Loading…

Suppressive Mechanisms Induced by Tregs in Celiac Disease

Celiac disease (CD) is a systemic immune-mediated disorder caused by the dietary gluten in individuals who are genetically susceptible to the disease. In fact, CD is a T cell-mediated immune disease in which gluten-derived peptides activate the lamina propria CD4+ Teff cells, and these T-cell subset...

Full description

Saved in:
Bibliographic Details
Published in:Iranian biomedical journal 2020-05, Vol.24 (3), p.140-147
Main Authors: Asri, Nastaran, Rostami-Nejad, Mohammad, Barzegar, Mohammad, Nikzamir, Abdolrahim, Rezaei-Tavirani, Mostafa, Razzaghi, Mohammadreza, Zali, Mohammad Reza
Format: Article
Language:English
Subjects:
Citations: 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-c3960-7ec0abfd0b36c81fbe16c0b71c196982dce6b528b53e2fc5f3ea14728cb8ac9e3
cites
container_end_page 147
container_issue 3
container_start_page 140
container_title Iranian biomedical journal
container_volume 24
creator Asri, Nastaran
Rostami-Nejad, Mohammad
Barzegar, Mohammad
Nikzamir, Abdolrahim
Rezaei-Tavirani, Mostafa
Razzaghi, Mohammadreza
Zali, Mohammad Reza
description Celiac disease (CD) is a systemic immune-mediated disorder caused by the dietary gluten in individuals who are genetically susceptible to the disease. In fact, CD is a T cell-mediated immune disease in which gluten-derived peptides activate the lamina propria CD4+ Teff cells, and these T-cell subsets can cause the intestinal tissue damages. Also, there are additional subsets of CD4+ T cells with suppressor functions. These subsets express the master transcription factor, FOXP3, and include Tr1 cells and CD4+CD25+ regulatory T cells (Tregs), which are the main population involved in maintaining the peripheral tolerance, preventing the autoimmune diseases and limiting the chronic inflammatory diseases such as CD. The suppressive function of Tregs is important to maintain the immune homeostasis. This paper examined the features and the basic mechanisms used by Tregs to mediate the suppression in CD.
doi_str_mv 10.29252/ibj.24.3.140
format article
fullrecord <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_881ef7a834214d2a9f17523dba982c31</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_881ef7a834214d2a9f17523dba982c31</doaj_id><sourcerecordid>2380648161</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3960-7ec0abfd0b36c81fbe16c0b71c196982dce6b528b53e2fc5f3ea14728cb8ac9e3</originalsourceid><addsrcrecordid>eNpdkU1r3DAQhkVpabZpj70WQy-9eKsZSZZ8KZTt10JKDkkhNyHJ440Wr72V1oH8-4hsGpKeNEgPz4zmZew98CW2qPBz9NslyqVYguQv2AI5N7VBcfWSLYBjqRVenbA3OW85Fwq0fs1OBLQKpYAFay_m_T5RzvGGqt8Urt0Y8y5X67GbA3WVv60uE21yFcdqRUN0ofoWM7lMb9mr3g2Z3j2cp-zPj--Xq1_12fnP9errWR1E2_BaU-DO9x33ogkGek_QBO41BGib1mAXqPEKjVeCsA-qF-RAajTBGxdaEqdsffR2k9vafYo7l27t5KK9v5jSxrp0iGEgawxQr50REkF26NoetELReVcaBQHF9eXo2s9-R6X1eEhueCZ9_jLGa7uZbqxGrRoURfDpQZCmvzPlg93FHGgY3EjTnC0KCQ2UJLCgH_9Dt9OcxrKqQhneSFPIQtVHKqQp50T94zDA7X3AtgRsUVphi7bwH57-4JH-l6i4AwkloKM</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2380648161</pqid></control><display><type>article</type><title>Suppressive Mechanisms Induced by Tregs in Celiac Disease</title><source>Freely Accessible Journals</source><source>Open Access: PubMed Central</source><creator>Asri, Nastaran ; Rostami-Nejad, Mohammad ; Barzegar, Mohammad ; Nikzamir, Abdolrahim ; Rezaei-Tavirani, Mostafa ; Razzaghi, Mohammadreza ; Zali, Mohammad Reza</creator><creatorcontrib>Asri, Nastaran ; Rostami-Nejad, Mohammad ; Barzegar, Mohammad ; Nikzamir, Abdolrahim ; Rezaei-Tavirani, Mostafa ; Razzaghi, Mohammadreza ; Zali, Mohammad Reza ; Proteomics Research Center, Faculty of Paramedical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran ; Gastroenterology and Liver Diseases Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran ; Department of Clinical Biochemistry, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran ; School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran ; Laser Application in Medical Sciences Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran</creatorcontrib><description>Celiac disease (CD) is a systemic immune-mediated disorder caused by the dietary gluten in individuals who are genetically susceptible to the disease. In fact, CD is a T cell-mediated immune disease in which gluten-derived peptides