Source:http://linkedlifedata.com/resource/pubmed/id/16493084
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2006-2-22
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pubmed:abstractText |
The genetic predisposition to many autoimmune diseases is inherited as a polygenic trait. It is conceivable that some of the causative alleles in these diseases became prevalent in the population by conferring a survival benefit against environmental assaults, such as infections. We used mice cogenic for genetic loci predisposing to systemic lupus erythomatosus to test the hypothesis that some of these genetic loci protect the host from bacterial infections. Mice with the Sle3 lupus-susceptibility locus on a wild-type background were found to have enhanced antibacterial responses in the context of pneumonia and intra-abdominal sepsis than wild-type animals. This was associated with markedly augmented accumulation of neutrophils in infected tissues, and was bone marrow transferable and dependent on the presence of neutrophils, but not lymphocytes. There was no difference in in vitro leukocyte killing of bacteria nor influx of phagocytes between lupus-susceptible and wild-type animals, but neutrophils from lupus-susceptible mice displayed markedly reduced rate of apoptosis, associated with altered expression of Bcl-2 family proteins, contributing to their greater accumulation. Importantly, deliberate inhibition of apoptosis in wild-type animals significantly boosted the accumulation of neutrophils at the site of infection and resulted in an enhanced antimicrobial response. These observations support the concept that some of the genetic loci that mediate autoimmunity may also confer augmented antimicrobial innate immunity.
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pubmed:grant | |
pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
176
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3233-9
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:16493084-Adjuvants, Immunologic,
pubmed-meshheading:16493084-Animals,
pubmed-meshheading:16493084-Apoptosis,
pubmed-meshheading:16493084-Genetic Markers,
pubmed-meshheading:16493084-Genetic Predisposition to Disease,
pubmed-meshheading:16493084-Klebsiella pneumoniae,
pubmed-meshheading:16493084-Lupus Erythematosus, Systemic,
pubmed-meshheading:16493084-Mice,
pubmed-meshheading:16493084-Mice, Congenic,
pubmed-meshheading:16493084-Mice, Inbred C57BL,
pubmed-meshheading:16493084-Mice, Inbred NZB,
pubmed-meshheading:16493084-Mice, Knockout,
pubmed-meshheading:16493084-Neutrophils,
pubmed-meshheading:16493084-Pneumonia, Bacterial
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pubmed:year |
2006
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pubmed:articleTitle |
The lupus-susceptibility locus, Sle3, mediates enhanced resistance to bacterial infections.
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pubmed:affiliation |
Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA. Borna.Mehrad@UTSouthwestern.edu
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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