Jessica Le Bérichel

ORCID: 0000-0003-0846-3280
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About
Contact & Profiles
Research Areas
  • Cancer Immunotherapy and Biomarkers
  • Epigenetics and DNA Methylation
  • Cancer Research and Treatments
  • Immune cells in cancer
  • Immunotherapy and Immune Responses
  • Immune Cell Function and Interaction
  • Phagocytosis and Immune Regulation
  • Single-cell and spatial transcriptomics
  • CAR-T cell therapy research
  • Kawasaki Disease and Coronary Complications
  • Immune responses and vaccinations
  • Pediatric health and respiratory diseases
  • Disaster Response and Management
  • Histiocytic Disorders and Treatments
  • Ferroptosis and cancer prognosis
  • Cancer Cells and Metastasis
  • COVID-19 Impact on Reproduction
  • Diabetes and associated disorders
  • Extracellular vesicles in disease
  • Long-Term Effects of COVID-19
  • COVID-19 epidemiological studies
  • Neuroinflammation and Neurodegeneration Mechanisms
  • CRISPR and Genetic Engineering
  • Intensive Care Unit Cognitive Disorders
  • Lung Cancer Research Studies

Icahn School of Medicine at Mount Sinai
2020-2025

Tisch Hospital
2023-2024

Tisch Cancer Institute
2021-2023

Mount Sinai Health System
2021

Immunologie et Neurogénétique Expérimentales et Moléculaires
2016-2018

Université d'Orléans
2016-2018

Centre National de la Recherche Scientifique
2016-2018

University of Cape Town
2016

Abstract It is currently accepted that cancer-associated fibroblasts (CAF) participate in T-cell exclusion from tumor nests. To unbiasedly test this, we used single-cell RNA sequencing coupled with multiplex imaging on a large cohort of lung tumors. We identified four main CAF populations, two which are associated exclusion: (i) MYH11+αSMA+ CAF, present early-stage tumors and form single cell layer lining cancer aggregates, (ii) FAP+αSMA+ appear more advanced organize patches within the...

10.1158/2159-8290.cd-21-1714 article EN Cancer Discovery 2022-08-26

Age is a major risk factor for cancer, but how aging impacts tumor control remains unclear. In this study, we establish that of the immune system, regardless age stroma and tumor, drives lung cancer progression. Hematopoietic enhances emergency myelopoiesis, resulting in local accumulation myeloid progenitor–like cells tumors. These are source interleukin (IL)–1⍺, which enhanced response. The age-associated decline DNA methyltransferase 3A IL-1⍺ production, disrupting IL-1 receptor 1...

10.1126/science.adn0327 article EN Science 2024-09-05

Inflammatory cytokines are fundamental mediators of the organismal response to injury, infection, or other harmful stimuli. To elucidate early and mostly direct transcriptional signatures inflammatory cytokines, we profiled all immunologic cell types by RNAseq after systemic exposure IL1β, IL6, TNFα. Our results revealed a significant overlap in responses, with broad divergence between myeloid lymphoid cells, but very few cell-type-specific responses. Pathway motif analysis identified...

