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Increased population of CD4 super(+)CD25 super(high) regulatory T cells with their higher apoptotic and proliferating status in peripheral blood of acute myeloid leukemia patients
Purpose: Regulatory T cells (T-reg) that control harmful autoimmune T cells in the periphery may also suppress the immune response against cancer. In this study we investigated the possible involvement of CD4 super(+)CD25 super(high) T-reg in the immune impairment of patients with acute myeloid leuk...
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Published in: | European journal of haematology 2005-12, Vol.75 (6), p.468-476 |
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container_title | European journal of haematology |
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creator | Wang, Xingbing Zheng, Jine Liu, Jun Yao, Junxia He, Yanli Li, Xiaoqing Yu, Jingming Yang, Jing Liu, Zhongping Huang, Shiang |
description | Purpose: Regulatory T cells (T-reg) that control harmful autoimmune T cells in the periphery may also suppress the immune response against cancer. In this study we investigated the possible involvement of CD4 super(+)CD25 super(high) T-reg in the immune impairment of patients with acute myeloid leukemia (AML). Experimental design: The frequencies and phenotypes of CD4 super(+)CD25 super(high) T cells in the peripheral blood of AML patients were determined by flow cytometry. To assess the functional activity of CD4 super(+)CD25 super(high) T cells, CD4 super(+)CD25 super(high), and CD4 super(+)CD25 super(-) T cells were sorted from peripheral blood mononuclear cells with FACS Vantage. The immunoregulatory properties of CD4 super(+)CD25 super(high) and CD4 super(+)CD25 super(-) T cells were characterized by proliferation assays and cytokine production assays. In addition, the frequency of apoptotic and proliferating cells in CD4 super(+)CD25 super(high) T cells were respectively evaluated by 7AAD and ki67 binding cells using flow cytometry. Results: Compared with healthy controls, AML patients had a higher proportion of CD4 super(+)CD25 super(high) T cells in peripheral blood. These cells were CD45-RA(-), CD69(-), CD45-RO(+), CD95(+), and intercellular CTLA-4(+), and secreted low levels of TNF- alpha and IL-10, but no IL-2, IL-4, IL-5, and IFN- gamma . They inhibited the proliferation and cytokine production (IL-2, IFN- gamma ) of CD4 super(+)CD25 super(-) T cells, but improved IL-10 production under the co-culture of both subsets with stimulation, thus behaving as T-reg. Notably, CD4 super(+)CD25 super(high) T cells in AML patients presented significantly higher apoptosis and proliferation than that of healthy individuals. Conclusions: The frequency of CD4 super(+)CD25 super(high) T-reg in peripheral blood in AML patients is significantly higher when compared with healthy individuals, likely due to the increasing proliferation of CD4 super(+)CD25 super(high) T cells. |
doi_str_mv | 10.1111/j.1600-0609.2005.00537.x |
format | article |
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In this study we investigated the possible involvement of CD4 super(+)CD25 super(high) T-reg in the immune impairment of patients with acute myeloid leukemia (AML). Experimental design: The frequencies and phenotypes of CD4 super(+)CD25 super(high) T cells in the peripheral blood of AML patients were determined by flow cytometry. To assess the functional activity of CD4 super(+)CD25 super(high) T cells, CD4 super(+)CD25 super(high), and CD4 super(+)CD25 super(-) T cells were sorted from peripheral blood mononuclear cells with FACS Vantage. The immunoregulatory properties of CD4 super(+)CD25 super(high) and CD4 super(+)CD25 super(-) T cells were characterized by proliferation assays and cytokine production assays. In addition, the frequency of apoptotic and proliferating cells in CD4 super(+)CD25 super(high) T cells were respectively evaluated by 7AAD and ki67 binding cells using flow cytometry. Results: Compared with healthy controls, AML patients had a higher proportion of CD4 super(+)CD25 super(high) T cells in peripheral blood. These cells were CD45-RA(-), CD69(-), CD45-RO(+), CD95(+), and intercellular CTLA-4(+), and secreted low levels of TNF- alpha and IL-10, but no IL-2, IL-4, IL-5, and IFN- gamma . They inhibited the proliferation and cytokine production (IL-2, IFN- gamma ) of CD4 super(+)CD25 super(-) T cells, but improved IL-10 production under the co-culture of both subsets with stimulation, thus behaving as T-reg. Notably, CD4 super(+)CD25 super(high) T cells in AML patients presented significantly higher apoptosis and proliferation than that of healthy individuals. Conclusions: The frequency of CD4 super(+)CD25 super(high) T-reg in peripheral blood in AML patients is significantly higher when compared with healthy individuals, likely due to the increasing proliferation of CD4 super(+)CD25 super(high) T cells.