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Reduced frequency of circulating regulatory T cells and their related immunosuppressive mediators in treated celiac patients
Background Regulatory T cells (Tregs) have an important role in the control of the immune responses. This study aimed to compare the frequency of peripheral blood (PB) CD4+ CD25+ FoxP3+ Treg cells and PB and duodenal expression levels of pro- and anti-inflammatory mediators in treated celiac disease...
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Published in: | Molecular biology reports 2022-09, Vol.49 (9), p.8527-8535 |
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description | Background
Regulatory T cells (Tregs) have an important role in the control of the immune responses. This study aimed to compare the frequency of peripheral blood (PB) CD4+ CD25+ FoxP3+ Treg cells and PB and duodenal expression levels of pro- and anti-inflammatory mediators in treated celiac disease (CD) patients and healthy controls.
Methods and results
Duodenal biopsy specimens and PB samples were collected from 60 treated CD patients and 60 controls. Flow cytometry analysis was conducted on peripheral blood mononuclear cell (PBMC) specimens and relative PB and duodenal mRNA expression levels of CD25, forkhead box P3 (Foxp3), interleukin (IL)-10 and granzyme B (GrzB) were evaluated using quantitative real-time PCR. The levels of serum IL-10 and IL-6 were tested with sandwich enzyme-linked immunosorbent assay kits. p values 0.05). IL-10 PB mRNA and protein expression did not differ between the groups (p > 0.05), and GrzB PB expression was significantly reduced in CD patients (p = 0.001). In duodenal specimens of CD patients, while significantly increased CD25, Foxp3 mRNA expression (p = 0.01 and 0.001, respectively) and decreased IL-10 mRNA expression (p = 0.02) were observed, GrzB mRNA expression did not differ between groups (p > 0.05). Moreover, a high serum level of IL-6 was observed in CD patients (p = 0.001).
Conclusions
Despite following the gluten free diet, there may still be residual inflammation in the intestine of CD patients. Accordingly, finding a therapeutic approach based on strengthening the function of Treg cells in CD might be helpful. |
doi_str_mv | 10.1007/s11033-022-07674-w |
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Regulatory T cells (Tregs) have an important role in the control of the immune responses. This study aimed to compare the frequency of peripheral blood (PB) CD4+ CD25+ FoxP3+ Treg cells and PB and duodenal expression levels of pro- and anti-inflammatory mediators in treated celiac disease (CD) patients and healthy controls.
Methods and results
Duodenal biopsy specimens and PB samples were collected from 60 treated CD patients and 60 controls. Flow cytometry analysis was conducted on peripheral blood mononuclear cell (PBMC) specimens and relative PB and duodenal mRNA expression levels of CD25, forkhead box P3 (Foxp3), interleukin (IL)-10 and granzyme B (GrzB) were evaluated using quantitative real-time PCR. The levels of serum IL-10 and IL-6 were tested with sandwich enzyme-linked immunosorbent assay kits. p values < 0.05 were considered significant. Flow cytometry analysis showed a significant decrease in the number of Tregs in CD patients’ PBMC specimens (p = 0.012). CD25 and Foxp3 PB mRNA expressions were also lower in CD patients without reaching the significance level (p > 0.05). IL-10 PB mRNA and protein expression did not differ between the groups (p > 0.05), and GrzB PB expression was significantly reduced in CD patients (p = 0.001). In duodenal specimens of CD patients, while significantly increased CD25, Foxp3 mRNA expression (p = 0.01 and 0.001, respectively) and decreased IL-10 mRNA expression (p = 0.02) were observed, GrzB mRNA expression did not differ between groups (p > 0.05). Moreover, a high serum level of IL-6 was observed in CD patients (p = 0.001).
