Tristan Courau

ORCID: 0000-0003-1819-9516
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About
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Research Areas
  • Immune cells in cancer
  • Immune Cell Function and Interaction
  • Cancer Immunotherapy and Biomarkers
  • Single-cell and spatial transcriptomics
  • COVID-19 Clinical Research Studies
  • Reproductive System and Pregnancy
  • Immunotherapy and Immune Responses
  • T-cell and B-cell Immunology
  • CAR-T cell therapy research
  • SARS-CoV-2 and COVID-19 Research
  • Cancer Cells and Metastasis
  • Wound Healing and Treatments
  • Phagocytosis and Immune Regulation
  • Pancreatic and Hepatic Oncology Research
  • Respiratory Support and Mechanisms
  • Immune responses and vaccinations
  • Advanced Biosensing Techniques and Applications
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Long-Term Effects of COVID-19
  • TGF-β signaling in diseases
  • Cell Image Analysis Techniques
  • Inflammation biomarkers and pathways
  • Respiratory viral infections research
  • Planarian Biology and Electrostimulation
  • Cancer Research and Treatments

University of California, San Francisco
2020-2024

Pollinator Partnership
2023

Sorbonne Université
2013-2023

Inserm
2013-2023

Université Paris Cité
2016-2022

Universidad Católica de Santa Fe
2022

Institut de recherche Saint-Louis
2019-2020

University of London Institute in Paris
2020

Centre National de la Recherche Scientifique
2015

Although infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has pleiotropic and systemic effects in some individuals1-3, many others experience milder symptoms. Here, to gain a more comprehensive understanding of the distinction between mild phenotypes pathology disease 2019 (COVID-19) its origins, we performed whole-blood-preserving single-cell analysis protocol integrate contributions from all major immune cell types blood-including neutrophils, monocytes,...

10.1038/s41586-021-03234-7 article EN other-oa Nature 2021-01-25

<h3>Background</h3> Immunotherapies still fail to benefit colorectal cancer (CRC) patients. Relevant functional assays aimed at studying these failures and the efficacy of immunotherapy in human are scarce. 3D tumor cultures, called organoids or spheroids, represent interesting models study treatments could help challenge issues. <h3>Methods</h3> We analyzed heterotypic cocultures colon tumor-derived spheroids with immune cells assess infiltration, activation function T NK toward tumors...

10.1186/s40425-019-0553-9 article EN cc-by Journal for ImmunoTherapy of Cancer 2019-03-14

Regulatory T cells (Tregs) play crucial roles in both fetal and tumor development. We recently showed that immunosurveillance by pre-existing CD44(high)CD62L(low) activated/memory Tregs (amTregs) specific for self-Ags protects emergent mice. This Treg response of a memory type is more rapid than dominates the antitumor tumor-specific effector cells. In this study, we report striking similarities between early responses to embryo implantation. are rapidly recruited uterus-draining lymph nodes...

10.4049/jimmunol.1202413 article EN The Journal of Immunology 2013-08-03

Tregs imprint an early immunotolerant tumor environment that prevents effective antitumor immune responses. Using transcriptomics of tissues, we identified upregulation VEGF and TGF-β pathways compatible with tolerance imprinting. Silencing or in cells induced pleiotropic modulation immune-related transcriptome signatures tissues. These were surprisingly similar for both silenced tumors related to common downstream effects on Tregs. resulted dramatically delayed growth, associated decreased...

