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Gene expression profiling in peripheral blood mononuclear cells of patients with common variable immunodeficiency: modulation of adaptive immune response following intravenous immunoglobulin therapy
Regular intravenous immunoglobulin treatment is used to replace antibody deficiency in primary immunodeficiency diseases; however the therapeutic effect seems to be related not only to antibody replacement but also to an active role in the modulation of the immune response. Common variable immunodef...
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Published in: | PloS one 2014-05, Vol.9 (5), p.e97571-e97571 |
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creator | Dolcino, Marzia Patuzzo, Giuseppe Barbieri, Alessandro Tinazzi, Elisa Rizzi, Monica Beri, Ruggero Argentino, Giuseppe Ottria, Andrea Lunardi, Claudio Puccetti, Antonio |
description | Regular intravenous immunoglobulin treatment is used to replace antibody deficiency in primary immunodeficiency diseases; however the therapeutic effect seems to be related not only to antibody replacement but also to an active role in the modulation of the immune response. Common variable immunodeficiency is the most frequent primary immunodeficiency seen in clinical practice.
We have studied the effect of intravenous immunoglobulin replacement in patients with common variable immunodeficiency by evaluating the gene-expression profiles from Affimetrix HG-U133A. Some of the gene array results were validated by real time RT-PCR and by the measurement of circulating cytokines and chemokines by ELISA. Moreover we performed FACS analysis of blood mononuclear cells from the patients enrolled in the study.
A series of genes involved in innate and acquired immune responses were markedly up- or down-modulated before therapy. Such genes included CD14, CD36, LEPR, IRF-5, RGS-1, CD38, TNFRSF25, IL-4, CXCR4, CCR3, IL-8. Most of these modulated genes showed an expression similar to that of normal controls after immunoglobulin replacement. Real time RT-PCR of selected genes and serum levels of IL-4, CXCR4 before and after therapy changed accordingly to gene array results. Interestingly, serum levels of IL-8 remained unchanged, as the corresponding gene, before and after treatment. FACS analysis showed a marked decrease of CD8+T cells and an increase of CD4+T cells following treatment. Moreover we observed a marked increase of CD23⁻CD27⁻IgM⁻IgG⁻ B cells (centrocytes).
Our results are in accordance with previous reports and provide further support to the hypothesis that the benefits of intravenous immunoglobulin therapy are not only related to antibody replacement but also to its ability to modulate the immune response in common variable immunodeficiency. |
doi_str_mv | 10.1371/journal.pone.0097571 |
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We have studied the effect of intravenous immunoglobulin replacement in patients with common variable immunodeficiency by evaluating the gene-expression profiles from Affimetrix HG-U133A. Some of the gene array results were validated by real time RT-PCR and by the measurement of circulating cytokines and chemokines by ELISA. Moreover we performed FACS analysis of blood mononuclear cells from the patients enrolled in the study.
A series of genes involved in innate and acquired immune responses were markedly up- or down-modulated before therapy. Such genes included CD14, CD36, LEPR, IRF-5, RGS-1, CD38, TNFRSF25, IL-4, CXCR4, CCR3, IL-8. Most of these modulated genes showed an expression similar to that of normal controls after immunoglobulin replacement. Real time RT-PCR of selected genes and serum levels of IL-4, CXCR4 before and after therapy changed accordingly to gene array results. Interestingly, serum levels of IL-8 remained unchanged, as the corresponding gene, before and after treatment. FACS analysis showed a marked decrease of CD8+T cells and an increase of CD4+T cells following treatment. Moreover we observed a marked increase of CD23⁻CD27⁻IgM⁻IgG⁻ B cells (centrocytes).
