Human herpesvirus-8 infection of umbilical cord-blood-derived CD34+ stem cells enhances the immunostimulatory function of their dendritic cell progeny

:  CD34+ progenitor cells carrying human herpesvirus‐8, Kaposi's sarcoma‐associated herpesvirus (HHV‐8/KSHV), have been described in the peripheral blood of AIDS patients suffering from Kaposi's sarcoma (KS). In this study, we investigated the influence of HHV‐8 on the differentiation of C...

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Veröffentlicht in:Experimental dermatology 2005-01, Vol.14 (1), p.41-49
Hauptverfasser: Larcher, C., Nguyen, V. A., Fürhapter, C., Ebner, S., Sölder, E., Stössel, H., Romani, N., Sepp, N.
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container_end_page 49
container_issue 1
container_start_page 41
container_title Experimental dermatology
container_volume 14
creator Larcher, C.
Nguyen, V. A.
Fürhapter, C.
Ebner, S.
Sölder, E.
Stössel, H.
Romani, N.
Sepp, N.
description :  CD34+ progenitor cells carrying human herpesvirus‐8, Kaposi's sarcoma‐associated herpesvirus (HHV‐8/KSHV), have been described in the peripheral blood of AIDS patients suffering from Kaposi's sarcoma (KS). In this study, we investigated the influence of HHV‐8 on the differentiation of CD34+ progenitor cells. Native CD34+ cells derived from cord blood could be infected by a laboratory strain of HHV‐8, as shown by immunofluorescence staining and polymerase chain reaction, but no significant initial maturation/differentiation effects were observed. In addition, these infected cells were differentiated into immature and mature dendritic cells (DCs) using cytokine induction with recombinant human granulocyte‐macrophage colony‐stimulating factor (rhGm‐CSF), recombinant human tumor necrosis factor (rhTNF‐α) and recombinant human stem cell factor (rhSCF). Double immunofluorescence and flow cytometry studies demonstrated that virus infection did not impair the development of immature and mature DC populations. Subsequently, the immunostimulating capacity of DC populations was tested in a mixed lymphocyte reaction using allogeneic T‐cells. The HHV‐8‐infected CD34+ progenitor cell‐derived mature DC population showed a significantly enhanced antigen‐presenting capacity, compared to non‐infected DCs, which was not observed with the immature DCs. This suggests stimulation of DC function by HHV‐8 infection. Because there are only a small percentage of HHV‐8‐positive DCs in the preparations and because it is not clear whether infection is abortive or productive to some extent, this seems to be most likely due to an indirect viral effect.
doi_str_mv 10.1111/j.0906-6705.2005.00234.x
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A. ; Fürhapter, C. ; Ebner, S. ; Sölder, E. ; Stössel, H. ; Romani, N. ; Sepp, N.</creator><creatorcontrib>Larcher, C. ; Nguyen, V. A. ; Fürhapter, C. ; Ebner, S. ; Sölder, E. ; Stössel, H. ; Romani, N. ; Sepp, N.</creatorcontrib><description>:  CD34+ progenitor cells carrying human herpesvirus‐8, Kaposi's sarcoma‐associated herpesvirus (HHV‐8/KSHV), have been described in the peripheral blood of AIDS patients suffering from Kaposi's sarcoma (KS). In this study, we investigated the influence of HHV‐8 on the differentiation of CD34+ progenitor cells. Native CD34+ cells derived from cord blood could be infected by a laboratory strain of HHV‐8, as shown by immunofluorescence staining and polymerase chain reaction, but no significant initial maturation/differentiation effects were observed. In addition, these infected cells were differentiated into immature and mature dendritic cells (DCs) using cytokine induction with recombinant human granulocyte‐macrophage colony‐stimulating factor (rhGm‐CSF), recombinant human tumor necrosis factor (rhTNF‐α) and recombinant human stem cell factor (rhSCF). Double immunofluorescence and flow cytometry studies demonstrated that virus infection did not impair the development of immature and mature DC populations. Subsequently, the immunostimulating capacity of DC populations was tested in a mixed lymphocyte reaction using allogeneic T‐cells. The HHV‐8‐infected CD34+ progenitor cell‐derived mature DC population showed a significantly enhanced antigen‐presenting capacity, compared to non‐infected DCs, which was not observed with the immature DCs. This suggests stimulation of DC function by HHV‐8 infection. 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A.</creatorcontrib><creatorcontrib>Fürhapter, C.</creatorcontrib><creatorcontrib>Ebner, S.