activate the lamina propria CD4+ Teff cells, and these T-cell subsets can cause the intestinal tissue damages. Also, there are additional subsets of CD4+ T cells with suppressor functions. These subsets express the master transcription factor, FOXP3, and include Tr1 cells and CD4+CD25+ regulatory T cells (Tregs), which are the main population involved in maintaining the peripheral tolerance, preventing the autoimmune diseases and limiting the chronic inflammatory diseases such as CD. The suppressive function of Tregs is important to maintain the immune homeostasis. This paper examined the features and the basic mechanisms used by Tregs to mediate the suppression in CD.</description><identifier>ISSN: 1028-852X</identifier><identifier>EISSN: 2008-823X</identifier><identifier>DOI: 10.29252/ibj.24.3.140</identifier><identifier>PMID: 31952431</identifier><language>eng</language><publisher>Iran: Pasteur Institute of Iran</publisher><subject>Antigen-Presenting Cells - immunology ; Autoimmune diseases ; Biomarkers - metabolism ; CD25 antigen ; CD4 antigen ; Celiac disease ; Celiac Disease - immunology ; Cytokines - metabolism ; Diet ; Disease ; Forkhead protein ; Foxp3 protein ; Gluten ; glutens ; Homeostasis ; Humans ; immune tolerance ; Immunological diseases ; Immunological tolerance ; Immunoregulation ; Immunosuppression ; Inflammatory diseases ; Intestine ; Lamina propria ; Lymphocytes ; Lymphocytes T ; Peptides ; Review ; t-lymphocytes ; T-Lymphocytes, Regulatory - immunology ; Transcription factors</subject><ispartof>Iranian biomedical journal, 2020-05, Vol.24 (3), p.140-147</ispartof><rights>2020. This work is published under https://creativecommons.org/licenses/by-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3960-7ec0abfd0b36c81fbe16c0b71c196982dce6b528b53e2fc5f3ea14728cb8ac9e3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275623/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275623/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31952431$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Asri, Nastaran</creatorcontrib><creatorcontrib>Rostami-Nejad, Mohammad</creatorcontrib><creatorcontrib>Barzegar, Mohammad</creatorcontrib><creatorcontrib>Nikzamir, Abdolrahim</creatorcontrib><creatorcontrib>Rezaei-Tavirani, Mostafa</creatorcontrib><creatorcontrib>Razzaghi, Mohammadreza</creatorcontrib><creatorcontrib>Zali, Mohammad Reza</creatorcontrib><creatorcontrib>Proteomics Research Center, Faculty of Paramedical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran</creatorcontrib><creatorcontrib>Gastroenterology and Liver Diseases Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran</creatorcontrib><creatorcontrib>Department of Clinical Biochemistry, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran</creatorcontrib><creatorcontrib>School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran</creatorcontrib><creatorcontrib>Laser Application in Medical Sciences Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran</creatorcontrib><title>Suppressive Mechanisms Induced by Tregs in Celiac Disease</title><title>Iranian biomedical journal</title><addtitle>Iran Biomed J</addtitle><description>Celiac disease (CD) is a systemic immune-mediated disorder caused by the dietary gluten in individuals who are genetically susceptible to the disease. In fact, CD is a T cell-mediated immune disease in which gluten-derived peptides activate the lamina propria CD4+ Teff cells, and these T-cell subsets can cause the intestinal tissue damages. Also, there are additional subsets of CD4+ T cells with suppressor functions. These subsets express the master transcription factor, FOXP3, and include Tr1 cells and CD4+CD25+ regulatory T cells (Tregs), which are the main population involved in maintaining the peripheral tolerance, preventing the autoimmune diseases and limiting the chronic inflammatory diseases such as CD. The suppressive function of Tregs is important to maintain the immune homeostasis. This paper examined the features and the basic mechanisms used by Tregs to mediate the suppression in CD.