10.1084/jem.20241207 article EN The Journal of Experimental Medicine 2025-01-28
Ryan C. Thompson Nicole W. Simons Lillian Wilkins Esther Cheng Diane M. Del Valle and 95 more Gabriel E. Hoffman Carlo Cervia Brian Fennessy Konstantinos Mouskas Nancy Francoeur Jessica Johnson Lauren Lepow Jessica Le Bérichel Christie Chang Aviva G. Beckmann Ying‐Chih Wang Kai Nie Nicholas Zaki Kevin Tuballes Vanessa Barcessat Mario A. Cedillo Dan Yuan Laura M. Huckins Panos Roussos Thomas U. Marron Charuta Agashe Priyal Agrawal Alara Akyatan Kasey Alesso-Carra Eziwoma Alibo Kelvin Alvarez Angelo Amabile Carmen Argmann Kimberly Argueta Steven Ascolillo Rasheed Bailey Craig Batchelor Noam D. Beckmann Priya Begani Dusan Bogunovic Swaroop Bose Cansu Cimen Bozkus Paloma Bravo Stacey-Ann Whittaker Brown Mark Buckup Larissa Burka Sharlene Calorossi Lena Cambron Guillermo Carbonell Gina Carrara Mario A. Cedillo Christie Chang Serena Chang Steven T. Chen Jonathan Chien Mashkura Chowdhury Jonathan Chung Phillip Comella Dana Cosgrove Francesca Cossarini Liam Cotter Arpit Dave Travis Dawson Bheesham D. Dayal Maxime Dhainaut Rebecca Dornfeld Katie Dul Melody Eaton Nissan Eber Cordelia Elaiho Ethan Ellis Frank Fabris Jeremiah J. Faith Dominique Falci Susie Feng Marie Fernandes Nataly Fishman Nancy Francoeur Sandeep Gangadharan Daniel Geanon Bruce D. Gelb Benjamin S. Glicksberg Sacha Gnjatic Edgar Gonzalez‐Kozlova Joanna Grabowska Gavin Gyimesi Maha Hamdani Diana Handler Jocelyn Harris Matthew Hartnett Sandra Hatem Manon Herbinet Elva Herrera Arielle Hochman Gabriel E. Hoffman Jaime L. Hook Laila Horta Étienne Humblin Suraj K. Jaladanki Hajra Jamal

Abstract Post-acute sequelae of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection are debilitating, clinically heterogeneous and unknown molecular etiology. A transcriptome-wide investigation was performed in 165 acutely infected hospitalized individuals who were followed into the post-acute period. Distinct gene expression signatures already present whole blood during infection, with innate adaptive immune cells implicated different symptoms. Two clusters exhibited...

10.1038/s41591-022-02107-4 article EN cc-by Nature Medicine 2022-12-08

Tissue-resident macrophages (TRMs) populate all tissues and play key roles in homeostasis, immunity repair. TRMs express a molecular program that is mostly shaped by tissue cues. However, TRM identity the mechanisms maintain remain poorly understood. We recently found serous-cavity (LPMs) are highly enriched RXR transcripts RXR-response elements. Here, we show RXRs control mouse serous-macrophage regulating chromatin accessibility transcriptional regulation of canonical macrophage genes....

10.1038/s41467-020-15371-0 article EN cc-by Nature Communications 2020-04-03

Multisystem inflammatory syndrome in children (MIS-C) presents with fever, inflammation and pathology of multiple organs individuals under 21 years age the weeks following severe acute respiratory coronavirus 2 (SARS-CoV-2) infection. Although an autoimmune pathogenesis has been proposed, genes, pathways cell types causal to this new disease remain unknown. Here we perform RNA sequencing blood from patients MIS-C controls find disease-associated genes clustered a co-expression module annotated CD56

10.1038/s41467-021-24981-1 article EN cc-by Nature Communications 2021-08-11
Alexander W. Charney Nicole W. Simons Konstantinos Mouskas Lauren Lepow Esther Cheng and 95 more Jessica Le Bérichel Christie Chang Robert Marvin Diane M. Del Valle Sharlene Calorossi Alona Lansky Laura Walker Manishkumar Patel Hui Xie Nancy Yi Alex W. Yu Gurpawan Kang Anthony Mendoza Lora E. Liharska Emily Moya Matthew Hartnett Sandra Hatem Lillian Wilkins Melody Eaton Hajra Jamal Kevin Tuballes Steven T. Chen Alexandra Tabachnikova Jonathan H. Chung Jocelyn Harris Craig Batchelor Jose Lacunza Mahlet Yishak Kimberly Argueta Neha Karekar Brian Lee Geoffrey Kelly Daniel Geanon Diana Handler John Leech Hiyab Stefanos Travis Dawson Ieisha Scott Nancy Francoeur Jessica Johnson Akhil Vaid Benjamin S. Glicksberg Girish N. Nadkarni Eric E. Schadt Bruce D. Gelb Adeeb Rahman Robert Sebra Glenn Martin Charuta Agashe Priyal Agrawal Alara Akyatan Kasey Alesso-Carra Eziwoma Alibo Kelvin Alvarez Angelo Amabile Steven Ascolillo Rasheed Bailey Priya Begani Paloma Bravo Correra Stacey-Ann Whittaker Brown Mark Buckup Larissa Burka Lena Cambron Gina Carrara Serena Chang Jonathan Chien Mashkura Chowdhury Cansu Cimen Bozkus Phillip Comella Dana Cosgrove Francesca Cossarini Liam Cotter Arpit Dave Bheesham D. Dayal Maxime Dhainaut Rebecca Dornfeld Katie Dul Nissan Eber Cordelia Elaiho Frank Fabris Jeremiah J. Faith Dominique Falci Susie Feng Brian Fennessy Marie Fernandes Sandeep Gangadharan Joanna Grabowska Gavin Gyimesi Maha Hamdani Manon Herbinet Elva Herrera Arielle Hochman Gabriel E. Hoffman Jaime L. Hook Laila Horta

