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  1. Article ; Online: Stem Cell Factor Neutralization Protects From Severe Anaphylaxis in a Murine Model of Food Allergy.

    Ptaschinski, Catherine / Rasky, Andrew J / Fonseca, Wendy / Lukacs, Nicholas W

    Frontiers in immunology

    2021  Volume 12, Page(s) 604192

    Abstract: Food allergy is a growing public health problem with ~15 million people affected in the United States. In allergic food disease, IgE on mast cells bind to ingested antigens leading to the activation and degranulation of mast cells. Stem cell factor (SCF) ...

    Abstract Food allergy is a growing public health problem with ~15 million people affected in the United States. In allergic food disease, IgE on mast cells bind to ingested antigens leading to the activation and degranulation of mast cells. Stem cell factor (SCF) is mast cell growth and activation factor that is required for peripheral tissue mast cells. We targeted a specific isoform of SCF, the larger 248 amino acid form, that drives peripheral tissue mast cell differentiation using a specific monoclonal antibody in a model of food allergy. Ovalbumin sensitized and intragastrically challenged mice were monitored for symptoms of anaphylaxis including respiratory distress, diarrhea, and a reduction in body temperature. During the second week of challenges, allergic mice were injected with an antibody to block SCF248 or given IgG control. Mice treated with α-SCF248 had a decreased incidence of diarrhea and no reduction in body temperature suggesting a reduction in anaphylaxis compared to IgG control treated animals. Re-stimulated mesenteric lymph nodes indicated that α-SCF248 treated mice had decreased OVA-specific Th2 cytokine production compared to IgG control treated allergic animals. The reduction of food induced anaphylaxis was accompanied by a significant reduction in gut leak. The mesenteric lymph node cells were analyzed by flow cytometry and showed a decrease in the number of type 2 innate lymphoid cells in mice injected with α-SCF248. Morphometric enumeration of esterase+ mast cells demonstrated a significant reduction throughout the small intestine. Using a more chronic model of persistent food-induced anaphylaxis, short term therapeutic treatment with α-SCF248 during established disease effectively blocked food induced anaphylaxis. Together, these data suggest that therapeutically blocking SCF248 in food allergic animals can reduce the severity of food allergy by reducing mast cell mediated disease activation.
    MeSH term(s) Allergens/immunology ; Anaphylaxis/diagnosis ; Anaphylaxis/drug therapy ; Anaphylaxis/immunology ; Anaphylaxis/prevention & control ; Animals ; Antibodies, Monoclonal/pharmacokinetics ; Antibodies, Monoclonal/therapeutic use ; Antibodies, Neutralizing/pharmacology ; Antibodies, Neutralizing/therapeutic use ; Biomarkers ; Biopsy ; Chemokine CCL2/metabolism ; Disease Models, Animal ; Female ; Food Hypersensitivity/diagnosis ; Food Hypersensitivity/drug therapy ; Food Hypersensitivity/immunology ; Immunoglobulin E/immunology ; Immunophenotyping ; Intestinal Mucosa/immunology ; Intestinal Mucosa/metabolism ; Mast Cells/drug effects ; Mast Cells/immunology ; Mast Cells/metabolism ; Mice ; Stem Cell Factor/antagonists & inhibitors ; Th2 Cells/immunology ; Th2 Cells/metabolism
    Chemical Substances Allergens ; Antibodies, Monoclonal ; Antibodies, Neutralizing ; Biomarkers ; Chemokine CCL2 ; Stem Cell Factor ; Immunoglobulin E (37341-29-0)
    Language English
    Publishing date 2021-03-09
    Publishing country Switzerland
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2606827-8
    ISSN 1664-3224 ; 1664-3224
    ISSN (online) 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2021.604192
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Early-life pulmonary viral infection leads to long-term functional and lower airway structural changes in the lungs.