</description><subject>Antigen-Presenting Cells - immunology</subject><subject>Autoimmune diseases</subject><subject>Biomarkers - metabolism</subject><subject>CD25 antigen</subject><subject>CD4 antigen</subject><subject>Celiac disease</subject><subject>Celiac Disease - immunology</subject><subject>Cytokines - metabolism</subject><subject>Diet</subject><subject>Disease</subject><subject>Forkhead protein</subject><subject>Foxp3 protein</subject><subject>Gluten</subject><subject>glutens</subject><subject>Homeostasis</subject><subject>Humans</subject><subject>immune tolerance</subject><subject>Immunological diseases</subject><subject>Immunological tolerance</subject><subject>Immunoregulation</subject><subject>Immunosuppression</subject><subject>Inflammatory diseases</subject><subject>Intestine</subject><subject>Lamina propria</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Peptides</subject><subject>Review</subject><subject>t-lymphocytes</subject><subject>T-Lymphocytes, Regulatory - immunology</subject><subject>Transcription factors</subject><issn>1028-852X</issn><issn>2008-823X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpdkU1r3DAQhkVpabZpj70WQy-9eKsZSZZ8KZTt10JKDkkhNyHJ440Wr72V1oH8-4hsGpKeNEgPz4zmZew98CW2qPBz9NslyqVYguQv2AI5N7VBcfWSLYBjqRVenbA3OW85Fwq0fs1OBLQKpYAFay_m_T5RzvGGqt8Urt0Y8y5X67GbA3WVv60uE21yFcdqRUN0ofoWM7lMb9mr3g2Z3j2cp-zPj--Xq1_12fnP9errWR1E2_BaU-DO9x33ogkGek_QBO41BGib1mAXqPEKjVeCsA-qF-RAajTBGxdaEqdsffR2k9vafYo7l27t5KK9v5jSxrp0iGEgawxQr50REkF26NoetELReVcaBQHF9eXo2s9-R6X1eEhueCZ9_jLGa7uZbqxGrRoURfDpQZCmvzPlg93FHGgY3EjTnC0KCQ2UJLCgH_9Dt9OcxrKqQhneSFPIQtVHKqQp50T94zDA7X3AtgRsUVphi7bwH57-4JH-l6i4AwkloKM</recordid><startdate>202005</startdate><enddate>202005</enddate><creator>Asri, Nastaran</creator><creator>Rostami-Nejad, Mohammad</creator><creator>Barzegar, Mohammad</creator><creator>Nikzamir, Abdolrahim</creator><creator>Rezaei-Tavirani, Mostafa</creator><creator>Razzaghi, Mohammadreza</creator><creator>Zali, Mohammad Reza</creator><general>Pasteur Institute of Iran</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>3V.</scope><scope>7QO</scope><scope>7T5</scope><scope>7TO</scope><scope>7U7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>CWDGH</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>202005</creationdate><title>Suppressive Mechanisms Induced by Tregs in Celiac Disease</title><author>Asri, Nastaran ; Rostami-Nejad, Mohammad ; Barzegar, Mohammad ; Nikzamir, Abdolrahim ; Rezaei-Tavirani, Mostafa ; Razzaghi, Mohammadreza ; Zali, Mohammad Reza</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3960-7ec0abfd0b36c81fbe16c0b71c196982dce6b528b53e2fc5f3ea14728cb8ac9e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Antigen-Presenting Cells - immunology</topic><topic>Autoimmune diseases</topic><topic>Biomarkers - metabolism</topic><topic>CD25 antigen</topic><topic>CD4 antigen</topic><topic>Celiac disease</topic><topic>Celiac Disease - immunology</topic><topic>Cytokines - metabolism</topic><topic>Diet</topic><topic>Disease</topic><topic>Forkhead protein</topic><topic>Foxp3 protein</topic><topic>Gluten</topic><topic>glutens</topic><topic>Homeostasis</topic><topic>Humans</topic><topic>immune tolerance</topic><topic>Immunological diseases</topic><topic>Immunological tolerance</topic><topic>Immunoregulation</topic><topic>Immunosuppression</topic><topic>Inflammatory diseases</topic><topic>Intestine</topic><topic>Lamina propria</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Peptides</topic><topic>Review</topic><topic>t-lymphocytes</topic><topic>T-Lymphocytes, Regulatory - immunology</topic><topic>Transcription factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Asri, Nastaran</creatorcontrib><creatorcontrib>Rostami-Nejad, Mohammad</creatorcontrib><creatorcontrib>Barzegar, Mohammad</creatorcontrib><creatorcontrib>Nikzamir, Abdolrahim</creatorcontrib><creatorcontrib>Rezaei-Tavirani, Mostafa</creatorcontrib><creatorcontrib>Razzaghi, Mohammadreza</creatorcontrib><creatorcontrib>Zali, Mohammad Reza</creatorcontrib><creatorcontrib>Proteomics Research Center, Faculty of Paramedical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran</creatorcontrib><creatorcontrib>Gastroenterology and Liver Diseases Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran</creatorcontrib><creatorcontrib>Department of Clinical Biochemistry, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran</creatorcontrib><creatorcontrib>School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran</creatorcontrib><creatorcontrib>Laser Application in Medical