CD4+ T cells of schistosomiasis naturally resistant individuals living in an endemic area produce interferon-gamma and tumour necrosis factor-alpha in response to the recombinant 14KDA Schistosoma mansoni fatty acid-binding protein
Cellular immune responses to recombinant (r) Sm14 were examined in chronic, treated patients and uninfected individuals living in an endemic area for schistosomiasis. The lymphocyte proliferative responses and cytokine profile to this antigen were evaluated. Peripheral blood mononuclear cells (PBMC)...
Gespeichert in:
Veröffentlicht in: | Scandinavian journal of immunology 2000-06, Vol.51 (6), p.595-601 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 601 |
---|---|
container_issue | 6 |
container_start_page | 595 |
container_title | Scandinavian journal of immunology |
container_volume | 51 |
creator | Brito, C F Caldas, I R Coura Filho, P Correa-Oliveira, R Oliveira, S C |
description | Cellular immune responses to recombinant (r) Sm14 were examined in chronic, treated patients and uninfected individuals living in an endemic area for schistosomiasis. The lymphocyte proliferative responses and cytokine profile to this antigen were evaluated. Peripheral blood mononuclear cells (PBMC) of all groups studied proliferated to rSm14. However, the highest proliferation index to rSm14 was detected in uninfected endemic normal (EN) individuals who are naturally resistant to schistosomiasis. Regarding the cytokines produced, the levels of interleukin (IL)-5 and IL-10, known as Th2 cytokines, were not statistically different among all groups studied. In contrast, interferon (IFN)-gamma and tumour necrosis factor (TNF)-alpha were produced in significantly higher amounts by PBMC of EN individuals following rSm14 stimulation. Additionally, we have determined by flow cytometry that CD4+ T cells from these individuals are the main lymphocyte subpopulation producing IFN-gamma and TNF-alpha. Moreover, we have used rIL-10 or rIFN-gamma, or monoclonal antibodies (MoAb) against these two cytokines to determine their role on cellular reactivity to rSm14. Exogenous IL-10 suppressed T-cell proliferation and neutralization of endogenous IL-10 restored lymphocyte activation and enhanced IFN-gamma and TNF-alpha production in chronically infected patients. In contrast, the addition of anti-IFN-gamma totally abrogated the PBMC proliferation within the EN group. This study demonstrated that IL-10 is an important cytokine down-regulating T-cell responses in chronic schistosomiasis, whereas lymphocyte proliferation in the uninfected resistant group is dependent on IFN-gamma. Taken together these results suggest that Th1 type of immune response induced in EN individuals to a specific schistosome antigen might be associated with resistance to infection and also highlighted the importance of Sm14 as a potential vaccine candidate. |
doi_str_mv | 10.1046/j.1365-3083.2000.00710.x |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_71171896</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>71171896</sourcerecordid><originalsourceid>FETCH-LOGICAL-p207t-65b14584f928b12846f0a59009c0e76c703b40fcbf4be24b41fe1796507cd83</originalsourceid><addsrcrecordid>eNo9kcFu1DAQhnMA0VJ4BTQnLijLOHbi5FhtKSAqcWjvq4kz6bqK7WA7iH1iXgOvKJw84_n9_588VQUCdwJV9_FpJ2TX1hJ7uWsQcYeoy-zXi-oSJWI9KN1eVK9TekIUstHyVXUhsFeD1HhZ_d7fqA_wAIaXJUGYIZmjTTmk4Cwlm8BT3iItywkilz6Tz2D9ZH_aaaPyZCmVfyxXQB7YT-ysAYpMsMYwbYbLKHOcOQZfP5JzVIQT5M2FLYJnE8M5ZiaTQ6xpWY90Nitha_CJIQfIRy69CW60_hwv1Leba7j_D0rgyKfgbXHJ-QRk7FSPZ8gCVigyW_-mejkXXH77fF5V97efHvZf6rvvn7_ur-_qtUGd664dhWp7NQ9NP4qmV92M1A6Ig0HWndEoR4WzGWc1cqNGJWYWeuha1Gbq5VX1_q9rSf2xccoHZ9P5a8lz2NJBC6FFP3RF-O5ZuI2Op8MaraN4OvxbjPwDcM2Vng</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>71171896</pqid></control><display><type>article</type><title>CD4+ T cells of schistosomiasis naturally resistant individuals living in an endemic area produce interferon-gamma