    Malinczak, Carrie-Anne / Fonseca, Wendy / Hrycaj, Steven M / Morris, Susan B / Rasky, Andrew J / Yagi, Kazuma / Wellik, Deneen M / Ziegler, Steven F / Zemans, Rachel L / Lukacs, Nicholas W

    American journal of physiology. Lung cellular and molecular physiology

    2024  Volume 326, Issue 3, Page(s) L280–L291

    Abstract: Early-life respiratory virus infections have been correlated with enhanced development of childhood asthma. In particular, significant numbers of respiratory syncytial virus (RSV)-hospitalized infants go on to develop lung disease. It has been suggested ... ...

    Abstract Early-life respiratory virus infections have been correlated with enhanced development of childhood asthma. In particular, significant numbers of respiratory syncytial virus (RSV)-hospitalized infants go on to develop lung disease. It has been suggested that early-life viral infections may lead to altered lung development or repair that negatively impacts lung function later in life. Our data demonstrate that early-life RSV infection modifies lung structure, leading to decreased lung function. At 5 wk postneonatal RSV infection, significant defects are observed in baseline pulmonary function test (PFT) parameters consistent with decreased lung function as well as enlarged alveolar spaces. Lung function changes in the early-life RSV-infected group continue at 3 mo of age. The altered PFT and structural changes induced by early-life RSV were mitigated in
    MeSH term(s) Humans ; Infant ; Animals ; Mice ; Respiratory Syncytial Virus Infections ; Lung/pathology ; Pneumonia/complications ; Lung Diseases/complications ; Respiratory Syncytial Virus, Human ; Mice, Inbred BALB C
    Language English
    Publishing date 2024-01-30
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1013184-x
    ISSN 1522-1504 ; 1040-0605
    ISSN (online) 1522-1504
    ISSN 1040-0605
    DOI 10.1152/ajplung.00300.2023
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: A steroid-resistant cockroach allergen model is associated with lung and cecal microbiome changes.

    Asai, Nobuhiro / Ethridge, Alexander D / Fonseca, Wendy / Yagi, Kazuma / Rasky, Andrew J / Morris, Susan B / Falkowski, Nicole R / Huang, Yvonne J / Huffnagle, Gary B / Lukacs, Nicholas W

    Physiological reports

    2023  Volume 11, Issue 13, Page(s) e15761

    Abstract: The pathogenesis of asthma has been partially linked to lung and gut microbiome. We utilized a steroid-resistant chronic model of cockroach antigen-induced (CRA) asthma with corticosteroid (fluticasone) treatment to examine lung and gut microbiome during ...

    Abstract The pathogenesis of asthma has been partially linked to lung and gut microbiome. We utilized a steroid-resistant chronic model of cockroach antigen-induced (CRA) asthma with corticosteroid (fluticasone) treatment to examine lung and gut microbiome during disease. The pathophysiology assessment demonstrated that mucus and airway hyperresponsiveness were increased in the chronic CRA with no alteration in the fluticasone (Flut)-treated group, demonstrating steroid resistance. Analysis of mRNA from lungs showed no decrease of MUC5AC or Gob5 in the Flut-treated group. Furthermore, flow-cytometry in lung tissue showed eosinophils and neutrophils were not significantly reduced in the Flut-treated group compared to the chronic CRA group. When the microbiome profiles were assessed, data showed that only the Flut-treated animals were significantly different in the gut microbiome. Finally, a functional analysis of cecal microbiome metabolites using PiCRUSt showed several biosynthetic pathways were significantly enriched in the Flut-treated group, with tryptophan pathway verified by ELISA with increased kynurenine in homogenized cecum samples. While the implications of these data are unclear, they may suggest a significant impact of steroid treatment on future disease pathogenesis through microbiome and associated metabolite pathway changes.
    MeSH term(s) Animals ; Lung/pathology ; Asthma/etiology ; Allergens ; Fluticasone ; Microbiota ; Cockroaches
    Chemical Substances Allergens ; Fluticasone (CUT2W21N7U)
    Language English
    Publishing date 2023-07-05
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2724325-4
    ISSN 2051-817X ; 2051-817X
    ISSN (online) 2051-817X
    ISSN 2051-817X
    DOI 10.14814/phy2.15761
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Sex-associated early-life viral innate immune response is transcriptionally associated with chromatin remodeling of type-I IFN-inducible genes.