Our results are in accordance with previous reports and provide further support to the hypothesis that the benefits of intravenous immunoglobulin therapy are not only related to antibody replacement but also to its ability to modulate the immune response in common variable immunodeficiency.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0097571</identifier><identifier>PMID: 24831519</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adaptive Immunity ; Adult ; Age ; Analysis ; B cells ; Biology and Life Sciences ; Blood ; Care and treatment ; CD14 antigen ; CD23 antigen ; CD27 antigen ; CD36 antigen ; CD38 antigen ; CD4 antigen ; CD8 antigen ; Cell Separation ; Chemokines ; Common variable immunodeficiency ; Common Variable Immunodeficiency - genetics ; CXCR4 protein ; Cytokines ; DNA microarrays ; Enzyme-Linked Immunosorbent Assay ; Female ; Flow Cytometry ; Gene Expression ; Gene Expression Profiling ; Genes ; Genomes ; Health aspects ; Humans ; Immune response ; Immune system ; Immunoglobulin E ; Immunoglobulin G ; Immunoglobulin M ; Immunoglobulins ; Immunoglobulins, Intravenous - therapeutic use ; Immunologic deficiency syndromes ; Immunology ; Immunomodulation ; Infections ; Interleukin 4 ; Interleukin 8 ; Intravenous administration ; Leptin ; Leukocytes (mononuclear) ; Leukocytes, Mononuclear - cytology ; Lymphocytes ; Lymphocytes B ; Lymphocytes T ; Male ; Medicine ; Medicine and Health Sciences ; Middle Aged ; Modulation ; Oligonucleotide Array Sequence Analysis ; Patients ; Peripheral blood mononuclear cells ; Polymerase chain reaction ; Primary immunodeficiencies ; Real time ; Research and Analysis Methods ; RNA, Complementary - metabolism ; Serum levels ; T cell receptors ; T cells ; Therapy</subject><ispartof>PloS one, 2014-05, Vol.9 (5), p.e97571-e97571</ispartof><rights>COPYRIGHT 2014 Public Library of Science</rights><rights>2014. This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-e33587cd12eed09fb9a54746647d8c834431fc05f8a2a70a573218023e8a85513</citedby><cites>FETCH-LOGICAL-c692t-e33587cd12eed09fb9a54746647d8c834431fc05f8a2a70a573218023e8a85513</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1524876169/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1524876169?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24831519$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Kaveri, Srinivas</contributor><creatorcontrib>Dolcino, Marzia</creatorcontrib><creatorcontrib>Patuzzo, Giuseppe</creatorcontrib><creatorcontrib>Barbieri, Alessandro</creatorcontrib><creatorcontrib>Tinazzi, Elisa</creatorcontrib><creatorcontrib>Rizzi, Monica</creatorcontrib><creatorcontrib>Beri, Ruggero</creatorcontrib><creatorcontrib>Argentino, Giuseppe</creatorcontrib><creatorcontrib>Ottria, Andrea</creatorcontrib><creatorcontrib>Lunardi, Claudio</creatorcontrib><creatorcontrib>Puccetti, Antonio</creatorcontrib><title>Gene expression profiling in peripheral blood mononuclear cells of patients with common variable immunodeficiency: modulation of adaptive immune response following intravenous immunoglobulin therapy</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Regular intravenous immunoglobulin treatment is used to replace antibody deficiency in primary immunodeficiency diseases; however the therapeutic effect seems to be related not only to antibody replacement but also to an active role in the modulation of the immune response. Common variable immunodeficiency is the most frequent primary immunodeficiency seen in clinical practice.
We have studied the effect of intravenous immunoglobulin replacement in patients with common variable immunodeficiency by evaluating the gene-expression profiles from Affimetrix HG-U133A. Some of the gene array results were validated by real time RT-PCR and by the measurement of circulating cytokines and chemokines by ELISA. Moreover we performed FACS analysis of blood mononuclear cells from the patients enrolled in the study.
