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      Molecular degree of perturbation of plasma inflammatory markers associated with tuberculosis reveals distinct disease profiles between Indian and Chinese populations

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          Abstract

          Tuberculosis (TB) is a chronic inflammatory disease caused by Mycobacterium tuberculosis infection which causes tremendous morbidity and mortality worldwide. Clinical presentation of TB patients is very diverse and disease heterogeneity is associated with changes in biomarker signatures. Here, we compared at the molecular level the extent of individual inflammatory perturbation of plasma protein and lipid mediators associated with TB in patients in China versus India. We performed a cross-sectional study analyzing the overall degree of inflammatory perturbation in treatment-naïve pulmonary TB patients and uninfected individuals from India (TB: n = 97, healthy: n = 20) and China (TB: n = 100, healthy: n = 11). We employed the molecular degree of perturbation (MDP) adapted to plasma biomarkers to examine the overall changes in inflammation between these countries. M. tuberculosis infection caused a significant degree of molecular perturbation in patients from both countries, with higher perturbation detected in India. Interestingly, there were differences in biomarker perturbation patterns and the overall degree of inflammation. Patients with severe TB exhibited increased MDP values and Indian patients with this condition exhibited even higher degree of perturbation compared to Chinese patients. Network analyses identified IFN-α, IFN-β, IL-1RI and TNF-α as combined biomarkers that account for the overall molecular perturbation in the entire study population. Our results delineate the magnitude of the systemic inflammatory perturbation in pulmonary TB and reveal qualitative changes in inflammatory profiles between two countries with high disease prevalence.

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          Most cited references28

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          Race and gender differences in C-reactive protein levels.

          This study sought to determine whether there are race and gender differences in the distribution of C-reactive protein (CRP) levels. Few data are available comparing CRP distributions in different race and gender groups. Recent clinical practice recommendations for CRP testing for cardiovascular risk assessment suggest a uniform threshold to define high relative risk (>3 mg/l). We measured CRP in 2,749 white and black subjects ages 30 to 65 participating in the Dallas Heart Study, a multiethnic, population-based, probability sample, and compared levels of CRP between different race and gender groups. Black subjects had higher CRP levels than white subjects (median, 3.0 vs. 2.3 mg/l; p 3 mg/l was 31%, 40%, 51%, and 58% in white men, black men, white women, and black women, respectively (p 3 mg/l remained more common in white women (odds ratio [OR] 1.6; 95% confidence interval [CI] 1.1 to 2.5) and black women (OR 1.7; 95% CI 1.2 to 2.6) but not in black men (OR, 1.3; 95% CI, 0.8 to 1.9) when compared with white men. Significant race and gender differences exist in the population distribution of CRP. Further research is needed to determine whether race and gender differences in CRP levels contribute to differences in cardiovascular outcomes, and whether thresholds for cardiovascular risk assessment should be adjusted for different race and gender groups.
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            Innate and adaptive interferons suppress IL-1α and IL-1β production by distinct pulmonary myeloid subsets during Mycobacterium tuberculosis infection.

            Interleukin-1 (IL-1) receptor signaling is necessary for control of Mycobacterium tuberculosis (Mtb) infection, yet the role of its two ligands, IL-1α and IL-1β, and their regulation in vivo are poorly understood. Here, we showed that both IL-1α and IL-1β are critically required for host resistance and identified two multifunctional inflammatory monocyte-macrophage and DC populations that coexpressed both IL-1 species at the single-cell level in lungs of Mtb-infected mice. Moreover, we demonstrated that interferons (IFNs) played important roles in regulating IL-1 production by these cells in vivo. Type I interferons inhibited IL-1 production by both subsets whereas CD4(+) T cell-derived IFN-γ selectively suppressed monocyte-macrophages. These data provide a cellular basis for both the anti-inflammatory effects of IFNs and probacterial functions of type I IFNs during Mtb infection and reveal differential regulation of IL-1 production by distinct cell populations as an additional layer of complexity in the activity of IL-1 in vivo. Copyright © 2011 Elsevier Inc. All rights reserved.
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              Mycobacterium tuberculosis evades macrophage defenses by inhibiting plasma membrane repair

