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Immune Dysregulation in Tuberculosis-Diabetes Comorbidity: A Systematic Review of Mechanistic Insights

https://doi.org/10.2139/ssrn.5368715
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A murine model of tuberculosis/type 2 diabetes comorbidity for investigating the microbiome, metabolome and associated immune parameters
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Impaired resolution of blood transcriptomes through tuberculosis treatment with diabetes comorbidity
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Coincident diabetes mellitus modulates Th1‐, Th2‐, and Th17‐cell responses in latent tuberculosis in an IL‐10‐ and TGF‐β‐dependent manner
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Hyperglycaemia is inversely correlated with live M. bovis BCG‐specific CD4+ T cell responses in Tanzanian adults with latent or active tuberculosis
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A multifaceted approach to modeling the immune response in tuberculosis
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The role of interferon-gamma in the increased tuberculosis risk in type 2 diabetes mellitus
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Patients with type 1 diabetes mellitus have impaired IL-1β production in response to Mycobacterium tuberculosis
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Resuscitation Promoting Factors: a Family of Microbial Proteins in Survival and Resuscitation of Dormant Mycobacteria
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Increased Severity of Tuberculosis in Guinea Pigs with Type 2 Diabetes
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Analysis of CD4 and CD8 expression in multidrug-resistant tuberculosis infection with diabetes mellitus: An experimental study in mice
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Expression of CD64, CD206, and RAGE in Adherent Cells of Diabetic Patients Infected with Mycobacterium tuberculosis
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Molecular mechanism of interaction of Mycobacterium tuberculosis with host macrophages under high glucose conditions
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Enumeration of lymphocyte subsets during follow-up in the pulmonary tuberculosis patients with co morbid diabetes mellitus
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Adipsin Is an Adipokine that Improves β Cell Function in Diabetes
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Defining a Research Agenda to Address the Converging Epidemics of Tuberculosis and Diabetes
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TGFβ restricts expansion, survival, and function of T cells within the tuberculous granuloma
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Effect of anticoagulants on multiplexed measurement of cytokine/chemokines in healthy subjects
inferredcites →https://doi.org/10.1016/j.cyto.2015.12.026openalex-snapshot
Type 2 diabetes mellitus coincident with pulmonary or latent tuberculosis results in modulation of adipocytokines
inferredcites →https://doi.org/10.1016/j.cyto.2016.03.009openalex-snapshot
Effect of IFN-γ, IL-12 and IL-10 cytokine production and mRNA expression in tuberculosis patients with diabetes mellitus and their household contacts
inferredcites →https://doi.org/10.1016/j.cyto.2017.05.014openalex-snapshot
Effect of the anticoagulant, storage time and temperature of blood samples on the concentrations of 27 multiplex assayed cytokines – Consequences for defining reference values in healthy humans
inferredcites →https://doi.org/10.1016/j.cyto.2019.154824openalex-snapshot
Heterogeneity in the cytokine profile of tuberculosis – diabetes co-morbidity
inferredcites →https://doi.org/10.1016/j.cyto.2020.155333openalex-snapshot
Anti-inflammatory cytokines IL-27, IL-10, IL-1Ra and TGF-β in subjects with increasing grades of glucose intolerence (DM-LTB-2)
inferredcites →https://doi.org/10.1016/j.diabres.2009.10.011openalex-snapshot
Macrophage foam cell formation is augmented in serum from patients with diabetic angiopathy
