The Peripheral T-Cell Lymphomas. Группа авторов

The Peripheral T-Cell Lymphomas - Группа авторов


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Birmingham, UK

      Francesca Montanari Center for Lymphoid Malignancies, Columbia University Medical Center, New York, NY, USA

      Katharine B. Moosic Department of Medicine and Department of Pathology, Division of Hematology and Oncology, University of Virginia Cancer Center, Charlottesville, VA, USA

      Franck Morschhauser Department of Hematology, Lille University Hospital, Lille, France

      Wataru Munakata Department of Hematology, National Cancer Center Hospital, Tokyo, Japan

      Owen A. O’Connor Department of Medicine, Division of Hematology and Oncology, University of Virginia Cancer Center, Charlottesville, VA, USA, and Program for T‐Cell Lymphoma Research, Department of Microbiology, Immunology and Cancer Research University of Virginia Cancer Center, Charlottesville, VA, USA

      Kristine C. Olson Department of Medicine, Division of Hematology and Oncology, University of Virginia Cancer Center, Charlottesville, VA, USA

      Juan Alejandro Ospina‐Idárraga Los Cobos Medical Center, Instituto Nacional de Cancerología, Universidad El Bosque, Bogotá, Colombia

      Neval Ozkaya Hematopathology Section, Laboratory of Pathology, Center for Cancer Research, NCI, Bethesda, MD, USA

      Pier Paolo Piccaluga Department of Experimental, Diagnostic, and Specialty Medicine, Bologna University School of Medicine, Bologna, Italy

      Stefano A. Pileri Hematopathology Division, European Institute of Oncology, IRCCS, Milan, Italy

      H. Miles Prince Epworth Healthcare and Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, Victoria, Australia

      Barbara Pro Division of Hematology and Oncology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA, and Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL, USA

      Dejan Radjeski Sir Charles Gardner Hospital, Perth, Western Australia, Australia

      Bethanie Rooke Department of Dermatology, University Hospital, Birmingham, UK

      Tatsuhiro Sakamoto Department of Hematology, Faculty of Medicine, University of Tsukuba Hospital, Tsukuba, Japan, and Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba, Japan

      Ahmed Sawas Center for Lymphoid Malignancies, Columbia University Medical Center, New York, NY, USA

      Julia Scarisbrick Department of Dermatology, University Hospital, Birmingham, UK

      Luigi Scotto Center for Lymphoid Malignancies, Columbia University Medical Center, New York, NY, USA

      Jennifer Shingleton Duke Cancer Institute, Center for Genomic and Computational Biology, Duke University, Durham, NC, USA

      Raksha Shrestha Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba, Japan

      Andrei Shustov Division of Hematology, Department of Medicine, University of Washington, Seattle, WA, USA; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA; and Seattle Cancer Care Alliance, Seattle, WA, USA

      Tetiana Skrypets Department of Surgical, Medical and Dental Sciences Related to Transplant, Oncology and Regenerative Medicine, University of Modena and Reggio Emilia, Reggio Emilia, Italy

      Craig R. Soderquist Division of Hematopathology, Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY, USA

      Robert N. Stuver Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA, USA

      Ritsuro Suzuki Department of Oncology and Hematology, Shimane University Hospital, Izumo, Japan

      Kensei Tobinai Department of Hematology, National Cancer Center Hospital, Tokyo, Japan

      Claudio Tripodo Tumor Immunology Unit, Department of Health Sciences, University of Palermo, Palermo, Italy, and Histopathology Unit, FIRC Institute of Molecular Oncology, Milan, Italy

      Lorenz Truempe Department of Hematology and Medical Oncology, University Medical Center Goettingen, Goettingen, Germany

      Sean Whittaker Guy’s and St Thomas’ National Health Service Foundation Trust, London, UK

      Mina Xu Department Pathology, Yale University School of Medicine, New Haven, CT, USA

      Amulya Yellala Division of Oncology‐Hematology, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE, USA

      Anas Younes Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA

      Jasmine Zain Department of Hematology/Hematopoietic Cell Transplantation, City of Hope Medical Center, Duarte, CA, USA

      Pier Luigi Zinzani IRCCS Azienda Ospedaliero‐Universitaria di Bologna Istituto di Ematologia “Seràgnoli”, Dipartimento di Medicina Specialistica, Diagnostica e Sperimentale Università degli Studi, Bologna, Italia

      Don’t forget to visit the companion web site for this book:

      www.wiley.com/go/OConnor/Peripheral_T‐cell_Lymphomas images

      There you will find valuable materials, including:

       Figures and Tables from within the book

      Scan this QR code to visit the companion website:

images
Part I Biological Basis of the Peripheral T‐cell Lymphomas

       Claudio Tripodo1,2 and Stefano A. Pileri3

       1 Tumor Immunology Unit, Department of Health Sciences, University of Palermo, Palermo, Italy

       2 Histopathology Unit, FIRC Institute of Molecular Oncology, Milan, Italy

       3 Hematopathology Division, European Institute of Oncology, IRCCS, Milan, Italy

      TAKE HOME MESSAGES

       The natural diversity of T cells in normal immune system functions contributes – in part – to the diversity of T‐cell malignancies.

       CD4‐positive T lymphocytes, also called T helper (Th) cells, are divided into a diverse repertoire of T lymphocytes (e.g. Th1, Th2, and Th17), in part defined by the cytokine profile they elaborate.

       Th1 and Th2 lymphocytes can also be classified based on the expression of the transcription factors T‐bet and GATA3. These factors can be prognostic in peripheral T‐cell non‐Hodgkin lymphomas derived from these cells (with GATA3 being associated with a poor prognosis).


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