10.1038/s41591-020-1004-3 article EN other-oa Nature Medicine 2020-07-27

Monocyte-derived macrophages (mo-macs) drive immunosuppression in the tumor microenvironment (TME) and tumor-enhanced myelopoiesis bone marrow (BM) fuels these populations. Here, we performed paired transcriptome chromatin analysis over continuum of BM myeloid progenitors, circulating monocytes, tumor-infiltrating mo-macs mice patients with lung cancer to identify progenitor programs that fuel pro-tumorigenic mo-macs. Analyzing accessibility histone mark changes, show tumors prime for Nfe2l2...

10.1101/2024.06.24.600383 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2024-06-28

Multiplex immunostaining analysis remains fragmented, underperforming, and labor-intensive despite tissue proteomic methodologies achieving ever-increasing marker complexity. Here we propose an open-source, semi-supervised automated pipeline that streamlines start-to-finish, single-cell resolution of whole-slide tissue, named Multiplex-imaging Analysis, Registration, Quantification, Overlaying (MARQO). We compared validated MARQO using Immunohistochemical Consecutive Staining on a Single...

10.1101/2025.04.24.650539 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2025-04-26

Allergic asthma is characterized by a strong Th2 response with inflammatory cell recruitment and structural changes in the lung. Papain protease allergen disrupting airway epithelium triggering rapid inflammation eosinophilia mediated innate lymphoid activation (ILC2) leading to immune response. In this study, we focused on responses single exposure papain showed that intranasal administration of results cells, including neutrophils eosinophils production IL-1α, IL-1β, IL-33. The abrogated...

10.1002/eji.201646366 article EN European Journal of Immunology 2016-08-29

Allergic asthma is characterized by a strong Th2 and Th17 response with inflammatory cell recruitment, airways hyperreactivity structural changes in the lung. The protease allergen papain disrupts airway epithelium triggering rapid eosinophilic inflammation innate lymphoid type 2 (ILC2) activation, leading to immune response. Here we asked whether daily oral administrations of probiotic Escherichia coli strain Nissle 1917 (ECN) might affect outcome induced allergic lung BL6 mice. We find...

10.1038/s41598-018-29689-9 article EN cc-by Scientific Reports 2018-07-20

Abstract Tertiary lymphoid structures (TLS) are organized immune cell aggregates that arise in chronic inflammatory conditions. In cancer, TLS associated with better prognosis and enhanced response to immunotherapy, making these attractive therapeutic targets. However, the mechanisms regulating formation maintenance cancer incompletely understood. Using spatial transcriptomics multiplex imaging across various human tumors, we found an enrichment of mature dendritic cells (DC) expressing high...

10.1101/2024.12.27.628014 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2024-12-27

Summary We previously found that uptake of cellular debris prompts conventional dendritic cells (cDCs) to undergo maturation. This transformation results in DCs entering the molecular state termed ‘mregDC’. In this state, mregDCs dampen their ability acquire new antigens, upregulate chemokine receptors migrate lymphoid organs, and MHC-I -II, co-stimulatory, -inhibitory molecules promote differentiation antigen-specific T cells. Here, we show cholesterol mobilization – through both de novo...

10.1101/2023.12.25.573303 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2023-12-25
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