    Malinczak, Carrie-Anne / Fonseca, Wendy / Mire, Mohamed M / Parolia, Abhijit / Chinnaiyan, Arul / Rasky, Andrew J / Morris, Susan / Yagi, Kazuma / Bermick, Jennifer R / Lukacs, Nicholas W

    Mucosal immunology

    2023  Volume 16, Issue 5, Page(s) 578–592

    Abstract: This study investigates sex-associated systemic innate immune differences by examining bone marrow-derived dendritic cells (BMDCs). BMDC grown from 7-day-old mice show enhanced type-I interferon (IFN) signaling in female compared to male BMDC. Upon ... ...

    Abstract This study investigates sex-associated systemic innate immune differences by examining bone marrow-derived dendritic cells (BMDCs). BMDC grown from 7-day-old mice show enhanced type-I interferon (IFN) signaling in female compared to male BMDC. Upon respiratory syncytial virus (RSV) infection of 7-day-old mice, a significantly altered phenotype of BMDC at 4 weeks post-infection is observed in a sex-dependent manner. The alterations include heightened Ifnb/ interleukin (Il12a) and enhanced IFNAR1+ expression in BMDC from early-life RSV-infected female mice that leads to increased IFN-γ production by T cells. Phenotypic differences were verified upon pulmonary sensitization whereby EL-RSV male-derived BMDC promoted enhanced T helper 2/17 responses and exacerbated disease upon RSV infection while EL-RSV/F BMDC sensitization was relatively protective. Assay for transposase-accessible chromatin using sequencing analysis (ATAC-seq) demonstrated that EL-RSV/F BMDC had enhanced chromatin accessibility near type-I immune genes with JUN, STAT1/2, and IRF1/8 transcription factors predicted to have binding sites in accessible regions. Importantly, ATAC-seq of human cord blood-derived monocytes displayed a similar sex-associated chromatin landscape with female-derived monocytes having more accessibility in type-I immune genes. These studies enhance our understanding of sex-associated differences in innate immunity by epigenetically controlled transcriptional programs amplified by early-life infection in females via type-I immunity.
    MeSH term(s) Male ; Mice ; Female ; Humans ; Animals ; Chromatin Assembly and Disassembly ; Respiratory Syncytial Virus Infections ; Immunity, Innate ; Lung ; Interferon Type I/metabolism ; Chromatin/genetics ; Chromatin/metabolism
    Chemical Substances Interferon Type I ; Chromatin
    Language English
    Publishing date 2023-06-10
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2411370-0
    ISSN 1935-3456 ; 1933-0219
    ISSN (online) 1935-3456
    ISSN 1933-0219
    DOI 10.1016/j.mucimm.2023.06.002
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: NLRP3-Inflammasome Inhibition during Respiratory Virus Infection Abrogates Lung Immunopathology and Long-Term Airway Disease Development.

    Malinczak, Carrie-Anne / Schuler, Charles F / Duran, Angela J / Rasky, Andrew J / Mire, Mohamed M / Núñez, Gabriel / Lukacs, Nicholas W / Fonseca, Wendy

    Viruses

    2021  Volume 13, Issue 4

    Abstract: Respiratory syncytial virus (RSV) infects most infants by two years of age. It can cause severe disease leading to an increased risk of developing asthma later in life. Previously, our group has shown that RSV infection in mice and infants promotes IL-1β ...

