Differential expansion of circulating human MDSC subsets in patients with cancer, infection and inflammation

Autor: Ana Godinho-Santos, Monika Kapinska-Mrowiecka, Magdalena Król, Michael Dixon, Karin Loré, Luca Cassetta, Derya Karakoc, Verena Müller, Bartłomiej Taciak, Elisabeth Ersvær, Ida Marie Rundgren, Jochen Utikal, Jeffrey W. Pollard, Kirsten Bruderek, Esther D. Kers-Rebel, Thalia Garcia-Tellez, Gunes Esendagli, Utku Horzum, Mark ter Laan, Benedikt Höing, Kerim Bora Yilmaz, Kim C. M. Santegoets, Stephan Lang, Mirjana Gotic, Lubomir Bodnar, Michaela Müller-Trutwin, Christine Bourgeois, Olympia E. Anastasiou, Oktawia Osiecka, Suncica Bjelica, Joanna Skrzeczynska-Moncznik, Viktor Umansky, Sven Brandau, Juan F. Santibanez, Robert Badura, Ang Lin, Joanna Cichy, Gennadiy Zelinskyy, Emilia Górka, Astrid Olsnes Kittang, Ulf Dittmer, Xiaoying Hu, Ana E. Sousa, Gosse J. Adema
Přispěvatelé: Repositório da Universidade de Lisboa
Rok vydání: 2020
Předmět:
Male
Cancer Research
tumor
Myeloid
Cancer development and immune defence Radboud Institute for Molecular Life Sciences [Radboudumc 2]
Immunology
Medizin
Inflammation
Disease
03 medical and health sciences
0302 clinical medicine
Immune system
Immunophenotyping
head and neck neoplasms
Neoplasms
Immunotherapy Biomarkers
medicine
Immunology and Allergy
Humans
immunoassay
RC254-282
030304 developmental biology
Pharmacology
0303 health sciences
business.industry
Myeloid-Derived Suppressor Cells
Cancer
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
biomarkers
medicine.disease
myeloid-derived suppressor cells
immunity
3. Good health
Reconstructive and regenerative medicine Radboud Institute for Health Sciences [Radboudumc 10]
VDP::Medisinske Fag: 700::Klinisk medisinske fag: 750::Onkologi: 762
Chronic infection
medicine.anatomical_structure
Oncology
030220 oncology & carcinogenesis
Myeloid-derived Suppressor Cell
Molecular Medicine
Female
medicine.symptom
business
cellular
Zdroj: Journal for Immunotherapy of Cancer
Journal for ImmunoTherapy of Cancer, Vol 8, Iss 2 (2020)
Journal for ImmunoTherapy of Cancer (JITC)
e001223
Journal for ImmunoTherapy of Cancer
Journal for Immunotherapy of Cancer, 8, 2
8:e001223
Cassetta, L, Bruderek, K, Skrzeczynska-Moncznik, J, Osiecka, O, Hu, X, Rundgren, I M, Lin, A, Santegoets, K, Horzum, U, Godinho-Santos, A, Zelinskyy, G, Garcia-Tellez, T, Bjelica, S, Taciak, B, Olsnes Kittang, A, Hoing, B, Lang, S, Dixon, M, Muller, V, Utikal, J, Karakoc, D, Bora Yilmaz, K, Gorka, E, Bodnar, L, Anastasiou, O, Bourgeois, C, Badura, R, Kapinska-Mrowiecka, M, Gotic, M, ter Laan, M, Kers-Rebel, E, Krol, M, Francisco Santibanez, J, Muller-Trutwin, M, Dittmer, U, Sousa, A E, Esendagli, G, Adema, G, Lore, K, Ersvaer, E, Umansky, V, Pollard, J W, Cichy, J & Brandau, S 2020, ' Differential expansion of circulating human MDSC subsets in patients with cancer, infection and inflammation ', British Medical Journal (BMJ) . https://doi.org/10.1136/jitc-2020-001223
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Journal for Immunotherapy of Cancer, 8
ISSN: 2051-1426
DOI: 10.1136/jitc-2020-001223
Popis: © Author(s) (or their employer(s)) 2020. Re- use permitted under CC BY- NC. No commercial re- use. See rights and permissions. Published by BMJ.
Background: Myeloid-derived suppressor cells (MDSC) are a functional myeloid cell subset that includes myeloid cells with immune suppressive properties. The presence of MDSC has been reported in the peripheral blood of patients with several malignant and non-malignant diseases. So far, direct comparison of MDSC across different diseases and Centers is hindered by technical pitfalls and a lack of standardized methodology. To overcome this issue, we formed a network through the COST Action Mye-EUNITER (www.mye-euniter.eu) with the goal to standardize and facilitate the comparative analysis of human circulating MDSC in cancer, inflammation and infection. In this manuscript, we present the results of the multicenter study Mye-EUNITER MDSC Monitoring Initiative, that involved 13 laboratories and compared circulating MDSC subsets across multiple diseases, using a common protocol for the isolation, identification and characterization of these cells. Methods: We developed, tested, executed and optimized a standard operating procedure for the isolation and immunophenotyping of MDSC using blood from healthy donors. We applied this procedure to the blood of almost 400 patients and controls with different solid tumors and non-malignant diseases. The latter included viral infections such as HIV and hepatitis B virus, but also psoriasis and cardiovascular disorders. Results: We observed that the frequency of MDSC in healthy donors varied substantially between centers and was influenced by technical aspects such as the anticoagulant and separation method used. Expansion of polymorphonuclear (PMN)-MDSC exceeded the expansion of monocytic MDSC (M-MDSC) in five out of six solid tumors. PMN-MDSC expansion was more pronounced in cancer compared with infection and inflammation. Programmed death-ligand 1 was primarily expressed in M-MDSC and e-MDSC and was not upregulated as a consequence of disease. LOX-1 expression was confined to PMN-MDSC. Conclusions: This study provides improved technical protocols and workflows for the multi-center analysis of circulating human MDSC subsets. Application of these workflows revealed a predominant expansion of PMN-MDSC in solid tumors that exceeds expansion in chronic infection and inflammation.
Lab10: This work was funded by the following grants: PTDC/MED- IMU/30474/2017 – project cofunded by FEDER LISBOA-01–0145- FEDER-030474, through Programa Operacional Regional de Lisboa, do PORTUGAL 2020, and Fundação para a Ciência e a Tecnologia and by Gilead Genesis to AES.
Databáze: OpenAIRE