Ph. Nibbering et al., BACTERIOSTATIC ACTIVITY OF BCG PPD-ACTIVATED MACROPHAGES AGAINST MYCOBACTERIUM-FORTUITUM DOES NOT INVOLVE REACTIVE NITROGEN OR OXYGEN INTERMEDIATES/, Scandinavian journal of immunology, 40(2), 1994, pp. 187-194
Mycobacteria preferentially reside in resident macrophages whereas act
ivated macrophages are presumed to eliminate the bacteria effectively.
The aim of the present study was to determine the antibacterial activ
ities of resident and activated murine peritoneal macrophages against
Mycobacterium fortuitum and the intracellular mechanisms involved. Aft
er phagocytosis M. fortuitum could not be killed by either BCG/PPD-act
ivated and IFN-gamma-activated macrophages and resident macrophages. T
he mycobacteria did not multiply in BCG/PPD-activated macrophages and
the rate of proliferation of M. fortuitum in IFN-gamma-activated macro
phages was only slightly inhibited compared to that in resident macrop
hages. Experiments with selective inhibitors of the production of reac
tive nitrogen intermediates (RNI) and reactive oxygen intermediates (R
OI) demonstrated that these factors are not essential for the mycobact
eriostatic activity of BCG/PPD-activated macrophages. After phagocytos
is of M. fortuitum, BCG/PPD-activated and IFN-gamma-activated macropha
ges produced substantial amounts of both RNI and ROI. No correlation w
as found between the levels of these intermediates and the proliferati
on of M. fortuitum in the macrophages. In conclusion, BCG/PPD-activate
d macrophages are bacteriostatic, but not bacteriocidal for M. fortuit
um and the former does not involve reactive nitrogen and oxygen interm
ediates.