نتایج جستجو برای: natural treg

تعداد نتایج: 487853  

2013
Nicole Bacher Verena Raker Claudia Hofmann Edith Graulich Melanie Schwenk Ria Baumgrass Tobias Bopp Ulrich Zechner Luzie Merten Christian Becker Kerstin Steinbrink

IFN-a is an antineoplastic agent in the treatment of several solid and hematologic malignancies that exerts strong immuneand autoimmune-stimulating activity. However, themechanisms of immune activation by IFN-a remain incompletely understood, particularly with regard to CD4þCD25highFoxpþ regulatory T cells (Treg). Here, we show that IFN-a deactivates the suppressive function of human Treg by do...

Journal: :Cancer research 2013
Nicole Bacher Verena Raker Claudia Hofmann Edith Graulich Melanie Schwenk Ria Baumgrass Tobias Bopp Ulrich Zechner Luzie Merten Christian Becker Kerstin Steinbrink

IFN-α is an antineoplastic agent in the treatment of several solid and hematologic malignancies that exerts strong immune- and autoimmune-stimulating activity. However, the mechanisms of immune activation by IFN-α remain incompletely understood, particularly with regard to CD4(+)CD25(high)Foxp(+) regulatory T cells (Treg). Here, we show that IFN-α deactivates the suppressive function of human T...

Journal: :Arthritis Research & Therapy 2011

Journal: :Journal of immunology 2008
Mohit Kashyap Angela M Thornton Sarah Kennedy Norton Brian Barnstein Matthew Macey Jennifer Brenzovich Ethan Shevach Warren J Leonard John J Ryan

Mast cell activation is associated with atopic and inflammatory diseases, but the natural controls of mast cell homeostasis are poorly understood. We hypothesized that CD4(+)CD25(+) regulatory T cells (Treg) could function in mast cell homeostasis. In this study, we demonstrate that mast cells can recruit both Treg and conventional CD4(+) T cells (Tconv). Furthermore, Treg, but not Tconv, suppr...

2014
Reiko Takahashi Akihiko Yoshimura

Several reports have suggested that natural regulatory T cells (Tregs) lose Forkhead box P3 (Foxp3) expression and suppression activity under certain inflammatory conditions. Treg plasticity has been studied because it may be associated with the pathogenesis of autoimmunity. Some studies showed that a minor uncommitted Foxp3(+) T cell population, which lacks hypomethylation at Treg-specific dem...

2013
Sari Lehtimäki Riitta Lahesmaa

Regulatory T cells (Treg) are needed in the control of immune responses and to maintain immune homeostasis. Of this subtype of regulatory lymphocytes, the most potent are Foxp3 expressing CD4+ T cells, which can be roughly divided into two main groups; natural Treg cells (nTreg), developing in the thymus, and induced or adaptive Treg cells (iTreg), developing in the periphery from naïve, conven...

2015
Hongfei Lou Jugao Fang Pingdong Li Weiguo Zhou Yang Wang Erzhong Fan Ying Li Hong Wang Zhongyan Liu Lei Xiao Chengshuo Wang Luo Zhang Pranela Rameshwar

BACKGROUND Sinonasal squamous cell carcinoma (SSCC) and nasal inverted papilloma (NIP) represent the predominant type of malignant and benign tumors in sinonasal tract, respectively. CD4+ CD25+ Foxp3+ natural regulatory T (Treg) cells might play critical role(s) in the suppression of anti-tumor immune response and thus shed light on tumor progression from benign to malignant. OBJECTIVE This s...

Journal: :Journal of immunology 2008
Sayuri Yamazaki Diana Dudziak Gordon F Heidkamp Christopher Fiorese Anthony J Bonito Kayo Inaba Michel C Nussenzweig Ralph M Steinman

Foxp3(+)CD25(+)CD4(+) regulatory T cells (Treg) mediate immunological self-tolerance and suppress immune responses. A subset of dendritic cells (DCs) in the intestine is specialized to induce Treg in a TGF-beta- and retinoic acid-dependent manner to allow for oral tolerance. In this study we compare two major DC subsets from mouse spleen. We find that CD8(+) DEC-205/CD205(+) DCs, but not the ma...

Journal: :Journal of immunology 2012
Guoyan Cheng Xiaomei Yuan Matthew S Tsai Eckhard R Podack Aixin Yu Thomas R Malek

Thymic-derived natural T regulatory cells (Tregs) are characterized by functional and phenotypic heterogeneity. Recently, a small fraction of peripheral Tregs has been shown to express Klrg1, but it remains unclear as to what extent Klrg1 defines a unique Treg subset. In this study, we show that Klrg1(+) Tregs represent a terminally differentiated Treg subset derived from Klrg1(-) Tregs. This s...

Journal: :International immunology 2009
Shimon Sakaguchi Kajsa Wing Yasushi Onishi Paz Prieto-Martin Tomoyuki Yamaguchi

Regulatory T cells (Tregs), either natural or induced, suppress a variety of physiological and pathological immune responses. One of the key issues for understanding Treg function is to determine how they suppress other lymphocytes at the molecular level in vivo and in vitro. Here we propose that there may be a key suppressive mechanism that is shared by every forkhead box p3 (Foxp3)(+) Treg in...

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