10.1172/jci.insight.85974 article EN JCI Insight 2016-06-15
Aartik Sarma Stephanie A. Christenson Ashley Byrne Eran Mick Angela Oliveira Pisco and 95 more Catherine DeVoe Thomas Deiss Rajani Ghale Beth Shoshana Zha Alexandra Tsitsiklis Alejandra Jáuregui Farzad Moazed Angela M. Detweiler Natasha Spottiswoode Pratik Sinha Norma Neff Michelle Tan Paula Hayakawa Serpa Andrew Willmore K. Mark Ansel Jennifer G. Wilson Aleksandra Leligdowicz Emily R. Siegel Marina Sirota Joseph L. DeRisi Michael A. Matthay Yumiko Abe‐Jones Saurabh Asthana Alexander J. Beagle Tanvi Bhakta Sharvari Bhide Cathy Cai Saharai Caldera Carolyn S. Calfee Lorena Espinar Sidney Carrillo Adithya Cattamanchi Suzanna Chak Vincent Chan Nayvin W. Chew Stephanie A. Christenson Zachary Collins Alexis J. Combes Tristan Courau Spyros Darmanis David Erle Armond M. Esmaili Gabriela K. Fragiadakis Rajani Ghale Jeremy Giberson Ana Gonzalez Paula Hayakawa Serpa Carolyn M. Hendrickson Kamir Hiam Kenneth H. Hu Billy Huang Alejandra Jáuregui Chayse Jones Norman G. Jones Kirsten N. Kangelaris Matthew F. Krummel Nitasha Kumar Divya Kushnoor Tasha Lea Deanna Lee David S. Lee Kathleen D. Liu Yale Liu Salman Mahboob Michael A. Matthay Jeff Milush Priscila Muñoz-Sandoval Nguyễn Hoàng Việt Gabe Ortiz Randy Parada Maíra Phelps Logan Pierce Priya A. Prasad Arjun A. Rao Sadeed Rashid Gabriella C. Reeder Nicklaus Rodriguez Bushra Samad Diane Scarlet Cole Shaw Alan Shen Austin Sigman Matthew H. Spitzer Yang Sun Sara Sunshine Kevin Tang Luz Torres Altamirano Jessica Tsui Erden Tumurbaatar Kathleen Turner Alyssa Ward Andrew Willmore Michael R. Wilson Juliane Winkler Reese Withers

Abstract The immunological features that distinguish COVID-19-associated acute respiratory distress syndrome (ARDS) from other causes of ARDS are incompletely understood. Here, we report the results comparative lower tract transcriptional profiling tracheal aspirate 52 critically ill patients with COVID-19 or etiologies, as well controls without ARDS. In contrast to a “cytokine storm,” observe reduced proinflammatory gene expression in when compared due causes. is characterized by...

10.1038/s41467-021-25040-5 article EN cc-by Nature Communications 2021-08-26

Tissue-resident macrophages adapt to local signals within tissues acquire specific functions. Neoplasia transforms the tissue, raising question as how environmental perturbations contribute tumor-associated macrophage (TAM) identity and Combining single-cell RNA sequencing (scRNA-seq) with spatial localization of distinct TAM subsets by imaging, we discover that transcriptomic programs follow two main differentiation paths according their in stroma or neoplastic epithelium mammary duct....

10.1016/j.celrep.2022.110865 article EN cc-by Cell Reports 2022-05-01

Intestinal tissue-resident memory CD8 T cells (Trm) are non-recirculating effector ideally positioned to detect and react microbial infections in the gut mucosa. There is an emerging understanding of Trm cell differentiation functions, but their implication inflammatory bowel diseases, such as Crohn's disease (CD), still unknown. Here, we describe human intestine expressing KLRG1 or CD103, two receptors E-cadherin. While CD103 present high numbers mucosa CD patients controls, increased...

10.3389/fimmu.2020.00896 article EN cc-by Frontiers in Immunology 2020-05-12

Abstract Dexamethasone is the standard of care for critically ill patients with COVID-19, but mechanisms by which it decreases mortality and its immunological effects in this setting are not understood. Here we perform bulk single-cell RNA sequencing samples from lower respiratory tract blood, assess plasma cytokine profiling to study dexamethasone on both systemic pulmonary immune cell compartments. In blood samples, associated decreased expression genes T activation, including TNFSFR4...

10.1038/s41467-024-49756-2 article EN cc-by Nature Communications 2024-06-28

Objective T cells are major effectors of the antitumoural immune response. Their activation by tumour-associated antigens can unleash their proliferation and cytotoxic functions, leading to tumour cell elimination. However, tumour-related immunosuppressive mechanisms including overexpression checkpoints like programmed death protein-1 (PD-1), also engaged, promoting escape. Current immunotherapies targeting these pathways have demonstrated weak efficacy in colorectal cancer (CRC). It is thus...

