Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2006-7-24
pubmed:abstractText
Immune responses against monocytotropic ehrlichiosis during infection with a strain of Ehrlichia from Ixodes ovatus (IOE) were evaluated using a model that closely reproduces the pathology and immunity associated with tick-transmitted human monocytotropic ehrlichiosis. C57BL/6 mice were inoculated intradermally or intraperitoneally with high-dose highly virulent IOE or intraperitoneally with mildly virulent Ehrlichia muris. Intradermal (i.d.) infection with IOE established mild, self-limited disease associated with minimal hepatic apoptosis, and all mice survived past 30 days. Intraperitoneal (i.p.) infection with IOE resulted in acute, severe toxic shock-like syndrome and severe multifocal hepatic apoptosis and necrosis, and all mice succumbed to disease. Compared to i.p. infection with IOE, intradermally infected mice had a 100- to 1,000-fold lower bacterial load in the spleen with limited dissemination. Compared to mice infected intraperitoneally with IOE, i.d. infection stimulated a stronger protective type-1 cell-mediated response on day 7 of infection, characterized by increased percentages of both CD4+ and CD8+ splenic T cells, generation of a greater number of IOE-specific, gamma interferon-producing CD4+ Th1 cells, and higher levels of tumor necrosis factor (TNF-alpha) in the spleen but lower concentrations of serum TNF-alpha and interleukin-10. These data suggest that under the conditions of natural route of challenge (i.e., i.d. inoculation), the immune response has the capacity to confer complete protection against monocytotropic ehrlichiosis, which is associated with a strong cell-mediated type-1 response and decreased systemic production of pro- and anti-inflammatory cytokines.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-10485258, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-10747103, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-11067936, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-11159213, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-11181643, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-11337387, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-11591786, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-11770046, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-11982308, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-12097412, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-12496190, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-12922099, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-14688093, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-14720399, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-14734762, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-15153508, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-15186397, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-15331423, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-15516632, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-15619234, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-15867407, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-15885364, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-15940820, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-16413927, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-16495559, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-7664785, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-8377780, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-8491479, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-9278605, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-9351183, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-9611619, http://linkedlifedata.com/resource/pubmed/commentcorrection/16861674-9673277
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0019-9567
pubmed:author
pubmed:issnType
Print
pubmed:volume
74
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
4856-64
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
2006
pubmed:articleTitle
An intradermal environment promotes a protective type-1 response against lethal systemic monocytotropic ehrlichial infection.
pubmed:affiliation
Department of Pathology and Center for Biodefense and Emerging Infectious Diseases, University of Texas Medical Branch, 301 University Blvd., Galveston, Texas 77555-0609, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, N.I.H., Extramural