Source:http://linkedlifedata.com/resource/pubmed/id/15448711
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions |
umls-concept:C0022688,
umls-concept:C0023690,
umls-concept:C0026809,
umls-concept:C0033119,
umls-concept:C0034117,
umls-concept:C0085358,
umls-concept:C0332325,
umls-concept:C0333668,
umls-concept:C0521375,
umls-concept:C0552510,
umls-concept:C1314792,
umls-concept:C1332717,
umls-concept:C1413244,
umls-concept:C1706438,
umls-concept:C2698600
|
pubmed:issue |
12
|
pubmed:dateCreated |
2004-11-16
|
pubmed:abstractText |
We previously showed that beta 2 microglobulin knockout mice depleted of NK cells by treatment with anti-asialoGM1 (beta2MKO/alphaAsGM1 mice) are resistant to sepsis caused by cecal ligation and puncture (CLP). beta2MKO mice possess multiple immunological defects including depletion of CD8+ T cells. This study was designed to determine the contribution of CD8+ T and NK cell deficiency to the resistance of beta2MKO/alphaAsGM1 mice to CLP-induced injury. beta2MKO/alphaAsGM1 mice and CD8 knockout mice treated with anti-asialoGM1 (CD8KO/alphaAsGM1 mice) survived significantly longer than wild-type mice following CLP. Improved long-term survival was also observed in wild-type mice rendered CD8+ T/NK cell-deficient by treatment with both anti-CD8alpha and anti-asialoGM1. Blood gas analysis and body temperature measurements showed that CD8+ T and NK cell-deficient mice have significantly reduced metabolic acidosis and less hypothermia compared to control mice at 18 h after CLP. CD8+ T/NK cell-deficient mice also showed an attenuated proinflammatory response as indicated by decreased expression of mRNAs for IL-1, IL-6 and MIP-2 in spleen and heart. IL-6, KC and MIP-2 levels in blood and peritoneal fluid were also significantly decreased CD8+ T/NK cell-deficient mice compared to controls. CD8+ T/NK cell-deficient mice exhibited decreased bacterial concentrations in blood, but not in peritoneal fluid or lung, compared to wild-type controls. These data show that mice depleted of CD8+ T and NK cells exhibit survival benefit, improved physiologic function and an attenuated proinflammatory response following CLP that is comparable to beta2M/alphaAsGM1 mice.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Dec
|
pubmed:issn |
0023-6837
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
84
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1655-65
|
pubmed:dateRevised |
2007-11-14
|
pubmed:meshHeading |
pubmed-meshheading:15448711-Acidosis,
pubmed-meshheading:15448711-Animals,
pubmed-meshheading:15448711-Antigens, CD8,
pubmed-meshheading:15448711-CD8-Positive T-Lymphocytes,
pubmed-meshheading:15448711-Cecum,
pubmed-meshheading:15448711-Cytokines,
pubmed-meshheading:15448711-Female,
pubmed-meshheading:15448711-Hypothermia,
pubmed-meshheading:15448711-Killer Cells, Natural,
pubmed-meshheading:15448711-Lymphocyte Depletion,
pubmed-meshheading:15448711-Mice,
pubmed-meshheading:15448711-Mice, Inbred C57BL,
pubmed-meshheading:15448711-Mice, Knockout,
pubmed-meshheading:15448711-Sepsis,
pubmed-meshheading:15448711-beta 2-Microglobulin
|
pubmed:year |
2004
|
pubmed:articleTitle |
Mice depleted of CD8+ T and NK cells are resistant to injury caused by cecal ligation and puncture.
|
pubmed:affiliation |
Department of Anesthesiology, The University of Texas Medical Branch, Shriners Hospital for Children, Galveston, TX 77555-0591, USA. ersherwo@utmb.edu
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|