Recent thymic emigrants, T regulatory cells, and BAFF level in children with X-linked agammaglobulinaemia in association with chronic respiratory disease

Abstract Background X-linked agammaglobulinaemia (XLA) is a genetic disorder affecting B cell maturation, which is characterised by a low number of B cells, agammaglobulinaemia and increased susceptibility to a variety of bacterial infections. This study was performed to assess T cell subpopulations...

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Veröffentlicht in:Allergologia et immunopathologia 2018-01, Vol.46 (1), p.58-66
Hauptverfasser: Sharapova, S.O, Pashchenko, O.E, Guryanova, I.E, Migas, A.A, Kondratenko, I.V, Aleinikova, O.V
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container_title Allergologia et immunopathologia
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creator Sharapova, S.O
Pashchenko, O.E
Guryanova, I.E
Migas, A.A
Kondratenko, I.V
Aleinikova, O.V
description Abstract Background X-linked agammaglobulinaemia (XLA) is a genetic disorder affecting B cell maturation, which is characterised by a low number of B cells, agammaglobulinaemia and increased susceptibility to a variety of bacterial infections. This study was performed to assess T cell subpopulations in a group of children with XLA in association with chronic respiratory disease (CRD). Methods Numbers of T cell subpopulations (CD3+, CD4+, CD8+, CD3+DR+, naïve, memory, recent thymic emigrants (RTE), regulatory T cells, follicular T helpers) were measured by eight-colour flow cytometry in 22 XLA patients and 50 controls. BAFF level was measured by ELISA. Results XLA patients with CRD had a significantly lower percentage of RTE numbers and Tregs, while significantly higher absolute counts of lymphocytes, CD3+, CD8+, CD3+DR+ and CD4+CD45RO+ T cells were detected as compared with healthy controls. In patients with XLA without CRD, the number of follicular T helper cells was altered significantly (percentage and absolute), as compared with healthy controls. Additionally, they had significantly higher counts (percentage and absolute) of CD4+CD45RA+ cells and lower percentage of CD4+CD45RO+ cells in comparison with healthy controls. Conclusions Our study affords new information concerning CRD and T cell subsets that differentiate or are maintained in the absence of B cells in children with XLA. T cell's homeostasis depends on the presence of chronic respiratory disease that may be caused by the delay in diagnosis.
doi_str_mv 10.1016/j.aller.2017.01.011
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This study was performed to assess T cell subpopulations in a group of children with XLA in association with chronic respiratory disease (CRD). Methods Numbers of T cell subpopulations (CD3+, CD4+, CD8+, CD3+DR+, naïve, memory, recent thymic emigrants (RTE), regulatory T cells, follicular T helpers) were measured by eight-colour flow cytometry in 22 XLA patients and 50 controls. BAFF level was measured by ELISA. Results XLA patients with CRD had a significantly lower percentage of RTE numbers and Tregs, while significantly higher absolute counts of lymphocytes, CD3+, CD8+, CD3+DR+ and CD4+CD45RO+ T cells were detected as compared with healthy controls. In patients with XLA without CRD, the number of follicular T helper cells was altered significantly (percentage and absolute), as compared with healthy controls. Additionally, they had significantly higher counts (percentage and absolute) of CD4+CD45RA+ cells and lower percentage of CD4+CD45RO+ cells in comparison with healthy controls. Conclusions Our study affords new information concerning CRD and T cell subsets that differentiate or are maintained in the absence of B cells in children with XLA. T cell's homeostasis depends on the presence of chronic respiratory disease that may be caused by the delay in diagnosis.