Loading…
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...
Saved in:
Published in: | Immunobiology (1979) 2019-03, Vol.224 (2), p.231-241 |
---|---|
Main Authors: | , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
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 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2155962813</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0171298518302146</els_id><sourcerecordid>2155962813</sourcerecordid><originalsourceid>FETCH-LOGICAL-c359t-383d186e172afaebd0cd5e76d25321fcfc77586f8124f7711219faa2e1a567de3</originalsourceid><addsrcrecordid>eNp9kMtOwzAQRS0EoqXwBUgoSzYJHhvHzoJFxaNUKmIBrC3XngiXPIqdVurfkz5gyWo0mjMzuoeQS6AZUMhvFpmv577NGAWVAWQU4IgMQUmVciaLYzKkICFlhRIDchbjglIomFSnZMCpYEwVMCSTlw1WrXeJaVxSberl566xnV-bzrdNUpvwhSEmvknG04e3Hde0TbprlgEjNl0_PycnpakiXhzqiHw8Pb7fP6ez18n0fjxLLRdFl3LFHagcQTJTGpw7ap1AmTsmOIPSllZKofJSAbstpQRgUJTGMAQjcumQj8j1_u4ytN8rjJ2ufbRYVabBdhU1AyGKnCngPcr3qA1tjAFLvQy-j7PRQPXWoF7onUG9NagBdG-w37o6PFjNa3R_O7_KeuBuD2Afc-0x6Gg9NhadD2g77Vr_74MfDM2B2w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2155962813</pqid></control><display><type>article</type><title>Myeloid and lymphoid activation markers in AIDS and non-AIDS presenters</title><source>ScienceDirect Freedom Collection</source><source>Elsevier ScienceDirect Journals</source><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</creator><creatorcontrib>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</creatorcontrib><description><![CDATA[•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 < 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. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c359t-383d186e172afaebd0cd5e76d25321fcfc77586f8124f7711219faa2e1a567de3</citedby><cites>FETCH-LOGICAL-c359t-383d186e172afaebd0cd5e76d25321fcfc77586f8124f7711219faa2e1a567de3</cites><orcidid>0000-0002-6938-8627 ; 0000-0002-1286-467X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0171298518302146$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3549,27924,27925,45780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30522891$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Iannetta, Marco</creatorcontrib><creatorcontrib>Savinelli, Stefano</creatorcontrib><creatorcontrib>Rossi, Raffaella</creatorcontrib><creatorcontrib>Mascia, Claudia</creatorcontrib><creatorcontrib>Marocco, Raffaella</creatorcontrib><creatorcontrib>Vita, Serena</creatorcontrib><creatorcontrib>Zuccalà, Paola</creatorcontrib><creatorcontrib>Zingaropoli, Maria Antonella</creatorcontrib><creatorcontrib>Mengoni, Fabio</creatorcontrib><creatorcontrib>Massetti, Anna Paola</creatorcontrib><creatorcontrib>Falciano, Mario</creatorcontrib><creatorcontrib>d’Ettorre, Gabriella</creatorcontrib><creatorcontrib>Ciardi, Maria Rosa</creatorcontrib><creatorcontrib>Mastroianni, Claudio Maria</creatorcontrib><creatorcontrib>Vullo, Vincenzo</creatorcontrib><creatorcontrib>Lichtner, Miriam</creatorcontrib><title>Myeloid and lymphoid activation markers in AIDS and non-AIDS presenters</title><title>Immunobiology (1979)</title><addtitle>Immunobiology</addtitle><description><![CDATA[•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 < 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><subject>Acquired Immunodeficiency Syndrome - immunology</subject><subject>Acquired Immunodeficiency Syndrome - metabolism</subject><subject>Acquired Immunodeficiency Syndrome - virology</subject><subject>Adult</subject><subject>Biomarkers</subject><subject>CD4 Lymphocyte Count</subject><subject>Dendritic cell</subject><subject>Dendritic Cells - immunology</subject><subject>Dendritic Cells - metabolism</subject><subject>Disease Progression</subject><subject>Female</subject><subject>HAART</subject><subject>HIV</subject><subject>HIV-1 - immunology</subject><subject>Humans</subject><subject>Leukocyte Count</subject><subject>Lymphocyte Activation - immunology</subject><subject>Lymphocyte Count</subject><subject>Lymphocytes - immunology</subject><subject>Lymphocytes - metabolism</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Monocyte</subject><subject>Monocytes - immunology</subject><subject>Monocytes - metabolism</subject><subject>Myeloid Cells - immunology</subject><subject>Myeloid Cells - metabolism</subject><subject>sCD14</subject><subject>sCD163</subject><subject>slanDC</subject><subject>Viral Load</subject><issn>0171-2985</issn><issn>1878-3279</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kMtOwzAQRS0EoqXwBUgoSzYJHhvHzoJFxaNUKmIBrC3XngiXPIqdVurfkz5gyWo0mjMzuoeQS6AZUMhvFpmv577NGAWVAWQU4IgMQUmVciaLYzKkICFlhRIDchbjglIomFSnZMCpYEwVMCSTlw1WrXeJaVxSberl566xnV-bzrdNUpvwhSEmvknG04e3Hde0TbprlgEjNl0_PycnpakiXhzqiHw8Pb7fP6ez18n0fjxLLRdFl3LFHagcQTJTGpw7ap1AmTsmOIPSllZKofJSAbstpQRgUJTGMAQjcumQj8j1_u4ytN8rjJ2ufbRYVabBdhU1AyGKnCngPcr3qA1tjAFLvQy-j7PRQPXWoF7onUG9NagBdG-w37o6PFjNa3R_O7_KeuBuD2Afc-0x6Gg9NhadD2g77Vr_74MfDM2B2w</recordid><startdate>201903</startdate><enddate>201903</enddate><creator>Iannetta, Marco</creator><creator>Savinelli, Stefano</creator><creator>Rossi, Raffaella</creator><creator>Mascia, Claudia</creator><creator>Marocco, Raffaella</creator><creator>Vita, Serena</creator><creator>Zuccalà, Paola</creator><creator>Zingaropoli, Maria