M. Susa et al., LEGIONELLA-PNEUMOPHILA INFECTION IN INTRATRACHEALLY INOCULATED T-CELL-DEPLETED OR T-CELL-NONDEPLETED A J MICE/, The Journal of immunology, 160(1), 1998, pp. 316-321
The inflammatory response and influence of T cell depletion on the pat
hogenesis of an experimental Legionella infection were studied, A/J mi
ce were infected with 10(6) CFU of Legionella pneumophila intratrachea
lly, With this dose all infected animals survived the infection and ba
cteria were cleared from lung, spleen, liver, and kidney within 10 to
11 days, leaving no residual changes in the affected organs. Inflammat
ory cells were recruited into the lung on the second day of infection,
reaching a maximum on the third day and filling out predominantly the
interstitial areas. During the first 3 days after inoculation, mainly
macrophages, B cells, NK cells, and large mononuclear cells of an unk
nown phenotype were attracted into the lung interstitium, whereas T ly
mphocytes infiltrated subsequently. During the early phase of infectio
n, serum concentrations of IFN-gamma, TNF-alpha, IL-1 beta, IL-4, and
IL-6 but not IL-2 increased dramatically, The cytokine secretion decre
ased on the third day after infection although bacteria were still pre
sent in the lung or even disseminated in different organs. Successful
clearance of bacteria from the lung was not observed before recruitmen
t of T cells into the lung, in mice depleted of both CD4(+) and CD8(+)
T cells, control of infection was impaired and lethality of infection
increased. Depletion of either subset left residual antibacterial mec
hanisms, which, however, were not sufficient to clear the Legionella a
s rapidly as in undepleted mice.