and tumour necrosis factor-alpha in response to the recombinant 14KDA Schistosoma mansoni fatty acid-binding protein</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Wiley Free Content</source><source>IngentaConnect Free/Open Access Journals</source><creator>Brito, C F ; Caldas, I R ; Coura Filho, P ; Correa-Oliveira, R ; Oliveira, S C</creator><creatorcontrib>Brito, C F ; Caldas, I R ; Coura Filho, P ; Correa-Oliveira, R ; Oliveira, S C</creatorcontrib><description>Cellular immune responses to recombinant (r) Sm14 were examined in chronic, treated patients and uninfected individuals living in an endemic area for schistosomiasis. The lymphocyte proliferative responses and cytokine profile to this antigen were evaluated. Peripheral blood mononuclear cells (PBMC) of all groups studied proliferated to rSm14. However, the highest proliferation index to rSm14 was detected in uninfected endemic normal (EN) individuals who are naturally resistant to schistosomiasis. Regarding the cytokines produced, the levels of interleukin (IL)-5 and IL-10, known as Th2 cytokines, were not statistically different among all groups studied. In contrast, interferon (IFN)-gamma and tumour necrosis factor (TNF)-alpha were produced in significantly higher amounts by PBMC of EN individuals following rSm14 stimulation. Additionally, we have determined by flow cytometry that CD4+ T cells from these individuals are the main lymphocyte subpopulation producing IFN-gamma and TNF-alpha. Moreover, we have used rIL-10 or rIFN-gamma, or monoclonal antibodies (MoAb) against these two cytokines to determine their role on cellular reactivity to rSm14. Exogenous IL-10 suppressed T-cell proliferation and neutralization of endogenous IL-10 restored lymphocyte activation and enhanced IFN-gamma and TNF-alpha production in chronically infected patients. In contrast, the addition of anti-IFN-gamma totally abrogated the PBMC proliferation within the EN group. This study demonstrated that IL-10 is an important cytokine down-regulating T-cell responses in chronic schistosomiasis, whereas lymphocyte proliferation in the uninfected resistant group is dependent on IFN-gamma. Taken together these results suggest that Th1 type of immune response induced in EN individuals to a specific schistosome antigen might be associated with resistance to infection and also highlighted the importance of Sm14 as a potential vaccine candidate.</description><identifier>ISSN: 0300-9475</identifier><identifier>DOI: 10.1046/j.1365-3083.2000.00710.x</identifier><identifier>PMID: 10849370</identifier><language>eng</language><publisher>England</publisher><subject>Adjuvants, Immunologic - physiology ; Adolescent ; Adult ; Aged ; Animals ; Carrier Proteins - pharmacology ; CD4-Positive T-Lymphocytes - immunology ; Cell Division ; Cytokines - biosynthesis ; Fatty Acid Transport Proteins ; Fatty Acid-Binding Protein 7 ; Fatty Acid-Binding Proteins ; Fatty Acids - metabolism ; Female ; Helminth Proteins - immunology ; Humans ; Immunity, Innate ; Interferon-gamma - biosynthesis ; Interleukin-10 - immunology ; Leukocytes, Mononuclear - immunology ; Leukocytes, Mononuclear - metabolism ; Lymphocyte Activation ; Lymphocyte Subsets - metabolism ; Male ; Membrane Transport Proteins ; Middle Aged ; Myelin P2 Protein - pharmacology ; Neoplasm Proteins ; Recombinant Proteins - pharmacology ; Schistosoma mansoni - immunology ; Schistosomiasis mansoni - epidemiology ; Schistosomiasis mansoni - immunology ; Tumor Necrosis Factor-alpha - biosynthesis ; Tumor Suppressor Proteins</subject><ispartof>Scandinavian journal of immunology, 2000-06, Vol.51 (6), p.595-601</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></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/10849370$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Brito, C F</creatorcontrib><creatorcontrib>Caldas, I R</creatorcontrib><creatorcontrib>Coura