Regulatory T cells and IgE expression in duodenal mucosa of Strongyloides stercoralis and human T lymphotropic virus type 1 co-infected patients

Strongyloides stercoralis is an intestinal nematode unique in its ability to replicate in the human host, allowing ongoing cycles of autoinfection, persisting for decades within the same host. Although usually asymptomatic, overwhelming infections can occur in Strongyloides and HTLV-1 co-infected in...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:PLoS neglected tropical diseases 2019-06, Vol.13 (6), p.e0007415-e0007415
Hauptverfasser: Malpica, Luis, White, Jr, A Clinton, Leguia, Cristina, Freundt, Natalia, Barros, Nicolas, Chian, Cesar, Antunez, E Antonio, Montes, Martin
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page e0007415
container_issue 6
container_start_page e0007415
container_title PLoS neglected tropical diseases
container_volume 13
creator Malpica, Luis
White, Jr, A Clinton
Leguia, Cristina
Freundt, Natalia
Barros, Nicolas
Chian, Cesar
Antunez, E Antonio
Montes, Martin
description Strongyloides stercoralis is an intestinal nematode unique in its ability to replicate in the human host, allowing ongoing cycles of autoinfection, persisting for decades within the same host. Although usually asymptomatic, overwhelming infections can occur in Strongyloides and HTLV-1 co-infected individuals (SS/HTLV-1). Regulatory T cells (Tregs) are able to blunt specific Th2 responses necessary to control the parasite. We previously reported that peripheral blood Tregs are increased in SS/HTLV-1 and correlate with low Th2 responses. We hypothesized that Tregs are also increased at the site of infection in duodenal mucosa. Paraffin embedded duodenal biopsies were obtained from 10 SS/HTLV-1 patients, 3 controls with non-parasitic chronic duodenitis, and 2 healthy controls. Immunohistochemistry was performed using monoclonal antibodies against human CD3, CD8, IgE and FoxP3. The number of cells were counted using a conventional light microscope. The number of CD3+, CD8+, FoxP3+ and IgE positive cells per 0.35 mm2 was measured using ImagePro Plus software comparing areas adjacent or distant from parasite material. In patients with SS/HTLV-1, T lymphocyte counts and CD8+ cells were lower in areas adjacent to the parasite compared to non-adjacent areas (CD3+: adjacent: 6.5 [Interquartile range (IQR: 2.8-12.3)]; non-adjacent: 24.5 [IQR: 20.9-34.4]; Mann-Whitney p = 0.0003; CD8+: adjacent: 4.5 [IQR: 2.3-11.8]; non-adjacent: 21 [IQR: 15.3-42.9]; Mann-Whitney p = 0.0011). Tregs cells in the intestines (FoxP3+ expressing cells) were increased in patients with SS/HTLV-1 compared with patients with chronic duodenitis (SS/HTLV-1: 1.5 [IQR: 0.7-2.3]; duodenitis controls: 0 [range 0-0.7]; healthy controls: 0; Mann-Whitney p = 0.034). There was also a trend towards fewer eosinophils adjacent to the parasites. Among SS/HTLV-1 patients the number of IgE expressing cells was increased for in areas not adjacent to the parasite compared to non-adjacent areas (ANOVA, p = 0.001). Our data shows increased Treg cell numbers localized adjacent to the parasites in the duodenum SS/HTLV-1 patients. In addition, other T lymphocytes and IgE expressing cells were decreased adjacent to the parasites, suggesting an important role for Tregs in down-regulating local parasite effector responses.
