Michael D. Claiborne

ORCID: 0000-0002-7633-0159
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About
Contact & Profiles
Research Areas
  • Immune Cell Function and Interaction
  • Biochemical and Molecular Research
  • Cancer, Hypoxia, and Metabolism
  • T-cell and B-cell Immunology
  • interferon and immune responses
  • Historical and Environmental Studies
  • Pancreatic function and diabetes
  • Historical Economic and Social Studies
  • Cancer Research and Treatments
  • Epigenetics and DNA Methylation
  • Historical and socio-economic studies of Spain and related regions
  • Protein Degradation and Inhibitors
  • Cancer Immunotherapy and Biomarkers
  • Immune cells in cancer
  • Immunotherapy and Immune Responses

Sidney Kimmel Comprehensive Cancer Center
2023

Johns Hopkins University
2020-2023

Bloomberg (United States)
2021-2023

Cancer Research Center
2023

Scripps Clinic
2022-2023

Scripps Green Hospital
2022-2023

Johns Hopkins Medicine
2020

Washington University in St. Louis
2011

Memory CD8+ T cells are characterized by their ability to persist long after the initial antigen encounter and capacity generate a rapid recall response. Recent studies have identified role for metabolic reprogramming mitochondrial function in promoting longevity of memory cells. However, detailed mechanisms involved response incompletely understood. Here, we identify continued activation trifunctional rate-limiting enzyme de novo pyrimidine synthesis pathway CAD (carbamoyl-phosphate...

10.1126/sciimmunol.abh4271 article EN Science Immunology 2022-05-27

Abstract In order to study mechanistic/mammalian target of rapamycin’s role in T cell differentiation, we generated mice which Rheb is selectively deleted cells (T-Rheb−/− C57BL/6J background). During these studies, noted that T-Rheb−/− were consistently heavier but had improved glucose tolerance and insulin sensitivity as well a marked increase beige fat. Microarray analysis Rheb−/− revealed expression kallikrein 1–related peptidase b22 (Klk1b22). Overexpression KLK1b22 vitro enhanced...

10.4049/immunohorizons.2300016 article EN cc-by ImmunoHorizons 2023-06-01

Abstract While the exquisite specificity of T-cell receptor (TCR) MHC + peptide interaction heralds recognition, it is ultimately cues from immune microenvironment that dictate outcome this recognition. Our lab has proposed mTOR plays a critical role in integrating signals and thus determining antigen Indeed, we have demonstrated mTORC1 mTORC2 signaling can selectively guide CD4+ effector regulatory differentiation function as well CD8+ memory function. Recent studies revealed performs part...

10.1158/1557-3125.pi3k-mtor18-ia14 article EN Molecular Cancer Research 2020-10-01

Abstract Memory CD8+ T cells are characterized by their ability to persist long after the initial antigen encounter and generate a rapid recall response. Recent studies have identified role for metabolic reprogramming mitochondrial function in promoting longevity of memory cells. However, detailed mechanisms involved response incompletely understood. Here we identify novel continued activation trifunctional rate-limiting enzyme de novo pyrimidine synthesis pathway CAD (carbamoyl-phosphate...

10.1101/2021.11.10.468070 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2021-11-11
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