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Cytokines Involved in Resistance to Mycobacterium avium in a Mouse Model of Infection.
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- Medical Principles & Practice, 1997, v. 6, n. 2, p. 97, doi. 10.1159/000157433
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- Article
Lipoarabinomannan mannose caps do not affect mycobacterial virulence or the induction of protective immunity in experimental animal models of infection and have minimal impact on in vitro inflammatory responses.
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- Cellular Microbiology, 2013, v. 15, n. 4, p. 660, doi. 10.1111/cmi.12065
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Cathelicidin is involved in the intracellular killing of mycobacteria in macrophages.
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- Cellular Microbiology, 2011, v. 13, n. 10, p. 1601, doi. 10.1111/j.1462-5822.2011.01644.x
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Nitric oxide inhibits the accumulation of CD4<sup>+</sup> CD44<sup>hi</sup> Tbet<sup>+</sup> CD69<sup>lo</sup> T cells in mycobacterial infection.
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- European Journal of Immunology, 2012, v. 42, n. 12, p. 3267, doi. 10.1002/eji.201142158
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Studies in the mouse model identify strain variability as a major determinant of disease outcome in Leishmania infantum infection.
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- Parasites & Vectors, 2015, v. 8, n. 1, p. 1, doi. 10.1186/s13071-015-1259-6
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IFNγ and iNOS-Mediated Alterations in the Bone Marrow and Thymus and Its Impact on Mycobacterium avium -Induced Thymic Atrophy.
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- Frontiers in Immunology, 2021, v. 12, p. 1, doi. 10.3389/fimmu.2021.696415
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Iron in intracellular infection: to provide or to deprive?
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- Frontiers in Cellular & Infection Microbiology, 2013, v. 3, n. 12, p. 1, doi. 10.3389/fcimb.2013.00096
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Iron in intracellular infection: to provide or to deprive?
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- Frontiers in Cellular & Infection Microbiology, 2013, v. 3, p. 1, doi. 10.3389/fcimb.2013.00096
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Predominant role of interferon-γ in the host protective effect of CD8<sup>+</sup> T cells against Neospora caninum infection.
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- Scientific Reports, 2015, p. 1, doi. 10.1038/srep14913
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<i>Mycobacterium avium</i> Infection Induces H-Ferritin Expression in Mouse Primary Macrophages by Activating Toll-Like Receptor 2.
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- PLoS ONE, 2013, v. 8, n. 12, p. 1, doi. 10.1371/journal.pone.0082874
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The Effect of the Host's Iron Status on Tuberculosis.
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- Journal of Infectious Diseases, 2007, v. 195, n. 12, p. 1745, doi. 10.1086/518040
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Genetic control of immune-mediated necrosis of Mycobacterium avium granulomas.
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- Immunology, 2006, v. 118, n. 1, p. 122, doi. 10.1111/j.1365-2567.2006.02350.x
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- Article
CD40 is required for the optimal induction of protective immunity to Mycobacterium avium.
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- Immunology, 2004, v. 111, n. 3, p. 323, doi. 10.1111/j.1365-2567.2004.01812.x
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- Article
Limited role of the Toll-like receptor-2 in resistance to Mycobacterium avium.
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- Immunology, 2004, v. 111, n. 2, p. 179, doi. 10.1111/j.0019-2805.2003.01807.x
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Immunological basis of the development of necrotic lesions following Mycobacterium avium infection.
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- Immunology, 2002, v. 106, n. 4, p. 590, doi. 10.1046/j.1365-2567.2002.01459.x
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Failure to induce enhanced protection against tuberculosis by increasing T-cell-dependent interferon-γ generation.
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- Immunology, 2001, v. 104, n. 2, p. 157, doi. 10.1046/j.1365-2567.2001.01305.x
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Interleukin-12 primes CD4<sup>+</sup> T cells for interferon-γ production and protective immunity during Mycobacterium avium infection.
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- Immunology, 2001, v. 103, n. 3, p. 368, doi. 10.1046/j.1365-2567.2001.01237.x
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Interleukin-6 regulates the phenotype of the immune response to a tuberculosis subunit vaccine.
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- Immunology, 2001, v. 103, n. 3, p. 375, doi. 10.1046/j.1365-2567.2001.01244.x
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Leishmania Mitochondrial Peroxiredoxin Plays a Crucial Peroxidase-Unrelated Role during Infection: Insight into Its Novel Chaperone Activity.
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- PLoS Pathogens, 2011, v. 7, n. 10, p. 1, doi. 10.1371/journal.ppat.1002325
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Endogenous cathelicidin production limits inflammation and protective immunity to Mycobacterium avium in mice.
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- Immunity, Inflammation & Disease, 2014, v. 2, n. 1, p. 1, doi. 10.1002/iid3.7
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Increased viability but decreased culturability of Mycobacterium avium subsp. paratuberculosis in macrophages from inflammatory bowel disease patients under Infliximab treatment.
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- Medical Microbiology & Immunology, 2015, v. 204, n. 6, p. 647, doi. 10.1007/s00430-015-0393-2
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Prevalence of Mycobacterium avium subsp. paratuberculosis and Escherichia coli in blood samples from patients with inflammatory bowel disease.
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- Medical Microbiology & Immunology, 2015, v. 204, n. 6, p. 681, doi. 10.1007/s00430-015-0420-3
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Iron Overload Favors the Elimination of Leishmania infantum from Mouse Tissues through Interaction with Reactive Oxygen and Nitrogen Species.
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- PLoS Neglected Tropical Diseases, 2013, v. 7, n. 2, p. 1, doi. 10.1371/journal.pntd.0002061
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Iron Overload Favors the Elimination of Leishmania infantum from Mouse Tissues through Interaction with Reactive Oxygen and Nitrogen Species.
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- PLoS Neglected Tropical Diseases, 2013, v. 7, n. 2, p. 1, doi. 10.1371/journal.pntd.0002061
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Regulation of granuloma fibrosis by nitric oxide during Mycobacterium avium experimental infection.
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- International Journal of Experimental Pathology, 2006, v. 87, n. 4, p. 307, doi. 10.1111/j.1365-2613.2006.00487.x
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Myeloid HIF‐1α regulates pulmonary inflammation during experimental Mycobacterium tuberculosis infection.
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- Immunology, 2020, v. 159, n. 1, p. 121, doi. 10.1111/imm.13131
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The Warburg effect in mycobacterial granulomas is dependent on the recruitment and activation of macrophages by interferon- γ.
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- Immunology, 2015, v. 145, n. 4, p. 498, doi. 10.1111/imm.12464
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IL-17A promotes intracellular growth of Mycobacterium by inhibiting apoptosis of infected macrophages.
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- Frontiers in Immunology, 2015, p. 1, doi. 10.3389/fimmu.2015.00498
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Engagement of Toll-like receptor 2 in mouse macrophages infected with Mycobacterium avium induces non-oxidative and TNF-independent anti-mycobacterial activity.
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- European Journal of Immunology, 2008, v. 38, n. 8, p. 2180, doi. 10.1002/eji.200737954
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