Selective recruitment of Th I cells induced by re-infection of succeptible and resistant mice with Pseudomonas aerugionosa in the lungs indicates protective role of IL-12.
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Selective recruitment of Th I cells induced by re-infection of succeptible and resistant mice with Pseudomonas aerugionosa in the lungs indicates protective role of IL-12. / Moser, C; Jensen, P O; Kobayashi, O; Hougen, H P; Song, Z; Rygaard, J; Kharazmi, A; Høiby, Niels.
In: Clinical and Experimental Immunology, Vol. 127, No. 2, 2002, p. 206-213.Research output: Contribution to journal › Journal article › Research › peer-review
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T1 - Selective recruitment of Th I cells induced by re-infection of succeptible and resistant mice with Pseudomonas aerugionosa in the lungs indicates protective role of IL-12.
AU - Moser, C
AU - Jensen, P O
AU - Kobayashi, O
AU - Hougen, H P
AU - Song, Z
AU - Rygaard, J
AU - Kharazmi, A
AU - Høiby, Niels
PY - 2002
Y1 - 2002
N2 - Repeated challenge with antigen is involved in the pathogenesis of a variety of pulmonary diseases. Patients with cystic fibrosis (CF) experience recurrent pulmonary colonization with Pseudomonas aeruginosa before establishment of chronic lung infection. To mimic recurrent lung infections in CF patients, the lungs of susceptible BALB/c mice were re-infected with P. aeruginosa 14 days after the initial infection. Singly-infected BALB/c mice, as well as non-infected mice, were used as controls. Decreased mortality and milder lung inflammation in re-infected BALB/c mice, as well as a tendency for improved clearance of bacteria, was observed when compared with singly-infected mice. The improved outcome in re-infected mice correlated with changes in CD4 cell numbers. Surface expression of LFA-1 on pulmonary CD4 cells was increased in re-infected compared with singly-infected mice. Moreover, resistance to re-infection was paralleled by a shift towards a Th1-dominated response and increased IL-12 production. No significant increase in serum IgG was observed in the re-infected mice. In conclusion, these results indicate a protective role for a Th1-dominated response, independent of antibody production, in chronic P. aeruginosa lung infection in CF.
AB - Repeated challenge with antigen is involved in the pathogenesis of a variety of pulmonary diseases. Patients with cystic fibrosis (CF) experience recurrent pulmonary colonization with Pseudomonas aeruginosa before establishment of chronic lung infection. To mimic recurrent lung infections in CF patients, the lungs of susceptible BALB/c mice were re-infected with P. aeruginosa 14 days after the initial infection. Singly-infected BALB/c mice, as well as non-infected mice, were used as controls. Decreased mortality and milder lung inflammation in re-infected BALB/c mice, as well as a tendency for improved clearance of bacteria, was observed when compared with singly-infected mice. The improved outcome in re-infected mice correlated with changes in CD4 cell numbers. Surface expression of LFA-1 on pulmonary CD4 cells was increased in re-infected compared with singly-infected mice. Moreover, resistance to re-infection was paralleled by a shift towards a Th1-dominated response and increased IL-12 production. No significant increase in serum IgG was observed in the re-infected mice. In conclusion, these results indicate a protective role for a Th1-dominated response, independent of antibody production, in chronic P. aeruginosa lung infection in CF.
KW - Agar
KW - Alginates
KW - Animals
KW - Antibodies, Bacterial
KW - Bronchoalveolar Lavage Fluid
KW - CD4 Lymphocyte Count
KW - Chronic Disease
KW - Cytokines
KW - Female
KW - Glucuronic Acid
KW - Hexuronic Acids
KW - Immunoglobulin G
KW - Interferon-gamma
KW - Interleukin-12
KW - Interleukin-4
KW - Lymphocyte Function-Associated Antigen-1
KW - Mice
KW - Mice, Inbred BALB C
KW - Models, Animal
KW - Pneumonia, Bacterial
KW - Pseudomonas Infections
KW - Pseudomonas aeruginosa
KW - Recurrence
KW - Th1 Cells
M3 - Journal article
C2 - 11876741
VL - 127
SP - 206
EP - 213
JO - Clinical and Experimental Immunology, Supplement
JF - Clinical and Experimental Immunology, Supplement
SN - 0964-2536
IS - 2
ER -
ID: 44353420