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Myeloid and lymphoid activation markers in AIDS and non-AIDS presenters

•Circulating dendritic cells were impaired in number or phenotype in untreated HIV+ subjects, especially in AIDS presenters.•In HIV+ subjects, HLA-DR expression on myeloid and slan-dendritic cells tended to normalise after antiretroviral treatment.•Intermediate monocyte absolute counts were increase...

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Published in:Immunobiology (1979) 2019-03, Vol.224 (2), p.231-241
Main Authors: Iannetta, Marco, Savinelli, Stefano, Rossi, Raffaella, Mascia, Claudia, Marocco, Raffaella, Vita, Serena, Zuccalà, Paola, Zingaropoli, Maria Antonella, Mengoni, Fabio, Massetti, Anna Paola, Falciano, Mario, d’Ettorre, Gabriella, Ciardi, Maria Rosa, Mastroianni, Claudio Maria, Vullo, Vincenzo, Lichtner, Miriam
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cited_by cdi_FETCH-LOGICAL-c359t-383d186e172afaebd0cd5e76d25321fcfc77586f8124f7711219faa2e1a567de3
cites cdi_FETCH-LOGICAL-c359t-383d186e172afaebd0cd5e76d25321fcfc77586f8124f7711219faa2e1a567de3
container_end_page 241
container_issue 2
container_start_page 231
container_title Immunobiology (1979)
container_volume 224
creator Iannetta, Marco
Savinelli, Stefano
Rossi, Raffaella
Mascia, Claudia
Marocco, Raffaella
Vita, Serena
Zuccalà, Paola
Zingaropoli, Maria Antonella
Mengoni, Fabio
Massetti, Anna Paola
Falciano, Mario
d’Ettorre, Gabriella
Ciardi, Maria Rosa
Mastroianni, Claudio Maria
Vullo, Vincenzo
Lichtner, Miriam
description •Circulating dendritic cells were impaired in number or phenotype in untreated HIV+ subjects, especially in AIDS presenters.•In HIV+ subjects, HLA-DR expression on myeloid and slan-dendritic cells tended to normalise after antiretroviral treatment.•Intermediate monocyte absolute counts were increased in AIDS and non-AIDS presenters and decreased after treatment.•Antiretroviral treatment reduced myeloid and lymphoid activation in advanced and non-advanced HIV+ patients.•Antiretroviral treatment can prevent disease progression and immune activation associated non-AIDS events. HIV infection is characterized by a state of chronic activation of the immune system, which is not completely reversed by antiretroviral treatment (ART). The aim of this study was to assess myeloid and lymphoid activation markers during HIV infection, before and one year after ART initiation, in AIDS and non-AIDS presenters. Treatment naïve HIV positive patients were enrolled in this study. Myeloid dendritic cell (mDC), plasmacytoid dendritic cell (pDC), slanDC, monocyte and T-lymphocyte cell counts and activation status, were assessed by flow cytometry in peripheral blood samples. Soluble (s)CD14 and sCD163 were assessed in plasma samples using ELISA assays. Statistical analyses were performed using GraphPad Prism and Minitab Express. Thirty-four ART naïve HIV-1 infected subjects were enrolled in this study (22 non-AIDS and 12 AIDS presenters). Seventeen healthy donors (HD) were included as control group. Although circulating mDC levels resulted unchanged, HLA-DR expression was decreased on mDCs of HIV positive subjects compared to HD (p 
doi_str_mv 10.1016/j.imbio.2018.11.011
