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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.
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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,
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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
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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 < 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
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Mycobacterium tuberculosis
T cells
Activation
Flowctometry
CFSE
Proliferation
Biomedicine
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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 < 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.
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Mycobacterium tuberculosis
T cells
Activation
Flowctometry
CFSE
Proliferation
Biomedicine
general
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Life Sciences
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