Issue Archive
Table of Contents
INSIDE BLOOD
BLOOD WORK
PERSPECTIVES
CLINICAL TRIALS AND OBSERVATIONS
Increasing levels of free thyroxine as a risk factor for a first venous thrombosis: a case-control study
Clinical Trials & Observations
GENE THERAPY
HEMATOPOIESIS AND STEM CELLS
IMMUNOBIOLOGY
Increasing the efficacy of CD20 antibody therapy through the engineering of a new type II anti-CD20 antibody with enhanced direct and immune effector cell–mediated B-cell cytotoxicity
The post sepsis-induced expansion and enhanced function of regulatory T cells create an environment to potentiate tumor growth
LYMPHOID NEOPLASIA
High expression of AID and active class switch recombination might account for a more aggressive disease in unmutated CLL patients: link with an activated microenvironment in CLL disease
MYELOID NEOPLASIA
Pim2 cooperates with PML-RARα to induce acute myeloid leukemia in a bone marrow transplantation model
The JAK2 46/1 haplotype predisposes to MPL-mutated myeloproliferative neoplasms
Use of chromosome engineering to model a segmental deletion of chromosome band 7q22 found in myeloid malignancies
PHAGOCYTES, GRANULOCYTES, AND MYELOPOIESIS
PLATELETS AND THROMBOPOIESIS
RED CELLS, IRON, AND ERYTHROPOIESIS
CpG-ODN 2006 and human parvovirus B19 genome consensus sequences selectively inhibit growth and development of erythroid progenitor cells
THROMBOSIS AND HEMOSTASIS
TRANSFUSION MEDICINE
TRANSPLANTATION
Novel pharmacokinetic behavior of intravenous busulfan in children with thalassemia undergoing hematopoietic stem cell transplantation: a prospective evaluation of pharmacokinetic and pharmacodynamic profile with therapeutic drug monitoring
VASCULAR BIOLOGY
Endothelial cell–specific chemotaxis receptor (ecscr) promotes angioblast migration during vasculogenesis and enhances VEGF receptor sensitivity
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Cover Image
Cover Image
Composite confocal overlay series of images demonstrating that type I CD20
antibody rituximab binds differently to lymphoma cells as compared with the type II CD20 antibody GA101. Each pair of images shows a Ramos cell exposed to GA101 (left) and rituximab (right), along with a lipid raft marker. The green panels show the distribution of lipid rafts (labeled with CTB-Alexa 488 cholera toxin subunit B, which binds to the membrane ganglioside GMI in lipid rafts) and the red panels the distribution of the CD20 antibodies (labeled with Cy3), and the bottom panels in each set show the overlay of the green and red images. The overlays confirm that the binding of the type I antibody rituximab to CD20 results in accumulation of CD20 clusters in lipid rafts as shown by colocalization with CTB-Alexa 488 (yellow fluorescence), whereas CD20 molecules do not redistribute to lipid rafts upon binding of the type II CD20 antibody GA101 and do not colocalize with CTB-Alexa 488. To illustrate the different localizations of rituximab and GA101, 3 different image-processing algorithms from Jasc Paint Shop Pro (Version 9.01) were applied to the original confocal pictures shown on the top left (Figure 2C, Mössner et al on page 4397) and are shown on the top right, and bottom left and right. This composite cover was prepared by Christian Klein with help from Claudia Kirstenpfad. See the article by Mössner et al on page 4393. - PDF Icon PDF LinkFront Matter
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