</creatorcontrib><creatorcontrib>Sölder, E.</creatorcontrib><creatorcontrib>Stössel, H.</creatorcontrib><creatorcontrib>Romani, N.</creatorcontrib><creatorcontrib>Sepp, N.</creatorcontrib><title>Human herpesvirus-8 infection of umbilical cord-blood-derived CD34+ stem cells enhances the immunostimulatory function of their dendritic cell progeny</title><title>Experimental dermatology</title><addtitle>Exp Dermatol</addtitle><description>:  CD34+ progenitor cells carrying human herpesvirus‐8, Kaposi's sarcoma‐associated herpesvirus (HHV‐8/KSHV), have been described in the peripheral blood of AIDS patients suffering from Kaposi's sarcoma (KS). In this study, we investigated the influence of HHV‐8 on the differentiation of CD34+ progenitor cells. Native CD34+ cells derived from cord blood could be infected by a laboratory strain of HHV‐8, as shown by immunofluorescence staining and polymerase chain reaction, but no significant initial maturation/differentiation effects were observed. In addition, these infected cells were differentiated into immature and mature dendritic cells (DCs) using cytokine induction with recombinant human granulocyte‐macrophage colony‐stimulating factor (rhGm‐CSF), recombinant human tumor necrosis factor (rhTNF‐α) and recombinant human stem cell factor (rhSCF). Double immunofluorescence and flow cytometry studies demonstrated that virus infection did not impair the development of immature and mature DC populations. Subsequently, the immunostimulating capacity of DC populations was tested in a mixed lymphocyte reaction using allogeneic T‐cells. The HHV‐8‐infected CD34+ progenitor cell‐derived mature DC population showed a significantly enhanced antigen‐presenting capacity, compared to non‐infected DCs, which was not observed with the immature DCs. This suggests stimulation of DC function by HHV‐8 infection. 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A.</au><au>Fürhapter, C.</au><au>Ebner, S.</au><au>Sölder, E.</au><au>Stössel, H.</au><au>Romani, N.</au><au>Sepp, N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Human herpesvirus-8 infection of umbilical cord-blood-derived CD34+ stem cells enhances the immunostimulatory function of their dendritic cell progeny</atitle><jtitle>Experimental dermatology</jtitle><addtitle>Exp Dermatol</addtitle><date>2005-01</date><risdate>2005</risdate><volume>14</volume><issue>1</issue><spage>41</spage><epage>49</epage><pages>41-49</pages><issn>0906-6705</issn><eissn>1600-0625</eissn><abstract>:  CD34+ progenitor cells carrying human herpesvirus‐8, Kaposi's sarcoma‐associated herpesvirus (HHV‐8/KSHV), have been described in the peripheral blood of AIDS patients suffering from Kaposi's sarcoma (KS). In this study, we investigated the influence of HHV‐8 on the differentiation of CD34+ progenitor cells. 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The HHV‐8‐infected CD34+ progenitor cell‐derived mature DC population showed a significantly enhanced antigen‐presenting capacity, compared to non‐infected DCs, which was not observed with the immature DCs. This suggests stimulation of DC function by HHV‐8 infection. Because there are only a small percentage of HHV‐8‐positive DCs in the preparations and because it is not clear whether infection is abortive or productive to some extent, this seems to be most likely due to an indirect viral effect.</abstract><cop>Oxford, UK; Malden, USA</cop><pub>Munksgaard International Publishers</pub><pmid>15660918</pmid><doi>10.1111/j.0906-6705.2005.00234.x</doi><tpages>9</tpages></addata></record>
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subjects Antibodies, Monoclonal - immunology
Antigens, CD - analysis
Antigens, CD34 - immunology
Biological and medical sciences
Cell Differentiation - drug effects
Cytokines - pharmacology
dendritic cells
Dendritic Cells - immunology
Dendritic Cells - ultrastructure
Dendritic Cells - virology
Dermatology
DNA, Viral - analysis
Fetal Blood - cytology
Herpesvirus 8, Human - genetics
Herpesvirus 8, Human - immunology
HHV-8
Humans
Immunohistochemistry
KSHV
Lymphocyte Activation - immunology
Lymphocyte Culture Test, Mixed
Medical sciences
Microscopy, Electron, Transmission
Stem Cells - chemistry
Stem Cells - immunology
Stem Cells - virology
T-Lymphocytes - immunology
umbilical cord-blood-derived CD34+ cells
title Human herpesvirus-8 infection of umbilical cord-blood-derived CD34+ stem cells enhances the immunostimulatory function of their dendritic cell progeny
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