              Induction of macrophage necrosis is an important strategy used by virulent Mycobacterium tuberculosis (Mtb) to avoid innate host defense. In contrast, attenuated Mtb causes apoptosis, which limits bacterial replication and promotes T cell cross priming by antigen presenting cells. Here we demonstrated that Mtb infection causes plasma membrane microdisruptions. Resealing of these lesions—a process crucial for preventing necrosis and promoting apoptosis—required the translocation of lysosome and Golgi apparatus-derived vesicles to the plasma membrane. Plasma membrane repair depended on prostaglandin E2 (PGE2), which regulates synaptotagmin 7, the Ca++ sensor involved in the lysosome-mediated repair mechanism. By inducing production of lipoxin A4 (LXA4), which blocks PGE2 biosynthesis, virulent Mtb prevented membrane repair and induced necrosis. Thus, virulent Mtb impairs macrophage plasma membrane repair to evade host defenses.
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                Author and article information

                Contributors
                bruno.andrade@fiocruz.br
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                29 May 2019
                29 May 2019
                2019
                : 9
                : 8002
                Affiliations
                [1 ]ISNI 0000 0001 0723 0931, GRID grid.418068.3, Instituto Gonçalo Moniz, , Fundação Oswaldo Cruz, ; Salvador, 40296-710 Brazil
                [2 ]Multinational Organization Network Sponsoring Translational and Epidemiological Research (MONSTER) Initiative, Fundação José Silveira, Salvador, 40210-320 Brazil
                [3 ]ISNI 0000 0004 0471 7789, GRID grid.467298.6, Curso de Medicina, , Faculdade de Tecnologia e Ciências (FTC), ; Salvador, 40290-150 Brazil
                [4 ]National Institutes of Health- National Institute for Research in Tuberculosis, International Center for Excellence in Research, Chennai, 600031 India
                [5 ]Henan Chest Hospital, Zhengzhou, 450000 China
                [6 ]Sino-US International Research Center for Tuberculosis, and Henan Public Health Center, Zhengzhou, 450000 China
                [7 ]Laboratory of Clinical Immunology and Microbiology, NIAID, NIH, Bethesda, 20892 USA
                [8 ]Laboratory of Parasitic Diseases, NIAID, NIH, Bethesda, 20892 USA
                [9 ]ISNI 0000 0004 1937 0722, GRID grid.11899.38, Department of Pathophysiology and Toxicology, , School of Pharmaceutical Sciences, University of São Paulo, ; São Paulo, 05508 Brazil
                [10 ]ISNI 0000 0001 2264 7217, GRID grid.152326.1, Division of Infectious Diseases, Department of Medicine, , Vanderbilt University School of Medicine, ; Nashville, TN 37232 USA
                [11 ]ISNI 0000 0001 0166 9177, GRID grid.442056.1, Universidade Salvador (UNIFACS), Laureate Universities, ; Salvador, 41720-200 Brazil
                Author information
                http://orcid.org/0000-0002-0311-3233
                http://orcid.org/0000-0001-5297-9108
                http://orcid.org/0000-0003-2223-0918
                http://orcid.org/0000-0001-6833-3811
                Article
                44513
                10.1038/s41598-019-44513-8
                6541651
                31142816
                689cd4b6-153e-4f48-b75d-77d34265fd9e
                © The Author(s) 2019

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 19 February 2019
                : 17 May 2019
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100003593, Ministry of Science, Technology and Innovation | Conselho Nacional de Desenvolvimento Científico e Tecnológico (National Council for Scientific and Technological Development);
                Funded by: FundRef https://doi.org/10.13039/100006492, Division of Intramural Research, National Institute of Allergy and Infectious Diseases (Division of Intramural Research of the NIAID);
                Funded by: FundRef https://doi.org/10.13039/100000060, U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID);
                Award ID: U01AI115940
                Award ID: R01AI069923-08
                Award ID: R01AI20790-02
                Award Recipient :
                Categories
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                © The Author(s) 2019

                Uncategorized
                infection,interleukins
                Uncategorized
                infection, interleukins

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