Jake A. Gertie

ORCID: 0000-0002-3867-1884
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About
Contact & Profiles
Research Areas
  • interferon and immune responses
  • RNA regulation and disease
  • Asthma and respiratory diseases
  • RNA Research and Splicing
  • Food Allergy and Anaphylaxis Research
  • T-cell and B-cell Immunology
  • Immune Cell Function and Interaction
  • Celiac Disease Research and Management
  • Immunotherapy and Immune Responses
  • Transgenic Plants and Applications
  • Immune Response and Inflammation
  • Cytomegalovirus and herpesvirus research
  • Diabetes and associated disorders
  • Neutrophil, Myeloperoxidase and Oxidative Mechanisms
  • Eosinophilic Esophagitis
  • Immunodeficiency and Autoimmune Disorders

Columbia University
2023-2025

Columbia University Irving Medical Center
2023-2024

Yale University
2019-2023

Cross-linking of high-affinity immunoglobulin E (IgE) results in the life-threatening allergic reaction anaphylaxis. Yet cellular mechanisms that induce B cells to produce IgE response allergens remain poorly understood. T follicular helper (TFH) direct affinity and isotype antibodies produced by cells. Although TFH cell-derived interleukin-4 (IL-4) is necessary for production, it not sufficient. We report a rare population IL-13-producing present mice humans with allergens, but when...

10.1126/science.aaw6433 article EN Science 2019-08-01

Loss of RNA homeostasis underlies numerous neurodegenerative and neuroinflammatory diseases. However, the molecular mechanisms that trigger neuroinflammation are poorly understood. Viral double-stranded (dsRNA) triggers innate immune responses when sensed by host pattern recognition receptors (PRRs) present in all cell types. Here, we report human neurons intrinsically carry exceptionally high levels immunostimulatory dsRNAs identify long 3'UTRs as giving rise to neuronal dsRNA structures....

10.1126/sciimmunol.adg2979 article EN Science Immunology 2023-10-20

Summary Ku70 and Ku80 form Ku, a ring-shaped protein that initiates the non-homologous end-joining (NHEJ) DNA repair pathway. 1 Specifically, Ku binds to double-stranded (dsDNA) ends recruits other NHEJ factors ( e.g. , DNA-PKcs LIG4). While RNA (dsRNA) 2 traps mutated-DNA-PKcs on ribosomal in vivo, 3,4 physiological significance of Ku-dsRNA interactions otherwise wild-type cells remains elusive. Intriguingly, while dispensable for murine development, 5,6 is essential human cells. 7 Despite...

10.1101/2025.01.31.633084 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2025-02-01
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