Filho, P</creatorcontrib><creatorcontrib>Correa-Oliveira, R</creatorcontrib><creatorcontrib>Oliveira, S C</creatorcontrib><title>CD4+ T cells of schistosomiasis naturally resistant individuals living in an endemic area produce interferon-gamma and tumour necrosis factor-alpha in response to the recombinant 14KDA Schistosoma mansoni fatty acid-binding protein</title><title>Scandinavian journal of immunology</title><addtitle>Scand J Immunol</addtitle><description>Cellular immune responses to recombinant (r) Sm14 were examined in chronic, treated patients and uninfected individuals living in an endemic area for schistosomiasis. The lymphocyte proliferative responses and cytokine profile to this antigen were evaluated. Peripheral blood mononuclear cells (PBMC) of all groups studied proliferated to rSm14. However, the highest proliferation index to rSm14 was detected in uninfected endemic normal (EN) individuals who are naturally resistant to schistosomiasis. Regarding the cytokines produced, the levels of interleukin (IL)-5 and IL-10, known as Th2 cytokines, were not statistically different among all groups studied. In contrast, interferon (IFN)-gamma and tumour necrosis factor (TNF)-alpha were produced in significantly higher amounts by PBMC of EN individuals following rSm14 stimulation. Additionally, we have determined by flow cytometry that CD4+ T cells from these individuals are the main lymphocyte subpopulation producing IFN-gamma and TNF-alpha. Moreover, we have used rIL-10 or rIFN-gamma, or monoclonal antibodies (MoAb) against these two cytokines to determine their role on cellular reactivity to rSm14. Exogenous IL-10 suppressed T-cell proliferation and neutralization of endogenous IL-10 restored lymphocyte activation and enhanced IFN-gamma and TNF-alpha production in chronically infected patients. In contrast, the addition of anti-IFN-gamma totally abrogated the PBMC proliferation within the EN group. This study demonstrated that IL-10 is an important cytokine down-regulating T-cell responses in chronic schistosomiasis, whereas lymphocyte proliferation in the uninfected resistant group is dependent on IFN-gamma. Taken together these results suggest that Th1 type of immune response induced in EN individuals to a specific schistosome antigen might be associated with resistance to infection and also highlighted the importance of Sm14 as a potential vaccine candidate.</description><subject>Adjuvants, Immunologic - physiology</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Animals</subject><subject>Carrier Proteins - pharmacology</subject><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>Cell Division</subject><subject>Cytokines - biosynthesis</subject><subject>Fatty Acid Transport Proteins</subject><subject>Fatty Acid-Binding Protein 7</subject><subject>Fatty Acid-Binding Proteins</subject><subject>Fatty Acids - metabolism</subject><subject>Female</subject><subject>Helminth Proteins - immunology</subject><subject>Humans</subject><subject>Immunity, Innate</subject><subject>Interferon-gamma - biosynthesis</subject><subject>Interleukin-10 - immunology</subject><subject>Leukocytes, Mononuclear - immunology</subject><subject>Leukocytes, Mononuclear - metabolism</subject><subject>Lymphocyte Activation</subject><subject>Lymphocyte Subsets - metabolism</subject><subject>Male</subject><subject>Membrane Transport Proteins</subject><subject>Middle Aged</subject><subject>Myelin P2 Protein - pharmacology</subject><subject>Neoplasm Proteins</subject><subject>Recombinant Proteins - pharmacology</subject><subject>Schistosoma mansoni - immunology</subject><subject>Schistosomiasis mansoni - epidemiology</subject><subject>Schistosomiasis mansoni - immunology</subject><subject>Tumor Necrosis Factor-alpha - biosynthesis</subject><subject>Tumor Suppressor