Heme on innate immunity and inflammation

FF Dutra, MT Bozza - Frontiers in pharmacology, 2014 - frontiersin.org
Heme is an essential molecule expressed ubiquitously all through our tissues. Heme plays
major functions in cellular physiology and metabolism as the prosthetic group of diverse …

[HTML][HTML] Beyond HIV infection: neglected and varied impacts of CCR5 and CCR5Δ32 on viral diseases

JH Ellwanger, B Kulmann-Leal, V de Lima Kaminski… - Virus research, 2020 - Elsevier
The interactions between chemokine receptors and their ligands may affect susceptibility to
infectious diseases as well as their clinical manifestations. These interactions mediate both …

Hemopexin therapy reverts heme-induced proinflammatory phenotypic switching of macrophages in a mouse model of sickle cell disease

F Vinchi, M Costa da Silva, G Ingoglia… - Blood, The Journal …, 2016 - ashpublications.org
Hemolytic diseases, such as sickle cell anemia and thalassemia, are characterized by
enhanced release of hemoglobin and heme into the circulation, heme-iron loading of …

Recipient inflammation affects the frequency and magnitude of immunization to transfused red blood cells

JE Hendrickson, M Desmarets, SS Deshpande… - …, 2006 - Wiley Online Library
BACKGROUND: Most alloantigens on transfused red blood cells (RBCs) are weakly
immunogenic, with only a 2 to 6 percent overall immunization rate even in patients receiving …

Energy expenditure, inflammation, and oxidative stress in steady-state adolescents with sickle cell anemia

SA Akohoue, S Shankar, GL Milne, J Morrow… - Pediatric …, 2007 - nature.com
Sickle cell anemia (HbSS) is characterized by hypermetabolism, chronic inflammation, and
increased oxidative stress, but the relationship between these factors is undefined. In this …

Biologically active CD40 ligand is elevated in sickle cell anemia: potential role for platelet-mediated inflammation

SP Lee, KI Ataga, EP Orringer, DR Phillips… - … , and vascular biology, 2006 - ahajournals.org
Objective—After activation, platelets expose CD40 ligand (CD40L) on their surface, then
subsequently release the inflammatory mediator as a soluble fragment (sCD40L). Because …

[PDF][PDF] Asthma is associated with increased mortality in individuals with sickle cell anemia

JH Boyd, EA Macklin, RC Strunk, MR DeBaun - 2007 - digitalcommons.wustl.edu
An analysis of a prospective cohort of individuals with sickle cell anemia (SCA), enrolled
from birth through adulthood, was conducted to determine if asthma is a risk factor for death …

Infections in thalassemia and hemoglobinopathies: focus on therapy-related complications

BM Ricerca, A Di Girolamo… - Mediterranean journal of …, 2009 - pmc.ncbi.nlm.nih.gov
The clinical approach to thalassemia and hemoglobinopathies, specifically Sickle Cell
Disease (SCD), based on transfusions, iron chelation and bone marrow transplantation has …

Red blood cell alloimmunization in patients with sickle cell disease: correlation with HLA and cytokine gene polymorphisms

EÂ Sippert, JEL Visentainer, HV Alves… - …, 2017 - Wiley Online Library
BACKGROUND The reason for the difference in susceptibility to red blood cell (RBC)
alloimmunization among patients with sickle cell disease (SCD) is not clearly understood …

Heme oxygenase-1 gene promoter polymorphism is associated with reduced incidence of acute chest syndrome among children with sickle cell disease

CJ Bean, SL Boulet, D Ellingsen… - Blood, The Journal …, 2012 - ashpublications.org
Sickle cell disease is a common hemolytic disorder with a broad range of complications,
including vaso-occlusive episodes, acute chest syndrome (ACS), pain, and stroke. Heme …