نتایج جستجو برای: foxp3

تعداد نتایج: 7965  

2012
Ekaterina Yurchenko Marina T. Shio Tony C. Huang Maria Da Silva Martins Moshe Szyf Megan K. Levings Martin Olivier Ciriaco A. Piccirillo

While natural CD4(+)Foxp3(+) regulatory T (nT(REG)) cells have long been viewed as a stable and distinct lineage that is committed to suppressive functions in vivo, recent evidence supporting this notion remains highly controversial. We sought to determine whether Foxp3 expression and the nT(REG) cell phenotype are stable in vivo and modulated by the inflammatory microenvironment. Here, we show...

2005
Bryan D. Carson Jared E. Lopes David M. Soper Steven F. Ziegler Virginia Mason

1. Abstract 2. The Fox family of transcription factors 3. Fox Family Members in the Immune System 3.1. FoxD1/2 3.2. FoxN1 3.3. FoxJ1 3.4. FoxO 4. Discovery of the FoxP subfamily 5. Role of FOXP subfamily members in human disease 6. FoxP3: the black sheep of the FoxP subfamily 6.1 Identification of FoxP3 6.2. FoxP3 function 6.3. Role of transcriptional co-repressors in FoxP function 6.4. Structu...

2016
Hiroko Fujii Julie Josse Miki Tanioka Yoshiki Miyachi François Husson Masahiro Ono

CD4(+) T cells that express the transcription factor FOXP3 (FOXP3(+) T cells) are commonly regarded as immunosuppressive regulatory T cells (Tregs). FOXP3(+) T cells are reported to be increased in tumor-bearing patients or animals and are considered to suppress antitumor immunity, but the evidence is often contradictory. In addition, accumulating evidence indicates that FOXP3 is induced by ant...

2012
Abdul Mannan Baru Christopher Untucht Venkateswaran Ganesh Christina Hesse Christian T. Mayer Tim Sparwasser

Foxp3 reporter mice including DEREG (DEpletion of REGulatory T cells) mice have greatly helped in exploring the biology of Foxp3(+) Tregs. DEREG mice express a DTR-eGFP fusion protein under the control of a bacterial artificial chromosome (BAC)-encoded Foxp3 promoter, allowing the viable isolation and inducible depletion of Foxp3(+) Tregs. Adaptive Tregs differentiated in vitro to express Foxp3...

2013
Teresa Lozano Noelia Casares Juan José Lasarte

FOXP3 is a multifaceted transcription factor with a major role in the control of immune homeostasis mediated by T regulatory cells (Treg). The immunoregulatory function of FOXP3 may hinder the induction of immune responses against cancer and infectious agents, and thus, development of inhibitors of its functions might give new therapeutic opportunities for these diseases. But also, FOXP3 is an ...

Journal: :Cell 2012
Robert M. Samstein Aaron Arvey Steven Z. Josefowicz Xiao Peng Alex Reynolds Richard Sandstrom Shane Neph Peter Sabo Jeong M. Kim Will Liao Ming O. Li Christina Leslie John A. Stamatoyannopoulos Alexander Y. Rudensky

Regulatory T (Treg) cells, whose identity and function are defined by the transcription factor Foxp3, are indispensable for immune homeostasis. It is unclear whether Foxp3 exerts its Treg lineage specification function through active modification of the chromatin landscape and establishment of new enhancers or by exploiting a pre-existing enhancer landscape. Analysis of the chromatin accessibil...

2014
Christel Devaud Carmen S. M. Yong Liza B. John Jennifer A. Westwood Connie P. M. Duong Colin M. House Delphine Denoyer Jason Li Phillip K. Darcy Michael H. Kershaw Derya Unutmaz

The transcription factor Foxp3 represents the most specific functional marker of CD4+ regulatory T cells (TRegs). However, previous reports have described Foxp3 expression in other cell types including some subsets of macrophages, although there are conflicting reports and Foxp3 expression in cells other than Treg is not well characterized. We performed detailed investigations into Foxp3 expres...

2008
Fabiola Osorio Salomé LeibundGut-Landmann Matthias Lochner Katharina Lahl Tim Sparwasser Gérard Eberl Caetano Reis e Sousa

Th cells producing IL-17 play a pro-inflammatory role at mucosal surfaces. Treg at the same sites dampen inflammation and prevent immunopathology. Th cells producing IL-17 (Th17) and Treg are thought to be distinct populations defined by expression of the transcription factors ROR-gammat and Foxp3, respectively. Here, we show that mouse CD25(+)Foxp3(+) Treg can be converted into a hybrid T-cell...

2012
Cristina Camperio Silvana Caristi Giorgia Fanelli Marzia Soligo Paola Del Porto Enza Piccolella

Considerable evidence supports the prediction that CD25 is directly regulated by the forkhead transcription factor FOXP3. However, given that CD25 is normally upregulated in activated T cells, regardless of whether they express FOXP3, this issue has still to be definitively demonstrated. Here we describe that FOXP3, induced by CD28 signals in human CD4(+)CD25(-) T lymphocytes, synergizes with R...

Journal: :iranian journal of immunology 0
mahboobeh razmkhah shiraz institute for cancer research nadieh abedi shiraz institute for cancer research ahmad hosseini shiraz institute for cancer research mohammad taghi imani department of plastic surgery abdol-rasoul talei department of surgery abbas ghaderi shiraz institute for cancer research

background: adipose derived stem cells (ascs) provoke the accumulation and expansion of regulatory t cells, leading to the modulation of immune responses in tumor microenvironment. objective: to assess the effect of tumoral ascs on the trend of regulatory t cells differentiation. methods: peripheral blood naïve cd4+ t cells were co-cultured with ascs derived from breast cancer or normal breast ...

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