Proteins</subject><issn>0300-9475</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kcFu1DAQhnMA0VJ4BTQnLijLOHbi5FhtKSAqcWjvq4kz6bqK7WA7iH1iXgOvKJw84_n9_588VQUCdwJV9_FpJ2TX1hJ7uWsQcYeoy-zXi-oSJWI9KN1eVK9TekIUstHyVXUhsFeD1HhZ_d7fqA_wAIaXJUGYIZmjTTmk4Cwlm8BT3iItywkilz6Tz2D9ZH_aaaPyZCmVfyxXQB7YT-ysAYpMsMYwbYbLKHOcOQZfP5JzVIQT5M2FLYJnE8M5ZiaTQ6xpWY90Nitha_CJIQfIRy69CW60_hwv1Leba7j_D0rgyKfgbXHJ-QRk7FSPZ8gCVigyW_-mejkXXH77fF5V97efHvZf6rvvn7_ur-_qtUGd664dhWp7NQ9NP4qmV92M1A6Ig0HWndEoR4WzGWc1cqNGJWYWeuha1Gbq5VX1_q9rSf2xccoHZ9P5a8lz2NJBC6FFP3RF-O5ZuI2Op8MaraN4OvxbjPwDcM2Vng</recordid><startdate>20000601</startdate><enddate>20000601</enddate><creator>Brito, C F</creator><creator>Caldas, I R</creator><creator>Coura Filho, P</creator><creator>Correa-Oliveira, R</creator><creator>Oliveira, S C</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20000601</creationdate><title>CD4+ T cells of schistosomiasis naturally resistant individuals living in an endemic area produce interferon-gamma and tumour necrosis factor-alpha in response to the recombinant 14KDA Schistosoma mansoni fatty acid-binding protein</title><author>Brito, C F ; Caldas, I R ; Coura Filho, P ; Correa-Oliveira, R ; Oliveira, S C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p207t-65b14584f928b12846f0a59009c0e76c703b40fcbf4be24b41fe1796507cd83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Adjuvants, Immunologic - physiology</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Animals</topic><topic>Carrier Proteins - pharmacology</topic><topic>CD4-Positive T-Lymphocytes - immunology</topic><topic>Cell Division</topic><topic>Cytokines - biosynthesis</topic><topic>Fatty Acid Transport Proteins</topic><topic>Fatty Acid-Binding Protein 7</topic><topic>Fatty Acid-Binding Proteins</topic><topic>Fatty Acids - metabolism</topic><topic>Female</topic><topic>Helminth Proteins - immunology</topic><topic>Humans</topic><topic>Immunity, Innate</topic><topic>Interferon-gamma - biosynthesis</topic><topic>Interleukin-10 - immunology</topic><topic>Leukocytes, Mononuclear - immunology</topic><topic>Leukocytes, Mononuclear - metabolism</topic><topic>Lymphocyte Activation</topic><topic>Lymphocyte Subsets - metabolism</topic><topic>Male</topic><topic>Membrane Transport Proteins</topic><topic>Middle Aged</topic><topic>Myelin P2 Protein - pharmacology</topic><topic>Neoplasm Proteins</topic><topic>Recombinant Proteins - pharmacology</topic><topic>Schistosoma mansoni - immunology</topic><topic>Schistosomiasis mansoni - epidemiology</topic><topic>Schistosomiasis mansoni - immunology</topic><topic>Tumor Necrosis Factor-alpha - biosynthesis</topic><topic>Tumor Suppressor Proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brito, C F</creatorcontrib><creatorcontrib>Caldas, I R</creatorcontrib><creatorcontrib>Coura Filho, P</creatorcontrib><creatorcontrib>Correa-Oliveira, R</creatorcontrib><creatorcontrib>Oliveira, S C</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Scandinavian journal of immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brito, C F</au><au>Caldas, I R</au><au>Coura Filho, P</au><au>Correa-Oliveira, R</au><au>Oliveira, S C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CD4+ T cells of schistosomiasis naturally resistant individuals living in an endemic area produce interferon-gamma and tumour necrosis factor-alpha in response to the recombinant 14KDA Schistosoma mansoni fatty acid-binding protein</atitle><jtitle>Scandinavian journal of immunology</jtitle><addtitle>Scand J Immunol</addtitle><date>2000-06-01</date><risdate>2000</risdate><volume>51</volume><issue>6</issue><spage>595</spage><epage>601</epage><pages>595-601</pages><issn>0300-9475</issn><abstract>Cellular immune responses to recombinant (r) Sm14 were examined in chronic, treated patients and uninfected individuals living in an endemic area for schistosomiasis. The lymphocyte proliferative responses and cytokine profile to this antigen were evaluated. Peripheral blood mononuclear cells (PBMC) of all groups studied proliferated to rSm14. However, the