Lindsey Call

ORCID: 0000-0003-0059-5107
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About
Contact & Profiles
Research Areas
  • CAR-T cell therapy research
  • Immune Cell Function and Interaction
  • Acute Lymphoblastic Leukemia research
  • Immunotherapy and Immune Responses
  • Acute Myeloid Leukemia Research
  • CRISPR and Genetic Engineering
  • RNA Interference and Gene Delivery
  • Venous Thromboembolism Diagnosis and Management
  • Macrophage Migration Inhibitory Factor
  • Virus-based gene therapy research
  • Chronic Myeloid Leukemia Treatments
  • Chronic Lymphocytic Leukemia Research
  • Viral Infectious Diseases and Gene Expression in Insects
  • Renal and related cancers
  • Intracranial Aneurysms: Treatment and Complications
  • Acute Ischemic Stroke Management
  • Ion channel regulation and function

Fred Hutch Cancer Center
2019-2023

University of Colorado Denver
2020

University of Washington
2020

The CBFA2T3-GLIS2 (C/G) fusion is a product of cryptic translocation primarily seen in infants and early childhood associated with dismal outcome. Here, we demonstrate that the expression C/G oncogenic protein promotes transformation human cord blood hematopoietic stem progenitor cells (CB HSPCs) an endothelial cell coculture system recapitulates transcriptome, morphology, immunophenotype acute myeloid leukemia (AML) induces highly aggressive xenograft models. Interrogating transcriptome...

10.1172/jci157101 article EN cc-by Journal of Clinical Investigation 2022-09-22

Background Blunt cerebrovascular injury (BCVI) is associated with increased stroke and mortality risk. However, the most appropriate follow-up strategy remains uncertain. Purpose To better understand natural history of BCVI help define optimal timing length imaging. Materials Methods In this retrospective HIPAA-compliant study, data from all patients treated for at a level I trauma center between April 1, 2005, June 30, 2015, were reviewed. For least one time-to-event analysis was performed...

10.1148/radiol.2020192866 article EN Radiology 2020-09-08

Abstract Purpose: We previously identified mesothelin (MSLN) as highly expressed in a significant fraction of acute myeloid leukemia (AML) but entirely silent normal hematopoiesis, providing promising antigen for immunotherapeutic targeting that avoids hematopoietic toxicity. Given T cells genetically modified to express chimeric receptors (CAR) are effective at eradicating relapsed/refractory lymphocytic leukemia, we developed MSLN-directed CAR preclinical evaluation AML. Experimental...

10.1158/1078-0432.ccr-21-1546 article EN cc-by-nc-nd Clinical Cancer Research 2021-08-11

<div>AbstractPurpose:<p>We previously identified mesothelin (MSLN) as highly expressed in a significant fraction of acute myeloid leukemia (AML) but entirely silent normal hematopoiesis, providing promising antigen for immunotherapeutic targeting that avoids hematopoietic toxicity. Given T cells genetically modified to express chimeric receptors (CAR) are effective at eradicating relapsed/refractory lymphocytic leukemia, we developed MSLN-directed CAR preclinical evaluation...

10.1158/1078-0432.c.7524149 preprint EN 2024-11-04

Abstract Fusion oncoproteins are the initiating event in AML pathogenesis, although they thought to require additional cooperating mutations for leukemic transformation. CBFA2T3-GLIS2 (C/G) fusion occurs exclusively infants and is associated with highly aggressive disease 1-4 . Here we report that lentiviral transduction of C/G sufficient induce malignant transformation human cord blood hematopoietic stem progenitor cells (CB HSPCs) fully recapitulates AML. Engineered CB HSPCs co-cultured...

10.21203/rs.3.rs-757279/v1 preprint EN cc-by Research Square (Research Square) 2021-08-12
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