PMC:1064873 / 15966-16822 JSONTXT

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    LappsTest

    {"project":"LappsTest","denotations":[{"id":"T12195","span":{"begin":833,"end":837},"obj":"Protein"},{"id":"T12194","span":{"begin":811,"end":816},"obj":"Protein"},{"id":"T12193","span":{"begin":715,"end":719},"obj":"Protein"},{"id":"T12192","span":{"begin":455,"end":460},"obj":"Protein"},{"id":"T12191","span":{"begin":253,"end":256},"obj":"Protein"},{"id":"T12190","span":{"begin":196,"end":199},"obj":"Protein"},{"id":"T12189","span":{"begin":51,"end":55},"obj":"Protein"}],"text":"We thus compared the levels of IFN-γ production by CD4+ T cells after CD3 and CD28 costimulation in the presence of 1 ng/ml IL-10 in RA patients with active disease (multiple inflammatory joints, CRP level ≥ 10 mg/l) and inactive disease (in remission, CRP level \u003c 10 mg/l) [26] and in healthy controls. There were no statistically significant differences in IFN-γ production without IL-10 among these three groups (Fig. 2a), but the inhibitory effect of IL-10 on IFN-γ production was significantly limited in the active RA group as compared with the inactive RA group and healthy controls (percentage decrease: active RA, 2.9 ± 14.4%; inactive RA, 45.6 ± 14.4%; controls, 65.8 ± 7.9%) (Fig. 2b). As a consequence, CD4+ T cells from active RA patients produced higher levels of IFN-γ in the presence of 1 ng/ml IL-10 than did normal CD4+ T cells (Fig. 2a)."}

    2_test

    {"project":"2_test","denotations":[{"id":"15535835-7306232-4156889","span":{"begin":275,"end":277},"obj":"7306232"}],"text":"We thus compared the levels of IFN-γ production by CD4+ T cells after CD3 and CD28 costimulation in the presence of 1 ng/ml IL-10 in RA patients with active disease (multiple inflammatory joints, CRP level ≥ 10 mg/l) and inactive disease (in remission, CRP level \u003c 10 mg/l) [26] and in healthy controls. There were no statistically significant differences in IFN-γ production without IL-10 among these three groups (Fig. 2a), but the inhibitory effect of IL-10 on IFN-γ production was significantly limited in the active RA group as compared with the inactive RA group and healthy controls (percentage decrease: active RA, 2.9 ± 14.4%; inactive RA, 45.6 ± 14.4%; controls, 65.8 ± 7.9%) (Fig. 2b). As a consequence, CD4+ T cells from active RA patients produced higher levels of IFN-γ in the presence of 1 ng/ml IL-10 than did normal CD4+ T cells (Fig. 2a)."}

    biosemtest

    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thus compared the levels of IFN-γ production by CD4+ T cells after CD3 and CD28 costimulation in the presence of 1 ng/ml IL-10 in RA patients with active disease (multiple inflammatory joints, CRP level ≥ 10 mg/l) and inactive disease (in remission, CRP level \u003c 10 mg/l) [26] and in healthy controls. There were no statistically significant differences in IFN-γ production without IL-10 among these three groups (Fig. 2a), but the inhibitory effect of IL-10 on IFN-γ production was significantly limited in the active RA group as compared with the inactive RA group and healthy controls (percentage decrease: active RA, 2.9 ± 14.4%; inactive RA, 45.6 ± 14.4%; controls, 65.8 ± 7.9%) (Fig. 2b). As a consequence, CD4+ T cells from active RA patients produced higher levels of IFN-γ in the presence of 1 ng/ml IL-10 than did normal CD4+ T cells (Fig. 2a)."}

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thus compared the levels of IFN-γ production by CD4+ T cells after CD3 and CD28 costimulation in the presence of 1 ng/ml IL-10 in RA patients with active disease (multiple inflammatory joints, CRP level ≥ 10 mg/l) and inactive disease (in remission, CRP level \u003c 10 mg/l) [26] and in healthy controls. There were no statistically significant differences in IFN-γ production without IL-10 among these three groups (Fig. 2a), but the inhibitory effect of IL-10 on IFN-γ production was significantly limited in the active RA group as compared with the inactive RA group and healthy controls (percentage decrease: active RA, 2.9 ± 14.4%; inactive RA, 45.6 ± 14.4%; controls, 65.8 ± 7.9%) (Fig. 2b). As a consequence, CD4+ T cells from active RA patients produced higher levels of IFN-γ in the presence of 1 ng/ml IL-10 than did normal CD4+ T cells (Fig. 2a)."}

