1993
DOI: 10.1128/iai.61.2.491-497.1993
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Gamma interferon-induced nitric oxide production reduces Chlamydia trachomatis infectivity in McCoy cells

Abstract: McCoy cells, murine-derived cells commonly used for propagation of chlamydiae, were found to be efficient producers of nitric oxide (NO) when primed with murine gamma interferon (IFN-y) and then exposed to the second signals provided by Escherichia coli lipopolysaccharide, human interleukin-la, murine tumor necrosis factor a, or Chlamydia trachomatis type H. Murine recombinant IFN-y over a range of 0 to 50 U/mi inhibited infectivity of C. trachomatis type H in a dose-dependent fashion in McCoy cells while simu… Show more

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Cited by 91 publications
(44 citation statements)
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References 42 publications
(29 reference statements)
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“…DNA damage by nitric oxide and other free radicals released by bacterial infection activated inflammatory cells has been suggested to be oncogenic (Oshima & Bartsch, 1994;Rosin et al, 1994). The liberation of nitric oxide has been demonstrated in chlamydial infections (Mayer et al, 1993), but is not plausible in the lymphoma context.…”
Section: Discussionmentioning
confidence: 97%
“…DNA damage by nitric oxide and other free radicals released by bacterial infection activated inflammatory cells has been suggested to be oncogenic (Oshima & Bartsch, 1994;Rosin et al, 1994). The liberation of nitric oxide has been demonstrated in chlamydial infections (Mayer et al, 1993), but is not plausible in the lymphoma context.…”
Section: Discussionmentioning
confidence: 97%
“…The same mechanism has been suggested for the role of schistosomiasis in the development of urinary bladder carcinoma (Rosin et al, 1994). The liberation of nitric oxide has also been shown to occur in chlamydial infections (Mayer et al, 1993). The possibility that chronic C. pneumoniae infection induces carcinogenesis in the lung through mediators of inflammation could thus be a logical consequence from a chronic infection.…”
Section: Discussionmentioning
confidence: 98%
“…After appropriate stimulation, macrophages produce NO and its metabolites (reactive nitrogen intermediates (RNI)) [16], and express their antimicrobial capabilities [17] by inhibiting cytochrome P450 activity [18] and causing changes in DNA [19]. Several recent studies have demonstrated that RNI play an important role in host defence against infections caused by various pathogens, including parasites [20][21][22][23], fungi [15,[24][25][26], bacteria [27][28][29][30][31], chlamydia [32] and mycobacteria [33][34][35]. In the present study, we examine the role of RNI in the anti-fungal activity of IFN-g-stimulated murine peritoneal macrophages.…”
Section: Introductionmentioning
confidence: 99%