Paper Review Records
All Paper Review Records
15 valid samples · Newest publication first
Review days = acceptance date − received date. PDF, DOI, and publisher-page sources are retained.
Collaborative functionality between three types of inflammation in idiopathic pulmonary fibrosis
AuthorsThomas Fabre; Thomas A. Wynn; Kevin M. Hart
Affiliations1. Pfizer, Cambridge, USA
Progenitor T cells drive chronic pulmonary type 2 inflammation
AuthorsRadomir Kratchmarov; Xiaojiong Jia; Jun Nagai; Gaspar A. Pacheco; Alexander Perniss; Madeleine R. Bell; Ersin Gül; Thornton W. Thompson; Hiroaki Hayashi; Shahab Saghaei; Caitlin Wong; Madeline M. Hastings; Kinan Alhallak; Juying Lai; Chunli Feng; Lora Bankova; Duane R. Wesemann; Jakob von Moltke; Joshua A. Boyce; Patrick J. Brennan
Affiliations1. Division of Allergy and Clinical Immunology, Department of Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, USA; 2. Division of Allergy and Clinical Immunology & Division of Genetics, Department of Medicine, Brigham and Women’s Hospital Boston, Harvard Medical School, Boston, USA; 3. The Broad Institute of MIT and Harvard, Cambridge, USA; 4. The Ragon Institute of MGH, MIT and Harvard, Cambridge, USA; 5. Department of Immunology, University of Washington School of Medicine, Seattle, USA
Hallmarks of the multidimensional immune response to trauma in humans
AuthorsMarkus Huber-Lang; Tianmeng Chen; Rebecca Halbgebauer; Timothy Billiar
Affiliations1. Institute of Clinical and Experimental Trauma Immunology, Ulm University Medical Center, Ulm, Germany; 2. Department of Surgery, University of Pittsburgh, Pittsburgh, USA
Potent type-specific de novo antibodies complement broadly reactive imprinted antibodies in immune responses to SARS-CoV-2 variants
AuthorsTimothy S. Johnston; Shuk Hang Li; Mark M. Painter; Divya Swaminathan; Reilly K. Atkinson; Bernadeta Dadonaite; Shuishu Wang; Naomi R. Douek; Lucas Kampman; Robin Schlesinger; Rachel Kazmierski; Bob C. Lin; Leonid A. Serebryannyy; Haijuan Du; Amy R. Henry; Sarah C. Smith; Farida Laboune; I-Ting Teng; Lingshu Wang; Nicole A. Doria-Rose; Chaim A. Schramm; Theodore C. Pierson; Tongqing Zhou; Jesse D. Bloom; E. John Wherry; Scott E. Hensley; Daniel C. Douek
Affiliations1. Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, USA; 2. Department of Microbiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, USA; 3. Institute for Immunology and Immune Health, University of Pennsylvania Perelman School of Medicine, Philadelphia, USA; 4. Department of Systems Pharmacology and Translational Therapeutics, University of Pennsylvania Perelman School of Medicine, Philadelphia, USA; 5. Basic Sciences Division and Computational Biology Program, Fred Hutchinson Cancer Center, Seattle, USA; 6. Howard Hughes Medical Institute, Seattle, USA
Peyer’s patch M cells organize an epithelial niche that sustains group 3 innate lymphoid cells and IL-22
AuthorsWang H. J. Cao; Yue You; Nancy Wang; M. Zeeshan Chaudhry; Huiyang Yu; Peter T. Bell; Ellesandra C. Noye; Renae Denman; Byungchul Lee; Abbey Waddington; Junpeng Ye; Jaring Schreuder; Qiutong Huang; Julie Tellier; Sophie Curio; James Santiago; Daniela Amann-Zalcenstein; Nicolas Jacquelot; Peter Hickey; Stephen L. Nutt; Cyril Seillet; Philip M. Hansbro; Verena C. Wimmer; Richard A. Strugnell; Zewen Kelvin Tuong; Matthew E. Ritchie; Gabrielle T. Belz
Affiliations1. The University of Queensland Frazer Institute, University of Queensland, Woolloongabba, Australia; 2. Walter and Eliza Hall Institute of Medical Research, Parkville, Australia; 3. Department of Medical Biology, University of Melbourne, Parkville, Australia; 4. Department of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia; 5. Department of Biochemistry & Molecular Biology; Department of Microbiology, Immunology & Infectious Diseases; Riddell Centre for Cancer Immunotherapy, Arnie Charbonneau Cancer Institute, Arthur J.E. Child Comprehensive Cancer Centre, Calvin, Phoebe, and Joan Snyder Institute for Chronic Diseases, Alberta Children’s Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, Canada; 6. Department of Immunology, University of Monash, Melbourne, Australia; 7. Centre for Inflammation, Centenary Institute and University of Technology Sydney, Faculty of Science, School of Life Sciences, Sydney, Australia; 8. Ian Frazer Centre for Children’s Immunotherapy Research, Child Health Research Centre, Faculty of Medicine, The University of Queensland, Brisbane, Australia