inferredcites →https://doi.org/10.1016/j.diabres.2012.11.006openalex-snapshot
By the numbers: New estimates from the IDF Diabetes Atlas Update for 2012
inferredcites →https://doi.org/10.1016/j.diabres.2018.02.023openalex-snapshot
IDF Diabetes Atlas: Global estimates of diabetes prevalence for 2017 and projections for 2045
inferredcites →https://doi.org/10.1016/j.ebiom.2022.104173openalex-snapshot
Transcriptional profiles predict treatment outcome in patients with tuberculosis and diabetes at diagnosis and at two weeks after initiation of anti-tuberculosis treatment
inferredcites →https://doi.org/10.1016/j.ebiom.2025.106050openalex-snapshot
Human alveolar macrophage function is impaired in tuberculosis contacts with diabetes
inferredcites →https://doi.org/10.1016/j.imlet.2017.03.017openalex-snapshot
Immunological response to Mycobacterium tuberculosis infection in blood from type 2 diabetes patients
inferredcites →https://doi.org/10.1016/j.jdiacomp.2018.07.001openalex-snapshot
Serum levels of chemokines IP-10, IL-8 and SDF-1 serve as good biomarkers for diabetes-tuberculosis nexus
inferredcites →https://doi.org/10.1016/j.jdiacomp.2022.108133openalex-snapshot
Serum levels of novel anti-inflammatory cytokine Interleukin-38 in diabetes patients infected with latent tuberculosis (DM-LTB-3)
inferredcites →https://doi.org/10.1016/j.jeas.2006.10.003openalex-snapshot
Hereditary hyperglycaemia and pancreatic degeneration in Guinea pigs
inferredcites →https://doi.org/10.1016/j.jmii.2019.10.008openalex-snapshot
How mycobacteria take advantage of the weakness in human immune system in the modern world
inferredcites →https://doi.org/10.1016/j.micinf.2005.08.014openalex-snapshot
Intragranulomatous necrosis in lungs of mice infected by aerosol with Mycobacterium tuberculosis is related to bacterial load rather than to any one cytokine or T cell type
inferredcites →https://doi.org/10.1016/j.micinf.2014.11.009openalex-snapshot
Increased resistin may suppress reactive oxygen species production and inflammasome activation in type 2 diabetic patients with pulmonary tuberculosis infection
inferredcites →https://doi.org/10.1016/j.micinf.2020.03.004openalex-snapshot
Increased susceptibility to Mycobacterium tuberculosis infection in a diet-induced murine model of type 2 diabetes
inferredcites →https://doi.org/10.1016/j.micpath.2016.06.002openalex-snapshot
Glucose levels affect LL-37 expression in monocyte-derived macrophages altering the Mycobacterium tuberculosis intracellular growth control
inferredcites →https://doi.org/10.1016/j.tube.2010.05.003openalex-snapshot
Regulatory T cell frequency and modulation of IFN-gamma and IL-17 in active and latent tuberculosis
inferredcites →https://doi.org/10.1016/j.tube.2012.10.003openalex-snapshot
Reduced Mycobacterium tuberculosis association with monocytes from diabetes patients that have poor glucose control
inferredcites →https://doi.org/10.1016/j.tube.2013.09.004openalex-snapshot
Damaging role of neutrophilic infiltration in a mouse model of progressive tuberculosis
inferredcites →https://doi.org/10.1016/j.tube.2015.06.004openalex-snapshot
Type 2 diabetes – Tuberculosis co-morbidity is associated with diminished circulating levels of IL-20 subfamily of cytokines
inferredcites →https://doi.org/10.1016/j.tube.2016.09.001openalex-snapshot
An adverse immune-endocrine profile in patients with tuberculosis and type 2 diabetes
inferredcites →https://doi.org/10.1016/j.tube.2016.10.004openalex-snapshot
Modulation of dendritic cell and monocyte subsets in tuberculosis-diabetes co-morbidity upon standard tuberculosis treatment
inferredcites →https://doi.org/10.1016/j.tube.2016.12.002openalex-snapshot
Anti-mycobacterial function of macrophages is impaired in a diet induced model of type 2 diabetes
inferredcites →https://doi.org/10.1016/j.tube.2018.06.009openalex-snapshot
Association between IL-15 and insulin plasmatic concentrations in patients with pulmonary tuberculosis and type 2 diabetes
inferredcites →https://doi.org/10.1016/j.tube.2018.08.007openalex-snapshot
Diabetes screen during tuberculosis contact investigations highlights opportunity for new diabetes diagnosis and reveals metabolic differences between ethnic groups
