author_facet Stevenson, Heather L.
Jordan, Jeffrey M.
Peerwani, Ziad
Wang, Hui-Qun
Walker, David H.
Ismail, Nahed
Stevenson, Heather L.
Jordan, Jeffrey M.
Peerwani, Ziad
Wang, Hui-Qun
Walker, David H.
Ismail, Nahed
author Stevenson, Heather L.
Jordan, Jeffrey M.
Peerwani, Ziad
Wang, Hui-Qun
Walker, David H.
Ismail, Nahed
spellingShingle Stevenson, Heather L.
Jordan, Jeffrey M.
Peerwani, Ziad
Wang, Hui-Qun
Walker, David H.
Ismail, Nahed
Infection and Immunity
An Intradermal Environment Promotes a Protective Type-1 Response against Lethal Systemic Monocytotropic Ehrlichial Infection
Infectious Diseases
Immunology
Microbiology
Parasitology
author_sort stevenson, heather l.
spelling Stevenson, Heather L. Jordan, Jeffrey M. Peerwani, Ziad Wang, Hui-Qun Walker, David H. Ismail, Nahed 0019-9567 1098-5522 American Society for Microbiology Infectious Diseases Immunology Microbiology Parasitology http://dx.doi.org/10.1128/iai.00246-06 <jats:title>ABSTRACT</jats:title> <jats:p> Immune responses against monocytotropic ehrlichiosis during infection with a strain of <jats:italic>Ehrlichia</jats:italic> from <jats:italic>Ixodes ovatus</jats:italic> (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 <jats:italic>Ehrlichia muris</jats:italic> . 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 <jats:sup>+</jats:sup> and CD8 <jats:sup>+</jats:sup> splenic T cells, generation of a greater number of IOE-specific, gamma interferon-producing CD4 <jats:sup>+</jats:sup> Th1 cells, and higher levels of tumor necrosis factor (TNF-α) in the spleen but lower concentrations of serum TNF-α 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. </jats:p> An Intradermal Environment Promotes a Protective Type-1 Response against Lethal Systemic Monocytotropic Ehrlichial Infection Infection and Immunity
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title An Intradermal Environment Promotes a Protective Type-1 Response against Lethal Systemic Monocytotropic Ehrlichial Infection
title_unstemmed An Intradermal Environment Promotes a Protective Type-1 Response against Lethal Systemic Monocytotropic Ehrlichial Infection
title_full An Intradermal Environment Promotes a Protective Type-1 Response against Lethal Systemic Monocytotropic Ehrlichial Infection
title_fullStr An Intradermal Environment Promotes a Protective Type-1 Response against Lethal Systemic Monocytotropic Ehrlichial Infection
title_full_unstemmed An Intradermal Environment Promotes a Protective Type-1 Response against Lethal Systemic Monocytotropic Ehrlichial Infection
title_short An Intradermal Environment Promotes a Protective Type-1 Response against Lethal Systemic Monocytotropic Ehrlichial Infection
title_sort an intradermal environment promotes a protective type-1 response against lethal systemic monocytotropic ehrlichial infection
topic Infectious Diseases
Immunology
Microbiology
Parasitology
url http://dx.doi.org/10.1128/iai.00246-06
publishDate 2006
physical 4856-4864
description <jats:title>ABSTRACT</jats:title> <jats:p> Immune responses against monocytotropic ehrlichiosis during infection with a strain of <jats:italic>Ehrlichia</jats:italic> from <jats:italic>Ixodes ovatus</jats:italic> (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 <jats:italic>Ehrlichia muris</jats:italic> . 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 <jats:sup>+</jats:sup> and CD8 <jats:sup>+</jats:sup> splenic T cells, generation of a greater number of IOE-specific, gamma interferon-producing CD4 <jats:sup>+</jats:sup> Th1 cells, and higher levels of tumor necrosis factor (TNF-α) in the spleen but lower concentrations of serum TNF-α 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. </jats:p>
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author Stevenson, Heather L., Jordan, Jeffrey M., Peerwani, Ziad, Wang, Hui-Qun, Walker, David H., Ismail, Nahed
author_facet Stevenson, Heather L., Jordan, Jeffrey M., Peerwani, Ziad, Wang, Hui-Qun, Walker, David H., Ismail, Nahed, Stevenson, Heather L., Jordan, Jeffrey M., Peerwani, Ziad, Wang, Hui-Qun, Walker, David H., Ismail, Nahed
author_sort stevenson, heather l.