    bionlp-st-ge-2016-test-proteins

    {"project":"bionlp-st-ge-2016-test-proteins","denotations":[{"id":"T12913","span":{"begin":124,"end":129},"obj":"Protein"},{"id":"T12912","span":{"begin":78,"end":82},"obj":"Protein"},{"id":"T12911","span":{"begin":70,"end":73},"obj":"Protein"},{"id":"T12910","span":{"begin":51,"end":54},"obj":"Protein"},{"id":"T12909","span":{"begin":31,"end":36},"obj":"Protein"},{"id":"T12921","span":{"begin":833,"end":836},"obj":"Protein"},{"id":"T12920","span":{"begin":811,"end":816},"obj":"Protein"},{"id":"T12919","span":{"begin":778,"end":783},"obj":"Protein"},{"id":"T12918","span":{"begin":715,"end":718},"obj":"Protein"},{"id":"T12917","span":{"begin":464,"end":469},"obj":"Protein"},{"id":"T12916","span":{"begin":455,"end":460},"obj":"Protein"},{"id":"T12915","span":{"begin":384,"end":389},"obj":"Protein"},{"id":"T12914","span":{"begin":359,"end":364},"obj":"Protein"}],"namespaces":[{"prefix":"_base","uri":"http://bionlp.dbcls.jp/ontology/ge.owl#"}],"text":"We thus compared the levels of IFN-γ production by CD4+ T cells after CD3 and CD28 costimulation in the presence of 1 ng/ml IL-10 in RA patients with active disease (multiple inflammatory joints, CRP level ≥ 10 mg/l) and inactive disease (in remission, CRP level \u003c 10 mg/l) [26] and in healthy controls. There were no statistically significant differences in IFN-γ production without IL-10 among these three groups (Fig. 2a), but the inhibitory effect of IL-10 on IFN-γ production was significantly limited in the active RA group as compared with the inactive RA group and healthy controls (percentage decrease: active RA, 2.9 ± 14.4%; inactive RA, 45.6 ± 14.4%; controls, 65.8 ± 7.9%) (Fig. 2b). As a consequence, CD4+ T cells from active RA patients produced higher levels of IFN-γ in the presence of 1 ng/ml IL-10 than did normal CD4+ T cells (Fig. 2a)."}

    bionlp-st-ge-2016-uniprot

    {"project":"bionlp-st-ge-2016-uniprot","denotations":[{"id":"T13112","span":{"begin":70,"end":73},"obj":"http://www.uniprot.org/uniprot/P09693"},{"id":"T13109","span":{"begin":70,"end":73},"obj":"http://www.uniprot.org/uniprot/P07766"},{"id":"T13106","span":{"begin":70,"end":73},"obj":"http://www.uniprot.org/uniprot/P04234"},{"id":"T13103","span":{"begin":70,"end":73},"obj":"http://www.uniprot.org/uniprot/P20963"},{"id":"T13100","span":{"begin":78,"end":82},"obj":"http://www.uniprot.org/uniprot/P10747"},{"id":"T13094","span":{"begin":833,"end":836},"obj":"http://www.uniprot.org/uniprot/P01730"},{"id":"T13093","span":{"begin":715,"end":718},"obj":"http://www.uniprot.org/uniprot/P01730"},{"id":"T13092","span":{"begin":51,"end":54},"obj":"http://www.uniprot.org/uniprot/P01730"},{"id":"T13086","span":{"begin":778,"end":783},"obj":"http://www.uniprot.org/uniprot/P01579"},{"id":"T13085","span":{"begin":464,"end":469},"obj":"http://www.uniprot.org/uniprot/P01579"},{"id":"T13073","span":{"begin":384,"end":389},"obj":"http://www.uniprot.org/uniprot/P22301"},{"id":"T13072","span":{"begin":124,"end":129},"obj":"http://www.uniprot.org/uniprot/P22301"},{"id":"T13084","span":{"begin":359,"end":364},"obj":"http://www.uniprot.org/uniprot/P01579"},{"id":"T13083","span":{"begin":31,"end":36},"obj":"http://www.uniprot.org/uniprot/P01579"},{"id":"T13075","span":{"begin":811,"end":816},"obj":"http://www.uniprot.org/uniprot/P22301"},{"id":"T13074","span":{"begin":455,"end":460},"obj":"http://www.uniprot.org/uniprot/P22301"}],"namespaces":[{"prefix":"_base","uri":"http://www.uniprot.org/uniprot/"}],"text":"We thus compared the levels of IFN-γ production by CD4+ T cells after CD3 and CD28 costimulation in the presence of 1 ng/ml IL-10 in RA patients with active disease (multiple inflammatory joints, CRP level ≥ 10 mg/l) and inactive disease (in remission, CRP level \u003c 10 mg/l) [26] and in healthy controls. There were no statistically significant differences in IFN-γ production without IL-10 among these three groups (Fig. 2a), but the inhibitory effect of IL-10 on IFN-γ production was significantly limited in the active RA group as compared with the inactive RA group and healthy controls (percentage decrease: active RA, 2.9 ± 14.4%; inactive RA, 45.6 ± 14.4%; controls, 65.8 ± 7.9%) (Fig. 2b). As a consequence, CD4+ T cells from active RA patients produced higher levels of IFN-γ in the presence of 1 ng/ml IL-10 than did normal CD4+ T cells (Fig. 2a)."}