A series of genes involved in innate and acquired immune responses were markedly up- or down-modulated before therapy. Such genes included CD14, CD36, LEPR, IRF-5, RGS-1, CD38, TNFRSF25, IL-4, CXCR4, CCR3, IL-8. Most of these modulated genes showed an expression similar to that of normal controls after immunoglobulin replacement. Real time RT-PCR of selected genes and serum levels of IL-4, CXCR4 before and after therapy changed accordingly to gene array results. Interestingly, serum levels of IL-8 remained unchanged, as the corresponding gene, before and after treatment. FACS analysis showed a marked decrease of CD8+T cells and an increase of CD4+T cells following treatment. Moreover we observed a marked increase of CD23⁻CD27⁻IgM⁻IgG⁻ B cells (centrocytes).
Our results are in accordance with previous reports and provide further support to the hypothesis that the benefits of intravenous immunoglobulin therapy are not only related to antibody replacement but also to its ability to modulate the immune response in common variable immunodeficiency.</description><subject>Adaptive Immunity</subject><subject>Adult</subject><subject>Age</subject><subject>Analysis</subject><subject>B cells</subject><subject>Biology and Life Sciences</subject><subject>Blood</subject><subject>Care and treatment</subject><subject>CD14 antigen</subject><subject>CD23 antigen</subject><subject>CD27 antigen</subject><subject>CD36 antigen</subject><subject>CD38 antigen</subject><subject>CD4 antigen</subject><subject>CD8 antigen</subject><subject>Cell Separation</subject><subject>Chemokines</subject><subject>Common variable immunodeficiency</subject><subject>Common Variable Immunodeficiency - genetics</subject><subject>CXCR4 protein</subject><subject>Cytokines</subject><subject>DNA microarrays</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Female</subject><subject>Flow Cytometry</subject><subject>Gene Expression</subject><subject>Gene Expression Profiling</subject><subject>Genes</subject><subject>Genomes</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Immune response</subject><subject>Immune system</subject><subject>Immunoglobulin E</subject><subject>Immunoglobulin G</subject><subject>Immunoglobulin M</subject><subject>Immunoglobulins</subject><subject>Immunoglobulins, Intravenous - therapeutic use</subject><subject>Immunologic deficiency syndromes</subject><subject>Immunology</subject><subject>Immunomodulation</subject><subject>Infections</subject><subject>Interleukin 4</subject><subject>Interleukin 8</subject><subject>Intravenous administration</subject><subject>Leptin</subject><subject>Leukocytes (mononuclear)</subject><subject>Leukocytes, Mononuclear - cytology</subject><subject>Lymphocytes</subject><subject>Lymphocytes B</subject><subject>Lymphocytes T</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine and Health Sciences</subject><subject>Middle Aged</subject><subject>Modulation</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Patients</subject><subject>Peripheral blood mononuclear cells</subject><subject>Polymerase chain reaction</subject><subject>Primary immunodeficiencies</subject><subject>Real time</subject><subject>Research and Analysis Methods</subject><subject>RNA, Complementary - metabolism</subject><subject>Serum levels</subject><subject>T cell receptors</subject><subject>T 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expression profiling in peripheral blood mononuclear cells of patients with common variable immunodeficiency: modulation of adaptive immune response following intravenous immunoglobulin therapy</title><author>Dolcino, Marzia ; Patuzzo, Giuseppe ; Barbieri, Alessandro ; Tinazzi, Elisa ; Rizzi, Monica ; Beri, Ruggero ; Argentino, Giuseppe ; Ottria, Andrea ; Lunardi, Claudio ; Puccetti, Antonio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-e33587cd12eed09fb9a54746647d8c834431fc05f8a2a70a573218023e8a85513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adaptive Immunity</topic><topic>Adult</topic><topic>Age</topic><topic>Analysis</topic><topic>B cells</topic><topic>Biology and Life Sciences</topic><topic>Blood</topic><topic>Care and treatment</topic><topic>CD14 antigen</topic><topic>CD23 antigen</topic><topic>CD27 antigen</topic><topic>CD36 antigen</topic><topic>CD38 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one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dolcino, Marzia</au><au>Patuzzo, Giuseppe</au><au>Barbieri, Alessandro</au><au>Tinazzi, Elisa</au><au>Rizzi, Monica</au><au>Beri, Ruggero</au><au>Argentino, Giuseppe</au><au>Ottria, Andrea</au><au>Lunardi, Claudio</au><au>Puccetti, Antonio</au><au>Kaveri, Srinivas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gene expression profiling in peripheral blood mononuclear cells of patients with common variable immunodeficiency: modulation of adaptive immune response following intravenous immunoglobulin therapy</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2014-05-15</date><risdate>2014</risdate><volume>9</volume><issue>5</issue><spage>e97571</spage><epage>e97571</epage><pages>e97571-e97571</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Regular intravenous immunoglobulin treatment is used to replace antibody deficiency in primary immunodeficiency diseases; however the therapeutic effect seems to be related not only to antibody replacement but also to an active role in the modulation of the immune response. Common variable immunodeficiency is the most frequent primary immunodeficiency seen in clinical practice.
