Chronic Pseudomonas aeruginosa lung infection is more severe in Th2 responding BALB/c mice compared to Th1 responding C3H/HeN mice. NLM AIDSLINE Important note: Information in this article was accurate in 1998. The state of the art may have changed since the publication date.

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Chronic Pseudomonas aeruginosa lung infection is more severe in Th2 responding BALB/c mice compared to Th1 responding C3H/HeN mice.

APMIS. 1997 Nov;105(11):838-42. Unique Identifier : AIDSLINE MED/98055272
Moser C; Johansen HK; Song Z; Hougen HP; Rygaard J; Hoiby N; Department of Clinical Microbiology, Rigshospitalet, Copenhagen,; Denmark.


Abstract: The chronic Pseudomonas aeruginosa lung infection in cystic fibrosis (CF) is characterized by a pronounced antibody response and microcolonies surrounded by numerous polymorphonuclear neutrophils (PMN). Poor prognosis is correlated with a high antibody response to P. aeruginosa antigens. An animal model of this infection was established in two strains of mice: C3H/HeN and BALB/c, generally known as Th1 and Th2 responders, respectively, which were challenged with alginate-embedded P. aeruginosa. Mortality was significantly lower in C3H/HeN compared to BALB/c mice (p < 0.025). P. aeruginosa was cleared more efficiently in C3H/HeN mice and significantly more C3H/HeN mice showed normal lung histopathology (p < 0.02), and we found significantly fewer microabscesses in C3H/HeN mice than in BALB/c mice (p < 0.005). In supernatants from P. aeruginosa antigen and concanavalin A-stimulated spleen cells from the two strains of mice, the interferon-(IFN-) gamma levels were higher, whereas IL-4 levels were lower in C3H/HeN mice than in BALB/c mice. The implications of these findings for CF patients with chronic P. aeruginosa lung infection are discussed.
Keywords: Animal Chronic Disease Female Interferon Type II/METABOLISM Interleukin-4/METABOLISM Lymphocyte Transformation Mice Mice, Inbred BALB C/IMMUNOLOGY Mice, Inbred C3H/IMMUNOLOGY Pneumonia, Bacterial/*IMMUNOLOGY/MICROBIOLOGY Pseudomonas aeruginosa/*PATHOGENICITY Pseudomonas Infections/*IMMUNOLOGY Spleen/IMMUNOLOGY Support, Non-U.S. Gov't Th1 Cells/*IMMUNOLOGY Th2 Cells/*IMMUNOLOGY JOURNAL ARTICLEKWDanimalchronicdiseasefemaleinterferontypeii/metabolisminterleukin-4/metabolismlymphocytetransformationmicemice,inbredbalbc/immunologymice,inbredc3h/immunologypneumonia,bacterial/KWDimmunology/microbiologypseudomonasaeruginosa/KWDpathogenicitypseudomonasinfections/KWDimmunologyspleen/immunologysupport,non-uKWDsKWDgov'tth1cells/KWDimmunologyth2cells/KWDimmunologyjournalarticle
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M9820738

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