    GO-CC

    {"project":"GO-CC","denotations":[{"id":"T12958","span":{"begin":840,"end":845},"obj":"http://purl.obolibrary.org/obo/GO_0005623"},{"id":"T12957","span":{"begin":722,"end":727},"obj":"http://purl.obolibrary.org/obo/GO_0005623"},{"id":"T12956","span":{"begin":58,"end":63},"obj":"http://purl.obolibrary.org/obo/GO_0005623"}],"text":"We thus compared the levels of IFN-γ production by CD4+ T cells after CD3 and CD28 costimulation in the presence of 1 ng/ml IL-10 in RA patients with active disease (multiple inflammatory joints, CRP level ≥ 10 mg/l) and inactive disease (in remission, CRP level \u003c 10 mg/l) [26] and in healthy controls. There were no statistically significant differences in IFN-γ production without IL-10 among these three groups (Fig. 2a), but the inhibitory effect of IL-10 on IFN-γ production was significantly limited in the active RA group as compared with the inactive RA group and healthy controls (percentage decrease: active RA, 2.9 ± 14.4%; inactive RA, 45.6 ± 14.4%; controls, 65.8 ± 7.9%) (Fig. 2b). As a consequence, CD4+ T cells from active RA patients produced higher levels of IFN-γ in the presence of 1 ng/ml IL-10 than did normal CD4+ T cells (Fig. 2a)."}

    GO-MF

    {"project":"GO-MF","denotations":[{"id":"T12940","span":{"begin":811,"end":816},"obj":"http://purl.obolibrary.org/obo/GO_0005141"},{"id":"T12939","span":{"begin":455,"end":460},"obj":"http://purl.obolibrary.org/obo/GO_0005141"},{"id":"T12938","span":{"begin":384,"end":389},"obj":"http://purl.obolibrary.org/obo/GO_0005141"},{"id":"T12937","span":{"begin":124,"end":129},"obj":"http://purl.obolibrary.org/obo/GO_0005141"}],"text":"We thus compared the levels of IFN-γ production by CD4+ T cells after CD3 and CD28 costimulation in the presence of 1 ng/ml IL-10 in RA patients with active disease (multiple inflammatory joints, CRP level ≥ 10 mg/l) and inactive disease (in remission, CRP level \u003c 10 mg/l) [26] and in healthy controls. There were no statistically significant differences in IFN-γ production without IL-10 among these three groups (Fig. 2a), but the inhibitory effect of IL-10 on IFN-γ production was significantly limited in the active RA group as compared with the inactive RA group and healthy controls (percentage decrease: active RA, 2.9 ± 14.4%; inactive RA, 45.6 ± 14.4%; controls, 65.8 ± 7.9%) (Fig. 2b). As a consequence, CD4+ T cells from active RA patients produced higher levels of IFN-γ in the presence of 1 ng/ml IL-10 than did normal CD4+ T cells (Fig. 2a)."}