10.1136/gutjnl-2021-326553 article EN Gut 2022-07-08

In the past decade, high-dimensional single-cell technologies have revolutionized basic and translational immunology research are now a key element of toolbox used by scientists to study immune system. However, analysis data generated these approaches often requires clustering algorithms dimensionality reduction representation, which computationally intense difficult evaluate optimize. Here, we present Cytometry Clustering Optimization Evaluation (Cyclone), an pipeline integrating reduction,...

10.3389/fimmu.2023.1167241 article EN cc-by Frontiers in Immunology 2023-09-04

Abstract Idiopathic Inflammatory Myopathies (IIMs) are a heterogeneous group of autoimmune diseases affecting skeletal muscle tissue homeostasis. They characterized by weakness and inflammatory infiltration with damage. Amongst the cells in infiltration, dendritic (DCs) potent antigen-presenting key components autoimmunity exhibiting an increased activation inflamed tissues. Since, IIMs focal necrosis/regeneration atrophy, we hypothesized that DCs may play role these processes. Due to...

10.1038/s41419-018-0426-z article EN cc-by Cell Death and Disease 2018-05-10

To further investigate the contribution of intercellular adhesion molecule-1 (ICAM-1) to adaptive immune responses, we analysed T-cell development and function in mice lacking full-length ICAM-1 (ICAM-1(tm1Jcgr) ). Compared with wild-type (ICAM-1(WT) ) mice, ICAM-1(tm1Jcgr) have impaired thymocyte development. Proportions numbers double negative, positive, mature CD4(+) CD8(+) thymocytes, as well regulatory T (Treg) cells were also significantly decreased. In periphery, had decreased...

10.1111/imm.12533 article EN Immunology 2015-09-15

Abstract Embryos and tumors are both masses of dividing cells expressing foreign Ags, but they not rejected by the immune system. We hypothesized that similar tolerogenic mechanisms prevent their rejection. Global comparison fetal tumor microenvironments through transcriptomics in mice revealed strikingly dramatic decreases expression numerous immune-related pathways, including Ag presentation T cell signaling. Unsupervised analyses highlighted parallel kinetics similarities signature...

10.4049/jimmunol.1501834 article EN The Journal of Immunology 2015-12-08

CD206 is a common marker of putative immunosuppressive “M2” state in tumor-associated macrophages (TAMs). We made novel conditional (Mrc1) knock-in mouse to specifically visualize and/or deplete CD206+ TAMs. Early depletion and monocytes (Mono/Macs) led the indirect loss conventional type I dendritic cells (cDC1), CD8 T cells, NK tumors. TAMs robustly expressed CXCL9, contrasting with stress-responsive Spp1-expressing immature monocytes, which became prominent early depletion. differentially...

10.1084/jem.20240957 article EN The Journal of Experimental Medicine 2024-11-27
Jason A. Hackney Haridha Shivram Jason A. Vander Heiden Christopher C. Overall Luz D. Orozco and 95 more Xia Gao Eugene S. Kim Nathaniel R. West Aditi Qamra Diana Chang Arindam Chakrabarti David F. Choy Alexis J. Combes Tristan Courau Gabriela K. Fragiadakis Arjun A. Rao Arja Ray Jessica Tsui Kenneth H. Hu Nicholas F. Kuhn Matthew F. Krummel David J. Erle Kirsten N. Kangelaris Aartik Sarma Zoe M. Lyon Carolyn S. Calfee Prescott G. Woodruff Rajani Ghale Eran Mick Ashley Byrne Beth Shoshana Zha Charles Langelier Carolyn M. Hendrickson Monique G.P. van der Wijst George C. Hartoularos Tianna Grant Raymund Bueno David S. Lee John R. Greenland Yang Sun Richard K. Perez Anton Ogorodnikov Alyssa Ward Chun Ye Yumiko Abe‐Jones Michael Adkisson K. Mark Ansel Saurabh Asthana Alexander J. Beagle Sharvari Bhide Cathy Cai Saharai Caldera Lorena Espinar Sidney Carrillo Suzanna Chak Stephanie A. Christenson Zachary Collins Spyros Darmanis Angela M. Detweiler Catherine DeVoe Walter L. Eckalbar Jeremy Giberson Ana Gonzalez Gracie Gordon Paula Hayakawa Serpa Alejandra Jáuregui Chayse Jones Serena Ke Divya Kushnoor Tasha Lea Deanna Lee Aleksandra Leligdowicz Yale Liu Salman Mahboob Lenka Maliskova Michael A. Matthay Elizabeth W. McCarthy Priscila Muñoz-Sandoval Norma Neff Nguyễn Hoàng Việt Nishita Nigam Randy Parada Maíra Phelps Logan Pierce Priya A. Prasad Sadeed Rashid Gabriella C. Reeder Nicklaus Rodriguez Bushra Samad Andrew Schroeder Cole Shaw Alan Shen Austin Sigman Pratik Sinha Matthew H. Spitzer Sara Sunshine Kevin Tang Luz Torres Altamirano Alexandra Tsitsiklis Erden Tumurbaatar

