نتایج جستجو برای: CD11c

تعداد نتایج: 2380  

2015
Lingjun Meng Wei Jin Xiaodong Wang Guosheng Liang

IMMUNOLOGY AND INFLAMMATION Correction for “RIP3-mediated necrotic cell death accelerates systematic inflammation and mortality,” by Lingjun Meng, Wei Jin, and Xiaodong Wang, which appeared in issue 35, September 1, 2015, of Proc Natl Acad Sci USA (112:11007–11012; first published August 17, 2015; 10.1073/pnas.1514730112). The authors note that on page 11010, left column, fifth full paragraph, ...

2014
Yanhong Chen Jie Tian Xinyu Tian Xinyi Tang Ke Rui Jia Tong Liwei Lu Huaxi Xu Shengjun Wang

BACKGROUND Obesity has become a global challenge for public health. It has been reported that obesity is associated with chronic inflammation. However, the mechanism for the chronic inflammation contributes to obesity remains elusive. METHODOLOGY/PRINCIPAL FINDINGS In our study, we found a novel CD11c+ dendritic cell subset existed in murine adipose tissues which was immature phenotype. Moreo...

Journal: :Blood 1993
R A Newman B Peterson F R Davey C Brabyn H Collins V L Brunetto D B Duggan R B Weiss I Royston F E Millard

The markers, CD11b, CD11c, CD14, CD21, CD23, CD25, CD38, and FMC7 were correlated with morphologic and other laboratory and clinical characteristics of 127 patients with untreated CD5+ chronic lymphocytic leukemia (CLL). Only CD38 and CD21 were significantly associated with atypical CLL morphology. The integrin associated markers CD11b and CD11c were associated with lower leukocyte count (white...

Journal: :Journal of immunology 2012
Masashi Ohtani Takayuki Hoshii Hideki Fujii Shigeo Koyasu Atsushi Hirao Satoshi Matsuda

The mammalian target of rapamycin (mTOR) controls cell growth and survival through two distinct complexes called mTOR complex 1 (mTORC1) and mTOR complex 2 (mTORC2). Although several reports have suggested the involvement of mTORC1 in development and function of dendritic cells (DCs), its physiological roles remain obscure. We therefore established mTORC1 signal-deficient mice lacking Raptor, a...

Journal: :Blood 2000
E Maraskovsky E Daro E Roux M Teepe C R Maliszewski J Hoek D Caron M E Lebsack H J McKenna

Dendritic cells (DCs) represent a family of ontogenically distinct leukocytes involved in immune response regulation. The ability of DCs to stimulate T-cell immunity has led to their use as vectors for immunotherapy vaccines. However, it is unclear whether and to what degree in vitro-generated DCs are representative of DCs that develop in vivo. Treatment of mice with human Flt3 ligand (FL) dram...

Journal: :Cell reports 2017
Kenta Moriwaki Sakthi Balaji John Bertin Peter J Gough Francis Ka-Ming Chan

Receptor interacting protein kinase 3 (RIPK3) induces necroptosis, a type of regulated necrosis, through its kinase domain and receptor interacting protein (RIP) homotypic interaction motif (RHIM). In addition, RIPK3 has been shown to regulate NLRP3 inflammasome and nuclear factor κB (NF-κB) activation. However, the relative contribution of these signaling pathways to RIPK3-dependent inflammati...

2012
Leanne M. Johnson-Huang Cara A. Pensabene Kejal R. Shah Katherine C. Pierson Toyoko Kikuchi Tim Lentini Patricia Gilleaudeau Mary Sullivan-Whalen Inna Cueto Artemis Khatcherian Luke A. Hyder Mayte Suárez-Fariñas James G. Krueger Michelle A. Lowes

UNLABELLED To understand the development of new psoriasis lesions, we studied a group of moderate-to-severe psoriasis patients who experienced a relapse after ceasing efalizumab (anti-CD11a, Raptiva, Genentech). There were increased CD3(+) T cells, neutrophils, CD11c(+) and CD83(+) myeloid dendritic cells (DCs), but no increase in CD1c(+) resident myeloid DCs. In relapsed lesions, there were ma...

Journal: :The Journal of Experimental Medicine 1999
Neil A. Fanger Charles R. Maliszewski Ken Schooley Thomas S. Griffith

TRAIL (TNF-related apoptosis-inducing ligand) is a member of the TNF family that induces apoptosis in a variety of cancer cells. In this study, we demonstrate that human CD11c(+) blood dendritic cells (DCs) express TRAIL after stimulation with either interferon (IFN)-gamma or -alpha and acquire the ability to kill TRAIL-sensitive tumor cell targets but not TRAIL-resistant tumor cells or normal ...

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