    sentences

    {"project":"sentences","denotations":[{"id":"T12803","span":{"begin":697,"end":856},"obj":"Sentence"},{"id":"T12802","span":{"begin":304,"end":696},"obj":"Sentence"},{"id":"T12801","span":{"begin":0,"end":303},"obj":"Sentence"},{"id":"T97","span":{"begin":0,"end":303},"obj":"Sentence"},{"id":"T98","span":{"begin":304,"end":696},"obj":"Sentence"},{"id":"T99","span":{"begin":697,"end":856},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"We thus compared the levels of IFN-γ production by CD4+ T cells after CD3 and CD28 costimulation in the presence of 1 ng/ml IL-10 in RA patients with active disease (multiple inflammatory joints, CRP level ≥ 10 mg/l) and inactive disease (in remission, CRP level \u003c 10 mg/l) [26] and in healthy controls. There were no statistically significant differences in IFN-γ production without IL-10 among these three groups (Fig. 2a), but the inhibitory effect of IL-10 on IFN-γ production was significantly limited in the active RA group as compared with the inactive RA group and healthy controls (percentage decrease: active RA, 2.9 ± 14.4%; inactive RA, 45.6 ± 14.4%; controls, 65.8 ± 7.9%) (Fig. 2b). As a consequence, CD4+ T cells from active RA patients produced higher levels of IFN-γ in the presence of 1 ng/ml IL-10 than did normal CD4+ T cells (Fig. 2a)."}

    simple1

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    BioNLP16_DUT

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    BioNLP16_Messiy

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    DLUT931

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    bionlp-st-ge-2016-test-ihmc

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thus compared the levels of IFN-γ production by CD4+ T cells after CD3 and CD28 costimulation in the presence of 1 ng/ml IL-10 in RA patients with active disease (multiple inflammatory joints, CRP level ≥ 10 mg/l) and inactive disease (in remission, CRP level \u003c 10 mg/l) [26] and in healthy controls. There were no statistically significant differences in IFN-γ production without IL-10 among these three groups (Fig. 2a), but the inhibitory effect of IL-10 on IFN-γ production was significantly limited in the active RA group as compared with the inactive RA group and healthy controls (percentage decrease: active RA, 2.9 ± 14.4%; inactive RA, 45.6 ± 14.4%; controls, 65.8 ± 7.9%) (Fig. 2b). As a consequence, CD4+ T cells from active RA patients produced higher levels of IFN-γ in the presence of 1 ng/ml IL-10 than did normal CD4+ T cells (Fig. 2a)."}

    bionlp-st-ge-2016-test-tees

    {"project":"bionlp-st-ge-2016-test-tees","denotations":[{"id":"T13055","span":{"begin":847,"end":854},"obj":"Protein"},{"id":"T13054","span":{"begin":833,"end":837},"obj":"Protein"},{"id":"T13053","span":{"begin":778,"end":783},"obj":"Protein"},{"id":"T13052","span":{"begin":715,"end":719},"obj":"Protein"},{"id":"T13051","span":{"begin":470,"end":480},"obj":"Gene_expression"},{"id":"T13050","span":{"begin":470,"end":480},"obj":"Gene_expression"},{"id":"T13049","span":{"begin":365,"end":375},"obj":"Gene_expression"},{"id":"T13048","span":{"begin":365,"end":375},"obj":"Gene_expression"},{"id":"T13047","span":{"begin":464,"end":469},"obj":"Protein"},{"id":"T13046","span":{"begin":455,"end":460},"obj":"Protein"},{"id":"T13045","span":{"begin":416,"end":423},"obj":"Protein"},{"id":"T13044","span":{"begin":359,"end":364},"obj":"Protein"},{"id":"T13043","span":{"begin":37,"end":47},"obj":"Gene_expression"},{"id":"T13042","span":{"begin":253,"end":256},"obj":"Protein"},{"id":"T13041","span":{"begin":196,"end":199},"obj":"Protein"},{"id":"T13040","span":{"begin":78,"end":82},"obj":"Protein"},{"id":"T13039","span":{"begin":70,"end":73},"obj":"Protein"},{"id":"T13038","span":{"begin":51,"end":55},"obj":"Protein"},{"id":"T13037","span":{"begin":31,"end":36},"obj":"Protein"}],"relations":[{"id":"R6408","pred":"themeOf","subj":"T13037","obj":"T13043"},{"id":"R6409","pred":"themeOf","subj":"T13044","obj":"T13048"},{"id":"R6410","pred":"themeOf","subj":"T13045","obj":"T13049"},{"id":"R6411","pred":"themeOf","subj":"T13046","obj":"T13050"},{"id":"R6412","pred":"themeOf","subj":"T13047","obj":"T13051"}],"text":"We thus compared the levels of IFN-γ production by CD4+ T cells after CD3 and CD28 costimulation in the presence of 1 ng/ml IL-10 in RA patients with active disease (multiple inflammatory joints, CRP level ≥ 10 mg/l) and inactive disease (in remission, CRP level \u003c 10 mg/l) [26] and in healthy controls. There were no statistically significant differences in IFN-γ production without IL-10 among these three groups (Fig. 2a), but the inhibitory effect of IL-10 on IFN-γ production was significantly limited in the active RA group as compared with the inactive RA group and healthy controls (percentage decrease: active RA, 2.9 ± 14.4%; inactive RA, 45.6 ± 14.4%; controls, 65.8 ± 7.9%) (Fig. 2b). As a consequence, CD4+ T cells from active RA patients produced higher levels of IFN-γ in the presence of 1 ng/ml IL-10 than did normal CD4+ T cells (Fig. 2a)."}

