecules liberated from damaged tissues and
accumulating phagocytic cells, and by participating in a feedback cont
rol mechanism that prevents an overload by the organisms' immune respo
nse, APP synthesis represents a non-specific response of the liver, in
somuch as different types of trauma elicit the production of the same
proteins, However, data obtained from different laboratory models and
clinical observations revealed a certain relationship between the seve
rity and type of trauma and the magnitude of activation of APP gene ex
pression, The observed variations of the overall pattern of APP synthe
sis point to the existence of different interplays between humoral and
cellular mediators capable of adjusting the production of individual
proteins to suit different traumas, Hence, changes in the serum concen
trations of some APPs have been shown to be useful in monitoring compl
ications such as infection or sepsis after surgery or trauma, and pred
icting the clinical course of malignant and other diseases, Of the APP
s studied in humans, information obtained on CRP and SAA has in partic
ular proved to be a useful indicator of the progression of different p
athological states.