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The Immunopathologic Effects of Mycoplasma pneumoniae and Community-acquired Respiratory Distress Syndrome Toxin. A Primate Model.
Maselli, Diego J; Medina, Jorge L; Brooks, Edward G; Coalson, Jacqueline J; Kannan, Thirumalai R; Winter, Vicki T; Principe, Molly; Cagle, Marianna P; Baseman, Joel B; Dube, Peter H; Peters, Jay I.
Afiliação
  • Maselli DJ; 1 Division of Pulmonary Diseases and Critical Care Medicine, Department of Medicine.
  • Medina JL; 2 Department of Microbiology and Immunology.
  • Brooks EG; 3 Center for Airway Inflammation Research.
  • Coalson JJ; 3 Center for Airway Inflammation Research.
  • Kannan TR; 4 Division of Immunology and Infectious Diseases, Department of Pediatrics, and.
  • Winter VT; 5 Department of Pathology, University of Texas Health Sciences Center at San Antonio, San Antonio, Texas.
  • Principe M; 2 Department of Microbiology and Immunology.
  • Cagle MP; 3 Center for Airway Inflammation Research.
  • Baseman JB; 5 Department of Pathology, University of Texas Health Sciences Center at San Antonio, San Antonio, Texas.
  • Dube PH; 4 Division of Immunology and Infectious Diseases, Department of Pediatrics, and.
  • Peters JI; 2 Department of Microbiology and Immunology.
Am J Respir Cell Mol Biol ; 58(2): 253-260, 2018 02.
Article em En | MEDLINE | ID: mdl-28915064
ABSTRACT
Mycoplasma pneumoniae infection has been linked to poor asthma outcomes. M. pneumoniae produces an ADP-ribosylating and vacuolating toxin called community-acquired respiratory distress syndrome (CARDS) toxin that has a major role in inflammation and airway dysfunction. The objective was to evaluate the immunopathological effects in primates exposed to M. pneumoniae or CARDS toxin. A total of 13 baboons were exposed to M. pneumoniae or CARDS toxin. At Days 7 and 14, BAL fluid was collected and analyzed for cell count, percent of each type of cell, CARDS toxin by PCR, CARDS toxin by antigen capture, eosinophilic cationic protein, and cytokine profiles. Serum IgM, IgG, and IgE responses to CARDS toxin were measured. All animals had a necropsy for analysis of the histopathological changes on lungs. No animal developed signs of infection. The serological responses to CARDS toxin were variable. At Day 14, four of seven animals exposed to M. pneumoniae and all four animals exposed to CARDS toxin developed histological "asthma-like" changes. T cell intracellular cytokine analysis revealed an increasing ratio of IL-4/IFN-γ over time. Both M. pneumoniae and CARDS toxin exposure resulted in similar histopathological pulmonary changes, suggesting that CARDS toxin plays a major role in the inflammatory response.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Asma / Proteínas de Bactérias / Toxinas Bacterianas / Pulmão / Mycoplasma pneumoniae Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Asma / Proteínas de Bactérias / Toxinas Bacterianas / Pulmão / Mycoplasma pneumoniae Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article