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Distinct systemic immune networks define severe vs. mild COVID-19 in hematologic and solid cancer patients.
Pignataro-Oshiro, Flávio; Figueiredo, Amanda B; Galdino, Nayane A L; Morais, Katia L P; Dutra, Walderez O; Silva, Bianca Grassi de Miranda; Feriani, Diego; Abrantes, Flávia de Azevedo; Silva, Ivan Leonardo Avelino França E; Filho, Jayr Schmidt; Framil, Juliana Valéria de Souza; Cesca, Marcelle Goldner; Riechelmann, Rachel Simões Pimenta; Batista, Marjorie V; Gollob, Kenneth J.
  • Pignataro-Oshiro F; International Research Center, Translational Immuno-oncology Group, A.C.Camargo Cancer Center, São Paulo, Brazil.
  • Figueiredo AB; International Research Center, Translational Immuno-oncology Group, A.C.Camargo Cancer Center, São Paulo, Brazil.
  • Galdino NAL; International Research Center, Translational Immuno-oncology Group, A.C.Camargo Cancer Center, São Paulo, Brazil.
  • Morais KLP; International Research Center, Translational Immuno-oncology Group, A.C.Camargo Cancer Center, São Paulo, Brazil.
  • Dutra WO; Department of Morphology, Federal University of Minas Gerais, Belo Horizonte, Brazil.
  • Silva BGM; Infectious Diseases Department, A.C.Camargo Cancer Center, Sao Paulo, Brazil.
  • Feriani D; Infectious Diseases Department, A.C.Camargo Cancer Center, Sao Paulo, Brazil.
  • Abrantes FA; Infectious Diseases Department, A.C.Camargo Cancer Center, Sao Paulo, Brazil.
  • Silva ILAFE; Infectious Diseases Department, A.C.Camargo Cancer Center, Sao Paulo, Brazil.
  • Filho JS; Hematology Department, A.C.Camargo Cancer Center, Sao Paulo, Brazil.
  • Framil JVS; Infectious Diseases Department, A.C.Camargo Cancer Center, Sao Paulo, Brazil.
  • Cesca MG; Clinical Oncology Department, A.C.Camargo Cancer Center, Sao Paulo, Brazil.
  • Riechelmann RSP; Clinical Oncology Department, A.C.Camargo Cancer Center, Sao Paulo, Brazil.
  • Batista MV; Infectious Diseases Department, A.C.Camargo Cancer Center, Sao Paulo, Brazil.
  • Gollob KJ; International Research Center, Translational Immuno-oncology Group, A.C.Camargo Cancer Center, São Paulo, Brazil.
Front Immunol ; 13: 1052104, 2022.
Article in English | MEDLINE | ID: covidwho-2276492
ABSTRACT

Introduction:

The COVID-19 pandemic, caused by the coronavirus SARS-CoV-2, has impacted health across all sectors of society. A cytokine-release syndrome, combined with an inefficient response of innate immune cells to directly combat the virus, characterizes the severe form of COVID-19. While immune factors involved in the development of severe COVID-19 in the general population are becoming clearer, identification of the immune mechanisms behind severe disease in oncologic patients remains uncertain.

Methods:

Here we evaluated the systemic immune response through the analysis of soluble blood immune factors and anti-SARS-CoV-2 antibodies within the early days of a positive SARS-CoV-2 diagnostic in oncologic patients.

Results:

Individuals with hematologic malignancies that went on to die from COVID-19 displayed at diagnosis severe leukopenia, low antibody production against SARS-CoV-2 proteins, and elevated production of innate immune cell recruitment and activation factors. These patients also displayed correlation networks in which IL-2, IL-13, TNF-alpha, IFN-gamma, and FGF2 were the focal points. Hematologic cancer patients that showed highly networked and coordinated anti-SARS-CoV-2 antibody production, with central importance of IL-4, IL-5, IL-12A, IL-15, and IL-17A, presented only mild COVID-19. Conversely, solid tumor patients that had elevated levels of inflammatory cytokines IL-6, CXCL8, and lost the coordinate production of anti-virus antibodies developed severe COVID-19 and died. Patients that displayed positive correlation networks between anti-virus antibodies, and a regulatory axis involving IL-10 and inflammatory cytokines recovered from the disease. We also provided evidence that CXCL8 is a strong predictor of death for oncologic patients and could be an indicator of poor prognosis within days of the positive diagnostic of SARS-CoV-2 infection.

Conclusion:

Our findings defined distinct systemic immune profiles associated with COVID-19 clinical outcome of patients with cancer and COVID-19. These systemic immune networks shed light on potential immune mechanisms involved in disease outcome, as well as identify potential clinically useful biomarkers.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Neoplasms Type of study: Experimental Studies / Prognostic study Topics: Long Covid Limits: Humans Language: English Journal: Front Immunol Year: 2022 Document Type: Article Affiliation country: Fimmu.2022.1052104

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Neoplasms Type of study: Experimental Studies / Prognostic study Topics: Long Covid Limits: Humans Language: English Journal: Front Immunol Year: 2022 Document Type: Article Affiliation country: Fimmu.2022.1052104