Epigenetic modulation of stromal cell states underpins pathological tissue niches in Crohn’s disease
AuthorsSimon Koplev; Osheen Sharma; Simon Woelfel; Ni Huang; Mathilde Pohin; Adrian Feile; Maria Warschinke; Mikel Rezola Artero; Sharujan Suthakaran; Ioannis Sarropoulos; J. Patrick Pett; Julia Nyman; Tom Thomas; Duy Pham; Bin Li; Moustafa Attar; Julia Pakpoor; Kate Milosevic-Hutton; Alistair Easton; Matt Butler; James Dunford; Martin Philpott; Mark Coles; Christopher D. Buckley; Calliope Dendrou; Khalid Shamiyah; Lorenz Kretschmer; Lisa Dratva; Fadi Issa; Joanna Hester; Jens Rittscher; Alissa Walsh; Simon P. Travis; Fränze Progatzky; Lukas W. Unger; Mark Bignell; Katherine Baker; Bruce George; Hussein Al-Mossawi; Paul Klenerman; Alexander S. Mosig; Udo Oppermann; Sarah A. Teichmann; Fiona M. Powrie; Matthias Friedrich
Affiliations1. Cambridge Stem Cell Institute, Jeffrey Cheah Biomedical Centre, Cambridge Biomedical Campus, Cambridge, UK; 2. Department of Gene Technology, KTH Royal Institute of Technology, Science for Life Laboratory, Stockholm, Sweden; 3. Translational Gastroenterology and Liver Unit, University of Oxford, Oxford, UK; 4. Wellcome Sanger Institute, Cambridge, UK; 5. ImmunoConcept University of Bordeaux, Immunology and Immunogenetic Unit University Hospital of Bordeaux, Bordeaux, France; 6. Kennedy Institute of Rheumatology, University of Oxford, Oxford, UK; 7. Institute of Biochemistry II, Jena University Hospital, Jena, Germany; 8. Big Data Institute/Li Ka Shing Centre for Health Information and Discovery, University of Oxford, Oxford, UK; 9. NIHR Oxford Biomedical Research Centre Oxford, Oxford, UK; 10. Department of Oncology, University of Oxford, Oxford, UK; 11. UCB Pharma, Slough, UK; 12. Botnar Institute, University of Oxford, Oxford, UK; 13. Oxford Translational Myeloma Centre, Botnar Research Centre, University of Oxford, Oxford, UK; 14. Nuffield Department of Orthopedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK; 15. Nuffield Department of Surgical Sciences, University of Oxford, Oxford, UK; 16. CAMS Oxford Institute, Chinese Academy of Medical Sciences & Peking Union Medical College, University of Oxford, Oxford, UK; 17. Institute of Biomedical Engineering (IBME), Department of Engineering Science, University of Oxford, Oxford, UK; 18. Ludwig Institute for Cancer Research (Oxford Branch), University of Oxford, Oxford, UK; 19. Department of Colorectal Surgery, Oxford University Hospitals, Oxford, UK; 20. Peter Medawar Building, South Parks Rd, University of Oxford, Oxford, UK; 21. Pandemic Sciences Institute, University of Oxford, Oxford, UK
A novel CAF population coordinates hyper-suppressive regulatory T cell recruitment and localization in lung cancer
AuthorsOlivia R. Ringham; Monica Rivera; Lucas F. Loffredo; Melih Arda Ozsoy; Christina M. Healy; Maye F. Cheng; Yinuo Jin; Noah Chen; Kenia de los Santos-Alexis; Elham Azizi; Anjali Saqi; Matthew B. Buechler; Carla P. Concepcion-Crisol; Nicholas Arpaia
Affiliations1. Department of Microbiology & Immunology, Columbia University Irving Medical Center, New York, USA; 2. Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, USA; 3. Department of Immunology, University of Toronto, Toronto, Canada; 4. Department of Biomedical Engineering, Columbia University, New York, USA; 5. Irving Institute for Cancer Dynamics, Columbia University, New York, USA; 6. Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, USA
TIF1γ regulates stability of regulatory T cells during inflammation
AuthorsEugenio Contreras-Castillo; Jesús Daniel Zambrano-Romero; Hober Nelson Núñez-Martínez; Ma. Cleofas Marcial-Medina; Javier Orozco-Cordoba; Diana Ríos-Ramírez; Ofelia Muñoz-Paleta; Diego Pérez-Vázquez; Andrés Felipe Sáenz-Cabezas; María Guadalupe García-Patiño; José Luis Ramos-Balderas; Gustavo Tapia-Urzúa; Luis Tenorio-Hernández; Georgina Guerrero; Nallely Cano-Domínguez; Diego Delgado-Zaldívar; Aurora Candelario-Martínez; Isaac Martínez-Racine; Ileana Licona-Limón; Iris Madera-Salcedo; Florencia Rosetti; José C. Crispín; Lilia G. Noriega; Porfirio Nava; Araceli Pérez-López; José Luis Maravillas-Montero; Félix Recillas-Targa; Victor Julián Valdés; Marina Macías-Silva; Martha Robles-Flores; Mayra Furlan-Magaril; Vesa Kaartinen; Jorge Henao-Mejía; Richard Flavell; Paula Licona-Limón