    Abstract Respiratory syncytial virus (RSV) infects most infants by two years of age. It can cause severe disease leading to an increased risk of developing asthma later in life. Previously, our group has shown that RSV infection in mice and infants promotes IL-1β production. Here, we characterized the role of NLRP3-Inflammasome activation during RSV infection in adult mice and neonates. We observed that the inhibition of NLRP3 activation using the small molecule inhibitor, MCC950, or in genetically modified NLRP3 knockout (
    MeSH term(s) Animals ; Animals, Newborn ; Cytokines/immunology ; Female ; Furans/administration & dosage ; Indenes/administration & dosage ; Inflammasomes/antagonists & inhibitors ; Inflammasomes/genetics ; Inflammasomes/immunology ; Lung/immunology ; Lung/pathology ; Lung/virology ; Mice ; Mice, Inbred BALB C ; Mice, Knockout ; NLR Family, Pyrin Domain-Containing 3 Protein/antagonists & inhibitors ; NLR Family, Pyrin Domain-Containing 3 Protein/genetics ; NLR Family, Pyrin Domain-Containing 3 Protein/immunology ; Respiratory Syncytial Virus Infections/immunology ; Respiratory Syncytial Virus, Human/immunology ; Respiratory Tract Diseases/immunology ; Respiratory Tract Diseases/prevention & control ; Respiratory Tract Diseases/virology ; Sulfonamides/administration & dosage
    Chemical Substances Cytokines ; Furans ; Indenes ; Inflammasomes ; NLR Family, Pyrin Domain-Containing 3 Protein ; Nlrp3 protein, mouse ; Sulfonamides ; N-(1,2,3,5,6,7-hexahydro-S-indacen-4-ylcarbamoyl)-4-(2-hydroxy-2-propanyl)-2-furansulfonamide (6RS86E2BWQ)
    Language English
    Publishing date 2021-04-16
    Publishing country Switzerland
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2516098-9
    ISSN 1999-4915 ; 1999-4915
    ISSN (online) 1999-4915
    ISSN 1999-4915
    DOI 10.3390/v13040692
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: ER stress protein PERK promotes inappropriate innate immune responses and pathogenesis during RSV infection.

    Narayanan, Samanthi / Elesela, Srikanth / Rasky, Andrew J / Morris, Susan H / Kumar, Surinder / Lombard, David / Lukacs, Nicholas W

    Journal of leukocyte biology

    2021  Volume 111, Issue 2, Page(s) 379–389

    Abstract: The activation of dendritic cells (DC) during respiratory viral infections is central to directing the immune response and the pathologic outcome. In these studies, the effect of RSV infection on development of ER stress responses and the impact on ... ...

    Abstract The activation of dendritic cells (DC) during respiratory viral infections is central to directing the immune response and the pathologic outcome. In these studies, the effect of RSV infection on development of ER stress responses and the impact on innate immunity was examined. The upregulation of ER stress was closely associated with the PERK pathway through the upregulation of CHOP in RSV infected DC. The inhibition of PERK corresponded with decreased EIF2a phosphorylation but had no significant effect on Nrf2 in DC, two primary pathways regulated by PERK. Subsequent studies identified that by blocking PERK activity in infected DC an altered ER stress response and innate cytokine profile was observed with the upregulation of IFNβ and IL-12, coincident to the down regulation of IL-1β. When mitochondria respiration was assessed in PERK deficient DC there were increased dysfunctional mitochondria after RSV infection that resulted in reduced oxygen consumption rates (OCR) and ATP production indicating altered cellular metabolism. Use of a CD11c targeted genetic deleted murine model, RSV infection was characterized by reduced inflammation and diminished mucus staining as well as reduced mucus-associated gene gob5 expression. The assessment of the cytokine responses showed decreased IL-13 and IL-17 along with diminished IL-1β in the lungs of PERK deficient infected mice. When PERK-deficient animals were assessed in parallel for lung leukocyte numbers, animals displayed significantly reduced myeloid and activated CD4 and CD8 T cell numbers. Thus, the PERK activation pathway may provide a rational target for altering the severe outcome of an RSV infection through modifying immune responses.
    MeSH term(s) Adenosine Triphosphate/metabolism ; Animals ; CD8-Positive T-Lymphocytes/immunology ; Cytokines/metabolism ; Dendritic Cells/immunology ; Endoplasmic Reticulum Stress ; Immunity, Innate ; Inflammation/immunology ; Inflammation/metabolism ; Inflammation/pathology ; Lung/immunology ; Lung/metabolism ; Lung/pathology ; Mice ; Mice, Inbred C57BL ; Oxygen Consumption ; Respiratory Syncytial Virus Infections/immunology ; Respiratory Syncytial Virus Infections/metabolism ; Respiratory Syncytial Virus Infections/pathology ; Respiratory Syncytial Viruses/immunology ; eIF-2 Kinase/genetics ; eIF-2 Kinase/metabolism
    Chemical Substances Cytokines ; Adenosine Triphosphate (8L70Q75FXE) ; PERK kinase (EC 2.7.11.1) ; eIF-2 Kinase (EC 2.7.11.1)
    Language English
    Publishing date 2021-04-18
    Publishing country United States
    Document type Journal Article
    ZDB-ID 605722-6
    ISSN 1938-3673 ; 0741-5400
    ISSN (online) 1938-3673
    ISSN 0741-5400
    DOI 10.1002/JLB.3A0520-322RR
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Intranasal delivery of allergen in a nanoemulsion adjuvant inhibits allergen-specific reactions in mouse models of allergic airway disease.

