Concurrent infection with Mycobacterium tuberculosis confers robust protection against secondary infection in macaques
Autor: | JoAnne L. Flynn, Constance J. Martin, Sarah M. Fortune, Allison F. Carey, Eileen A. Wong, Anthony M. Cadena, Pauline Maiello, Philana Ling Lin, Forrest F. Hopkins, Hannah P. Gideon, Peter Andersen, Robert M. DiFazio |
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Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
Monkeys Macaque Biochemistry Diagnostic Radiology White Blood Cells Animal Cells Medicine and Health Sciences DNA libraries Biology (General) Tuberculosis Vaccines Immune Response Mammals 0303 health sciences biology T Cells Coinfection Radiology and Imaging Vaccination Infection Imaging Eukaryota 3. Good health Actinobacteria Nucleic acids Granuloma Vertebrates Granulomas medicine.symptom Cellular Types Research Article Primates Tuberculosis Imaging Techniques QH301-705.5 Secondary infection Immune Cells 030106 microbiology Immunology Inflammation Research and Analysis Methods Microbiology Mycobacterium tuberculosis 03 medical and health sciences Immune system Immunity Diagnostic Medicine Virology biology.animal Old World monkeys medicine Genetics Animals Molecular Biology Tuberculosis Pulmonary 030304 developmental biology Blood Cells Biology and life sciences Bacteria 030306 microbiology business.industry Organisms Cell Biology DNA Pneumonia RC581-607 medicine.disease biology.organism_classification 030104 developmental biology Amniotes Macaca Parasitology Immunologic diseases. Allergy business |
Zdroj: | PLoS Pathogens, Vol 14, Iss 10, p e1007305 (2018) PLoS Pathogens |
ISSN: | 1553-7374 1553-7366 |
Popis: | For many pathogens, including most targets of effective vaccines, infection elicits an immune response that confers significant protection against reinfection. There has been significant debate as to whether natural Mycobacterium tuberculosis (Mtb) infection confers protection against reinfection. Here we experimentally assessed the protection conferred by concurrent Mtb infection in macaques, a robust experimental model of human tuberculosis (TB), using a combination of serial imaging and Mtb challenge strains differentiated by DNA identifiers. Strikingly, ongoing Mtb infection provided complete protection against establishment of secondary infection in over half of the macaques and allowed near sterilizing bacterial control for those in which a secondary infection was established. By contrast, boosted BCG vaccination reduced granuloma inflammation but had no impact on early granuloma bacterial burden. These findings are evidence of highly effective concomitant mycobacterial immunity in the lung, which may inform TB vaccine design and development. Author summary Tuberculosis (TB), a lung disease caused by the bacterial pathogen Mycobacterium tuberculosis, is endemic in many developing countries. This infection is transmitted from a person with active tuberculosis through coughing, talking, and singing. Exposure to this bacterium can result in a spectrum of infection outcomes, including in the majority of persons asymptomatic infection, known as latent TB. However, re-exposure to those with active disease occurs frequently, particularly in crowded conditions. Here we demonstrate that ongoing Mtb infection in a non-human primate model provides robust protection against reinfection and disease. This has important implications for vaccine development against this infection. |
Databáze: | OpenAIRE |
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