Altered myeloid inflammation and lymphopenia are hallmarks of severe infections. We identified the upregulated EN-RAGE gene program in airway blood cells from patients with acute lung injury SARS-CoV-2 or other causes across 7 cohorts. This was associated greater clinical severity predicted future mechanical ventilation death.

10.1016/j.isci.2023.107813 article EN cc-by-nc-nd iScience 2023-09-01

Abstract The anti-tumor function of CD8 T cells is limited through well-established pathways cell exhaustion (T EX ). Strategies to capture emergent functional states amongst this dominant trajectory dysfunction are necessary find durable immunity. By leveraging transcriptional reporting (by the fluorescent protein TFP) activation marker Cd69, related upstream AP-1 transcription factors, we define a classifier for potent versus sub-optimal CD69+ arising from stimulation. In tumors,...

10.1101/2023.09.26.559470 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2023-09-28

Tumor-associated macrophages (TAMs) are frequently categorized as being 'M1' or 'M2' polarized, even substantial data challenges this binary modeling of macrophage cell state. One molecule consistently referenced a delineator putative immunosuppressive state is the surface protein CD206. We thus made novel conditional CD206 (Mrc1) knock-in mouse to specifically visualize and/or deplete CD206+ 'M2-like' TAMs and assess their correspondence with pro-tumoral immunity. Early, but not late...

10.1101/2023.10.31.560822 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2023-11-02

Abstract While SARS-CoV-2 infection has pleiotropic and systemic effects in some patients, many others experience milder symptoms. We sought a holistic understanding of the severe/mild distinction COVID-19 pathology, its origins. performed wholeblood preserving single-cell analysis protocol to integrate contributions from all major cell types including neutrophils, monocytes, platelets, lymphocytes contents serum. Patients with mild disease display coordinated pattern interferonstimulated...

10.21203/rs.3.rs-97042/v1 preprint EN cc-by Research Square (Research Square) 2020-10-28

SUMMARY Cancers display significant heterogeneity with respect to tissue of origin, driver mutations and other features the surrounding tissue. It is likely that persistent tumors differentially engage inherent patterns–here ‘Archetypes’–of immune system, both benefit from a tumor microenvironment (TIME) disengage tumor-targeting. To discover dominant system archetypes, Immunoprofiler Initiative (IPI) processed 364 individual across 12 cancer types using standardized protocols. Computational...

10.1101/2021.04.26.441344 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2021-04-27

<h3>Background</h3> The idea that tumors co-opt elements of tissue repair and maintenance for growth immune evasion is a long-held one.<sup>1</sup> Cancer associated fibroblasts or CAFs can control the localization polarization state infiltrating cells, therefore they represent an enticing target clinical modulation.<sup>2–4</sup> Through mechanisms including ECM modulation, cytokine secretion even antigen presentation<sup>5</sup>, these relatively rare but powerful cells have potential to...

10.1136/jitc-2024-sitc2024.0876 article EN cc-by-nc Regular and Young Investigator Award Abstracts 2024-11-01
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