doi_str_mv 10.1371/journal.pntd.0007415
format Article
fullrecord <record><control><sourceid>gale_plos_</sourceid><recordid>TN_cdi_plos_journals_2258790042</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A592167394</galeid><doaj_id>oai_doaj_org_article_720177b99d70442c82709e24875ca44d</doaj_id><sourcerecordid>A592167394</sourcerecordid><originalsourceid>FETCH-LOGICAL-c585t-f5f5debb02780bc0f737c8739ee45f2e5b640314f66df426fdbf21b4a1bad7773</originalsourceid><addsrcrecordid>eNptkt-K1DAUh4so7rr6BqIBQbyZMUmTpr1ZWJZVBxYEXa9Dmj-dDGlTk3Rx3sJHNnW6y4x4lZJ--ZJzzq8oXiO4RiVDH3d-CoNw63FIag0hZATRJ8U5akq6wqykT4--z4oXMe4gpA2t0fPirESIQUTQefH7m-4mJ5IPe3AHpHYuAjEosOlugP41Bh2j9QOwA1CTVzpfCPpJ-iiAN-B7Cn7o9s5bpSOISQfpg3D2oNhOvRiy1O37ceszOloJ7m2YIkj7UQMEpF_ZwWiZtAKjSFYPKb4snhnhon61rBfFj083d9dfVrdfP2-ur25XktY0rQw1VOm2hZjVsJXQsJLJmpWN1oQarGlbEVgiYqpKGYIro1qDUUsEaoVijJUXxduDd3Q-8qWZkWNMa9ZASHAmNgdCebHjY7C9CHvuheV_N3zouAjJSqc5wxAx1jaNYpAQLGvMYKMxqRmVghCVXZfLbVPbayVzpblRJ9LTP4Pd8s7f8yoPDDOUBR8WQfA_Jx0T722cxyUG7af53aQkdZUbkNF3_6D_r26hOpELyGPIExJylvIr2mA0q0im3h9RWy1c2kbvppRDEU9BcgBl8DEGbR5rQ5DPeX14BJ_zype85mNvjvvyeOghoOUfZK3pYQ</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2258790042</pqid></control><display><type>article</type><title>Regulatory T cells and IgE expression in duodenal mucosa of Strongyloides stercoralis and human T lymphotropic virus type 1 co-infected patients</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>PubMed Central Open Access</source><source>Public Library of Science (PLoS)</source><creator>Malpica, Luis ; White, Jr, A Clinton ; Leguia, Cristina ; Freundt, Natalia ; Barros, Nicolas ; Chian, Cesar ; Antunez, E Antonio ; Montes, Martin</creator><creatorcontrib>Malpica, Luis ; White, Jr, A Clinton ; Leguia, Cristina ; Freundt, Natalia ; Barros, Nicolas ; Chian, Cesar ; Antunez, E Antonio ; Montes, Martin</creatorcontrib><description>Strongyloides stercoralis is an intestinal nematode unique in its ability to replicate in the human host, allowing ongoing cycles of autoinfection, persisting for decades within the same host. Although usually asymptomatic, overwhelming infections can occur in Strongyloides and HTLV-1 co-infected individuals (SS/HTLV-1). Regulatory T cells (Tregs) are able to blunt specific Th2 responses necessary to control the parasite. We previously reported that peripheral blood Tregs are increased in SS/HTLV-1 and correlate with low Th2 responses. We hypothesized that Tregs are also increased at the site of infection in duodenal mucosa. Paraffin embedded duodenal biopsies were obtained from 10 SS/HTLV-1 patients, 3 controls with non-parasitic chronic duodenitis, and 2 healthy controls. Immunohistochemistry was performed using monoclonal antibodies against human CD3, CD8, IgE and FoxP3. The number of cells were counted using a conventional light microscope. The number of CD3+, CD8+, FoxP3+ and IgE positive cells per 0.35 mm2 was measured using ImagePro Plus software comparing areas adjacent or distant from parasite material. In patients with SS/HTLV-1, T lymphocyte counts and CD8+ cells were lower in areas adjacent to the parasite compared to non-adjacent areas (CD3+: adjacent: 6.5 [Interquartile range (IQR: 2.8-12.3)]; non-adjacent: 24.5 [IQR: 20.9-34.4]; Mann-Whitney p = 0.0003; CD8+: adjacent: 4.5 [IQR: 2.3-11.8]; non-adjacent: 21 [IQR: 15.3-42.9]; Mann-Whitney p = 0.0011). Tregs cells in the intestines (FoxP3+ expressing cells) were increased in patients with SS/HTLV-1 compared with patients with chronic duodenitis (SS/HTLV-1: 1.5 [IQR: 0.7-2.3]; duodenitis controls: 0 [range 0-0.7]; healthy controls: 0; Mann-Whitney p = 0.034). There was also a trend towards fewer eosinophils adjacent to the parasites. Among SS/HTLV-1 patients the number of IgE expressing cells was increased for in areas not adjacent to the parasite compared to non-adjacent areas (ANOVA, p = 0.001). Our data shows increased Treg cell numbers localized adjacent to the parasites in the duodenum SS/HTLV-1 patients. In addition, other T lymphocytes and IgE expressing cells were decreased adjacent to the parasites, suggesting an important role for Tregs in down-regulating local parasite effector responses.