    Baker, James R / Rasky, Andrew J / Landers, Jeffrey J / Janczak, Katarzyna W / Totten, Tiffanie D / Lukacs, Nicholas W / O'Konek, Jessica J

    Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology

    2021  Volume 51, Issue 10, Page(s) 1361–1373

    Abstract: Background: Atopic diseases are an increasing problem that involve both immediate hypersensitivity reactions mediated by IgE and unique cellular inflammation. Many forms of specific immunotherapy involve the administration of allergen to suppress ... ...

    Abstract Background: Atopic diseases are an increasing problem that involve both immediate hypersensitivity reactions mediated by IgE and unique cellular inflammation. Many forms of specific immunotherapy involve the administration of allergen to suppress allergic immune responses but are focused on IgE-mediated reactions. In contrast, the effect of allergen-specific immunotherapy on allergic inflammation is complex, not entirely consistent and not well understood. We have previously demonstrated the ability of allergen administered in a nanoemulsion (NE) mucosal adjuvant to suppress IgE-mediated allergic responses and protect from allergen challenge in murine food allergy models. This activity was associated with decreases in allergen-specific IL-10 and reductions in allergic cytokines and increases in regulatory T cells.
    Objective: Here, we extend these studies to using 2 distinct models, the ovalbumin (OVA) and cockroach (CRA) models of allergic airway disease, which are based predominantly on allergic inflammation.
    Methods: Acute or chronic allergic airway disease was induced in mice using ovalbumin and cockroach allergen models. Mice received three therapeutic immunizations with allergen in NE, and reactivity to airway challenge was determined.
    Results: Therapeutic immunization with cockroach or OVA allergen in NE markedly reduced pathology after airway challenge. The 2 models demonstrated protection from allergen challenge-induced pathology that was associated with suppression of Th2-polarized immune responses in the lung. In addition, the reduction in ILC2 numbers in the lungs of allergic mice along with reduction in epithelial cell alarmins, IL-25 and IL-33, suggests an overall change in the lung immune environment induced by the NE immunization protocol.
    Conclusions and clinical relevance: These results demonstrate that suppression of allergic airway inflammation and bronchial hyper-reactivity can be achieved using allergen-specific immunotherapy without significant reductions in allergen-specific IgE and suggest that ILC2 cells may be critical targets for this activity.
    MeSH term(s) Allergens ; Animals ; Humans ; Hypersensitivity ; Immunity, Innate ; Immunoglobulin E ; Lymphocytes ; Mice
    Chemical Substances Allergens ; Immunoglobulin E (37341-29-0)
    Language English
    Publishing date 2021-05-29
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 645204-8
    ISSN 1365-2222 ; 0954-7894 ; 0960-2178
    ISSN (online) 1365-2222
    ISSN 0954-7894 ; 0960-2178
    DOI 10.1111/cea.13903
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  8. Article: NLRP3-Inflammasome Inhibition during Respiratory Virus Infection Abrogates Lung Immunopathology and Long-Term Airway Disease Development

