Calreticulin exposure by malignant blasts correlates with robust anticancer immunity and improved clinical outcome in AML patients
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
PubMed
27802968
PubMed Central
PMC5201098
DOI
10.1182/blood-2016-08-731737
PII: S0006-4971(20)33855-6
Knihovny.cz E-zdroje
- MeSH
- akutní myeloidní leukemie farmakoterapie genetika imunologie metabolismus MeSH
- alarminy metabolismus MeSH
- blastická krize imunologie patologie MeSH
- buněčná smrt MeSH
- CD8-pozitivní T-lymfocyty imunologie MeSH
- fenotyp MeSH
- genetická transkripce MeSH
- imunita MeSH
- kalretikulin metabolismus MeSH
- lidé středního věku MeSH
- lidé MeSH
- multivariační analýza MeSH
- proporcionální rizikové modely MeSH
- proteiny tepelného šoku HSP70 metabolismus MeSH
- proteiny tepelného šoku HSP90 metabolismus MeSH
- regulace genové exprese u leukemie MeSH
- stanovení celkové genové exprese MeSH
- Th1 buňky imunologie MeSH
- výsledek terapie MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- alarminy MeSH
- CALR protein, human MeSH Prohlížeč
- kalretikulin MeSH
- proteiny tepelného šoku HSP70 MeSH
- proteiny tepelného šoku HSP90 MeSH
Cancer cell death can be perceived as immunogenic by the host only when malignant cells emit immunostimulatory signals (so-called "damage-associated molecular patterns," DAMPs), as they die in the context of failing adaptive responses to stress. Accumulating preclinical and clinical evidence indicates that the capacity of immunogenic cell death to (re-)activate an anticancer immune response is key to the success of various chemo- and radiotherapeutic regimens. Malignant blasts from patients with acute myeloid leukemia (AML) exposed multiple DAMPs, including calreticulin (CRT), heat-shock protein 70 (HSP70), and HSP90 on their plasma membrane irrespective of treatment. In these patients, high levels of surface-exposed CRT correlated with an increased proportion of natural killer cells and effector memory CD4+ and CD8+ T cells in the periphery. Moreover, CRT exposure on the plasma membrane of malignant blasts positively correlated with the frequency of circulating T cells specific for leukemia-associated antigens, indicating that ecto-CRT favors the initiation of anticancer immunity in patients with AML. Finally, although the levels of ecto-HSP70, ecto-HSP90, and ecto-CRT were all associated with improved relapse-free survival, only CRT exposure significantly correlated with superior overall survival. Thus, CRT exposure represents a novel powerful prognostic biomarker for patients with AML, reflecting the activation of a clinically relevant AML-specific immune response.
Department of Radiation Oncology Weill Cornell Medical College New York NY
Department of Women's and Children's Health Karolinska University Hospital Stockholm Sweden
Gustave Roussy Cancer Campus Villejuif France
INSERM U1138 Centre de Recherche des Cordeliers Paris France
Institute of Hematology and Blood Transfusion Prague Czech Republic; and
Metabolomics and Cell Biology Platforms Gustave Roussy Cancer Campus Villejuif France
Pôle de Biologie Hôpital Européen Georges Pompidou AP HP Paris France
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