</description><identifier>ISSN: 1935-2735</identifier><identifier>ISSN: 1935-2727</identifier><identifier>EISSN: 1935-2735</identifier><identifier>DOI: 10.1371/journal.pntd.0007415</identifier><identifier>PMID: 31170141</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adolescent ; Adult ; Antibodies ; Biology and life sciences ; Biopsy ; Care and treatment ; CD3 antigen ; CD8 antigen ; Cells ; Coinfection - complications ; Coinfection - pathology ; Cytokines ; Development and progression ; Duodenitis ; Duodenum ; Duodenum - pathology ; Eosinophils ; Family medical history ; Female ; Foxp3 protein ; Gene Expression ; Genetic aspects ; Health aspects ; Hospitals ; HTLV-I infections ; HTLV-I Infections - complications ; HTLV-I Infections - pathology ; Humans ; Humboldt, Alexander von (1769-1859) ; Immune response ; Immunoglobulin E ; Immunoglobulin E - analysis ; Immunohistochemistry ; Immunologic Factors - analysis ; Immunoregulation ; Infection ; Infections ; Infectious diseases ; Internal medicine ; Intestinal Mucosa - pathology ; Intestine ; Intestines ; Leukocytes (eosinophilic) ; Lymphocytes ; Lymphocytes T ; Male ; Medicine and Health Sciences ; Microscopes ; Middle Aged ; Monoclonal antibodies ; Mucosa ; Nematodes ; Neutrophils ; Paraffin ; Paraffins ; Parasites ; Parasitic diseases ; Peripheral blood ; Roundworms ; Strongyloides stercoralis ; Strongyloidiasis ; Strongyloidiasis - complications ; Strongyloidiasis - pathology ; T cells ; T-Lymphocytes, Regulatory - immunology ; Tropical diseases ; Variance analysis ; Viruses ; Young Adult</subject><ispartof>PLoS neglected tropical diseases, 2019-06, Vol.13 (6), p.e0007415-e0007415</ispartof><rights>COPYRIGHT 2019 Public Library of Science</rights><rights>2019 Malpica et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2019 Malpica et al 2019 Malpica et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c585t-f5f5debb02780bc0f737c8739ee45f2e5b640314f66df426fdbf21b4a1bad7773</citedby><cites>FETCH-LOGICAL-c585t-f5f5debb02780bc0f737c8739ee45f2e5b640314f66df426fdbf21b4a1bad7773</cites><orcidid>0000-0002-9668-4632 ; 0000-0002-7082-1846</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6581271/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6581271/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79569,79570</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31170141$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Malpica, Luis</creatorcontrib><creatorcontrib>White, Jr, A Clinton</creatorcontrib><creatorcontrib>Leguia, Cristina</creatorcontrib><creatorcontrib>Freundt, Natalia</creatorcontrib><creatorcontrib>Barros, Nicolas</creatorcontrib><creatorcontrib>Chian, Cesar</creatorcontrib><creatorcontrib>Antunez, E Antonio</creatorcontrib><creatorcontrib>Montes, Martin</creatorcontrib><title>Regulatory T cells and IgE expression in duodenal mucosa of Strongyloides stercoralis and human T lymphotropic virus type 1 co-infected patients</title><title>PLoS neglected tropical diseases</title><addtitle>PLoS Negl Trop Dis</addtitle><description>Strongyloides stercoralis is an intestinal nematode unique in its ability to replicate in the human host, allowing ongoing cycles of autoinfection, persisting for decades within the same host. Although usually asymptomatic, overwhelming infections can occur in Strongyloides and HTLV-1 co-infected individuals (SS/HTLV-1). Regulatory T cells (Tregs) are able to blunt specific Th2 responses necessary to control the parasite. We previously reported that peripheral