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We are analyzing https://link.springer.com/article/10.1186/1743-422x-4-22.

Title:
Pathogeneses of respiratory infections with virulent and attenuated vaccinia viruses | Virology Journal
Description:
Background Respiratory infection with the neurovirulent vaccinia virus (VV) strain Western Reserve (WR) results in an acute infection of the lung followed by dissemination of the virus to other organs and causes lethality in mice. The mechanisms of lethality are not well-understood. In this study, we analyzed virus replication and host immune responses after intranasal infection with lethal and non-lethal doses of VV using the WR strain and the less virulent Wyeth strain. Results The WR strain replicated more vigorously in the lung and in the brain than the Wyeth strain. There were, however, no differences between the virus titers in the brains of mice infected with the higher lethal dose and the lower non-lethal dose of WR strain, suggesting that the amount of virus replication in the brain is unlikely to be the sole determining factor of lethality. The WR strain grew better in primary mouse lung cells than the Wyeth strain. Lethal infection with WR strain was associated with a reduced number of lymphocytes and an altered phenotype of the T cells in the lung compared to non-lethal infections with the WR or Wyeth strains. Severe thymus atrophy with a reduction of CD4 and CD8 double positive T cells was also observed in the lethal infection. Conclusion These results suggest that the lethality induced by intranasal infection with a high dose of the WR strain is caused by the higher replication of virus in lung cells and immune suppression during the early phase of the infection, resulting in uncontrolled virus replication in the lung.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Science
  • Pets
  • Education

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,016 visitors per month in the current month.

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How Does Link.springer.com Make Money? {💸}

We can't see how the site brings in money.

Not all websites focus on profit; some are designed to educate, connect people, or share useful tools. People create websites for numerous reasons. And this could be one such example. Link.springer.com might have a hidden revenue stream, but it's not something we can detect.

Keywords {🔍}

virus, cells, mice, infection, pubmed, strain, lung, google, scholar, article, wyeth, fig, postinfection, infected, days, mouse, pfu, respiratory, lethal, cell, thymus, strains, vaccinia, replication, titers, dose, immune, central, induced, lungs, infections, nonlethal, atrophy, high, uninfected, viruses, responses, intranasal, virol, lymphocytes, thymocytes, figure, brain, compared, authors, virology, number, primary, severe, control,

Topics {✒️}

sars-cov-2 n-specific cd8+ long-term airway hyperresponsiveness related subjects open access article 3β-hydroxysteroid dehydrogenase encoded fluorescent-labeled antibodies directed inhibits cell-cell fusion respiratory syncytial virus anti-apoptotic activity cd8 double positive recombinant vaccinia viruses t-cell subset recruitment scid-hu mouse leads abl-family tyrosine kinases article download pdf da cruz-hofling ma attenuated vaccinia viruses trans-sialidase-induced apoptosis hla-a2 transgenic mice c3h/hen male mice cd8+ t-cell mechanisms tumor necrosis factor-α immature cd4+cd8+ dp health grant u19-ai-057319 live cells vaccinia virus suppresses female c57bl/6j mice cd4+cd8+ dp cells t-dependent areas vaccinia virus induced privacy choices/manage cookies vaccine research vaccinia-immune igg cd4+cd8+ dp thymocytes endothelial specific markers authors’ original file alveolar fluid clearance cd4+cd8+ thymocyte depletion ennis & masanori terajima severe thymic atrophy smallpox vaccines vaccinia virus persistence cd4high cd8- cells full access respiratory virus infections surface phenotypic markers time points post-infection c57bl/6j mouse severe weight loss full size image

Questions {❓}

  • Jondal M, Pazirandeh A, Okret S: Different roles for glucocorticoids in thymocyte homeostasis?

Schema {🗺️}

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         headline:Pathogeneses of respiratory infections with virulent and attenuated vaccinia viruses
         description:Respiratory infection with the neurovirulent vaccinia virus (VV) strain Western Reserve (WR) results in an acute infection of the lung followed by dissemination of the virus to other organs and causes lethality in mice. The mechanisms of lethality are not well-understood. In this study, we analyzed virus replication and host immune responses after intranasal infection with lethal and non-lethal doses of VV using the WR strain and the less virulent Wyeth strain. The WR strain replicated more vigorously in the lung and in the brain than the Wyeth strain. There were, however, no differences between the virus titers in the brains of mice infected with the higher lethal dose and the lower non-lethal dose of WR strain, suggesting that the amount of virus replication in the brain is unlikely to be the sole determining factor of lethality. The WR strain grew better in primary mouse lung cells than the Wyeth strain. Lethal infection with WR strain was associated with a reduced number of lymphocytes and an altered phenotype of the T cells in the lung compared to non-lethal infections with the WR or Wyeth strains. Severe thymus atrophy with a reduction of CD4 and CD8 double positive T cells was also observed in the lethal infection. These results suggest that the lethality induced by intranasal infection with a high dose of the WR strain is caused by the higher replication of virus in lung cells and immune suppression during the early phase of the infection, resulting in uncontrolled virus replication in the lung.
         datePublished:2007-02-27T00:00:00Z
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            Double Positive
            Lethal Infection
            Virology
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      headline:Pathogeneses of respiratory infections with virulent and attenuated vaccinia viruses
      description:Respiratory infection with the neurovirulent vaccinia virus (VV) strain Western Reserve (WR) results in an acute infection of the lung followed by dissemination of the virus to other organs and causes lethality in mice. The mechanisms of lethality are not well-understood. In this study, we analyzed virus replication and host immune responses after intranasal infection with lethal and non-lethal doses of VV using the WR strain and the less virulent Wyeth strain. The WR strain replicated more vigorously in the lung and in the brain than the Wyeth strain. There were, however, no differences between the virus titers in the brains of mice infected with the higher lethal dose and the lower non-lethal dose of WR strain, suggesting that the amount of virus replication in the brain is unlikely to be the sole determining factor of lethality. The WR strain grew better in primary mouse lung cells than the Wyeth strain. Lethal infection with WR strain was associated with a reduced number of lymphocytes and an altered phenotype of the T cells in the lung compared to non-lethal infections with the WR or Wyeth strains. Severe thymus atrophy with a reduction of CD4 and CD8 double positive T cells was also observed in the lethal infection. These results suggest that the lethality induced by intranasal infection with a high dose of the WR strain is caused by the higher replication of virus in lung cells and immune suppression during the early phase of the infection, resulting in uncontrolled virus replication in the lung.
      datePublished:2007-02-27T00:00:00Z
      dateModified:2007-02-27T00:00:00Z
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