Effect of stimulation of human macrophages on intracellular survival of Mycobacterium bovis cacillus Calmette–Guerin
Autor: | Bonay, Marcel, BOUCHONNET, FRANCINE, Pelicic, V., LAGIER, BEATRICE, GRANDSAIGNE, MARTINE, Lecossier, Denise, Grodet, Alain, VOKURKA, MARTIN, Gicquel, Brigitte, HANCE, ALLAN J. |
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Přispěvatelé: | Génétique mycobactérienne - Mycobacterial genetics, Institut Pasteur [Paris] (IP), Institut National de la Santé et de la Recherche Médicale (INSERM), Faculte de Medecine Xavier Bichat, Université Paris Diderot - Paris 7 (UPD7), Supported by grants from Recherche et Partage and the Fondation pour la Recherche Medicale, France., Institut Pasteur [Paris] |
Jazyk: | angličtina |
Rok vydání: | 1999 |
Předmět: |
MESH: Mycobacterium bovis
MESH: Cytokines MESH: Intracellular Membranes MESH: Humans MESH: Interferon-gamma MESH: Genes Reporter MESH: Stimulation Chemical MESH: Macrophages MESH: Luciferases MESH: Colony Count Microbial [SDV.MP.BAC]Life Sciences [q-bio]/Microbiology and Parasitology/Bacteriology ComputingMilieux_MISCELLANEOUS |
Zdroj: | American Journal of Respiratory and Critical Care Medicine American Journal of Respiratory and Critical Care Medicine, 1999, 159 (5), pp.1629-1637. ⟨10.1164/ajrccm.159.5.9807021⟩ American Journal of Respiratory and Critical Care Medicine, American Thoracic Society, 1999, 159 (5), pp.1629-1637. ⟨10.1164/ajrccm.159.5.9807021⟩ |
ISSN: | 1073-449X 1535-4970 |
DOI: | 10.1164/ajrccm.159.5.9807021⟩ |
Popis: | International audience; The mechanisms through which immune and inflammatory responses stimulate the expression of antimycobacterial activity by human macrophages remain poorly defined. To study this question, we developed a method permitting the rapid quantification of viable mycobacteria, based on the detection of luciferase activity expressed by a Mycobacterium bovis Bacillus Calmette-Guerin (BCG) reporter strain, and used this approach to evaluate mycobacterial survival in human monocyte-derived macrophages following stimulation with cytokines and through crosslinking of costimulatory molecules expressed on the cell surface. Modest proliferation, followed by persistence of mycobacteria, was observed in unpretreated macrophages as assessed both by measurement of luciferase activity and by the evaluation of colony forming units. Of the 19 cytokines tested, only granulocyte-macrophage colony-stimulating factor (GM-CSF) and interleukin-3 (IL-3) were found to improve the mycobactericidal activity of monocyte-derived macrophages. In both cases, this effect was observed only when macrophages were pretreated with the cytokines prior to infection. In contrast, pretreatment of human macrophages with interferon-gamma, either alone or in combination with other mediators (including tumor necrosis factor-alpha and 1,25[OH]2-vitamin D3), did not improve mycobacterial killing. The stimulation of macrophages through several different costimulatory molecules known to participate in macrophage-lymphocyte interactions (CD4, CD40, CD45, CD86, CD95 [Fas/Apo-1]) also failed to improve mycobactericidal activity. This study shows that GM-CSF and IL-3, cytokines whose receptors are known to share a common subunit and to use common second messengers, may contribute to the stimulation of mycobactericidal activity in humans. The ability to rapidly screen the effects of different macrophage stimuli on mycobacterial survival through the detection of luciferase activity should help define additional signals required for optimal antimycobacterial responses. |
Databáze: | OpenAIRE |
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