Sciences Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health &amp; Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</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>AUTh Library subscriptions: ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Middle East &amp; Africa Database</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</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 China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Iranian biomedical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Asri, Nastaran</au><au>Rostami-Nejad, Mohammad</au><au>Barzegar, Mohammad</au><au>Nikzamir, Abdolrahim</au><au>Rezaei-Tavirani, Mostafa</au><au>Razzaghi, Mohammadreza</au><au>Zali, Mohammad Reza</au><aucorp>Proteomics Research Center, Faculty of Paramedical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran</aucorp><aucorp>Gastroenterology and Liver Diseases Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran</aucorp><aucorp>Department of Clinical Biochemistry, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran</aucorp><aucorp>School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran</aucorp><aucorp>Laser Application in Medical Sciences Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Suppressive Mechanisms Induced by Tregs in Celiac Disease</atitle><jtitle>Iranian biomedical journal</jtitle><addtitle>Iran Biomed J</addtitle><date>2020-05</date><risdate>2020</risdate><volume>24</volume><issue>3</issue><spage>140</spage><epage>147</epage><pages>140-147</pages><issn>1028-852X</issn><eissn>2008-823X</eissn><abstract>Celiac disease (CD) is a systemic immune-mediated disorder caused by the dietary gluten in individuals who are genetically susceptible to the disease. In fact, CD is a T cell-mediated immune disease in which gluten-derived peptides activate the lamina propria CD4+ Teff cells, and these T-cell subsets can cause the intestinal tissue damages. Also, there are additional subsets of CD4+ T cells with suppressor functions. These subsets express the master transcription factor, FOXP3, and include Tr1 cells and CD4+CD25+ regulatory T cells (Tregs), which are the main population involved in maintaining the peripheral tolerance, preventing the autoimmune diseases and limiting the chronic inflammatory diseases such as CD. The suppressive function of Tregs is important to maintain the immune homeostasis. This paper examined the features and the basic mechanisms used by Tregs to mediate the suppression in CD.</abstract><cop>Iran</cop><pub>Pasteur Institute of Iran</pub><pmid>31952431</pmid><doi>10.29252/ibj.24.3.140</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1028-852X
ispartof Iranian biomedical journal, 2020-05, Vol.24 (3), p.140-147
issn 1028-852X
2008-823X
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_881ef7a834214d2a9f17523dba982c31
source Freely Accessible Journals; Open Access: PubMed Central
subjects Antigen-Presenting Cells - immunology
Autoimmune diseases
Biomarkers - metabolism
CD25 antigen
CD4 antigen
Celiac disease
Celiac Disease - immunology
Cytokines - metabolism
Diet
Disease
Forkhead protein
Foxp3 protein
Gluten
glutens
Homeostasis
Humans
immune tolerance
Immunological diseases
Immunological tolerance
Immunoregulation
Immunosuppression
Inflammatory diseases
Intestine
Lamina propria
Lymphocytes
Lymphocytes T
Peptides
Review
t-lymphocytes
T-Lymphocytes, Regulatory - immunology
Transcription factors
title Suppressive Mechanisms Induced by Tregs in Celiac Disease
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T01%3A47%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Suppressive%20Mechanisms%20Induced%20by%20Tregs%20in%20Celiac%20Disease&rft.jtitle=Iranian%20biomedical%20journal&rft.au=Asri,%20Nastaran&rft.aucorp=Proteomics%20Research%20Center,%20Faculty%20of%20Paramedical%20Sciences,%20Shahid%20Beheshti%20University%20of%20Medical%20Sciences,%20Tehran,%20Iran&rft.date=2020-05&rft.volume=24&rft.issue=3&rft.spage=140&rft.epage=147&rft.pages=140-147&rft.issn=1028-852X&rft.eissn=2008-823X&rft_id=info:doi/10.29252/ibj.24.3.140&rft_dat=%3Cproquest_doaj_%3E2380648161%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3960-7ec0abfd0b36c81fbe16c0b71c196982dce6b528b53e2fc5f3ea14728cb8ac9e3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2380648161&rft_id=info:pmid/31952431&rfr_iscdi=true