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description <jats:title>ABSTRACT</jats:title> <jats:p> Immune responses against monocytotropic ehrlichiosis during infection with a strain of <jats:italic>Ehrlichia</jats:italic> from <jats:italic>Ixodes ovatus</jats:italic> (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 <jats:italic>Ehrlichia muris</jats:italic> . 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 <jats:sup>+</jats:sup> and CD8 <jats:sup>+</jats:sup> splenic T cells, generation of a greater number of IOE-specific, gamma interferon-producing CD4 <jats:sup>+</jats:sup> Th1 cells, and higher levels of tumor necrosis factor (TNF-α) in the spleen but lower concentrations of serum TNF-α 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. </jats:p>
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spelling Stevenson, Heather L. Jordan, Jeffrey M. Peerwani, Ziad Wang, Hui-Qun Walker, David H. Ismail, Nahed 0019-9567 1098-5522 American Society for Microbiology Infectious Diseases Immunology Microbiology Parasitology http://dx.doi.org/10.1128/iai.00246-06 <jats:title>ABSTRACT</jats:title> <jats:p> Immune responses against monocytotropic ehrlichiosis during infection with a strain of <jats:italic>Ehrlichia</jats:italic> from <jats:italic>Ixodes ovatus</jats:italic> (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 <jats:italic>Ehrlichia muris</jats:italic> . 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 <jats:sup>+</jats:sup> and CD8 <jats:sup>+</jats:sup> splenic T cells, generation of a greater number of IOE-specific, gamma interferon-producing CD4 <jats:sup>+</jats:sup> Th1 cells, and higher levels of tumor necrosis factor (TNF-α) in the spleen but lower concentrations of serum TNF-α 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. </jats:p> An Intradermal Environment Promotes a Protective Type-1 Response against Lethal Systemic Monocytotropic Ehrlichial Infection Infection and Immunity
spellingShingle Stevenson, Heather L., Jordan, Jeffrey M., Peerwani, Ziad, Wang, Hui-Qun, Walker, David H., Ismail, Nahed, Infection and Immunity, An Intradermal Environment Promotes a Protective Type-1 Response against Lethal Systemic Monocytotropic Ehrlichial Infection, Infectious Diseases, Immunology, Microbiology, Parasitology
title An Intradermal Environment Promotes a Protective Type-1 Response against Lethal Systemic Monocytotropic Ehrlichial Infection
title_full An Intradermal Environment Promotes a Protective Type-1 Response against Lethal Systemic Monocytotropic Ehrlichial Infection
title_fullStr An Intradermal Environment Promotes a Protective Type-1 Response against Lethal Systemic Monocytotropic Ehrlichial Infection
title_full_unstemmed An Intradermal Environment Promotes a Protective Type-1 Response against Lethal Systemic Monocytotropic Ehrlichial Infection
title_short An Intradermal Environment Promotes a Protective Type-1 Response against Lethal Systemic Monocytotropic Ehrlichial Infection
title_sort an intradermal environment promotes a protective type-1 response against lethal systemic monocytotropic ehrlichial infection
title_unstemmed An Intradermal Environment Promotes a Protective Type-1 Response against Lethal Systemic Monocytotropic Ehrlichial Infection
topic Infectious Diseases, Immunology, Microbiology, Parasitology
url http://dx.doi.org/10.1128/iai.00246-06