inferredcites →https://doi.org/10.1016/j.tube.2019.02.005openalex-snapshot
Dysregulation of key cytokines may contribute to increased susceptibility of diabetic mice to Mycobacterium bovis BCG infection
inferredcites →https://doi.org/10.1016/j.tube.2019.04.011openalex-snapshot
Diabetic trends and associated mortality in tuberculosis patients in Texas, a large population-based analysis
inferredcites →https://doi.org/10.1016/j.tube.2020.101935openalex-snapshot
Adults with Mycobacterium tuberculosis infection and pre-diabetes have increased levels of QuantiFERON interferon-gamma responses
inferredcites →https://doi.org/10.1016/s0962-8479(97)90016-2openalex-snapshot
Progression of chronic pulmonary tuberculosis in mice aerogenically infected with virulent Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1016/s1472-9792(02)00069-0openalex-snapshot
The mouse as a useful model of tuberculosis
inferredcites →https://doi.org/10.1016/s1472-9792(13)70015-5openalex-snapshot
Differential expression of monocyte surface markers among TB patients with diabetes co-morbidity
inferredcites →https://doi.org/10.1017/s0950268808000782openalex-snapshot
Impact of type 2 diabetes on manifestations and treatment outcome of pulmonary tuberculosis
inferredcites →https://doi.org/10.1038/nature09247openalex-snapshot
An interferon-inducible neutrophil-driven blood transcriptional signature in human tuberculosis
inferredcites →https://doi.org/10.1038/s41598-017-01767-4openalex-snapshot
Systems Immunology of Diabetes-Tuberculosis Comorbidity Reveals Signatures of Disease Complications
inferredcites →https://doi.org/10.1038/s41598-021-99257-1openalex-snapshot
Reactivation of latent tuberculosis through modulation of resuscitation promoting factors by diabetes
inferredcites →https://doi.org/10.1038/srep32484openalex-snapshot
High fat diet drives obesity regardless the composition of gut microbiota in mice
inferredcites →https://doi.org/10.1054/tuld.1998.0167openalex-snapshot
Hypodense alveolar macrophages in patients with diabetes mellitus and active pulmonary tuberculosis
inferredcites →https://doi.org/10.1086/590565openalex-snapshot
Tuberculosis in Poorly Controlled Type 2 Diabetes: Altered Cytokine Expression in Peripheral White Blood Cells
inferredcites →https://doi.org/10.1093/cid/ciaa751openalex-snapshot
Impact of Intermediate Hyperglycemia and Diabetes on Immune Dysfunction in Tuberculosis
inferredcites →https://doi.org/10.1093/infdis/jiac102openalex-snapshot
A Blunted GPR183/Oxysterol Axis During Dysglycemia Results in Delayed Recruitment of Macrophages to the Lung During Mycobacterium tuberculosis Infection
inferredcites →https://doi.org/10.1093/infdis/jit241openalex-snapshot
Expansion of Pathogen-Specific T-Helper 1 and T-Helper 17 Cells in Pulmonary Tuberculosis With Coincident Type 2 Diabetes Mellitus
inferredcites →https://doi.org/10.1093/infdis/jiu329openalex-snapshot
Diminished Systemic and Antigen-Specific Type 1, Type 17, and Other Proinflammatory Cytokines in Diabetic and Prediabetic Individuals With LatentMycobacterium tuberculosisInfection
inferredcites →https://doi.org/10.1093/infdis/jiv484openalex-snapshot
Impaired Cytokine but Enhanced Cytotoxic Marker Expression inMycobacterium tuberculosis–Induced CD8+T Cells in Individuals With Type 2 Diabetes and LatentMycobacterium tuberculosisInfection
inferredcites →https://doi.org/10.1093/infdis/jiw436openalex-snapshot
Impaired Recognition ofMycobacterium tuberculosisby Alveolar Macrophages From Diabetic Mice
inferredcites →https://doi.org/10.1093/ofid/ofz257openalex-snapshot
Plasma Proinflammatory Cytokines Are Markers of Disease Severity and Bacterial Burden in Pulmonary Tuberculosis
inferredcites →https://doi.org/10.1111/imcb.12497openalex-snapshot
Impact of type 2 diabetes on the capacity of human macrophages infected with Mycobacterium tuberculosis to modulate monocyte differentiation through a bystander effect
inferredcites →https://doi.org/10.1111/imm.12421openalex-snapshot
Type 2 diabetes mellitus is associated with altered CD 8+ T and natural killer cell function in pulmonary tuberculosis