Conclusions
Despite following the gluten free diet, there may still be residual inflammation in the intestine of CD patients. Accordingly, finding a therapeutic approach based on strengthening the function of Treg cells in CD might be helpful.</description><identifier>ISSN: 0301-4851</identifier><identifier>EISSN: 1573-4978</identifier><identifier>DOI: 10.1007/s11033-022-07674-w</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Animal Anatomy ; Animal Biochemistry ; Biomedical and Life Sciences ; Biopsy ; CD25 antigen ; CD4 antigen ; Celiac disease ; Enzyme-linked immunosorbent assay ; Flow cytometry ; Forkhead protein ; Foxp3 protein ; Gene expression ; Gluten ; Granzyme B ; Histology ; Immunoregulation ; Inflammation ; Interleukin 10 ; Interleukin 6 ; Life Sciences ; Lymphocytes T ; Morphology ; Original Article ; Peripheral blood mononuclear cells</subject><ispartof>Molecular biology reports, 2022-09, Vol.49 (9), p.8527-8535</ispartof><rights>The Author(s), under exclusive licence to Springer Nature B.V. 2022</rights><rights>The Author(s), under exclusive licence to Springer Nature B.V. 2022.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c282t-27a6cef5f7383a2ca73238d7ede084a82b2046652ed73c649cd4e321aeb6d5253</citedby><cites>FETCH-LOGICAL-c282t-27a6cef5f7383a2ca73238d7ede084a82b2046652ed73c649cd4e321aeb6d5253</cites><orcidid>0000-0003-2495-1831</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Asri, Nastaran</creatorcontrib><creatorcontrib>Rostami-Nejad, Mohammad</creatorcontrib><creatorcontrib>Nikzamir, Abdolrahim</creatorcontrib><creatorcontrib>Aghamohamadi, Elham</creatorcontrib><creatorcontrib>Asadzadeh-Aghdaei, Hamid</creatorcontrib><creatorcontrib>Zali, Mohammad Reza</creatorcontrib><title>Reduced frequency of circulating regulatory T cells and their related immunosuppressive mediators in treated celiac patients</title><title>Molecular biology reports</title><addtitle>Mol Biol Rep</addtitle><description>Background
Regulatory T cells (Tregs) have an important role in the control of the immune responses. This study aimed to compare the frequency of peripheral blood (PB) CD4+ CD25+ FoxP3+ Treg cells and PB and duodenal expression levels of pro- and anti-inflammatory mediators in treated celiac disease (CD) patients and healthy controls.
Methods and results
Duodenal biopsy specimens and PB samples were collected from 60 treated CD patients and 60 controls. Flow cytometry analysis was conducted on peripheral blood mononuclear cell (PBMC) specimens and relative PB and duodenal mRNA expression levels of CD25, forkhead box P3 (Foxp3), interleukin (IL)-10 and granzyme B (GrzB) were evaluated using quantitative real-time PCR. The levels of serum IL-10 and IL-6 were tested with sandwich enzyme-linked immunosorbent assay kits. p values < 0.05 were considered significant. Flow cytometry analysis showed a significant decrease in the number of Tregs in CD patients’ PBMC specimens (p = 0.012). CD25 and Foxp3 PB mRNA expressions were also lower in CD patients without reaching the significance level (p > 0.05). IL-10 PB mRNA and protein expression did not differ between the groups (p > 0.05), and GrzB PB expression was significantly reduced in CD patients (p = 0.001). In duodenal specimens of CD patients, while significantly increased CD25, Foxp3 mRNA expression (p = 0.01 and 0.001, respectively) and decreased IL-10 mRNA expression (p = 0.02) were observed, GrzB mRNA expression did not differ between groups (p > 0.05). Moreover, a high serum level of IL-6 was observed in CD patients (p = 0.001).
Conclusions
Despite following the gluten free diet, there may still be residual inflammation in the intestine of CD patients. Accordingly, finding a therapeutic approach based on strengthening the function of Treg cells in CD might be helpful.</description><subject>Animal Anatomy</subject><subject>Animal Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biopsy</subject><subject>CD25 antigen</subject><subject>CD4 antigen</subject><subject>Celiac disease</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Flow cytometry</subject><subject>Forkhead protein</subject><subject>Foxp3 protein</subject><subject>Gene expression</subject><subject>Gluten</subject><subject>Granzyme B</subject><subject>Histology</subject><subject>Immunoregulation</subject><subject>Inflammation</subject><subject>Interleukin 10</subject><subject>Interleukin 6</subject><subject>Life Sciences</subject><subject>Lymphocytes T</subject><subject>Morphology</subject><subject>Original Article</subject><subject>Peripheral blood mononuclear cells</subject><issn>0301-4851</issn><issn>1573-4978</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kV1LwzAUhoMoOKd_wKuAN95U89Wmu5ThFwwEmdchS05nRpvWpHUM_PGmmyB44VUOnOd5yeFF6JKSG0qIvI2UEs4zwlhGZCFFtj1CE5pLnomZLI_RhHBCM1Hm9BSdxbghhAgq8wn6egU7GLC4CvAxgDc73FbYuGCGWvfOr3GA9Ti2YYeX2EBdR6y9xf07uJCWaZVs1zSDb-PQdQFidJ-AG7ButCJ2HvcB9ljSnTa4S8ng-3iOTipdR7j4eafo7eF-OX_KFi-Pz_O7RWZYyfqMSV0YqPJK8pJrZrTkjJdWggVSCl2yFSOiKHIGVnJTiJmxAjijGlaFzVnOp-j6kNuFNh0Ze9W4OJ6iPbRDVKyQpRRUkCKhV3_QTTsEn36nmKSMUsolTRQ7UCa0MQaoVBdco8NOUaLGQtShEJUKUftC1DZJ_CDFBPs1hN_of6xvUEaQ7w</recordid><startdate>20220901</startdate><enddate>20220901</enddate><creator>Asri, Nastaran</creator><creator>Rostami-Nejad, Mohammad</creator><creator>Nikzamir, Abdolrahim</creator><creator>Aghamohamadi, Elham</creator><creator>Asadzadeh-Aghdaei, Hamid</creator><creator>Zali, Mohammad