Affiliations1. Departamento de Biología Celular y del Desarrollo, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, Mexico City, Mexico; 2. Departamento de Genética Molecular, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, Mexico City, Mexico; 3. Departamento de Inmunologia y Reumatologia, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico; 4. Departamento de Fisiología, Biofísica y Neurociencias, CINVESTAV-IPN, Mexico City, Mexico; 5. Departamento de Patología, Facultad de Medicina Veterinaria y Zootecnia, Universidad Nacional Autónoma de México, Mexico City, Mexico; 6. Department of Immunobiology, Yale University, New Haven, USA; 7. Escuela de Medicina y Ciencias de la Salud, Tecnológico de Monterrey, Monterrey, Mexico; 8. Departamento de Fisiología de la Nutrición, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico; 9. Unidad de Investigación en Biomedicina, Facultad de Estudios Superiores-Iztacala, Universidad Nacional Autónoma de México, Mexico City, Mexico; 10. Departamento de Medicina Molecular y Bioprocesos, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Cuernavaca, México; 11. Departamento de Bioquímica, Facultad de Medicina, Universidad Nacional Autónoma de México, Mexico City, Mexico; 12. Department of Biologic and Materials Sciences, University of Michigan School of Dentistry, Ann Arbor, USA; 13. Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, USA; 14. Institute for Immunology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, USA; 15. Division of Protective Immunity, Department of Pathology and Laboratory Medicine, Children’s Hospital of Pennsylvania, University of Pennsylvania, Philadelphia, USA; 16. Howard Hughes Medical Institute, Yale University, New Haven, USA
Loss of cellular RNA homeostasis contributes to MDA5 activation during virus infection
AuthorsNatália G. Sampaio; Tanja Davis; Linden J. Gearing; Antonio G. Dias Junior; Lise Chauveau; Georgie Wray-McCann; Valerie Odon; Vladyslava Liudkovska; Alexandra L. McAllan; Chiara Cursi; Alice Mayer; Madara Ratnadiwakara; Minna-Liisa Änkö; Maciej Cieśla; Paul J. Hertzog; Jan Rehwinkel
Affiliations1. Medical Research Council Translational Immune Discovery Unit, Medical Research Council Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK; 2. Centre for Innate Immunity and Infectious Diseases, Hudson Institute of Medical Research, Clayton, Australia; 3. Department of Molecular and Translational Sciences, School of Clinical Sciences, Monash University, Clayton, Australia; 4. RNA viruses and metabolism team, Institut de Recherche en Infectiologie de Montpellier (IRIM), CNRS, University of Montpellier, Montpellier, France; 5. IMol Polish Academy of Sciences, Warsaw, Poland; 6. Centre for Cancer Research, Hudson Institute of Medical Research, Clayton, Australia; 7. Faculty of Science and Engineering, Åbo Akademi University, Turku, Finland
Tissue-resident immune cells drive genetic risk in autoimmune and lung diseases
AuthorsBenjamin J. Schmiedel; Cristian Gonzalez-Colin; Vicente Fajardo-Rosas; Job Rocha; Hayley Simon; Johannes Ottensmeier; Ignacio E. Ramírez-Bernabé; April Cano; Angel De la Cruz Castillo; Elizabeth Márquez-Gómez; Brendan Ha; Jason A. Greenbaum; Lindsey Chudley; Judith Cave; Aiman Alzetani; Edwin Woo; Michael Shackcloth; Serena J. Chee; Vivek Chandra; Mitchell Kronenberg; Bjoern Peters; Christian H. Ottensmeier; Anusha-Preethi Ganesan; Pandurangan Vijayanand
Affiliations1. La Jolla Institute for Immunology, La Jolla, USA; 2. Bioinformatics and Systems Biology Graduate Program, University of California San Diego, La Jolla, USA; 3. Biological Sciences Graduate Program, University of California San Diego, La Jolla, USA; 4. Genomic Sciences Undergraduate Program, National Autonomous University of Mexico, Cuernavaca, Mexico; 5. Department of Molecular and Clinical Cancer Medicine, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, UK; 6. University Hospital Southampton NHS Foundation Trust, Southampton, UK; 7. NIHR Southampton Biomedical Research Centre, Southampton, UK; 8. Liverpool Heart and Chest Hospital NHS Foundation Trust, Liverpool, UK; 9. Department of Molecular Biology, University of California San Diego, La Jolla, USA; 10. Department of Medicine, University of California San Diego, La Jolla, USA; 11. Clatterbridge Cancer Center NHS Foundation Trust, Liverpool, UK; 12. Department of Pediatrics, Rady Children’s Hospital, University of California San Diego, La Jolla, USA
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