blood Tregs are increased in SS/HTLV-1 and correlate with low Th2 responses. We hypothesized that Tregs are also increased at the site of infection in duodenal mucosa. Paraffin embedded duodenal biopsies were obtained from 10 SS/HTLV-1 patients, 3 controls with non-parasitic chronic duodenitis, and 2 healthy controls. Immunohistochemistry was performed using monoclonal antibodies against human CD3, CD8, IgE and FoxP3. The number of cells were counted using a conventional light microscope. The number of CD3+, CD8+, FoxP3+ and IgE positive cells per 0.35 mm2 was measured using ImagePro Plus software comparing areas adjacent or distant from parasite material. In patients with SS/HTLV-1, T lymphocyte counts and CD8+ cells were lower in areas adjacent to the parasite compared to non-adjacent areas (CD3+: adjacent: 6.5 [Interquartile range (IQR: 2.8-12.3)]; non-adjacent: 24.5 [IQR: 20.9-34.4]; Mann-Whitney p = 0.0003; CD8+: adjacent: 4.5 [IQR: 2.3-11.8]; non-adjacent: 21 [IQR: 15.3-42.9]; Mann-Whitney p = 0.0011). Tregs cells in the intestines (FoxP3+ expressing cells) were increased in patients with SS/HTLV-1 compared with patients with chronic duodenitis (SS/HTLV-1: 1.5 [IQR: 0.7-2.3]; duodenitis controls: 0 [range 0-0.7]; healthy controls: 0; Mann-Whitney p = 0.034). There was also a trend towards fewer eosinophils adjacent to the parasites. Among SS/HTLV-1 patients the number of IgE expressing cells was increased for in areas not adjacent to the parasite compared to non-adjacent areas (ANOVA, p = 0.001). Our data shows increased Treg cell numbers localized adjacent to the parasites in the duodenum SS/HTLV-1 patients. In addition, other T lymphocytes and IgE expressing cells were decreased adjacent to the parasites, suggesting an important role for Tregs in down-regulating local parasite effector responses.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Antibodies</subject><subject>Biology and life sciences</subject><subject>Biopsy</subject><subject>Care and treatment</subject><subject>CD3 antigen</subject><subject>CD8 antigen</subject><subject>Cells</subject><subject>Coinfection - complications</subject><subject>Coinfection - pathology</subject><subject>Cytokines</subject><subject>Development and progression</subject><subject>Duodenitis</subject><subject>Duodenum</subject><subject>Duodenum - pathology</subject><subject>Eosinophils</subject><subject>Family medical history</subject><subject>Female</subject><subject>Foxp3 protein</subject><subject>Gene Expression</subject><subject>Genetic aspects</subject><subject>Health aspects</subject><subject>Hospitals</subject><subject>HTLV-I infections</subject><subject>HTLV-I Infections - complications</subject><subject>HTLV-I Infections - pathology</subject><subject>Humans</subject><subject>Humboldt, Alexander von (1769-1859)</subject><subject>Immune response</subject><subject>Immunoglobulin E</subject><subject>Immunoglobulin E - analysis</subject><subject>Immunohistochemistry</subject><subject>Immunologic Factors - analysis</subject><subject>Immunoregulation</subject><subject>Infection</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Internal medicine</subject><subject>Intestinal Mucosa - pathology</subject><subject>Intestine</subject><subject>Intestines</subject><subject>Leukocytes (eosinophilic)</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Male</subject><subject>Medicine and Health Sciences</subject><subject>Microscopes</subject><subject>Middle Aged</subject><subject>Monoclonal antibodies</subject><subject>Mucosa</subject><subject>Nematodes</subject><subject>Neutrophils</subject><subject>Paraffin</subject><subject>Paraffins</subject><subject>Parasites</subject><subject>Parasitic diseases</subject><subject>Peripheral blood</subject><subject>Roundworms</subject><subject>Strongyloides stercoralis</subject><subject>Strongyloidiasis</subject><subject>Strongyloidiasis - complications</subject><subject>Strongyloidiasis - pathology</subject><subject>T cells</subject><subject>T-Lymphocytes, Regulatory - immunology</subject><subject>Tropical diseases</subject><subject>Variance analysis</subject><subject>Viruses</subject><subject>Young Adult</subject><issn>1935-2735</issn><issn>1935-2727</issn><issn>1935-2735</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNptkt-K1DAUh4so7rr6BqIBQbyZMUmTpr1ZWJZVBxYEXa9Dmj-dDGlTk3Rx3sJHNnW6y4x4lZJ--ZJzzq8oXiO4RiVDH3d-CoNw63FIag0hZATRJ8U5akq6wqykT4--z4oXMe4gpA2t0fPirESIQUTQefH7m-4mJ5IPe3AHpHYuAjEosOlugP41Bh2j9QOwA1CTVzpfCPpJ-iiAN-B7Cn7o9s5bpSOISQfpg3D2oNhOvRiy1O37ceszOloJ7m2YIkj7UQMEpF_ZwWiZtAKjSFYPKb4snhnhon61rBfFj083d9dfVrdfP2-ur25XktY0rQw1VOm2hZjVsJXQsJLJmpWN1oQarGlbEVgiYqpKGYIro1qDUUsEaoVijJUXxduDd3Q-8qWZkWNMa9ZASHAmNgdCebHjY7C9CHvuheV_N3zouAjJSqc5wxAx1jaNYpAQLGvMYKMxqRmVghCVXZfLbVPbayVzpblRJ9LTP4Pd8s7f8yoPDDOUBR8WQfA_Jx0T722cxyUG7af53aQkdZUbkNF3_6D_r26hOpELyGPIExJylvIr2mA0q0im3h9RWy1c2kbvppRDEU9BcgBl8DEGbR5rQ5DPeX14BJ_zype85mNvjvvyeOghoOUfZK3pYQ</recordid><startdate>20190601</startdate><enddate>20190601</enddate><creator>Malpica, Luis</creator><creator>White, Jr, A Clinton</creator><creator>Leguia, Cristina</creator><creator>Freundt, Natalia</creator><creator>Barros, Nicolas</creator><creator>Chian, Cesar</creator><creator>Antunez, E Antonio</creator><creator>Montes, Martin</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>7QL</scope><scope>7SS</scope><scope>7T2</scope><scope>7T7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8C1</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>F1W</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>H95</scope><scope>H97</scope><scope>K9.</scope><scope>L.G</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>P64</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-9668-4632</orcidid><orcidid>https://orcid.org/0000-0002-7082-1846</orcidid></search><sort><creationdate>20190601</creationdate><title>Regulatory T cells and IgE expression in duodenal mucosa of Strongyloides stercoralis and human T lymphotropic virus type 1 co-infected patients</title><author>Malpica, Luis ; White, Jr, A Clinton ; Leguia, Cristina ; Freundt, Natalia ; Barros, Nicolas ; Chian, Cesar ; Antunez, E Antonio ; Montes, Martin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c585t-f5f5debb02780bc0f737c8739ee45f2e5b640314f66df426fdbf21b4a1bad7773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Antibodies</topic><topic>Biology and life sciences</topic><topic>Biopsy</topic><topic>Care and treatment</topic><topic>CD3 antigen</topic><topic>CD8 antigen</topic><topic>Cells</topic><topic>Coinfection - complications</topic><topic>Coinfection - pathology</topic><topic>Cytokines</topic><topic>Development and progression</topic><topic>Duodenitis</topic><topic>Duodenum</topic><topic>Duodenum - pathology</topic><topic>Eosinophils</topic><topic>Family medical history</topic><topic>Female</topic><topic>Foxp3 protein</topic><topic>Gene Expression</topic><topic>Genetic aspects</topic><topic>Health aspects</topic><topic>Hospitals</topic><topic>HTLV-I infections</topic><topic>HTLV-I Infections - complications</topic><topic>HTLV-I Infections - pathology</topic><topic>Humans</topic><topic>Humboldt, Alexander von (1769-1859)</topic><topic>Immune response</topic><topic>Immunoglobulin E</topic><topic>Immunoglobulin E - analysis</topic><topic>Immunohistochemistry</topic><topic>Immunologic Factors - analysis</topic><topic>Immunoregulation</topic><topic>Infection</topic><topic>Infections</topic><topic>Infectious diseases</topic><topic>Internal medicine</topic><topic>Intestinal Mucosa - pathology</topic><topic>Intestine</topic><topic>Intestines</topic><topic>Leukocytes (eosinophilic)</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Male</topic><topic>Medicine and