Issue Archive
Table of Contents
Inside Blood
The newest member of the VEGF family
In this issue of Blood, Singh et al establish the existence of a new soluble isoform of vascular endothelial growth factor receptor 3 (sVEGFR-3), which is synthesized and secreted by corneal epithelial cells; they show that sVEGFR-3 modulates lymphangiogenesis by impounding vascular endothelial growth factor (VEGF) C and rendering it unable to activate its cognate receptors, thereby maintaining the natural alymphatic disposition of the cornea (see figure).1
Jump-starting the T cells in CLL
In this issue of Blood, Shanafelt and colleagues demonstrate that T-cell immune synapse function can be increased in chronic lymphocytic leukemia (CLL), both by reducing tumor burden with immunochemotherapy and by lenalidomide.1
Gimme a brake: HPK1 regulates LFA-1 and neutrophil traction
In this issue of Blood, Jakob et al report that hematopoietic progenitor kinase 1 (HPK1) participates during signaling of neutrophil recruitment by acting as a regulator of the adhesiveness of the β2-integrin lymphocyte function-associated antigen 1 (LFA-1) during acute inflammation.1
SHPing in different directions in platelet production
In this issue of Blood, Mazharian and colleagues characterize Shp1 and Shp2 conditional knockout (KO) murine models, underscoring the role of these phosphatases not only on platelet function but also on megakaryocyte development and platelet counts and size.1
Blood Work
Plenary Paper
MYC/BCL2 protein coexpression contributes to the inferior survival of activated B-cell subtype of diffuse large B-cell lymphoma and demonstrates high-risk gene expression signatures: a report from The International DLBCL Rituximab-CHOP Consortium Program
CME
Blood Spotlight
Review Article
Clinical Trials and Observations
Intensity of factor VIII treatment and inhibitor development in children with severe hemophilia A: the RODIN study
Clinical Trials & Observations
MRD-directed risk stratification treatment may improve outcomes of t(8;21) AML in the first complete remission: results from the AML05 multicenter trial
Clinical Trials & Observations
Hematopoiesis and Stem Cells
Immunobiology
Naive B-cell trafficking is shaped by local chemokine availability and LFA-1–independent stromal interactions
Lymphoid Neoplasia
MAPK pathway activation leads to Bim loss and histone deacetylase inhibitor resistance: rationale to combine romidepsin with an MEK inhibitor
CD44 regulates the apoptotic response and promotes disease development in chronic lymphocytic leukemia
Long-term repair of T-cell synapse activity in a phase II trial of chemoimmunotherapy followed by lenalidomide consolidation in previously untreated chronic lymphocytic leukemia (CLL)
Brief Report
Myeloid Neoplasia
The shortest isoform of C/EBPβ, liver inhibitory protein (LIP), collaborates with Evi1 to induce AML in a mouse BMT model
Impact of isolated germline JAK2V617I mutation on human hematopoiesis
Prognostic impact and targeting of CRM1 in acute myeloid leukemia
Genomic instability may originate from imatinib-refractory chronic myeloid leukemia stem cells
Phagocytes, Granulocytes, and Myelopoiesis
Platelets and Thrombopoiesis
Thrombosis and Hemostasis
Transplantation
Host-derived CD8+ dendritic cells are required for induction of optimal graft-versus-tumor responses after experimental allogeneic bone marrow transplantation
Vascular Biology
Continuing Medical Education (CME) Questions
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Cover Image
Cover Image
Degradation-resistant HOXB4 protein augments the expansion of burst-forming erythroid (BFU-E) cells. Shown is a BFU-E colony derived from G-CSF-mobilized CD34+ cells following the administration of degradation-resistant recombinant HOXB4 protein and quantified using a colony-forming cell assay. Prolonging the half-life of transduced HOXB4 protein preferentially increases the size and number of BFU-E colonies compared with wild-type HOXB4 protein, indicating that attenuation of HOXB4 destruction by the CUL4 ubiquitin ligase helps maintain G-CSF-mobilized CD34+ cells in a primitive state. See the article by Lee et al on page 4082.
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