The Balance of Interferon-γ and Interleukin-10 during Influenza A Virus Infection Complicated by Methicillin-Resistant Staphylococcus aureus Superinfection

dc.contributor.advisorSun, Keer (kesun@utmb.edu)
dc.contributor.committeeMemberChopra, Ashok (achopra@utmb.edu)
dc.contributor.committeeMemberHuber, Victor (Victor.Huber@usd.edu)
dc.contributor.committeeMemberSoong, Lynn (Lysoong@utmb.edu)
dc.contributor.committeeMemberWalker, David (dwalker@utmb.edu)
dc.creatorMcKelvey, Michael Daniel 1997-
dc.creator.orcid0000-0002-5334-4005
dc.date.accessioned2024-09-04T18:01:21Z
dc.date.available2024-09-04T18:01:21Z
dc.date.created2024-12
dc.date.issued2024-12
dc.date.submittedDecember 2024
dc.date.updated2024-09-04T18:01:23Z
dc.description.abstractImmune activation is necessary to mount a protective immune response against viral and bacterial infections, but an overzealous response can lead to the development of acute respiratory distress syndrome (ARDS). ARDS is a highly lethal inflammatory lung injury that is associated with dysregulated cytokine production and decreased lung compliance. No specific treatment exists for ARDS due to the limited understanding of its pathogenesis. We have developed an influenza A virus (IAV) and methicillin-resistant Staphylococcus aureus (MRSA) superinfection model with antibiotic therapy that resembles severe secondary bacterial pneumonia in patients that often progresses to ARDS. Despite antibiotic therapy, mice still succumb to superinfection-induced inflammatory lung damage. Using single-cell RNA sequencing, we reveal significant transcriptome alterations prompted by interferon (IFN)-γ. Transgenic mouse studies demonstrate that IFN-γ receptor (IFN-γR) signaling in mononuclear phagocytes induces tumor necrosis factor (TNF)-α hyperproduction and lethal inflammatory lung damage, with no detectable benefit to viral or bacterial clearance. In contrast, we show that interleukin (IL)-10 is crucial to counteract the lethal IFN-γ-induced cytokine storm and preserve lung function. Transgenic mice with ablation of the IL-10 receptor α gene in mononuclear phagocytes have significantly higher levels of IFN-γ and TNF-α, and a higher mortality rate. This reveals the importance of mononuclear phagocytes in shifting the balance between immunopathology and protective immunity. By omitting antibiotic therapy from the superinfection model, we show that IL-10 also impairs bacterial clearance, specifically when the IL-10Rα gene is ablated in interferon-I-responsive monocytes. Collectively, this body of evidence demonstrates the dominant role played by hypercytokinemia and acute lung damage during post-influenza bacterial pneumonia and the balance of IFN-γ and IL-10 that shifts the balance between immunopathogenesis and bacterial outgrowth.
dc.format.mimetypeapplication/pdf
dc.identifier.uri
dc.identifier.urihttps://hdl.handle.net/2152.3/12476
dc.language.isoEnglish
dc.subject.otherInfluenza
dc.subject.otherStaphylococcus aureus
dc.subject.otherCo-infection
dc.subject.otherSuperinfection
dc.subject.otherRespiratory infection
dc.subject.otherAcute lung injury
dc.subject.otherAcute respiratory distress syndrome
dc.subject.otherInterleukin-10
dc.subject.otherInterferon-gamma
dc.titleThe Balance of Interferon-γ and Interleukin-10 during Influenza A Virus Infection Complicated by Methicillin-Resistant Staphylococcus aureus Superinfection
dc.typeThesis
dc.type.materialtext
thesis.degree.collegeUTMB Graduate School of Biomedical Sciences
thesis.degree.departmentExperimental Pathology
thesis.degree.grantorThe University of Texas Medical Branch at Galveston
thesis.degree.nameExperimental Pathology (Doctoral)
thesis.degree.schoolUniversity of Texas Medical Branch

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