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HIV infection is characterized by a state of chronic activation of the immune system, which is not completely reversed by antiretroviral treatment (ART). The aim of this study was to assess myeloid and lymphoid activation markers during HIV infection, before and one year after ART initiation, in AIDS and non-AIDS presenters. Treatment naïve HIV positive patients were enrolled in this study. Myeloid dendritic cell (mDC), plasmacytoid dendritic cell (pDC), slanDC, monocyte and T-lymphocyte cell counts and activation status, were assessed by flow cytometry in peripheral blood samples. Soluble (s)CD14 and sCD163 were assessed in plasma samples using ELISA assays. Statistical analyses were performed using GraphPad Prism and Minitab Express. Thirty-four ART naïve HIV-1 infected subjects were enrolled in this study (22 non-AIDS and 12 AIDS presenters). Seventeen healthy donors (HD) were included as control group. Although circulating mDC levels resulted unchanged, HLA-DR expression was decreased on mDCs of HIV positive subjects compared to HD (p < 0,0001). AIDS presenters showed the lowest level of expression of HLA-DR on mDCs. Circulating levels of pDCs were decreased in HIV patients compared to HD (p < 0,001), without any changes in HLA-DR expression. SlanDC cell counts were extremely reduced in AIDS presenters, compared to non-AIDS presenters and HD (p < 0,01 and p < 0,0001, respectively) and showed higher HLA-DR expression in HIV patients compared to HD (p < 0,01). Intermediate monocyte (IM) cell counts were increased in AIDS and non-AIDS presenters compared to HD (p < 0,001 and p < 0,001 respectively). Furthermore, IM expansion was directly correlated to HIV viral load (p = 0,036) and independent from CD4 cell counts and activation levels. Plasma concentrations of sCD14 and sCD163 resulted increased in HIV infected subjects compared to HD (p < 0,0001 and p < 0,001), with the highest levels observed in AIDS presenters. After 1 year, ART was able to increase pDC and decrease IM absolute cell counts and modify HLA-DR expression on mDCs and slanDCs, approaching the levels observed in HD. ART reduced also CD4 and CD8 activation levels. In conclusion, in untreated HIV infected subjects circulating dendritic cells resulted altered either in numbers or in HLA-DR expression, especially in AIDS presenters. IM absolute counts were equally increased in AIDS and non-AIDS presenters. ART was able to reduce myeloid and lymphoid inflammation in both advanced and non-advanced HIV patients, confirming the role of ART in hampering disease progression and immune activation associated non-AIDS events.]]></description><identifier>ISSN: 0171-2985</identifier><identifier>EISSN: 1878-3279</identifier><identifier>DOI: 10.1016/j.imbio.2018.11.011</identifier><identifier>PMID: 30522891</identifier><language>eng</language><publisher>Netherlands: Elsevier GmbH</publisher><subject>Acquired Immunodeficiency Syndrome - immunology ; Acquired Immunodeficiency Syndrome - metabolism ; Acquired Immunodeficiency Syndrome - virology ; Adult ; Biomarkers ; CD4 Lymphocyte Count ; Dendritic cell ; Dendritic Cells - immunology ; Dendritic Cells - metabolism ; Disease Progression ; Female ; HAART ; HIV ; HIV-1 - immunology ; Humans ; Leukocyte Count ; Lymphocyte Activation - immunology ; Lymphocyte Count ; Lymphocytes - immunology ; Lymphocytes - metabolism ; Male ; Middle Aged ; Monocyte ; Monocytes - immunology ; Monocytes - metabolism ; Myeloid Cells - immunology ; Myeloid Cells - metabolism ; sCD14 ; sCD163 ; slanDC ; Viral Load</subject><ispartof>Immunobiology (1979), 2019-03, Vol.224 (2), p.231-241</ispartof><rights>2018 Elsevier GmbH</rights><rights>Copyright © 2018 Elsevier GmbH. 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Plasma concentrations of sCD14 and sCD163 resulted increased in HIV infected subjects compared to HD (p < 0,0001 and p < 0,001), with the highest levels observed in AIDS presenters. After 1 year, ART was able to increase pDC and decrease IM absolute cell counts and modify HLA-DR expression on mDCs and slanDCs, approaching the levels observed in HD. ART reduced also CD4 and CD8 activation levels. In conclusion, in untreated HIV infected subjects circulating dendritic cells resulted altered either in numbers or in HLA-DR expression, especially in AIDS presenters. IM absolute counts were equally increased in AIDS and non-AIDS presenters. 