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We are analyzing https://link.springer.com/article/10.1186/1756-0500-4-247.

Title:
Dendritic Cells Activate and Mature after Infection with Mycobacterium tuberculosis | BMC Research Notes
Description:
Background Dendritic cells (DCs) can take up an array of different antigens, including microorganisms which they can process and present more effectively than any other antigen presenting cell. However, whether the interaction between the human DC and Mycobacterium tuberculosis represents a defense mechanism by the invaded host, or helping the invader to evade the defense mechanism of the host is still not clearly understood. Findings To analyze the interactions between M. tuberculosis and immune cells, human peripheral blood monocyte-derived immature DCs were infected with M. tuberculosis H37Rv wild type strain and flow cytometry was used to analyse cell surface expression markers. The ability of the M. tuberculosis infected DC to induce T cell proliferation using 5 and 6-carboxyfluorescein diacetate succinimidyl ester (CFSE) dilution technique was also investigated. DCs were found to internalize the mycobacteria and show dose dependent infection and necrosis with different multiplicity of infection. Flow cytometry analysis of cell surface expression markers CD40, CD54, CD80, CD83, CD86 and HLA DR in infected DC revealed significant (p < 0.05) up regulation following infection with M. tuberculosis in comparison to immature DC with no stimulation. Lipopolysaccharide (LPS) from Salmonella abortus equi, a known DC maturation agent, was used as a positive control and showed a comparable up regulation of cell surface markers as observed with M. tuberculosis infected DC. It was revealed that the M. tuberculosis infected DC induced T cell proliferation. Conclusion These data clearly demonstrate that M. tuberculosis induces activation and maturation of human monocyte-derived immature DC as well as induces T cell proliferation in vitro.
Website Age:
28 years and 1 months (reg. 1997-05-29).

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  • Science
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Custom-built

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Traffic Estimate {๐Ÿ“ˆ}

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๐ŸŒ  Phenomenal Traffic: 5M - 10M visitors per month


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How Does Link.springer.com Make Money? {๐Ÿ’ธ}

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Keywords {๐Ÿ”}

cells, cell, tuberculosis, infected, dendritic, infection, article, dcs, human, antigen, surface, maturation, positive, proliferation, pubmed, immature, expression, hrv, mouse, moi, google, scholar, mhc, lps, cas, regulation, molecules, clone, igg, antibody, data, mycobacterium, immune, cfse, response, low, medium, control, composition, ccr, study, cdi, addis, ababa, research, monocytederived, markers, activation, complete, aad,

Topics {โœ’๏ธ}

mixed dc-autologous-t-cell reaction dc-mediated t-cell stimulation rare autoantigen-specific human human monocyte-derived dcs anti-human tnf ฮฑ t-cell stimulatory capacity article download pdf monocyte-derived immature dc enzyme-linked immunosorbent assay intracellular adhesion molecule medical faculty research intracellular acid-fast bacteria monoclonal antibodies conjugated mycobacteria target dc-sign mixed leukocyte reaction human rgm-csf dendritic cells activate privacy choices/manage cookies mouse igg 2a human dendritic cells stimulatory surface molecules t-cell response middlebrook 7h10 agar immature human dc cd40 fitc/cd80 pe mhc class ii orchestrate signals derived measles virus [11] full access authorsโ€™ original file cd83 fitc/cd86 pe surface marker expression mycobacterium tuberculosis represents acid-fast bacteria cfse dilution technique tuberculosis strain leads mixed dc-autologous stimulatory molecules cd40 biomed central cell surface markers murine dendritic cells hla dr fitc article mihret virulent mycobacterium tuberculosis subsequently displayed phenotypic mentioned surface molecules tuberculosis induces activation cfsebright cd3+ cells cfse dilution techniques tuberculosis occurred annually

