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We are analyzing https://link.springer.com/article/10.1007/s13277-011-0254-6.

Title:
CD15+/CD16low human granulocytes from terminal cancer patients: granulocytic myeloid-derived suppressor cells that have suppressive function | Tumor Biology
Description:
Myeloid-derived suppressor cells (MDSCs) are a subpopulation of myeloid cells with immunosuppressive function whose numbers are increased in conditions such as chronic infection, trauma, and cancer. Unlike murine MDSCs defined as CD11b+/Gr-1+, there are no specific markers for human MDSCs. The goal of this study was to delineate a specific human MDSCs subpopulation in granulocytes from terminal cancer patients and investigate its clinical implications. Here, we show that the CD15+/CD16low subset was increased in terminal cancer patients compared with healthy donors (P = 0.009). Phorbol 12-myristate 13-acetate-activated granulocytes (CD16low/CD66b++/CD15+) that have a phenotype similar to MDSCs from cancer patients, effectively suppressed both proliferation and cytotoxicity of normal T cells. Among cancer patients, T-cell proliferation was highly suppressed by granulocytes isolated from terminal cancer patients with a high proportion of CD15+/CD16low cells. Patients with low peripheral blood levels of CD15+/CD16low cells had significantly longer survival than those with high levels (P = 0.0011). Patients with higher levels of CD15+/CD16low also tended to have poor performance status (P = 0.05). These data suggest that CD15+/CD16low granulocytes found in terminal cancer patients may play a role in the progression of cancer by inhibiting tumor immunity.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {πŸ“š}

  • Health & Fitness
  • Science
  • Education

Content Management System {πŸ“}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {πŸ“ˆ}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 8,280,528 visitors per month in the current month.

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How Does Link.springer.com Make Money? {πŸ’Έ}

We're unsure if the website is profiting.

Earning money isn't the goal of every website; some are designed to offer support or promote social causes. People have different reasons for creating websites. This might be one such reason. Link.springer.com could have a money-making trick up its sleeve, but it's undetectable for now.

Keywords {πŸ”}

article, cancer, cells, google, scholar, pubmed, cas, suppressor, myeloidderived, patients, immunol, cell, granulocytes, cdcdlow, myeloid, tumor, lee, seoul, research, human, terminal, mdscs, blood, privacy, cookies, function, content, dae, seog, heo, access, mechanism, res, apoptosis, inflammation, medicine, korea, data, publish, search, choi, ahn, tae, min, kim, sehoon, subpopulation, increased, subset, carcinoma,

Topics {βœ’οΈ}

myeloid-derived suppressor cells cd15+/cd16low human granulocytes month download article/chapter dae seog heo cd15+/cd16low granulocytes found granulocyte-derived hydrogen peroxide inhibiting tumor immunity myeloid suppressor cells cd15+/cd16low cells cd16low/cd66b++/cd15+ related subjects immature myeloid cells t-cell function t-cell proliferation cd15+/cd16low subset full article pdf independent prognostic factor renal cell carcinoma fc gamma riii metastatic tumor burden privacy choices/manage cookies myeloid cells tae min kim cd15+/cd16low proinflammatory myeloid subpopulation human neutrophils lose tumor-bearing mice cell-suppressive activity immune responses th2 cytokine interleukin-13 human granulocytes article choi check access instant access korea healthcare technology european economic area significantly longer survival poor performance status zea ah l-arginine metabolism reactive oxygen species doxorubicin-cyclophosphamide chemotherapy kurt-jones ea human mdscs adverse clinical outcomes van den bossche van den bergh yong-oon ahn inflammatory bowel disease crit care med