    Malinczak, Carrie-Anne / Schuler, Charles F / Duran, Angela J / Rasky, Andrew J / Mire, Mohamed M / Núñez, Gabriel / Lukacs, Nicholas W / Fonseca, Wendy

    Viruses. 2021 Apr. 16, v. 13, no. 4

    2021  

    Abstract: Respiratory syncytial virus (RSV) infects most infants by two years of age. It can cause severe disease leading to an increased risk of developing asthma later in life. Previously, our group has shown that RSV infection in mice and infants promotes IL-1β ...

    Abstract Respiratory syncytial virus (RSV) infects most infants by two years of age. It can cause severe disease leading to an increased risk of developing asthma later in life. Previously, our group has shown that RSV infection in mice and infants promotes IL-1β production. Here, we characterized the role of NLRP3-Inflammasome activation during RSV infection in adult mice and neonates. We observed that the inhibition of NLRP3 activation using the small molecule inhibitor, MCC950, or in genetically modified NLRP3 knockout (Nlrp3−/−) mice during in vivo RSV infection led to decreased lung immunopathology along with a reduced expression of the mucus-associated genes and reduced production of innate cytokines (IL-1β, IL-33 and CCL2) linked to severe RSV disease while leading to significant increases in IFN-β. NLRP3-inflammasome inhibition or deletion diminished Th2 cytokines and inflammatory cell infiltration into the lungs. Furthermore, NLRP3 inhibition or deletion during early-life RSV infection led to reducing viral-exacerbated allergic response in a mouse model of RSV-induced allergy exacerbation. Here, we demonstrated the critical role of NLRP3-inflammasome activation in RSV immunopathology and the related long-term airway alteration. Moreover, these findings suggest the NLRP3-inflammasome as a potential therapeutic target to attenuate severe RSV disease and limit childhood asthma development.
    Keywords Respiratory syncytial virus ; adults ; asthma ; childhood ; disease severity ; immunopathology ; lungs ; mice ; risk ; therapeutics ; viruses
    Language English
    Dates of publication 2021-0416
    Publishing place Multidisciplinary Digital Publishing Institute
    Document type Article
    Note NAL-AP-2-clean
    ZDB-ID 2516098-9
    ISSN 1999-4915
    ISSN 1999-4915
    DOI 10.3390/v13040692
    Database NAL-Catalogue (AGRICOLA)

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  9. Article ; Online: Inhibition of uric acid or IL-1β ameliorates respiratory syncytial virus immunopathology and development of asthma.

    Schuler, Charles F / Malinczak, Carrie-Anne / Best, Shannon K K / Morris, Susan B / Rasky, Andrew J / Ptaschinski, Catherine / Lukacs, Nicholas W / Fonseca, Wendy

    Allergy

    2020  Volume 75, Issue 9, Page(s) 2279–2293

    Abstract: Background: Respiratory syncytial virus (RSV) affects most infants early in life and is associated with increased asthma risk. The specific mechanism remains unknown.: Objective: To investigate the role of uric acid (UA) and IL-1β in RSV ... ...

