Chlamydia pneumoniae infection can exacerbate atherosclerosis in animals. T
o test the hypothesis that antibiotic therapy inhibits the atherogenic effe
cts of C. pneumoniae infection, 10-week-old apolipoprotein E (ApoE) null mi
ce were infected with C. pneumoniae or placebo, were treated for 2 weeks af
ter infection with azithromycin or placebo, and were killed at 20 weeks of
age. Infection did not affect the size of the aortic lesion, and antibiotic
treatment had no effect. Another group of mice, 12-week-old ApoE mice, wer
e infected with C. pneumoniae or placebo, were treated for 2 weeks after in
fection with azithromycin or placebo, and were killed at 26 weeks of age. C
. pneumoniae infection increased the size of the lesion in infected mice, b
ut azithromycin did not reduce the size of the aortic lesion in infected mi
ce. Therefore, immediate therapy of acute infection may be necessary to pre
vent the proatherogenic effects of C. pneumoniae infection.