inferredcites →https://doi.org/10.1111/imm.12496openalex-snapshot
Profiling leucocyte subsets in tuberculosis–diabetes co‐morbidity
inferredcites →https://doi.org/10.1111/imm.12632openalex-snapshot
Effect of standard tuberculosis treatment on naive, memory and regulatory T‐cell homeostasis in tuberculosis–diabetes co‐morbidity
inferredcites →https://doi.org/10.1111/imm.12762openalex-snapshot
Influence of diabetes mellitus on immunity to human tuberculosis
inferredcites →https://doi.org/10.1111/imm.13023openalex-snapshot
Elevated circulating levels of monocyte activation markers among tuberculosis patients with diabetes co‐morbidity
inferredcites →https://doi.org/10.1111/j.1365-2249.2009.04000.xopenalex-snapshot
Mycobacterial antigen-induced T helper type 1 (Th1) and Th2 reactivity of peripheral blood mononuclear cells from diabetic and non-diabetic tuberculosis patients and Mycobacterium bovis bacilli Calmette–Guérin (BCG)-vaccinated healthy subjects
inferredcites →https://doi.org/10.1111/j.1440-1843.2012.02184.xopenalex-snapshot
Significance of the frequency of CD4+CD25+CD127− T‐cells in patients with pulmonary tuberculosis and diabetes mellitus
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Immune dysfunction in patients with diabetes mellitus (DM)
inferredcites →https://doi.org/10.1128/iai.00611-13openalex-snapshot
The Intracellular Environment of Human Macrophages That Produce Nitric Oxide Promotes Growth of Mycobacteria
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Depressed immunological defence mechanisms in mice with experimentally induced diabetes
inferredcites →https://doi.org/10.1128/iai.32.1.42-47.1981openalex-snapshot
Differences in Response Among Inbred Mouse Strains to Infection with Small Doses of Mycobacterium bovis BCG
inferredcites →https://doi.org/10.1152/ajpendo.00256.2007openalex-snapshot
Nonobese, insulin-deficient Ins2Akitamice develop type 2 diabetes phenotypes including insulin resistance and cardiac remodeling
inferredcites →https://doi.org/10.1155/2012/139127openalex-snapshot
The Tuberculous Granuloma: An Unsuccessful Host Defence Mechanism Providing a Safety Shelter for the Bacteria?
inferredcites →https://doi.org/10.1155/2022/2422790openalex-snapshot
High Dimensionality Reduction and Immune Phenotyping of Natural Killer and Invariant Natural Killer Cells in Latent Tuberculosis-Diabetes Comorbidity
inferredcites →https://doi.org/10.1165/rcmb.2006-0478ocopenalex-snapshot
Tuberculosis Susceptibility of Diabetic Mice
inferredcites →https://doi.org/10.1165/rcmb.2010-0319ocopenalex-snapshot
IL-10 Blocks Phagosome Maturation in Mycobacterium tuberculosis– Infected Human Macrophages
inferredcites →https://doi.org/10.1172/jci23949openalex-snapshot
Host control of Mycobacterium tuberculosis is regulated by 5-lipoxygenase–dependent lipoxin production
inferredcites →https://doi.org/10.1177/20499361221095831openalex-snapshot
Tuberculosis and comorbidities: treatment challenges in patients with comorbid diabetes mellitus and depression
inferredcites →https://doi.org/10.1177/2058739219828628openalex-snapshot
RETRACTED: Detection and significance of TNF-α and hs-CRP in the pleural effusion of patients with diabetes and pulmonary tuberculosis
inferredcites →https://doi.org/10.1183/13993003.01891-2019openalex-snapshot
Diabetes is associated with genotypically drug-resistant tuberculosis
inferredcites →https://doi.org/10.1186/1741-7015-9-81openalex-snapshot
The impact of diabetes on tuberculosis treatment outcomes: A systematic review
inferredcites →https://doi.org/10.1186/1743-7075-3-17openalex-snapshot
Guinea pigs: A suitable animal model to study lipoprotein metabolism, atherosclerosis and inflammation
inferredcites →https://doi.org/10.1186/cc10021openalex-snapshot
Clinical review: Adiponectin biology and its role in inflammation and critical illness
inferredcites →https://doi.org/10.1186/s12879-017-2705-1openalex-snapshot
Low serum vitamin D levels in type 2 diabetes patients are associated with decreased mycobacterial activity
inferredcites →https://doi.org/10.1371/journal.pmed.0050152openalex-snapshot
