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https://hdl.handle.net/20.500.13003/20253 Circulating TNF-RII, IP-10 and HGF are associated with severity of COVID-19 in oncologic patients
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eISSN: 1096-0023
WOS ID: 001186375600001
Scopus EID: 2-s2.0-85185338942
PMID: 38364458
Embase PUI: L2030456714
Authors
Carrillo-García, Jaime
Lacerenza, Serena
Hindi, Nadia
Moura, David S
Marquina, Gloria
Parra Corral, Daniel
Olalla, Jennifer
María Cano Cano, Juana
Hoyos, Sergio
Renshaw, Marta
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Date of defense
Publication date
2024-05
Document type
research article
Citation
Carrillo-García J, Lacerenza S, Hindi N, Moura DS, Marquina G, Parra Corral D, et al. Circulating TNF-RII, IP-10 and HGF are associated with severity of COVID-19 in oncologic patients. Cytokine. 2024 Feb 15;177:156542.
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Abstract
The COVID-19 patients showed hyperinflammatory response depending on the severity of the disease but little have been reported about this response in oncologic patients that also were infected with the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Sixty-five circulating cytokines/chemokines were quantified in 15 oncologic patients, just after SARS-CoV-2 infection and fourteen days later, and their levels were compared in patients who required hospitalisation by COVID-19 versus non-hospitalised patients. A higher median age of 72 years (range 61-83) in oncologic patients after SARS-CoV-2 infection was associated with hospitalisation requirement by COVID-19 versus a median age of 49 years (20-75) observed in the non-hospitalised oncologic patients (p = 0.008). Moreover, oncologic patients at metastatic stage or with lung cancer were significantly associated with hospitalisation by COVID-19 (p = 0.044). None of these hospitalised patients required ICU treatment. Higher basal levels of tumour necrosis factor receptor II (TNF-RII), interferon-γ (IFNγ)-induced protein 10 (IP-10) and hepatocyte growth factor (HGF) in plasma were significantly observed in oncologic patients who required hospitalisation by COVID-19. Higher TNF-RII, IP-10 and HGF levels after the SARS-CoV-2 infection in oncologic patients could be used as biomarkers of COVID-19 severity associated with hospitalisation requirements.
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Keywords
MeSH
Aged
Aged, 80 and over
COVID-19* / diagnosis
COVID-19* / metabolism
Chemokine CXCL10 / blood
Chemokine CXCL10 / chemistry
Hepatocyte Growth Factor / blood
Hepatocyte Growth Factor / chemistry
Humans
Middle Aged
Neoplasms* / metabolism
Receptors, Tumor Necrosis Factor, Type II / blood
Receptors, Tumor Necrosis Factor, Type II / chemistry
SARS-CoV-2
Aged, 80 and over
COVID-19* / diagnosis
COVID-19* / metabolism
Chemokine CXCL10 / blood
Chemokine CXCL10 / chemistry
Hepatocyte Growth Factor / blood
Hepatocyte Growth Factor / chemistry
Humans
Middle Aged
Neoplasms* / metabolism
Receptors, Tumor Necrosis Factor, Type II / blood
Receptors, Tumor Necrosis Factor, Type II / chemistry
SARS-CoV-2
DeCS
Anciano
Humanos
Persona de Mediana Edad
SARS-CoV-2
Humanos
Persona de Mediana Edad
SARS-CoV-2







