P
Peter T. Sage
Researcher at Brigham and Women's Hospital
Publications - 70
Citations - 6738
Peter T. Sage is an academic researcher from Brigham and Women's Hospital. The author has contributed to research in topics: T cell & Germinal center. The author has an hindex of 26, co-authored 57 publications receiving 5284 citations. Previous affiliations of Peter T. Sage include Harvard University & Beth Israel Deaconess Medical Center.
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Journal ArticleDOI
The PD-1 pathway in tolerance and autoimmunity
TL;DR: This review highlights how PD‐1 and its ligands defend against potentially pathogenic self‐reactive effector T cells by simultaneously harnessing two mechanisms of peripheral tolerance: (i) the promotion of Treg development and function and (ii) the direct inhibition of potentially pathogen self-reactive T cells that have escaped into the periphery.
Journal ArticleDOI
Transcellular Diapedesis Is Initiated by Invasive Podosomes
Christopher V. Carman,Peter T. Sage,Tracey E. Sciuto,Miguel Angel de la Fuente,Raif S. Geha,Hans D. Ochs,Harold F. Dvorak,Ann M. Dvorak,Timothy A. Springer +8 more
TL;DR: It is demonstrated that lymphocytes usedpodosomes and extended "invasive podosomes" to palpate the surface of, and ultimately form transcellular pores through, the endothelium, providing insights into basic mechanisms for leukocyte trafficking and the functions of podosome.
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The receptor PD-1 controls follicular regulatory T cells in the lymph nodes and blood
Peter T. Sage,Loise M. Francisco,Loise M. Francisco,Christopher V. Carman,Arlene H. Sharpe,Arlene H. Sharpe +5 more
TL;DR: These findings demonstrate mechanisms by which the PD-1 pathway regulates antibody production and help reconcile inconsistencies surrounding the role of this pathway in humoral immunity.
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The Coinhibitory Receptor CTLA-4 Controls B Cell Responses by Modulating T Follicular Helper, T Follicular Regulatory, and T Regulatory Cells
Peter T. Sage,Alison M. Paterson,Alison M. Paterson,Scott B. Lovitch,Arlene H. Sharpe,Arlene H. Sharpe +5 more
TL;DR: It is found that non-Tfr Treg cells could suppress B cell responses through CTLA-4 and that Treg and/or Tfr cells might downregulate B7-2 on B cells outside germinal centers as a means of suppression.
Journal ArticleDOI
Control of PI(3) kinase in Treg cells maintains homeostasis and lineage stability
Alexandria Huynh,Michel DuPage,Bhavana Priyadharshini,Peter T. Sage,Jason Quiros,Christopher Borges,Natavudh Townamchai,Valerie A. Gerriets,Jeffrey C. Rathmell,Arlene H. Sharpe,Jeffrey A. Bluestone,Laurence A. Turka +11 more
TL;DR: Collectively, the data demonstrate that control of PI(3)K signaling by PTEN in Treg cells is critical for maintaining their homeostasis, function and stability.