CpG oligodeoxynucleotides enhance host defense during murine tuberculosis

N.P. Juffermans, J.C. Leemans, S. Florquin, A. Verbon, A.H. Kolk, P. Speelman, S.J. van Deventer, T. van der Poll*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review


Oligodeoxynucleotides (ODNs) containing unmethylated CpG motifs activate immune cells to produce cytokines. CpG ODNs protect mice against infections with intracellular bacteria by the induction of a T helper 1 (Th1) response. To determine the effect of CpG ODNs in pulmonary tuberculosis, mice were treated with CpG ODNs or control ODNs at the time of intranasal infection. CpG ODNs reduced mycobacterial outgrowth for up to 5 weeks after Mycobacterium tuberculosis infection and were associated with a decrease in inflammation in lung tissue. CpG treatment was also associated with elevated levels of gamma interferon (IFN-gamma) and decreased levels of interleukin 4 in the lungs and an increased capacity of splenocytes to secrete Th1-type cytokines. CpG ODNs given 2 weeks after infection were still able to reduce mycobacterial outgrowth and to enhance a Th1 response 5 weeks postinfection. Administration of CpG ODNs to IFN-gamma-gene-deficient mice failed to reduce mycobacterial outgrowth. These data suggest that CpG ODNs improve host defense during pulmonary tuberculosis by an IFN-gamma-dependent mechanism.
Original languageEnglish
Pages (from-to)147-152
Number of pages7
JournalInfection and Immunity
Issue number1
Publication statusPublished - 1 Jan 2002


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