Health Sciences</topic><topic>Microscopes</topic><topic>Middle Aged</topic><topic>Monoclonal antibodies</topic><topic>Mucosa</topic><topic>Nematodes</topic><topic>Neutrophils</topic><topic>Paraffin</topic><topic>Paraffins</topic><topic>Parasites</topic><topic>Parasitic diseases</topic><topic>Peripheral blood</topic><topic>Roundworms</topic><topic>Strongyloides stercoralis</topic><topic>Strongyloidiasis</topic><topic>Strongyloidiasis - complications</topic><topic>Strongyloidiasis - pathology</topic><topic>T cells</topic><topic>T-Lymphocytes, Regulatory - immunology</topic><topic>Tropical diseases</topic><topic>Variance analysis</topic><topic>Viruses</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Malpica, Luis</creatorcontrib><creatorcontrib>White, Jr, A Clinton</creatorcontrib><creatorcontrib>Leguia, Cristina</creatorcontrib><creatorcontrib>Freundt, Natalia</creatorcontrib><creatorcontrib>Barros, Nicolas</creatorcontrib><creatorcontrib>Chian, Cesar</creatorcontrib><creatorcontrib>Antunez, E Antonio</creatorcontrib><creatorcontrib>Montes, Martin</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>Bacteriology Abstracts (Microbiology B)</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Public Health Database</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 Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</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>Aquatic Science &amp; Fisheries Abstracts (ASFA) 1: Biological Sciences &amp; Living Resources</collection><collection>Aquatic Science &amp; Fisheries Abstracts (ASFA) 3: Aquatic Pollution &amp; Environmental Quality</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Aquatic Science &amp; Fisheries Abstracts (ASFA) Professional</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest Health &amp; Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health &amp; Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS neglected tropical diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Malpica, Luis</au><au>White, Jr, A Clinton</au><au>Leguia, Cristina</au><au>Freundt, Natalia</au><au>Barros, Nicolas</au><au>Chian, Cesar</au><au>Antunez, E Antonio</au><au>Montes, Martin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regulatory T cells and IgE expression in duodenal mucosa of Strongyloides stercoralis and human T lymphotropic virus type 1 co-infected patients</atitle><jtitle>PLoS neglected tropical diseases</jtitle><addtitle>PLoS Negl Trop Dis</addtitle><date>2019-06-01</date><risdate>2019</risdate><volume>13</volume><issue>6</issue><spage>e0007415</spage><epage>e0007415</epage><pages>e0007415-e0007415</pages><issn>1935-2735</issn><issn>1935-2727</issn><eissn>1935-2735</eissn><abstract>Strongyloides stercoralis is an intestinal nematode unique in its ability to replicate in the human host, allowing ongoing cycles of autoinfection, persisting for decades within the same host. Although usually asymptomatic, overwhelming infections can occur in Strongyloides and HTLV-1 co-infected individuals (SS/HTLV-1). Regulatory T cells (Tregs) are able to blunt specific Th2 responses necessary to control the parasite. We previously reported that peripheral blood Tregs are increased in SS/HTLV-1 and correlate with low Th2 responses. We hypothesized that Tregs are also increased at the site of infection in duodenal mucosa. Paraffin embedded duodenal biopsies were obtained from 10 SS/HTLV-1 patients, 3 controls with non-parasitic chronic duodenitis, and 2 healthy controls. Immunohistochemistry was performed using monoclonal antibodies against human CD3, CD8, IgE and FoxP3. The number of cells were counted using a conventional light microscope. The number of CD3+, CD8+, FoxP3+ and IgE positive cells per 0.35 mm2 was measured using ImagePro Plus software comparing areas adjacent or distant from parasite material. In patients