We have studied the effect of intravenous immunoglobulin replacement in patients with common variable immunodeficiency by evaluating the gene-expression profiles from Affimetrix HG-U133A. Some of the gene array results were validated by real time RT-PCR and by the measurement of circulating cytokines and chemokines by ELISA. Moreover we performed FACS analysis of blood mononuclear cells from the patients enrolled in the study.
A series of genes involved in innate and acquired immune responses were markedly up- or down-modulated before therapy. Such genes included CD14, CD36, LEPR, IRF-5, RGS-1, CD38, TNFRSF25, IL-4, CXCR4, CCR3, IL-8. Most of these modulated genes showed an expression similar to that of normal controls after immunoglobulin replacement. Real time RT-PCR of selected genes and serum levels of IL-4, CXCR4 before and after therapy changed accordingly to gene array results. Interestingly, serum levels of IL-8 remained unchanged, as the corresponding gene, before and after treatment. FACS analysis showed a marked decrease of CD8+T cells and an increase of CD4+T cells following treatment. Moreover we observed a marked increase of CD23⁻CD27⁻IgM⁻IgG⁻ B cells (centrocytes).
Our results are in accordance with previous reports and provide further support to the hypothesis that the benefits of intravenous immunoglobulin therapy are not only related to antibody replacement but also to its ability to modulate the immune response in common variable immunodeficiency.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>24831519</pmid><doi>10.1371/journal.pone.0097571</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2014-05, Vol.9 (5), p.e97571-e97571 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1524876169 |
source | Publicly Available Content (ProQuest); PubMed Central |
subjects | Adaptive Immunity Adult Age Analysis B cells Biology and Life Sciences Blood Care and treatment CD14 antigen CD23 antigen CD27 antigen CD36 antigen CD38 antigen CD4 antigen CD8 antigen Cell Separation Chemokines Common variable immunodeficiency Common Variable Immunodeficiency - genetics CXCR4 protein Cytokines DNA microarrays Enzyme-Linked Immunosorbent Assay Female Flow Cytometry Gene Expression Gene Expression Profiling Genes Genomes Health aspects Humans Immune response Immune system Immunoglobulin E Immunoglobulin G Immunoglobulin M Immunoglobulins Immunoglobulins, Intravenous - therapeutic use Immunologic deficiency syndromes Immunology Immunomodulation Infections Interleukin 4 Interleukin 8 Intravenous administration Leptin Leukocytes (mononuclear) Leukocytes, Mononuclear - cytology Lymphocytes Lymphocytes B Lymphocytes T Male Medicine Medicine and Health Sciences Middle Aged Modulation Oligonucleotide Array Sequence Analysis Patients Peripheral blood mononuclear cells Polymerase chain reaction Primary immunodeficiencies Real time Research and Analysis Methods RNA, Complementary - metabolism Serum levels T cell receptors T cells Therapy |
title | Gene expression profiling in peripheral blood mononuclear cells of patients with common variable immunodeficiency: modulation of adaptive immune response following intravenous immunoglobulin therapy |
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