</description><identifier>ISSN: 0902-4441</identifier><identifier>EISSN: 1600-0609</identifier><identifier>DOI: 10.1111/j.1600-0609.2005.00537.x</identifier><language>eng</language><ispartof>European journal of haematology, 2005-12, Vol.75 (6), p.468-476</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>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Wang, Xingbing</creatorcontrib><creatorcontrib>Zheng, Jine</creatorcontrib><creatorcontrib>Liu, Jun</creatorcontrib><creatorcontrib>Yao, Junxia</creatorcontrib><creatorcontrib>He, Yanli</creatorcontrib><creatorcontrib>Li, Xiaoqing</creatorcontrib><creatorcontrib>Yu, Jingming</creatorcontrib><creatorcontrib>Yang, Jing</creatorcontrib><creatorcontrib>Liu, Zhongping</creatorcontrib><creatorcontrib>Huang, Shiang</creatorcontrib><title>Increased population of CD4 super(+)CD25 super(high) regulatory T cells with their higher apoptotic and proliferating status in peripheral blood of acute myeloid leukemia patients</title><title>European journal of haematology</title><description>Purpose: Regulatory T cells (T-reg) that control harmful autoimmune T cells in the periphery may also suppress the immune response against cancer. In this study we investigated the possible involvement of CD4 super(+)CD25 super(high) T-reg in the immune impairment of patients with acute myeloid leukemia (AML). Experimental design: The frequencies and phenotypes of CD4 super(+)CD25 super(high) T cells in the peripheral blood of AML patients were determined by flow cytometry. To assess the functional activity of CD4 super(+)CD25 super(high) T cells, CD4 super(+)CD25 super(high), and CD4 super(+)CD25 super(-) T cells were sorted from peripheral blood mononuclear cells with FACS Vantage. The immunoregulatory properties of CD4 super(+)CD25 super(high) and CD4 super(+)CD25 super(-) T cells were characterized by proliferation assays and cytokine production assays. In addition, the frequency of apoptotic and proliferating cells in CD4 super(+)CD25 super(high) T cells were respectively evaluated by 7AAD and ki67 binding cells using flow cytometry. Results: Compared with healthy controls, AML patients had a higher proportion of CD4 super(+)CD25 super(high) T cells in peripheral blood. These cells were CD45-RA(-), CD69(-), CD45-RO(+), CD95(+), and intercellular CTLA-4(+), and secreted low levels of TNF- alpha and IL-10, but no IL-2, IL-4, IL-5, and IFN- gamma . They inhibited the proliferation and cytokine production (IL-2, IFN- gamma ) of CD4 super(+)CD25 super(-) T cells, but improved IL-10 production under the co-culture of both subsets with stimulation, thus behaving as T-reg. Notably, CD4 super(+)CD25 super(high) T cells in AML patients presented significantly higher apoptosis and proliferation than that of healthy individuals. 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In this study we investigated the possible involvement of CD4 super(+)CD25 super(high) T-reg in the immune impairment of patients with acute myeloid leukemia (AML). Experimental design: The frequencies and phenotypes of CD4 super(+)CD25 super(high) T cells in the peripheral blood of AML patients were determined by flow cytometry. To assess the functional activity of CD4 super(+)CD25 super(high) T cells, CD4 super(+)CD25 super(high), and CD4 super(+)CD25 super(-) T cells were sorted from peripheral blood mononuclear cells with FACS Vantage. The immunoregulatory properties of CD4 super(+)CD25 super(high) and CD4 super(+)CD25 super(-) T cells were characterized by proliferation assays and cytokine production assays. In addition, the frequency of apoptotic and proliferating cells in CD4 super(+)CD25 super(high) T cells were respectively evaluated by 7AAD and ki67 binding cells using flow cytometry. Results: Compared with healthy controls, AML patients had a higher proportion of CD4 super(+)CD25 super(high) T cells in peripheral blood. These cells were CD45-RA(-), CD69(-), CD45-RO(+), CD95(+), and intercellular CTLA-4(+), and secreted low levels of TNF- alpha and IL-10, but no IL-2, IL-4, IL-5, and IFN- gamma . They inhibited the proliferation and cytokine production (IL-2, IFN- gamma ) of CD4 super(+)CD25 super(-) T cells, but improved IL-10 production under the co-culture of both subsets with stimulation, thus behaving as T-reg. Notably, CD4 super(+)CD25 super(high) T cells in AML patients presented significantly higher apoptosis and proliferation than that of healthy individuals. Conclusions: The frequency of CD4 super(+)CD25 super(high) T-reg in peripheral blood in AML patients is significantly higher when compared with healthy individuals, likely due to the increasing proliferation of CD4 super(+)CD25 super(high) T cells.</abstract><doi>10.1111/j.1600-0609.2005.00537.x</doi></addata></record> |
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title | Increased population of CD4 super(+)CD25 super(high) regulatory T cells with their higher apoptotic and proliferating status in peripheral blood of acute myeloid leukemia patients |
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