Antonella</creator><creator>Mengoni, Fabio</creator><creator>Massetti, Anna Paola</creator><creator>Falciano, Mario</creator><creator>d’Ettorre, Gabriella</creator><creator>Ciardi, Maria Rosa</creator><creator>Mastroianni, Claudio Maria</creator><creator>Vullo, Vincenzo</creator><creator>Lichtner, Miriam</creator><general>Elsevier GmbH</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6938-8627</orcidid><orcidid>https://orcid.org/0000-0002-1286-467X</orcidid></search><sort><creationdate>201903</creationdate><title>Myeloid and lymphoid activation markers in AIDS and non-AIDS presenters</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-383d186e172afaebd0cd5e76d25321fcfc77586f8124f7711219faa2e1a567de3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Acquired Immunodeficiency Syndrome - immunology</topic><topic>Acquired Immunodeficiency Syndrome - metabolism</topic><topic>Acquired Immunodeficiency Syndrome - virology</topic><topic>Adult</topic><topic>Biomarkers</topic><topic>CD4 Lymphocyte Count</topic><topic>Dendritic cell</topic><topic>Dendritic Cells - immunology</topic><topic>Dendritic Cells - metabolism</topic><topic>Disease Progression</topic><topic>Female</topic><topic>HAART</topic><topic>HIV</topic><topic>HIV-1 - immunology</topic><topic>Humans</topic><topic>Leukocyte Count</topic><topic>Lymphocyte Activation - immunology</topic><topic>Lymphocyte Count</topic><topic>Lymphocytes - immunology</topic><topic>Lymphocytes - metabolism</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Monocyte</topic><topic>Monocytes - immunology</topic><topic>Monocytes - metabolism</topic><topic>Myeloid Cells - immunology</topic><topic>Myeloid Cells - metabolism</topic><topic>sCD14</topic><topic>sCD163</topic><topic>slanDC</topic><topic>Viral Load</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Iannetta, Marco</creatorcontrib><creatorcontrib>Savinelli, Stefano</creatorcontrib><creatorcontrib>Rossi, Raffaella</creatorcontrib><creatorcontrib>Mascia, Claudia</creatorcontrib><creatorcontrib>Marocco, Raffaella</creatorcontrib><creatorcontrib>Vita, Serena</creatorcontrib><creatorcontrib>Zuccalà, Paola</creatorcontrib><creatorcontrib>Zingaropoli, Maria Antonella</creatorcontrib><creatorcontrib>Mengoni, Fabio</creatorcontrib><creatorcontrib>Massetti, Anna Paola</creatorcontrib><creatorcontrib>Falciano, Mario</creatorcontrib><creatorcontrib>d’Ettorre, Gabriella</creatorcontrib><creatorcontrib>Ciardi, Maria Rosa</creatorcontrib><creatorcontrib>Mastroianni, Claudio Maria</creatorcontrib><creatorcontrib>Vullo, Vincenzo</creatorcontrib><creatorcontrib>Lichtner, Miriam</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Immunobiology (1979)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Iannetta, Marco</au><au>Savinelli, Stefano</au><au>Rossi, Raffaella</au><au>Mascia, Claudia</au><au>Marocco, Raffaella</au><au>Vita, Serena</au><au>Zuccalà, Paola</au><au>Zingaropoli, Maria Antonella</au><au>Mengoni, Fabio</au><au>Massetti, Anna Paola</au><au>Falciano, Mario</au><au>d’Ettorre, Gabriella</au><au>Ciardi, Maria Rosa</au><au>Mastroianni, Claudio Maria</au><au>Vullo, Vincenzo</au><au>Lichtner, Miriam</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Myeloid and lymphoid activation markers in AIDS and non-AIDS presenters</atitle><jtitle>Immunobiology (1979)</jtitle><addtitle>Immunobiology</addtitle><date>2019-03</date><risdate>2019</risdate><volume>224</volume><issue>2</issue><spage>231</spage><epage>241</epage><pages>231-241</pages><issn>0171-2985</issn><eissn>1878-3279</eissn><abstract><![CDATA[•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 < 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> |
fulltext | fulltext |
identifier | ISSN: 0171-2985 |
ispartof | Immunobiology (1979), 2019-03, Vol.224 (2), p.231-241 |
issn | 0171-2985 1878-3279 |
language | eng |
recordid | cdi_proquest_miscellaneous_2155962813 |
source | ScienceDirect Freedom Collection; Elsevier ScienceDirect Journals |
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 |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-24T14%3A05%3A17IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Myeloid%20and%20lymphoid%20activation%20markers%20in%20AIDS%20and%20non-AIDS%20presenters&rft.jtitle=Immunobiology%20(1979)&rft.au=Iannetta,%20Marco&rft.date=2019-03&rft.volume=224&rft.issue=2&rft.spage=231&rft.epage=241&rft.pages=231-241&rft.issn=0171-2985&rft.eissn=1878-3279&rft_id=info:doi/10.1016/j.imbio.2018.11.011&rft_dat=%3Cproquest_cross%3E2155962813%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c359t-383d186e172afaebd0cd5e76d25321fcfc77586f8124f7711219faa2e1a567de3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2155962813&rft_id=info:pmid/30522891&rfr_iscdi=true |