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HIV infection is characterized by a state of chronic activation of the immune system, which is not completely reversed by antiretroviral treatment (ART). The aim of this study was to assess myeloid and lymphoid activation markers during HIV infection, before and one year after ART initiation, in AIDS and non-AIDS presenters. Treatment naïve HIV positive patients were enrolled in this study. Myeloid dendritic cell (mDC), plasmacytoid dendritic cell (pDC), slanDC, monocyte and T-lymphocyte cell counts and activation status, were assessed by flow cytometry in peripheral blood samples. Soluble (s)CD14 and sCD163 were assessed in plasma samples using ELISA assays. Statistical analyses were performed using GraphPad Prism and Minitab Express. Thirty-four ART naïve HIV-1 infected subjects were enrolled in this study (22 non-AIDS and 12 AIDS presenters). Seventeen healthy donors (HD) were included as control group. Although circulating mDC levels resulted unchanged, HLA-DR expression was decreased on mDCs of HIV positive subjects compared to HD (p < 0,0001). AIDS presenters showed the lowest level of expression of HLA-DR on mDCs. Circulating levels of pDCs were decreased in HIV patients compared to HD (p < 0,001), without any changes in HLA-DR expression. SlanDC cell counts were extremely reduced in AIDS presenters, compared to non-AIDS presenters and HD (p < 0,01 and p < 0,0001, respectively) and showed higher HLA-DR expression in HIV patients compared to HD (p < 0,01). Intermediate monocyte (IM) cell counts were increased in AIDS and non-AIDS presenters compared to HD (p < 0,001 and p < 0,001 respectively). Furthermore, IM expansion was directly correlated to HIV viral load (p = 0,036) and independent from CD4 cell counts and activation levels. Plasma concentrations of sCD14 and sCD163 resulted increased in HIV infected subjects compared to HD (p < 0,0001 and p < 0,001), with the highest levels observed in AIDS presenters. After 1 year, ART was able to increase pDC and decrease IM absolute cell counts and modify HLA-DR expression on mDCs and slanDCs, approaching the levels observed in HD. ART reduced also CD4 and CD8 activation levels. In conclusion, in untreated HIV infected subjects circulating dendritic cells resulted altered either in numbers or in HLA-DR expression, especially in AIDS presenters. IM absolute counts were equally increased in AIDS and non-AIDS presenters. ART was able to reduce myeloid and lymphoid inflammation in both advanced and non-advanced HIV patients, confirming the role of ART in hampering disease progression and immune activation associated non-AIDS events.]]></abstract><cop>Netherlands</cop><pub>Elsevier GmbH</pub><pmid>30522891</pmid><doi>10.1016/j.imbio.2018.11.011</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-6938-8627</orcidid><orcidid>https://orcid.org/0000-0002-1286-467X</orcidid></addata></record>
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subjects Acquired Immunodeficiency Syndrome - immunology
Acquired Immunodeficiency Syndrome - metabolism
Acquired Immunodeficiency Syndrome - virology
Adult
Biomarkers
CD4 Lymphocyte Count
Dendritic cell
Dendritic Cells - immunology
Dendritic Cells - metabolism
Disease Progression
Female
HAART
HIV
HIV-1 - immunology
Humans
Leukocyte Count
Lymphocyte Activation - immunology
Lymphocyte Count
Lymphocytes - immunology
Lymphocytes - metabolism
Male
Middle Aged
Monocyte
Monocytes - immunology
Monocytes - metabolism
Myeloid Cells - immunology
Myeloid Cells - metabolism
sCD14
sCD163
slanDC
Viral Load
title Myeloid and lymphoid activation markers in AIDS and non-AIDS presenters
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