Despite the importance of tuberculosis as the leading cause of death d
ue to infectious disease in the world, it has only been recently that
an understanding of the human host response in this infection has begu
n to emerge. The key components of this response are cytokines and com
ponents of cellular immunity, predominantly T-lymphocytes and macropha
ges. Though the relationships among the components of the immune respo
nse are complex, it seems likely that in response to mycobacterial inf
ection associated with active disease, cytokines such as TNF-alpha and
IL-1 beta are produced; these cytokines serve to recruit more lymphoc
ytes, generally of the T-H (T helper) phenotype, which then produces s
ubstances such as the macrophage activating factor interferon-gamma. M
acrophages activated by IFN-gamma are thus stimulating to enhance intr
acellular killing of mycobacteria. The role of other cytokines, such a
s IL-6 and IL-8, both of which are induced by M. tuberculosis or its c
ell wall components, is less clear. Further elucidation of the human h
ost response to tuberculosis should help in the development of new vac
cines and treatment strategies.