S
Sivan Cohen
Researcher at Weizmann Institute of Science
Publications - 28
Citations - 1707
Sivan Cohen is an academic researcher from Weizmann Institute of Science. The author has contributed to research in topics: B cell & Transplantation. The author has an hindex of 16, co-authored 26 publications receiving 1350 citations. Previous affiliations of Sivan Cohen include Netherlands Cancer Institute & Duke University.
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Journal ArticleDOI
Foxp3 and Toll-like receptor signaling balance Treg cell anabolic metabolism for suppression
Valerie A. Gerriets,Rigel J. Kishton,Marc O. Johnson,Marc O. Johnson,Sivan Cohen,Peter J. Siska,Amanda G. Nichols,Marc O. Warmoes,Aguirre A. de Cubas,Nancie J. MacIver,Jason W. Locasale,Laurence A. Turka,Andrew D. Wells,Jeffrey C. Rathmell +13 more
TL;DR: Inflammatory signals and Foxp3 balance mTORC1 signaling and glucose metabolism to control the proliferation and suppressive function of Treg cells.
Journal ArticleDOI
mTORC1 and mTORC2 Kinase Signaling and Glucose Metabolism Drive Follicular Helper T Cell Differentiation.
Hu Zeng,Sivan Cohen,Cliff Guy,Sharad Shrestha,Geoffrey Neale,Scott A. Brown,Caryn Cloer,Rigel J. Kishton,Xia Gao,Ben Youngblood,Mytrang H. Do,Ming O. Li,Jason W. Locasale,Jeffrey C. Rathmell,Jeffrey C. Rathmell,Hongbo Chi +15 more
TL;DR: It is reported here that mTOR kinase complexes 1 and 2 (mTORC1 and mTORC2) are essential for Tfh cell differentiation and GC reaction under steady state and after antigen immunization and viral infection.
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AMPK is essential to balance glycolysis and mitochondrial metabolism to control T-ALL cell stress and survival
Rigel J. Kishton,Carson E. Barnes,Amanda G. Nichols,Sivan Cohen,Valerie A. Gerriets,Peter J. Siska,Andrew N. Macintyre,Pankuri Goraksha-Hicks,Aguirre A. de Cubas,Tingyu Liu,Marc O. Warmoes,E. Dale Abel,Allen Eng Juh Yeoh,Allen Eng Juh Yeoh,Timothy R. Gershon,W. Kimryn Rathmell,Kristy L. Richards,Jason W. Locasale,Jason W. Locasale,Jeffrey C. Rathmell +19 more
TL;DR: It is shown that aerobic glycolysis is surprisingly less active in T-ALL cells than proliferating normal T cells and that T-all cells are metabolically distinct, and that AMPK simultaneously inhibits anabolic growth signaling and is essential to promote mitochondrial pathways that mitigate metabolic stress and apoptosis inT-ALL.
Journal ArticleDOI
Deficiency of caspase recruitment domain family, member 11 (CARD11), causes profound combined immunodeficiency in human subjects
Polina Stepensky,Baerbel Keller,Mary Buchta,Anne-Kathrin Kienzler,Orly Elpeleg,Raz Somech,Sivan Cohen,Idit Shachar,Lisa A. Miosge,Michael Schlesier,Ilka Fuchs,Anselm Enders,Hermann Eibel,Bodo Grimbacher,Klaus Warnatz +14 more
TL;DR: In this article, the authors identify the genetic alteration in a patient with combined immunodeficiency and characterize human caspase recruitment domain family, member 11 (CARD11), deficiency, and reveal the crucial and nonredundant role of canonical NF-κB activation and specifically CARD11 in the antigen-specific immune response in human subjects.
Iconographies supplémentaires de l'article : Deficiency of caspase recruitment domain family, member 11 (CARD11), causes profound combined immunodeficiency in human subjects
Polina Stepensky,Baerbel Keller,Mary Buchta,Anne-Kathrin Kienzler,Orly Elpeleg,Raz Somech,Sivan Cohen,Idit Shachar,Lisa A. Miosge,Michael Schlesier,Ilka Fuchs,Anselm Enders,Hermann Eibel,Bodo Grimbacher,Klaus Warnatz +14 more
TL;DR: In patients with CARD11 deficiency, the combination of impaired activation and especially upregulation of inducible T- cell costimulator on T cells, together with severely disturbed peripheral B-cell differentiation, apparently leads to a defective T-cell/B-cell cooperation and probably germinal center formation and clinically results in severe immunodeficiency.