</description><identifier>ISSN: 0301-0546</identifier><identifier>EISSN: 1578-1267</identifier><identifier>DOI: 10.1016/j.aller.2017.01.011</identifier><identifier>PMID: 28477853</identifier><language>eng</language><publisher>Spain: Elsevier España, S.L.U</publisher><subject>Adolescent ; Agammaglobulinemia - complications ; Agammaglobulinemia - immunology ; Allergy and Immunology ; B-Cell Activating Factor - metabolism ; BAFF ; Bronchitis - complications ; Bronchitis - immunology ; Cell Separation ; Child ; Child, Preschool ; Chronic Disease ; Chronic lung infections ; Chronic sinusitis ; Female ; Flow Cytometry ; Genetic Diseases, X-Linked - complications ; Genetic Diseases, X-Linked - immunology ; Humans ; Immunologic Memory ; Immunophenotyping ; Internal Medicine ; Male ; Sinusitis - complications ; Sinusitis - immunology ; T cells ; T-Lymphocyte Subsets - immunology ; T-Lymphocytes, Regulatory - immunology ; Thymocytes - immunology ; X-linked agammaglobulinaemia</subject><ispartof>Allergologia et immunopathologia, 2018-01, Vol.46 (1), p.58-66</ispartof><rights>SEICAP</rights><rights>2017 SEICAP</rights><rights>Copyright © 2017 SEICAP. Published by Elsevier España, S.L.U. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c414t-f75b90c42d8083a78151f2d29f33cd8709daa208be0ccd1ba237ef1b751587173</citedby><cites>FETCH-LOGICAL-c414t-f75b90c42d8083a78151f2d29f33cd8709daa208be0ccd1ba237ef1b751587173</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28477853$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sharapova, S.O</creatorcontrib><creatorcontrib>Pashchenko, O.E</creatorcontrib><creatorcontrib>Guryanova, I.E</creatorcontrib><creatorcontrib>Migas, A.A</creatorcontrib><creatorcontrib>Kondratenko, I.V</creatorcontrib><creatorcontrib>Aleinikova, O.V</creatorcontrib><title>Recent thymic emigrants, T regulatory cells, and BAFF level in children with X-linked agammaglobulinaemia in association with chronic respiratory disease</title><title>Allergologia et immunopathologia</title><addtitle>Allergol Immunopathol (Madr)</addtitle><description>Abstract Background X-linked agammaglobulinaemia (XLA) is a genetic disorder affecting B cell maturation, which is characterised by a low number of B cells, agammaglobulinaemia and increased susceptibility to a variety of bacterial infections. This study was performed to assess T cell subpopulations in a group of children with XLA in association with chronic respiratory disease (CRD). Methods Numbers of T cell subpopulations (CD3+, CD4+, CD8+, CD3+DR+, naïve, memory, recent thymic emigrants (RTE), regulatory T cells, follicular T helpers) were measured by eight-colour flow cytometry in 22 XLA patients and 50 controls. BAFF level was measured by ELISA. Results XLA patients with CRD had a significantly lower percentage of RTE numbers and Tregs, while significantly higher absolute counts of lymphocytes, CD3+, CD8+, CD3+DR+ and CD4+CD45RO+ T cells were detected as compared with healthy controls. In patients with XLA without CRD, the number of follicular T helper cells was altered significantly (percentage and absolute), as compared with healthy controls. Additionally, they had significantly higher counts (percentage and absolute) of CD4+CD45RA+ cells and lower percentage of CD4+CD45RO+ cells in comparison with healthy controls. Conclusions Our study affords new information concerning CRD and T cell subsets that differentiate or are maintained in the absence of B cells in children with XLA. T cell's homeostasis depends on the presence of chronic respiratory disease that may be caused by the delay in diagnosis.