Photo of Tobias Schatton,  PhD

Tobias Schatton, PhD

Brigham And Women's Hospital

Brigham And Women's Hospital


tschatton@bwh.harvard.edu

Tobias Schatton, PhD

Brigham And Women's Hospital

EDUCATIONAL TITLES

  • Assistant Professor, Dermatology, Harvard Medical School
  • Research Associate, Dermatology, Brigham And Women's Hospital
  • Research Associate, Medicine, Boston Children's Hospital
  • Affiliated Faculty, Dermatology, HARVARD STEM CELL INSTITUTE - HSCI

DF/HCC PROGRAM AFFILIATION

Research Abstract

Dr. Tobias Schatton’s laboratory research centers on immune checkpoint pathways and homing mediators in skin cancer progression, skin disorders, and normal skin homeostasis. His objective is to mechanistically dissect how cell type-specific glycostructural modifications impact skin cancer immunobiology, normal skin physiology, therapeutic efficacy, and patient outcome. Major focuses of the Schatton laboratory include previously unrecognized cancer- versus immune cell subset-specific roles of glycoprotein receptors, such as PD-1 and Tim-3, homing molecules, and their roles in tumor immune evasion, growth, metastasis, and immunotherapy response. Dr. Schatton is the principal investigator on several NIH grants from the NCI and serves as the Co-Director of the Harvard Program of Glyco-Immunology and Oncology.

Publications from Harvard Catalyst Profiles

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  • Schatton T, Itoh Y, Martins C, Rasbach E, Singh P, Silva M, Mucciarone KN, Heppt MV, Geddes-Sweeney J, Stewart K, Brandenburg A, Liang J, Dimitroff CJ, Mihm MC, Landsberg J, Schlapbach C, Lian CG, Murphy GF, Kupper TS, Ramsey MR, Barthel SR. Inhibition of melanoma cell-intrinsic Tim-3 stimulates MAPK-dependent tumorigenesis. Cancer Res 2022. PubMed
  • Martins C, Silva M, Rasbach E, Singh P, Itoh Y, Williams JB, Statham E, Meurer A, Martinez DV, Brandenburg A, Heppt MV, Barthel SR, Schatton T. Distinct antibody clones detect PD-1 checkpoint expression and block PD-L1 interactions on live murine melanoma cells. Sci Rep 2022; 12:12491. PubMed
  • Sackstein R, Schatton T, Barthel SR. T-lymphocyte homing: an underappreciated yet critical hurdle for successful cancer immunotherapy. Lab Invest 2017. PubMed
  • Lee N, Zakka LR, Mihm MC, Schatton T. Tumour-infiltrating lymphocytes in melanoma prognosis and cancer immunotherapy. Pathology 2016; 48:177-87. PubMed
  • Kleffel S, Lee N, Lezcano C, Wilson BJ, Sobolewski K, Saab KR, Mueller H, Zhan Q, Posch C, Elco CP, DoRosario A, Garcia SS, Thakuria M, Wang YE, Wang LC, Murphy GF, Frank MH, Schatton T. ABCB5-targeted chemoresistance reversal inhibits Merkel cell carcinoma growth. J Invest Dermatol 2016. PubMed
  • Barthel SR, Schatton T. Homing in on the Sweet Side of Immune Checkpoint Biology. Immunity 2016; 44:1083-5. PubMed
  • Kleffel S, Posch C, Barthel SR, Mueller H, Schlapbach C, Guenova E, Elco CP, Lee N, Juneja VR, Zhan Q, Lian CG, Thomi R, Hoetzenecker W, Cozzio A, Dummer R, Mihm MC, Flaherty KT, Frank MH, Murphy GF, Sharpe AH, Kupper TS, Schatton T. Melanoma Cell-Intrinsic PD-1 Receptor Functions Promote Tumor Growth. Cell 2015; 162:1242-56. PubMed
  • Lee N, Barthel SR, Schatton T. Melanoma stem cells and metastasis: mimicking hematopoietic cell trafficking? Lab Invest 2014; 94:13-30. PubMed
  • Wilson BJ, Schatton T, Zhan Q, Gasser M, Ma J, Saab KR, Schanche R, Waaga-Gasser AM, Gold JS, Huang Q, Murphy GF, Frank MH, Frank NY. ABCB5 identifies a therapy-refractory tumor cell population in colorectal cancer patients. Cancer Res 2011. PubMed
  • Schatton T, Schütte U, Frank NY, Zhan Q, Hoerning A, Robles SC, Zhou J, Hodi FS, Spagnoli GC, Murphy GF, Frank MH. Modulation of T-Cell Activation by Malignant Melanoma Initiating Cells. Cancer Res 2010; 70:697-708. PubMed
  • Schatton T, Murphy GF, Frank NY, Yamaura K, Waaga-Gasser AM, Gasser M, Zhan Q, Jordan S, Duncan LM, Weishaupt C, Fuhlbrigge RC, Kupper TS, Sayegh MH, Frank MH. Identification of cells initiating human melanomas. Nature 2008; 451:345-9. PubMed