Schema {๐Ÿ—บ๏ธ}

WebPage:
      mainEntity:
         headline:Dendritic Cells Activate and Mature after Infection with Mycobacterium tuberculosis
         description:Dendritic cells (DCs) can take up an array of different antigens, including microorganisms which they can process and present more effectively than any other antigen presenting cell. However, whether the interaction between the human DC and Mycobacterium tuberculosis represents a defense mechanism by the invaded host, or helping the invader to evade the defense mechanism of the host is still not clearly understood. To analyze the interactions between M. tuberculosis and immune cells, human peripheral blood monocyte-derived immature DCs were infected with M. tuberculosis H37Rv wild type strain and flow cytometry was used to analyse cell surface expression markers. The ability of the M. tuberculosis infected DC to induce T cell proliferation using 5 and 6-carboxyfluorescein diacetate succinimidyl ester (CFSE) dilution technique was also investigated. DCs were found to internalize the mycobacteria and show dose dependent infection and necrosis with different multiplicity of infection. Flow cytometry analysis of cell surface expression markers CD40, CD54, CD80, CD83, CD86 and HLA DR in infected DC revealed significant (p &lt; 0.05) up regulation following infection with M. tuberculosis in comparison to immature DC with no stimulation. Lipopolysaccharide (LPS) from Salmonella abortus equi, a known DC maturation agent, was used as a positive control and showed a comparable up regulation of cell surface markers as observed with M. tuberculosis infected DC. It was revealed that the M. tuberculosis infected DC induced T cell proliferation. These data clearly demonstrate that M. tuberculosis induces activation and maturation of human monocyte-derived immature DC as well as induces T cell proliferation in vitro.
         datePublished:2011-07-21T00:00:00Z
         dateModified:2011-07-21T00:00:00Z
         pageStart:1
         pageEnd:7
         license:http://creativecommons.org/licenses/by/2.0
         sameAs:https://doi.org/10.1186/1756-0500-4-247
         keywords:
            Dendritic cells
            Mycobacterium tuberculosis
            T cells
            Activation
            Flowctometry
            CFSE
            Proliferation
            Biomedicine
            general
            Medicine/Public Health
            Life Sciences
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ScholarlyArticle:
      headline:Dendritic Cells Activate and Mature after Infection with Mycobacterium tuberculosis
      description:Dendritic cells (DCs) can take up an array of different antigens, including microorganisms which they can process and present more effectively than any other antigen presenting cell. However, whether the interaction between the human DC and Mycobacterium tuberculosis represents a defense mechanism by the invaded host, or helping the invader to evade the defense mechanism of the host is still not clearly understood. To analyze the interactions between M. tuberculosis and immune cells, human peripheral blood monocyte-derived immature DCs were infected with M. tuberculosis H37Rv wild type strain and flow cytometry was used to analyse cell surface expression markers. The ability of the M. tuberculosis infected DC to induce T cell proliferation using 5 and 6-carboxyfluorescein diacetate succinimidyl ester (CFSE) dilution technique was also investigated. DCs were found to internalize the mycobacteria and show dose dependent infection and necrosis with different multiplicity of infection. Flow cytometry analysis of cell surface expression markers CD40, CD54, CD80, CD83, CD86 and HLA DR in infected DC revealed significant (p &lt; 0.05) up regulation following infection with M. tuberculosis in comparison to immature DC with no stimulation. Lipopolysaccharide (LPS) from Salmonella abortus equi, a known DC maturation agent, was used as a positive control and showed a comparable up regulation of cell surface markers as observed with M. tuberculosis infected DC. It was revealed that the M. tuberculosis infected DC induced T cell proliferation. These data clearly demonstrate that M. tuberculosis induces activation and maturation of human monocyte-derived immature DC as well as induces T cell proliferation in vitro.
      datePublished:2011-07-21T00:00:00Z
      dateModified:2011-07-21T00:00:00Z
      pageStart:1
      pageEnd:7
      license:http://creativecommons.org/licenses/by/2.0
      sameAs:https://doi.org/10.1186/1756-0500-4-247
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         Dendritic cells
         Mycobacterium tuberculosis
         T cells
         Activation
         Flowctometry
         CFSE
         Proliferation
         Biomedicine
         general
         Medicine/Public Health
         Life Sciences
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            name:Adane Mihret
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      affiliation:
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               name:Armauer Hansen Research Institute (AHRI), Addis Ababa, Ethiopia
               type:PostalAddress
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            name:Addis Ababa, University
            address:
               name:Faculty of Veterinary Medicine, Addis Ababa, University, Addis Ababa, Ethiopia
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      name:Mesfin Tafesse
      affiliation:
            name:Armauer Hansen Research Institute (AHRI)
            address:
               name:Armauer Hansen Research Institute (AHRI), Addis Ababa, Ethiopia
               type:PostalAddress
            type:Organization
      name:Asrat Hailu
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      affiliation:
            name:Armauer Hansen Research Institute (AHRI)
            address:
               name:Armauer Hansen Research Institute (AHRI), Addis Ababa, Ethiopia
               type:PostalAddress
            type:Organization
            name:Max Planck Institute for Infection Biology
            address:
               name:Max Planck Institute for Infection Biology, Berlin, Germany
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Armauer Hansen Research Institute (AHRI), Addis Ababa, Ethiopia
      name:Faculty of Medicine, Addis Ababa University, Addis Ababa, Ethiopia
      name:Armauer Hansen Research Institute (AHRI), Addis Ababa, Ethiopia
      name:Faculty of Veterinary Medicine, Addis Ababa, University, Addis Ababa, Ethiopia
      name:Armauer Hansen Research Institute (AHRI), Addis Ababa, Ethiopia
      name:Faculty of Medicine, Addis Ababa University, Addis Ababa, Ethiopia
      name:Armauer Hansen Research Institute (AHRI), Addis Ababa, Ethiopia
      name:Max Planck Institute for Infection Biology, Berlin, Germany

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