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. 2015 Jun 9;7(6):637–646. doi: 10.1159/000430913

Table 2.

Inflammatory response

WT Vehicle WT rIFN-γ TRIF mutant vehicle TRIF mutant rIFN-γ
TNF-α 892 (245) 760 (57) 191 (48)** 501 (115)#
IL-1β 7,434 (642) 4,950 (753)* 4,168 (731)** 4,525 (557)**
IL-6 1,914 (451) 2,030 (624) 2,446 (398) 1,507 (216)#
IL-10 14 (2) 11 (1) 14 (2) b.d.
CXCL1 12,586 (1,899) 9,453 (1,645) 3,625 (871)** 4,255 (828)*
CXCL2 20,553 (6,546) 38,048 (7,157) 6,432 (1,532)* 28,943 (5,785)###
CCL2 4,619 (541) 3,718 (366) 1,841 (210)*** 2,126 (240)**' #

WT and TRIF mutant mice were infected with 1 × 104 CFU K. pneumoniae and 50 ng recombinant IFN-γ was administered intranasally upon infection and after 48 h. Homogenates were prepared from right lungs. Cytokine and chemokine levels are presented in pg/ml of lung homogenate. Data are mean (SE) of 7–8 mice per group. b.d. = Below detection.

*

p <0.05,

**

p <0.01,

***

p <0.001, vs. vehicle-treated WT mice.

#

p <0.05,

## p <0.01,

###

p <0.001, rIFN-γ-treated TRIF mutant mice vs. vehicle-treated TRIF mutant mice.