highest proliferation index to rSm14 was detected in uninfected endemic normal (EN) individuals who are naturally resistant to schistosomiasis. Regarding the cytokines produced, the levels of interleukin (IL)-5 and IL-10, known as Th2 cytokines, were not statistically different among all groups studied. In contrast, interferon (IFN)-gamma and tumour necrosis factor (TNF)-alpha were produced in significantly higher amounts by PBMC of EN individuals following rSm14 stimulation. Additionally, we have determined by flow cytometry that CD4+ T cells from these individuals are the main lymphocyte subpopulation producing IFN-gamma and TNF-alpha. Moreover, we have used rIL-10 or rIFN-gamma, or monoclonal antibodies (MoAb) against these two cytokines to determine their role on cellular reactivity to rSm14. Exogenous IL-10 suppressed T-cell proliferation and neutralization of endogenous IL-10 restored lymphocyte activation and enhanced IFN-gamma and TNF-alpha production in chronically infected patients. In contrast, the addition of anti-IFN-gamma totally abrogated the PBMC proliferation within the EN group. This study demonstrated that IL-10 is an important cytokine down-regulating T-cell responses in chronic schistosomiasis, whereas lymphocyte proliferation in the uninfected resistant group is dependent on IFN-gamma. Taken together these results suggest that Th1 type of immune response induced in EN individuals to a specific schistosome antigen might be associated with resistance to infection and also highlighted the importance of Sm14 as a potential vaccine candidate.</abstract><cop>England</cop><pmid>10849370</pmid><doi>10.1046/j.1365-3083.2000.00710.x</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0300-9475 |
ispartof | Scandinavian journal of immunology, 2000-06, Vol.51 (6), p.595-601 |
issn | 0300-9475 |
language | eng |
recordid | cdi_proquest_miscellaneous_71171896 |
source | MEDLINE; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Wiley Free Content; IngentaConnect Free/Open Access Journals |
subjects | Adjuvants, Immunologic - physiology Adolescent Adult Aged Animals Carrier Proteins - pharmacology CD4-Positive T-Lymphocytes - immunology Cell Division Cytokines - biosynthesis Fatty Acid Transport Proteins Fatty Acid-Binding Protein 7 Fatty Acid-Binding Proteins Fatty Acids - metabolism Female Helminth Proteins - immunology Humans Immunity, Innate Interferon-gamma - biosynthesis Interleukin-10 - immunology Leukocytes, Mononuclear - immunology Leukocytes, Mononuclear - metabolism Lymphocyte Activation Lymphocyte Subsets - metabolism Male Membrane Transport Proteins Middle Aged Myelin P2 Protein - pharmacology Neoplasm Proteins Recombinant Proteins - pharmacology Schistosoma mansoni - immunology Schistosomiasis mansoni - epidemiology Schistosomiasis mansoni - immunology Tumor Necrosis Factor-alpha - biosynthesis Tumor Suppressor Proteins |
title | CD4+ T cells of schistosomiasis naturally resistant individuals living in an endemic area produce interferon-gamma and tumour necrosis factor-alpha in response to the recombinant 14KDA Schistosoma mansoni fatty acid-binding protein |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-26T02%3A39%3A38IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=CD4+%20T%20cells%20of%20schistosomiasis%20naturally%20resistant%20individuals%20living%20in%20an%20endemic%20area%20produce%20interferon-gamma%20and%20tumour%20necrosis%20factor-alpha%20in%20response%20to%20the%20recombinant%2014KDA%20Schistosoma%20mansoni%20fatty%20acid-binding%20protein&rft.jtitle=Scandinavian%20journal%20of%20immunology&rft.au=Brito,%20C%20F&rft.date=2000-06-01&rft.volume=51&rft.issue=6&rft.spage=595&rft.epage=601&rft.pages=595-601&rft.issn=0300-9475&rft_id=info:doi/10.1046/j.1365-3083.2000.00710.x&rft_dat=%3Cproquest_pubme%3E71171896%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=71171896&rft_id=info:pmid/10849370&rfr_iscdi=true |