    test3

    {"project":"test3","denotations":[{"id":"T12290","span":{"begin":833,"end":836},"obj":"Protein"},{"id":"T12289","span":{"begin":811,"end":816},"obj":"Protein"},{"id":"T12288","span":{"begin":778,"end":783},"obj":"Protein"},{"id":"T12287","span":{"begin":752,"end":760},"obj":"Gene_expression"},{"id":"T12286","span":{"begin":715,"end":718},"obj":"Protein"},{"id":"T12285","span":{"begin":470,"end":480},"obj":"Gene_expression"},{"id":"T12284","span":{"begin":464,"end":469},"obj":"Protein"},{"id":"T12283","span":{"begin":455,"end":460},"obj":"Protein"},{"id":"T12282","span":{"begin":445,"end":451},"obj":"Regulation"},{"id":"T12281","span":{"begin":384,"end":389},"obj":"Protein"},{"id":"T12280","span":{"begin":365,"end":375},"obj":"Gene_expression"},{"id":"T12279","span":{"begin":359,"end":364},"obj":"Protein"},{"id":"T12278","span":{"begin":124,"end":129},"obj":"Protein"},{"id":"T12277","span":{"begin":78,"end":82},"obj":"Protein"},{"id":"T12276","span":{"begin":70,"end":73},"obj":"Protein"},{"id":"T12275","span":{"begin":51,"end":54},"obj":"Protein"},{"id":"T12274","span":{"begin":37,"end":47},"obj":"Gene_expression"},{"id":"T12273","span":{"begin":31,"end":36},"obj":"Protein"},{"id":"T12234","span":{"begin":833,"end":836},"obj":"Protein"},{"id":"T12233","span":{"begin":811,"end":816},"obj":"Protein"},{"id":"T12232","span":{"begin":778,"end":783},"obj":"Protein"},{"id":"T12231","span":{"begin":715,"end":718},"obj":"Protein"},{"id":"T12230","span":{"begin":464,"end":469},"obj":"Protein"},{"id":"T12229","span":{"begin":455,"end":460},"obj":"Protein"},{"id":"T12228","span":{"begin":384,"end":389},"obj":"Protein"},{"id":"T12227","span":{"begin":359,"end":364},"obj":"Protein"},{"id":"T12226","span":{"begin":124,"end":129},"obj":"Protein"},{"id":"T12225","span":{"begin":78,"end":82},"obj":"Protein"},{"id":"T12224","span":{"begin":70,"end":73},"obj":"Protein"},{"id":"T12223","span":{"begin":51,"end":54},"obj":"Protein"},{"id":"T12222","span":{"begin":31,"end":36},"obj":"Protein"}],"relations":[{"id":"R6344","pred":"themeOf","subj":"T12273","obj":"T12274"},{"id":"R6345","pred":"themeOf","subj":"T12279","obj":"T12280"},{"id":"R6346","pred":"themeOf","subj":"T12283","obj":"T12285"},{"id":"R6347","pred":"themeOf","subj":"T12284","obj":"T12285"},{"id":"R6348","pred":"themeOf","subj":"T12285","obj":"T12282"},{"id":"R6349","pred":"themeOf","subj":"T12288","obj":"T12287"}],"text":"We thus compared the levels of IFN-γ production by CD4+ T cells after CD3 and CD28 costimulation in the presence of 1 ng/ml IL-10 in RA patients with active disease (multiple inflammatory joints, CRP level ≥ 10 mg/l) and inactive disease (in remission, CRP level \u003c 10 mg/l) [26] and in healthy controls. There were no statistically significant differences in IFN-γ production without IL-10 among these three groups (Fig. 2a), but the inhibitory effect of IL-10 on IFN-γ production was significantly limited in the active RA group as compared with the inactive RA group and healthy controls (percentage decrease: active RA, 2.9 ± 14.4%; inactive RA, 45.6 ± 14.4%; controls, 65.8 ± 7.9%) (Fig. 2b). As a consequence, CD4+ T cells from active RA patients produced higher levels of IFN-γ in the presence of 1 ng/ml IL-10 than did normal CD4+ T cells (Fig. 2a)."}