</description><subject>Adolescent</subject><subject>Agammaglobulinemia - complications</subject><subject>Agammaglobulinemia - immunology</subject><subject>Allergy and Immunology</subject><subject>B-Cell Activating Factor - metabolism</subject><subject>BAFF</subject><subject>Bronchitis - complications</subject><subject>Bronchitis - immunology</subject><subject>Cell Separation</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Chronic Disease</subject><subject>Chronic lung infections</subject><subject>Chronic sinusitis</subject><subject>Female</subject><subject>Flow Cytometry</subject><subject>Genetic Diseases, X-Linked - complications</subject><subject>Genetic Diseases, X-Linked - immunology</subject><subject>Humans</subject><subject>Immunologic Memory</subject><subject>Immunophenotyping</subject><subject>Internal Medicine</subject><subject>Male</subject><subject>Sinusitis - complications</subject><subject>Sinusitis - immunology</subject><subject>T cells</subject><subject>T-Lymphocyte Subsets - immunology</subject><subject>T-Lymphocytes, Regulatory - immunology</subject><subject>Thymocytes - immunology</subject><subject>X-linked agammaglobulinaemia</subject><issn>0301-0546</issn><issn>1578-1267</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUsGKFDEQbURxZ1e_QJAcPdhjKunu9BwU1sVRYUHQFbyFdFI9k9l0Mpt0r8yn-LebdkYPXoSCguK9erx6VRQvgC6BQvNmt1TOYVwyCmJJIRc8KhZQi7YE1ojHxYJyCiWtq-asOE9pRymjrOFPizPWVkK0NV8Uv76iRj-ScXsYrCY42E1UfkyvyQ2JuJmcGkM8EI3O5Znyhry_XK-Jw3t0xHqit9aZiJ78tOOW_Cid9bdoiNqoYVAbF7opT1Req2a0Siloq0YbTgS9jcFn3Yhpb-NRy9iEKuGz4kmvXMLnp35RfF9_uLn6VF5_-fj56vK61BVUY9mLultRXTHT0pYr0UINPTNs1XOuTSvoyijFaNsh1dpApxgX2EMnaqhbAYJfFK-Oe_cx3E2YRjnYNPtVHsOUJLSrpspX5U2G8iNUx5BSxF7uox1UPEigcs5E7uTvTOSciaSQCzLr5Ulg6gY0fzl_QsiAt0cAZpv3NtOTtug1GhtRj9IE-x-Bd__wdT661crd4gHTLkzR5wtKkIlJKr_NbzF_RTZPaQ0VfwDPKbVc</recordid><startdate>20180101</startdate><enddate>20180101</enddate><creator>Sharapova, S.O</creator><creator>Pashchenko, O.E</creator><creator>Guryanova, I.E</creator><creator>Migas, A.A</creator><creator>Kondratenko, I.V</creator><creator>Aleinikova, O.V</creator><general>Elsevier España, S.L.U</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></search><sort><creationdate>20180101</creationdate><title>Recent thymic emigrants, T regulatory cells, and BAFF level in children with X-linked agammaglobulinaemia in association with chronic respiratory disease</title><author>Sharapova, S.O ; Pashchenko, O.E ; Guryanova, I.E ; Migas, A.A ; Kondratenko, I.V ; Aleinikova, O.V</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c414t-f75b90c42d8083a78151f2d29f33cd8709daa208be0ccd1ba237ef1b751587173</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adolescent</topic><topic>Agammaglobulinemia - complications</topic><topic>Agammaglobulinemia - immunology</topic><topic>Allergy and Immunology</topic><topic>B-Cell Activating Factor - metabolism</topic><topic>BAFF</topic><topic>Bronchitis - complications</topic><topic>Bronchitis - immunology</topic><topic>Cell Separation</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Chronic Disease</topic><topic>Chronic lung infections</topic><topic>Chronic sinusitis</topic><topic>Female</topic><topic>Flow Cytometry</topic><topic>Genetic Diseases, X-Linked - complications</topic><topic>Genetic Diseases, X-Linked - immunology</topic><topic>Humans</topic><topic>Immunologic Memory</topic><topic>Immunophenotyping</topic><topic>Internal Medicine</topic><topic>Male</topic><topic>Sinusitis - complications</topic><topic>Sinusitis - immunology</topic><topic>T cells</topic><topic>T-Lymphocyte Subsets - immunology</topic><topic>T-Lymphocytes, Regulatory - immunology</topic><topic>Thymocytes - immunology</topic><topic>X-linked agammaglobulinaemia</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sharapova, S.O</creatorcontrib><creatorcontrib>Pashchenko, O.E</creatorcontrib><creatorcontrib>Guryanova, I.E</creatorcontrib><creatorcontrib>Migas, A.A</creatorcontrib><creatorcontrib>Kondratenko, I.V</creatorcontrib><creatorcontrib>Aleinikova, O.V</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>Allergologia et immunopathologia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sharapova, S.O</au><au>Pashchenko, O.E</au><au>Guryanova, I.E</au><au>Migas, A.A</au><au>Kondratenko, I.V</au><au>Aleinikova, O.V</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Recent thymic emigrants, T regulatory cells, and BAFF level in children with X-linked agammaglobulinaemia in association with chronic respiratory disease</atitle><jtitle>Allergologia et immunopathologia</jtitle><addtitle>Allergol Immunopathol (Madr)</addtitle><date>2018-01-01</date><risdate>2018</risdate><volume>46</volume><issue>1</issue><spage>58</spage><epage>66</epage><pages>58-66</pages><issn>0301-0546</issn><eissn>1578-1267</eissn><abstract>Abstract Background X-linked agammaglobulinaemia (XLA) is a genetic disorder affecting B cell maturation, which is characterised by a low number of B cells, agammaglobulinaemia and increased susceptibility to a variety of bacterial infections. This study was performed to assess T cell subpopulations in a group of children with XLA in association with chronic respiratory disease (CRD). Methods Numbers of T cell subpopulations (CD3+, CD4+, CD8+, CD3+DR+, naïve, memory, recent thymic emigrants (RTE), regulatory T cells, follicular T helpers) were measured by eight-colour flow cytometry in 22 XLA patients and 50 controls. BAFF level was measured by ELISA. Results XLA patients with CRD had a significantly lower percentage of RTE numbers and Tregs, while significantly higher absolute counts of lymphocytes, CD3+, CD8+, CD3+DR+ and CD4+CD45RO+ T cells were detected as compared with healthy controls. In patients with XLA without CRD, the number of follicular T helper cells was altered significantly (percentage and absolute), as compared with healthy controls. Additionally, they had significantly higher counts (percentage and absolute) of CD4+CD45RA+ cells and lower percentage of CD4+CD45RO+ cells in comparison with healthy controls. Conclusions Our study affords new information concerning CRD and T cell subsets that differentiate or are maintained in the absence of B cells in children with XLA. T cell's homeostasis depends on the presence of chronic respiratory disease that may be caused by the delay in diagnosis.</abstract><cop>Spain</cop><pub>Elsevier España, S.L.U</pub><pmid>28477853</pmid><doi>10.1016/j.aller.2017.01.011</doi><tpages>9</tpages></addata></record>
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subjects Adolescent
Agammaglobulinemia - complications
Agammaglobulinemia - immunology
Allergy and Immunology
B-Cell Activating Factor - metabolism
BAFF
Bronchitis - complications
Bronchitis - immunology
Cell Separation
Child
Child, Preschool
Chronic Disease
Chronic lung infections
Chronic sinusitis
Female
Flow Cytometry
Genetic Diseases, X-Linked - complications
Genetic Diseases, X-Linked - immunology
Humans
Immunologic Memory
Immunophenotyping
Internal Medicine
Male
Sinusitis - complications
Sinusitis - immunology
T cells
T-Lymphocyte Subsets - immunology
T-Lymphocytes, Regulatory - immunology
Thymocytes - immunology
X-linked agammaglobulinaemia
title Recent thymic emigrants, T regulatory cells, and BAFF level in children with X-linked agammaglobulinaemia in association with chronic respiratory disease
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