Diabetes Mellitus Increases the Risk of Active Tuberculosis: A Systematic Review of 13 Observational Studies
inferredcites →https://doi.org/10.1371/journal.pone.0010030openalex-snapshot
Granuloma Encapsulation Is a Key Factor for Containing Tuberculosis Infection in Minipigs
inferredcites →https://doi.org/10.1371/journal.pone.0023366openalex-snapshot
Phagocytic Activity Is Impaired in Type 2 Diabetes Mellitus and Increases after Metabolic Improvement
inferredcites →https://doi.org/10.1371/journal.pone.0046824openalex-snapshot
Non-Diabetic Hyperglycemia Exacerbates Disease Severity in Mycobacterium tuberculosis Infected Guinea Pigs
inferredcites →https://doi.org/10.1371/journal.pone.0092977openalex-snapshot
Phagocytosis via Complement or Fc-Gamma Receptors Is Compromised in Monocytes from Type 2 Diabetes Patients with Chronic Hyperglycemia
inferredcites →https://doi.org/10.1371/journal.pone.0112108openalex-snapshot
Coincident Pre-Diabetes Is Associated with Dysregulated Cytokine Responses in Pulmonary Tuberculosis
inferredcites →https://doi.org/10.1371/journal.pone.0117941openalex-snapshot
The Effect of Hyperglycaemia on In Vitro Cytokine Production and Macrophage Infection with Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1371/journal.pone.0118436openalex-snapshot
Investigating the Causes for Decreased Levels of Glutathione in Individuals with Type II Diabetes
inferredcites →https://doi.org/10.1371/journal.pone.0173715openalex-snapshot
Hypervirulent Mycobacterium tuberculosis strain triggers necrotic lung pathology associated with enhanced recruitment of neutrophils in resistant C57BL/6 mice
inferredcites →https://doi.org/10.1371/journal.pone.0187967openalex-snapshot
Association between diabetes mellitus and active tuberculosis: A systematic review and meta-analysis
inferredcites →https://doi.org/10.1371/journal.ppat.1005972openalex-snapshot
NK-CD11c+ Cell Crosstalk in Diabetes Enhances IL-6-Mediated Inflammation during Mycobacterium tuberculosis Infection
inferredcites →https://doi.org/10.1371/journal.ppat.1008140openalex-snapshot
IL-22 produced by type 3 innate lymphoid cells (ILC3s) reduces the mortality of type 2 diabetes mellitus (T2DM) mice infected with Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1371/journal.ppat.1009578openalex-snapshot
Correction: IL-22 produced by type 3 innate lymphoid cells (ILC3s) reduces the mortality of type 2 diabetes mellitus (T2DM) mice infected with Mycobacterium tuberculosis
inferredcites →https://doi.org/10.14745/ccdr.v43i34a01openalex-snapshot
Latent tuberculosis infection: An overview
inferredcites →https://doi.org/10.1513/annalsats.201305-112ocopenalex-snapshot
Type 2 Diabetes Mellitus Coincident with Pulmonary Tuberculosis Is Associated with Heightened Systemic Type 1, Type 17, and Other Proinflammatory Cytokines
inferredcites →https://doi.org/10.1590/0074-02760170326openalex-snapshot
Type-2 diabetes alters the basal phenotype of human macrophages and diminishes their capacity to respond, internalise, and control Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1620/tjem.216.363openalex-snapshot
Higher Susceptibility of Type 1 Diabetic Rats to Mycobacterium tuberculosis Infection
inferredcites →https://doi.org/10.17615/grv0-jy81openalex-snapshot
The Guinea Pig as a Model of Infectious Diseases
inferredcites →https://doi.org/10.2147/rmhp.s354377openalex-snapshot
Impact of Diabetes Mellitus on the Immunity of Tuberculosis Patients: A Retrospective, Cross-Sectional Study
inferredcites →https://doi.org/10.3329/bjms.v17i1.35290openalex-snapshot
Comparative studies evaluating macrophage activity of pulmonary tuberculosis patients with and without diabetes mellitus (tb-dm and non tb-dm)
inferredcites →https://doi.org/10.3389/fcimb.2019.00335openalex-snapshot
Plasma Eicosanoid Levels in Tuberculosis and Tuberculosis-Diabetes Co-morbidity Are Associated With Lung Pathology and Bacterial Burden
inferredcites →https://doi.org/10.3389/fcimb.2019.00342openalex-snapshot
Changes in Host Response to Mycobacterium tuberculosis Infection Associated With Type 2 Diabetes: Beyond Hyperglycemia
inferredcites →https://doi.org/10.3389/fcimb.2021.640707openalex-snapshot