Reza</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-2495-1831</orcidid></search><sort><creationdate>20220901</creationdate><title>Reduced frequency of circulating regulatory T cells and their related immunosuppressive mediators in treated celiac patients</title><author>Asri, Nastaran ; Rostami-Nejad, Mohammad ; Nikzamir, Abdolrahim ; Aghamohamadi, Elham ; Asadzadeh-Aghdaei, Hamid ; Zali, Mohammad Reza</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c282t-27a6cef5f7383a2ca73238d7ede084a82b2046652ed73c649cd4e321aeb6d5253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Animal Anatomy</topic><topic>Animal Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biopsy</topic><topic>CD25 antigen</topic><topic>CD4 antigen</topic><topic>Celiac disease</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Flow cytometry</topic><topic>Forkhead protein</topic><topic>Foxp3 protein</topic><topic>Gene expression</topic><topic>Gluten</topic><topic>Granzyme B</topic><topic>Histology</topic><topic>Immunoregulation</topic><topic>Inflammation</topic><topic>Interleukin 10</topic><topic>Interleukin 6</topic><topic>Life Sciences</topic><topic>Lymphocytes T</topic><topic>Morphology</topic><topic>Original Article</topic><topic>Peripheral blood mononuclear cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Asri, Nastaran</creatorcontrib><creatorcontrib>Rostami-Nejad, Mohammad</creatorcontrib><creatorcontrib>Nikzamir, Abdolrahim</creatorcontrib><creatorcontrib>Aghamohamadi, Elham</creatorcontrib><creatorcontrib>Asadzadeh-Aghdaei, Hamid</creatorcontrib><creatorcontrib>Zali, Mohammad Reza</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular biology reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Asri, Nastaran</au><au>Rostami-Nejad, Mohammad</au><au>Nikzamir, Abdolrahim</au><au>Aghamohamadi, Elham</au><au>Asadzadeh-Aghdaei, Hamid</au><au>Zali, Mohammad Reza</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reduced frequency of circulating regulatory T cells and their related immunosuppressive mediators in treated celiac patients</atitle><jtitle>Molecular biology reports</jtitle><stitle>Mol Biol Rep</stitle><date>2022-09-01</date><risdate>2022</risdate><volume>49</volume><issue>9</issue><spage>8527</spage><epage>8535</epage><pages>8527-8535</pages><issn>0301-4851</issn><eissn>1573-4978</eissn><abstract>Background
Regulatory T cells (Tregs) have an important role in the control of the immune responses. This study aimed to compare the frequency of peripheral blood (PB) CD4+ CD25+ FoxP3+ Treg cells and PB and duodenal expression levels of pro- and anti-inflammatory mediators in treated celiac disease (CD) patients and healthy controls.
Methods and results
Duodenal biopsy specimens and PB samples were collected from 60 treated CD patients and 60 controls. Flow cytometry analysis was conducted on peripheral blood mononuclear cell (PBMC) specimens and relative PB and duodenal mRNA expression levels of CD25, forkhead box P3 (Foxp3), interleukin (IL)-10 and granzyme B (GrzB) were evaluated using quantitative real-time PCR. The levels of serum IL-10 and IL-6 were tested with sandwich enzyme-linked immunosorbent assay kits. p values < 0.05 were considered significant. Flow cytometry analysis showed a significant decrease in the number of Tregs in CD patients’ PBMC specimens (p = 0.012). CD25 and Foxp3 PB mRNA expressions were also lower in CD patients without reaching the significance level (p > 0.05). IL-10 PB mRNA and protein expression did not differ between the groups (p > 0.05), and GrzB PB expression was significantly reduced in CD patients (p = 0.001). In duodenal specimens of CD patients, while significantly increased CD25, Foxp3 mRNA expression (p = 0.01 and 0.001, respectively) and decreased IL-10 mRNA expression (p = 0.02) were observed, GrzB mRNA expression did not differ between groups (p > 0.05). Moreover, a high serum level of IL-6 was observed in CD patients (p = 0.001).
Conclusions
Despite following the gluten free diet, there may still be residual inflammation in the intestine of CD patients. Accordingly, finding a therapeutic approach based on strengthening the function of Treg cells in CD might be helpful.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s11033-022-07674-w</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-2495-1831</orcidid></addata></record> |
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subjects | Animal Anatomy Animal Biochemistry Biomedical and Life Sciences Biopsy CD25 antigen CD4 antigen Celiac disease Enzyme-linked immunosorbent assay Flow cytometry Forkhead protein Foxp3 protein Gene expression Gluten Granzyme B Histology Immunoregulation Inflammation Interleukin 10 Interleukin 6 Life Sciences Lymphocytes T Morphology Original Article Peripheral blood mononuclear cells |
title | Reduced frequency of circulating regulatory T cells and their related immunosuppressive mediators in treated celiac patients |
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