    Abstract Background: Respiratory syncytial virus (RSV) affects most infants early in life and is associated with increased asthma risk. The specific mechanism remains unknown.
    Objective: To investigate the role of uric acid (UA) and IL-1β in RSV immunopathology and asthma predisposition.
    Methods: Tracheal aspirates from human infants with and without RSV were collected and analyzed for pro-IL-1β mRNA and protein to establish a correlation in human disease. Neonatal mouse models of RSV were employed, wherein mice infected at 6-7 days of life were analyzed at 8 days postinfection, 5 weeks postinfection, or after a chronic cockroach allergen asthma model. A xanthine oxidase inhibitor or IL-1 receptor antagonist was administered during RSV infection.
    Results: Human tracheal aspirates from RSV-infected infants showed elevated pro-IL-1β mRNA and protein. Inhibition of UA or IL-1β during neonatal murine RSV infection decreased mucus production, reduced cellular infiltrates to the lung (especially ILC2s), and decreased type 2 immune responses. Inhibition of either UA or IL-1β during RSV infection led to chronic reductions in pulmonary immune cell composition and reduced type 2 immune responses and reduced similar responses after challenge with cockroach antigen.
    Conclusions: Inhibiting UA and IL-1β during RSV infection ameliorates RSV immunopathology, reduces the consequences of allergen-induced asthma, and presents new therapeutic targets to reduce early-life viral-induced asthma development.
    MeSH term(s) Animals ; Asthma ; Immunity, Innate ; Lung ; Lymphocytes ; Mice ; Mice, Inbred BALB C ; Respiratory Syncytial Virus Infections ; Respiratory Syncytial Viruses ; Uric Acid
    Chemical Substances Uric Acid (268B43MJ25)
    Language English
    Publishing date 2020-05-15
    Publishing country Denmark
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 391933-x
    ISSN 1398-9995 ; 0105-4538
    ISSN (online) 1398-9995
    ISSN 0105-4538
    DOI 10.1111/all.14310
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Loss of Hox5 function results in myofibroblast mislocalization and distal lung matrix defects during postnatal development.

    Hrycaj, Steven M / Marty-Santos, Leilani / Rasky, Andrew J / Lukacs, Nicholas W / Wellik, Deneen M

    Science China. Life sciences

    2018  Volume 61, Issue 9, Page(s) 1030–1038

    Abstract: Alveologenesis is the final stage of lung development and is responsible for the formation of the principle gas exchange units called alveoli. The lung mesenchyme, in particular the alveolar myofibroblasts, are drivers of alveolar development, however, ... ...

    Abstract Alveologenesis is the final stage of lung development and is responsible for the formation of the principle gas exchange units called alveoli. The lung mesenchyme, in particular the alveolar myofibroblasts, are drivers of alveolar development, however, few key regulators that govern the proper distribution and behavior of these cells in the distal lung during alveologenesis have been identified. While Hox5 triple mutants (Hox5 aabbcc) exhibit neonatal lethality, four-allele, compound mutant mice (Hox5 AabbCc) are born in Mendelian ratios and are phenotypically normal at birth. However, they exhibit defects in alveologenesis characterized by a BPD-like phenotype by early postnatal stages that becomes more pronounced at adult stages. Invasive pulmonary functional analyses demonstrate significant increases in total lung volume and compliance and a decrease in elastance in Hox5 compound mutants. SMA+ myofibroblasts in the distal lung are distributed abnormally during peak stages of alveologenesis and aggregate, resulting in the formation of a disrupted elastin network. Examination of other key components of the distal lung ECM, as well as other epithelial cells and lipofibroblasts reveal no differences in distribution. Collectively, these data indicate that Hox5 genes play a critical role in alveolar development by governing the proper cellular behavior of myofibroblasts during alveologenesis.
    MeSH term(s) Animals ; Congenital Abnormalities/genetics ; Homeodomain Proteins/genetics ; Homeodomain Proteins/metabolism ; Lung/abnormalities ; Lung/growth & development ; Mice ; Mutation/genetics ; Myofibroblasts/metabolism ; Myofibroblasts/pathology ; Pulmonary Alveoli/cytology ; Pulmonary Alveoli/growth & development ; Pulmonary Alveoli/metabolism
    Chemical Substances Homeodomain Proteins ; Hoxd1 protein, mouse
    Language English
    Publishing date 2018-04-27
    Publishing country China
    Document type Journal Article
    ZDB-ID 2546732-3
    ISSN 1869-1889 ; 1674-7305
    ISSN (online) 1869-1889
    ISSN 1674-7305
    DOI 10.1007/s11427-017-9290-1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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