Abstract |
The impact of L. monocytogenes infection on maternal immune responses as well as on the outcome of pregnancy was studied in a murine model of pregnancy-associated listeriosis. Mice infected i.v. with L. monocytogenes at day 15 of pregnancy showed a significantly impaired bacterial elimination, which resulted in a severe necrotizing hemorrhagic hepatitis. The aggravated course of the infection could be attributed to a suppressed transcription and production of anti-listerial, pro-inflammatory cytokines and chemokines, namely interferon-gamma, tumor necrosis factor, interleukin-12p40, inducible nitric oxide synthase, murine monokine induced by interferon-gamma, and interferon-gamma-inducible protein-10. In addition, listeriosis significantly increased the abortion rate. Infection of the placenta and fetuses was characterized by placental and fetal necrosis with unrestricted bacterial multiplication. A weak transcription of anti-listerial cytokines in the placenta in the absence of a cellular immune response could not prevent the fatal outcome of pregnancy-associated listeriosis.
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Authors | Maja Abram, Dirk Schlüter, Darinka Vuckovic, Branka Waber, Miljenko Doric, Martina Deckert |
Journal | Virchows Archiv : an international journal of pathology
(Virchows Arch)
Vol. 441
Issue 4
Pg. 368-79
(Oct 2002)
ISSN: 0945-6317 [Print] Germany |
PMID | 12404062
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Chemokines
- RNA, Messenger
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Topics |
- Animals
- Chemokines
(biosynthesis, genetics)
- Disease Models, Animal
- Embryo Loss
(immunology, microbiology, pathology)
- Female
- Hepatitis, Animal
(immunology, microbiology, pathology)
- Immunity, Cellular
(immunology)
- Immunocompromised Host
- Immunoenzyme Techniques
- Listeria monocytogenes
(immunology, pathogenicity)
- Listeriosis
(immunology, pathology)
- Mice
- Mice, Inbred BALB C
- Necrosis
- Placenta
(microbiology, pathology)
- Pregnancy
- Pregnancy Complications, Infectious
(immunology, microbiology, pathology)
- RNA, Messenger
(biosynthesis)
- Reverse Transcriptase Polymerase Chain Reaction
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