Issue Archive
Table of Contents
INSIDE BLOOD COMMENTARIES
Mitochondria on the move: BMSCs fuel AML energy
In this issue of Blood, Marlein et al1 identify a tumor-specific NOX2-dependent transfer of mitochondria from bone marrow stromal cells (BMSCs) to acute myeloid leukemia (AML) cells via AML-derived tunneling nanotubes (see figure), supporting inhibition of NOX2 as a novel therapeutic strategy in AML.
Maestro tissue factor reaches new hEIGHT
In this issue of Blood, Kamikubo et al broaden the already diverse tissue factor (TF) repertoire to include activation of anti–hemophilia A clotting factor VIII (FVIII), which amplifies coagulation initiation.1
REVIEW ARTICLE
CLINICAL TRIALS AND OBSERVATIONS
Phase 1 study of the anti-CD22 immunotoxin moxetumomab pasudotox for childhood acute lymphoblastic leukemia
Clinical Trials & Observations
IMMUNOBIOLOGY AND IMMUNOTHERAPY
HDAC6 inhibition upregulates CD20 levels and increases the efficacy of anti-CD20 monoclonal antibodies
LYMPHOID NEOPLASIA
Neutral tumor evolution in myeloma is associated with poor prognosis
Brief Report
Genomic analysis of hairy cell leukemia identifies novel recurrent genetic alterations
Brief Report
MYELOID NEOPLASIA
THROMBOSIS AND HEMOSTASIS
Selective factor VIII activation by the tissue factor–factor VIIa–factor Xa complex
Publisher's Note: There is an Inside Blood Commentary on this article in this issue.
LETTERS TO BLOOD
Pregnancy outcomes in inherited bone marrow failure syndromes
A multi-institutional outcomes analysis of patients with relapsed or refractory DLBCL treated with ibrutinib
BLOOD WORK
ERRATA
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Cover Image
Cover Image
Mitochondrial transfer from bone marrow stromal cells to acute myeloid leukemia (AML) blasts is driven by NOX2-derived superoxide. The cover image shows a tunneling nanotube formed by the AML blast (orange) and mitochondria (green) from bone marrow stromal cells in the tunneling nanotube. See the article by Marlein et al on page 1649.
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