Benign Hematology and Transfusion Medicine
The Section of Benign Hematology (Department of Medicine, Division of Hematology/Oncology) has 9 clinical Faculty members active in clinical and basic/translational research. This group represents one of the largest benign hematology programs in the U.S.
Areas of research excellence include hemophilia and bleeding disorders (Drs. Ragni, Seaman, and Machin), whose clinical and research activities are housed in the state-of-the-art Hemophilia Center of Western Pennsylvania (HCWP), which is funded by a 340B program. Another area of excellence is sickle cell disease (Drs. Novelli and De Castro). The UPMC Adult Sickle Cell Program is funded by the Pennsylvania Department of Health. In addition, blood banking and transfusion medicine benefit from a close collaboration between the Department of Pathology (Dr. Triulzi), and the Section of Benign Hematology (Dr. Kiss).
Areas of research focus in hemophilia and bleeding disorders include novel therapies and bleeding prophylaxis in bleeding disorders, gene therapy in hemophilia, inhibitor formation, bleeding disorders in women, and aging and biomarkers in von Willebrand disease.
Areas of research focus in sickle cell disease include neurocognitive dysfunction, new biomarker development, and designing and testing evidence-based mHealth tools for improving stress and pain management.
Areas of research focus in general hematology include clinical trials in thrombotic microangiopathies/thrombotic thrombocytopenic purpura (TTP) and autoimmune hemolytic anemias.
Areas of research focus in transfusion medicine include red cell storage, platelet transfusions, transfusion related acute lung injury (TRALI), transfusion associated circulatory overload (TACO), leukoreduction, and transfusion support of stem cell and solid organ transplant recipients.
Benign Hematology Clinical and Research Faculty and Programs
Vascular Biology, Platelets, and Hemostasis
Franklin Bontempo, MD
Clinical and Laboratory Hemostasis and Thrombosis
Mark Gladwin, MD
Donor genetic variations can affect hemolytic propensity and RBC storage recovery and function
Matthew Neal, MD
Hemostasis, Inflammation, Thrombosis, Trauma, and Transfusion Surgical Outcomes (HIT3S) Research Group
Margaret Ragni, MD, MPH
Novel therapies for hemophilia and Von Willebrand Disease (VWD)
Sruti Shiva, PhD
Mitochondria, Platelets, and Heme
Red Cells, Iron, and Hematopoiesis
Grant Bullock, MD, PhD
Aconitase: an iron-sensing regulator of mitochondrial oxidative metabolism and erythropoiesis
Paola Corti, PhD
Investigating the function of zebrafish globins in development and heart generation
Joseph Kiss, MD
Impact of Iron Status and Anemia in Blood Donors… Does it Matter for RBC Transfusion Therapy
Adam Straub, PhD
Mechanisms of heme redox regulation
Darrell Triulzi, MD
Anti-fibrinolytic Agents in the Management of Thrombocytopenia
Vitalant
Yvette Yien, PhD
Sickle Cell Disease
Laura De Castro, MD, MHSc
Translation from Biology to Clinical Trials in Sickle Cell Disease
Cheryl Hillery, MD
HMGB1 and TLR4 in Sickle Cell Disease
Charles Jonassaint, PhD
Using Mobile Technology to Bridge Gaps in Sickle Cell Disease Care
Enrico Novelli, MD, MS
Novel Biomarkers in Sickle Cell Anemia
Solomon Ofori-Acquah, PhD
Extracellular heme: a prototypical erythroid DAMP molecule and effector pathogen of sickle crisis
Tirthadipa Pradhan-Sundd, PhD
Hepatic complications in Sickle Cell Disease
Prithu Sundd, PhD
Role of platelet TLR4, NLRP3-inflammasome and extracellular vesicles in sickle cell disease
Yingze Zhang, PhD
Genetic Control of Thrombospondin Transcription and Vasculopathy in Sickle Cell Disease
Phagocytes, Granulocytes, and Myelopoiesis
Partha Dutta, PhD
Hematopoiesis in Cardiovascular Disease
Janet S. Lee, MD, MS
Translation from Biology to Clinical Trials in Sickle Cell Disease
Immunobiology
Lisa Borghesi, PhD
Role of Toll-like receptors in hematopoiesis