Mycobacterial Growth Inhibition Assay (MGIA) as a Host Directed Diagnostic Tool for the Evaluation of the Immune Response in Subjects Living With Type 2 Diabetes Mellitus
inferredcites →https://doi.org/10.3389/fcimb.2021.691823openalex-snapshot
Pre-Diabetes Increases Tuberculosis Disease Severity, While High Body Fat Without Impaired Glucose Tolerance Is Protective
inferredcites →https://doi.org/10.3389/fcimb.2021.756854openalex-snapshot
Decreased Frequencies of Gamma/Delta T Cells Expressing Th1/Th17 Cytokine, Cytotoxic, and Immune Markers in Latent Tuberculosis-Diabetes/Pre-Diabetes Comorbidity
inferredcites →https://doi.org/10.3389/fcimb.2022.957512openalex-snapshot
Immunological aspects of host–pathogen crosstalk in the co-pathogenesis of diabetes and latent tuberculosis
inferredcites →https://doi.org/10.3389/fendo.2020.00126openalex-snapshot
Evidence for a More Disrupted Immune-Endocrine Relation and Cortisol Immunologic Influences in the Context of Tuberculosis and Type 2 Diabetes Comorbidity
inferredcites →https://doi.org/10.3389/fimmu.2014.00219openalex-snapshot
The T-Cell Response to Lipid Antigens of Mycobacterium tuberculosis
inferredcites →https://doi.org/10.3389/fimmu.2017.01843openalex-snapshot
Deletion of TGF-β1 Increases Bacterial Clearance by Cytotoxic T Cells in a Tuberculosis Granuloma Model
inferredcites →https://doi.org/10.3389/fimmu.2018.00709openalex-snapshot
New Players in Immunity to Tuberculosis: The Host Microbiome, Lung Epithelium, and Innate Immune Cells
inferredcites →https://doi.org/10.3389/fimmu.2019.01142openalex-snapshot
Gut Microbiota Regulates Mincle Mediated Activation of Lung Dendritic Cells to Protect Against Mycobacterium tuberculosis
inferredcites →https://doi.org/10.3389/fimmu.2019.02464openalex-snapshot
Influence of Gut Microbiota on Progression to Tuberculosis Generated by High Fat Diet-Induced Obesity in C3HeB/FeJ Mice
inferredcites →https://doi.org/10.3389/fimmu.2020.601534openalex-snapshot
GPR183 Regulates Interferons, Autophagy, and Bacterial Growth During Mycobacterium tuberculosis Infection and Is Associated With TB Disease Severity
inferredcites →https://doi.org/10.3389/fimmu.2021.716819openalex-snapshot
Type 2 Diabetes Mellitus and Latent Tuberculosis Infection Moderately Influence Innate Lymphoid Cell Immune Responses in Uganda
inferredcites →https://doi.org/10.3389/fimmu.2022.973991openalex-snapshot
The impact of pulmonary tuberculosis on immunological and metabolic features of diabetic patients
inferredcites →https://doi.org/10.3389/fmicb.2022.884374openalex-snapshot
Unique Reciprocal Association Seen Between Latent Tuberculosis Infection and Diabetes Is Due to Immunoendocrine Modulation (DM-LTB-1)
inferredcites →https://doi.org/10.3390/biom11121763openalex-snapshot
High Glucose Concentrations Impair the Processing and Presentation of Mycobacterium tuberculosis Antigens In Vitro
inferredcites →https://doi.org/10.3390/life13010228openalex-snapshot
Diets Differently Regulate Pulmonary Pathogenesis and Immune Signaling in Mice during Acute and Chronic Mycobacterium tuberculosis Infection
inferredcites →https://doi.org/10.3390/pathogens11010087openalex-snapshot
Multi-Dimensionality Immunophenotyping Analyses of MAIT Cells Expressing Th1/Th17 Cytokines and Cytotoxic Markers in Latent Tuberculosis Diabetes Comorbidity
inferredcites →https://doi.org/10.3390/pathogens12010049openalex-snapshot
Mouse Models for Mycobacterium tuberculosis Pathogenesis: Show and Do Not Tell
inferredcites →https://doi.org/10.4046/trd.2016.79.4.201openalex-snapshot
Tuberculosis Infection and Latent Tuberculosis
inferredcites →https://doi.org/10.4049/jimmunol.1000304openalex-snapshot
Diabetic Mice Display a Delayed Adaptive Immune Response to Mycobacterium tuberculosis
inferredcites →https://doi.org/10.4269/ajtmh.2008.79.541openalex-snapshot
Mycobacterial Clearance from Sputum Is Delayed during the First Phase of Treatment in Patients with Diabetes
inferredcites →https://doi.org/10.7554/elife.46477openalex-snapshot
Persistent inflammation during anti-tuberculosis treatment with diabetes comorbidity
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