    testone

    {"project":"testone","denotations":[{"id":"T12168","span":{"begin":761,"end":767},"obj":"Positive_regulation"},{"id":"T12167","span":{"begin":752,"end":760},"obj":"Gene_expression"},{"id":"T12166","span":{"begin":499,"end":506},"obj":"Negative_regulation"},{"id":"T12165","span":{"begin":470,"end":480},"obj":"Gene_expression"},{"id":"T12164","span":{"begin":445,"end":451},"obj":"Regulation"},{"id":"T12163","span":{"begin":434,"end":444},"obj":"Negative_regulation"},{"id":"T12162","span":{"begin":365,"end":375},"obj":"Gene_expression"},{"id":"T12161","span":{"begin":37,"end":47},"obj":"Gene_expression"},{"id":"T12145","span":{"begin":833,"end":836},"obj":"Protein"},{"id":"T12144","span":{"begin":811,"end":816},"obj":"Protein"},{"id":"T12143","span":{"begin":778,"end":783},"obj":"Protein"},{"id":"T12142","span":{"begin":715,"end":718},"obj":"Protein"},{"id":"T12141","span":{"begin":464,"end":469},"obj":"Protein"},{"id":"T12140","span":{"begin":455,"end":460},"obj":"Protein"},{"id":"T12139","span":{"begin":384,"end":389},"obj":"Protein"},{"id":"T12138","span":{"begin":359,"end":364},"obj":"Protein"},{"id":"T12137","span":{"begin":124,"end":129},"obj":"Protein"},{"id":"T12136","span":{"begin":78,"end":82},"obj":"Protein"},{"id":"T12135","span":{"begin":70,"end":73},"obj":"Protein"},{"id":"T12134","span":{"begin":51,"end":54},"obj":"Protein"},{"id":"T12133","span":{"begin":31,"end":36},"obj":"Protein"}],"relations":[{"id":"R6311","pred":"themeOf","subj":"T12133","obj":"T12161"},{"id":"R6312","pred":"themeOf","subj":"T12138","obj":"T12162"},{"id":"R6313","pred":"themeOf","subj":"T12141","obj":"T12165"},{"id":"R6314","pred":"themeOf","subj":"T12143","obj":"T12167"},{"id":"R6315","pred":"themeOf","subj":"T12143","obj":"T12168"},{"id":"R6316","pred":"causeOf","subj":"T12144","obj":"T12168"},{"id":"R6323","pred":"themeOf","subj":"T12165","obj":"T12166"},{"id":"R6324","pred":"themeOf","subj":"T12165","obj":"T12164"},{"id":"R6325","pred":"themeOf","subj":"T12167","obj":"T12168"}],"text":"We thus compared the levels of IFN-γ production by CD4+ T cells after CD3 and CD28 costimulation in the presence of 1 ng/ml IL-10 in RA patients with active disease (multiple inflammatory joints, CRP level ≥ 10 mg/l) and inactive disease (in remission, CRP level \u003c 10 mg/l) [26] and in healthy controls. There were no statistically significant differences in IFN-γ production without IL-10 among these three groups (Fig. 2a), but the inhibitory effect of IL-10 on IFN-γ production was significantly limited in the active RA group as compared with the inactive RA group and healthy controls (percentage decrease: active RA, 2.9 ± 14.4%; inactive RA, 45.6 ± 14.4%; controls, 65.8 ± 7.9%) (Fig. 2b). As a consequence, CD4+ T cells from active RA patients produced higher levels of IFN-γ in the presence of 1 ng/ml IL-10 than did normal CD4+ T cells (Fig. 2a)."}