Schema {πŸ—ΊοΈ}

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         headline:CD15+/CD16low human granulocytes from terminal cancer patients: granulocytic myeloid-derived suppressor cells that have suppressive function
         description:Myeloid-derived suppressor cells (MDSCs) are a subpopulation of myeloid cells with immunosuppressive function whose numbers are increased in conditions such as chronic infection, trauma, and cancer. Unlike murine MDSCs defined as CD11b+/Gr-1+, there are no specific markers for human MDSCs. The goal of this study was to delineate a specific human MDSCs subpopulation in granulocytes from terminal cancer patients and investigate its clinical implications. Here, we show that the CD15+/CD16low subset was increased in terminal cancer patients compared with healthy donors (P = 0.009). Phorbol 12-myristate 13-acetate-activated granulocytes (CD16low/CD66b++/CD15+) that have a phenotype similar to MDSCs from cancer patients, effectively suppressed both proliferation and cytotoxicity of normal T cells. Among cancer patients, T-cell proliferation was highly suppressed by granulocytes isolated from terminal cancer patients with a high proportion of CD15+/CD16low cells. Patients with low peripheral blood levels of CD15+/CD16low cells had significantly longer survival than those with high levels (P = 0.0011). Patients with higher levels of CD15+/CD16low also tended to have poor performance status (P = 0.05). These data suggest that CD15+/CD16low granulocytes found in terminal cancer patients may play a role in the progression of cancer by inhibiting tumor immunity.
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      headline:CD15+/CD16low human granulocytes from terminal cancer patients: granulocytic myeloid-derived suppressor cells that have suppressive function
      description:Myeloid-derived suppressor cells (MDSCs) are a subpopulation of myeloid cells with immunosuppressive function whose numbers are increased in conditions such as chronic infection, trauma, and cancer. Unlike murine MDSCs defined as CD11b+/Gr-1+, there are no specific markers for human MDSCs. The goal of this study was to delineate a specific human MDSCs subpopulation in granulocytes from terminal cancer patients and investigate its clinical implications. Here, we show that the CD15+/CD16low subset was increased in terminal cancer patients compared with healthy donors (P = 0.009). Phorbol 12-myristate 13-acetate-activated granulocytes (CD16low/CD66b++/CD15+) that have a phenotype similar to MDSCs from cancer patients, effectively suppressed both proliferation and cytotoxicity of normal T cells. Among cancer patients, T-cell proliferation was highly suppressed by granulocytes isolated from terminal cancer patients with a high proportion of CD15+/CD16low cells. Patients with low peripheral blood levels of CD15+/CD16low cells had significantly longer survival than those with high levels (P = 0.0011). Patients with higher levels of CD15+/CD16low also tended to have poor performance status (P = 0.05). These data suggest that CD15+/CD16low granulocytes found in terminal cancer patients may play a role in the progression of cancer by inhibiting tumor immunity.
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            name:Seoul National University College of Medicine and Hospital
            address:
               name:Cancer Research Institute, Seoul National University College of Medicine and Hospital, Seoul, South Korea
               type:PostalAddress
            type:Organization
            name:Seoul National University College of Medicine and Hospital
            address:
               name:Innovative Research Institute for Cell Therapy, Seoul National University College of Medicine and Hospital, Seoul, South Korea
               type:PostalAddress
            type:Organization
            name:Seoul National University College of Medicine and Hospital
            address:
               name:Department of Internal Medicine, Seoul National University College of Medicine and Hospital, Seoul, South Korea
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Cancer Research Institute, Seoul National University College of Medicine and Hospital, Seoul, South Korea
      name:Innovative Research Institute for Cell Therapy, Seoul National University College of Medicine and Hospital, Seoul, South Korea
      name:Cancer Research Institute, Seoul National University College of Medicine and Hospital, Seoul, South Korea
      name:Cancer Research Institute, Seoul National University College of Medicine and Hospital, Seoul, South Korea
      name:Innovative Research Institute for Cell Therapy, Seoul National University College of Medicine and Hospital, Seoul, South Korea
      name:Cancer Research Institute, Seoul National University College of Medicine and Hospital, Seoul, South Korea
      name:Innovative Research Institute for Cell Therapy, Seoul National University College of Medicine and Hospital, Seoul, South Korea
      name:Department of Internal Medicine, Seoul National University College of Medicine and Hospital, Seoul, South Korea
      name:Cancer Research Institute, Seoul National University College of Medicine and Hospital, Seoul, South Korea
      name:Department of Internal Medicine, Seoul National University College of Medicine and Hospital, Seoul, South Korea
      name:Cancer Research Institute, Seoul National University College of Medicine and Hospital, Seoul, South Korea
      name:Innovative Research Institute for Cell Therapy, Seoul National University College of Medicine and Hospital, Seoul, South Korea
      name:Department of Internal Medicine, Seoul National University College of Medicine and Hospital, Seoul, South Korea
      name:Cancer Research Institute, Seoul National University College of Medicine and Hospital, Seoul, South Korea
      name:Innovative Research Institute for Cell Therapy, Seoul National University College of Medicine and Hospital, Seoul, South Korea
      name:Department of Internal Medicine, Seoul National University College of Medicine and Hospital, Seoul, South Korea
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