with SS/HTLV-1, T lymphocyte counts and CD8+ cells were lower in areas adjacent to the parasite compared to non-adjacent areas (CD3+: adjacent: 6.5 [Interquartile range (IQR: 2.8-12.3)]; non-adjacent: 24.5 [IQR: 20.9-34.4]; Mann-Whitney p = 0.0003; CD8+: adjacent: 4.5 [IQR: 2.3-11.8]; non-adjacent: 21 [IQR: 15.3-42.9]; Mann-Whitney p = 0.0011). Tregs cells in the intestines (FoxP3+ expressing cells) were increased in patients with SS/HTLV-1 compared with patients with chronic duodenitis (SS/HTLV-1: 1.5 [IQR: 0.7-2.3]; duodenitis controls: 0 [range 0-0.7]; healthy controls: 0; Mann-Whitney p = 0.034). There was also a trend towards fewer eosinophils adjacent to the parasites. Among SS/HTLV-1 patients the number of IgE expressing cells was increased for in areas not adjacent to the parasite compared to non-adjacent areas (ANOVA, p = 0.001). Our data shows increased Treg cell numbers localized adjacent to the parasites in the duodenum SS/HTLV-1 patients. In addition, other T lymphocytes and IgE expressing cells were decreased adjacent to the parasites, suggesting an important role for Tregs in down-regulating local parasite effector responses.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>31170141</pmid><doi>10.1371/journal.pntd.0007415</doi><orcidid>https://orcid.org/0000-0002-9668-4632</orcidid><orcidid>https://orcid.org/0000-0002-7082-1846</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1935-2735
ispartof PLoS neglected tropical diseases, 2019-06, Vol.13 (6), p.e0007415-e0007415
issn 1935-2735
1935-2727
1935-2735
language eng
recordid cdi_plos_journals_2258790042
source MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; PubMed Central Open Access; Public Library of Science (PLoS)
subjects Adolescent
Adult
Antibodies
Biology and life sciences
Biopsy
Care and treatment
CD3 antigen
CD8 antigen
Cells
Coinfection - complications
Coinfection - pathology
Cytokines
Development and progression
Duodenitis
Duodenum
Duodenum - pathology
Eosinophils
Family medical history
Female
Foxp3 protein
Gene Expression
Genetic aspects
Health aspects
Hospitals
HTLV-I infections
HTLV-I Infections - complications
HTLV-I Infections - pathology
Humans
Humboldt, Alexander von (1769-1859)
Immune response
Immunoglobulin E
Immunoglobulin E - analysis
Immunohistochemistry
Immunologic Factors - analysis
Immunoregulation
Infection
Infections
Infectious diseases
Internal medicine
Intestinal Mucosa - pathology
Intestine
Intestines
Leukocytes (eosinophilic)
Lymphocytes
Lymphocytes T
Male
Medicine and Health Sciences
Microscopes
Middle Aged
Monoclonal antibodies
Mucosa
Nematodes
Neutrophils
Paraffin
Paraffins
Parasites
Parasitic diseases
Peripheral blood
Roundworms
Strongyloides stercoralis
Strongyloidiasis
Strongyloidiasis - complications
Strongyloidiasis - pathology
T cells
T-Lymphocytes, Regulatory - immunology
Tropical diseases
Variance analysis
Viruses
Young Adult
title Regulatory T cells and IgE expression in duodenal mucosa of Strongyloides stercoralis and human T lymphotropic virus type 1 co-infected patients
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-20T14%3A54%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Regulatory%20T%20cells%20and%20IgE%20expression%20in%20duodenal%20mucosa%20of%20Strongyloides%20stercoralis%20and%20human%20T%20lymphotropic%20virus%20type%201%20co-infected%20patients&rft.jtitle=PLoS%20neglected%20tropical%20diseases&rft.au=Malpica,%20Luis&rft.date=2019-06-01&rft.volume=13&rft.issue=6&rft.spage=e0007415&rft.epage=e0007415&rft.pages=e0007415-e0007415&rft.issn=1935-2735&rft.eissn=1935-2735&rft_id=info:doi/10.1371/journal.pntd.0007415&rft_dat=%3Cgale_plos_%3EA592167394%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2258790042&rft_id=info:pmid/31170141&rft_galeid=A592167394&rft_doaj_id=oai_doaj_org_article_720177b99d70442c82709e24875ca44d&rfr_iscdi=true