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ssrn.4148192

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2 of the 71 references listed on this page are in the Retraction Watch database as retracted (export 2026-10-21): 10.1038/ncb3192 (notice 2024-03-04), 10.1073/pnas.1113421108 (notice 2025-08-04).

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/s10875-007-9084-0openalex-extracted

Host Innate Immune Response to Mycobacterium tuberculosis

inferredcites →https://doi.org/10.1016/j.biocel.2014.08.022openalex-extracted

IL-27 inhibits IFN-γ induced autophagy by concomitant induction of JAK/PI3 K/Akt/mTOR cascade and up-regulation of Mcl-1 in Mycobacterium tuberculosis H37Rv infected macrophages

inferredcites →https://doi.org/10.1016/j.cell.2004.11.038openalex-extracted

Autophagy Is a Defense Mechanism Inhibiting BCG and Mycobacterium tuberculosis Survival in Infected Macrophages

inferredcites →https://doi.org/10.1016/j.cellimm.2009.03.008openalex-extracted

TLR2 and its co-receptors determine responses of macrophages and dendritic cells to lipoproteins of Mycobacterium tuberculosis

inferredcites →https://doi.org/10.1016/j.chom.2009.08.004openalex-extracted

Vitamin D3 Induces Autophagy in Human Monocytes/Macrophages via Cathelicidin

inferredcites →https://doi.org/10.1016/j.chom.2012.07.009openalex-extracted

Neutrophils Exert Protection in the Early Tuberculous Granuloma by Oxidative Killing of Mycobacteria Phagocytosed from Infected Macrophages

inferredcites →https://doi.org/10.1016/j.cyto.2013.03.010openalex-extracted

Interleukin-27 inhibits phagosomal acidification by blocking vacuolar ATPases

inferredcites →https://doi.org/10.1016/j.freeradbiomed.2012.04.022openalex-extracted

Regulation of innate immunity by NADPH oxidase

inferredcites →https://doi.org/10.1016/j.imbio.2005.05.001openalex-extracted

Tuning of macrophage responses by Stat3-inducing cytokines: molecular mechanisms and consequences in infection

inferredcites →https://doi.org/10.1016/j.immuni.2007.07.022openalex-extracted

T Helper 2 Cytokines Inhibit Autophagic Control of Intracellular Mycobacterium tuberculosis

inferredcites →https://doi.org/10.1016/j.jmb.2017.08.012openalex-extracted

LC3-Associated Phagocytosis and Inflammation

inferredcites →https://doi.org/10.1016/j.smim.2014.09.010openalex-extracted

Macrophage immunoregulatory pathways in tuberculosis

inferredcites →https://doi.org/10.1016/j.tube.2019.04.008openalex-extracted

Dual activity of niclosamide to suppress replication of integrated HIV-1 and Mycobacterium tuberculosis (Beijing)

inferredcites →https://doi.org/10.1016/j.vaccine.2006.02.005openalex-extracted

Protection against an aerogenic Mycobacterium tuberculosis infection in BCG-immunized and DNA-vaccinated mice is associated with early type I cytokine responses

inferredcites →https://doi.org/10.1016/j.vaccine.2015.10.124openalex-extracted

Efficacy of parainfluenza virus 5 (PIV5)-based tuberculosis vaccines in mice

inferredcites →https://doi.org/10.1038/mi.2011.7openalex-extracted

The role of IL-10 in immune regulation during M. tuberculosis infection

inferredcites →https://doi.org/10.1038/ncb3192openalex-extracted

RETRACTED ARTICLE: Molecular characterization of LC3-associated phagocytosis reveals distinct roles for Rubicon, NOX2 and autophagy proteins

inferredcites →https://doi.org/10.1038/ni.3434openalex-extracted

Mycobacterium tuberculosis induces the miR-33 locus to reprogram autophagy and host lipid metabolism

inferredcites →https://doi.org/10.1038/s41598-017-07101-2openalex-extracted

Characterisation of lung macrophage subpopulations in COPD patients and controls

inferredcites →https://doi.org/10.1038/srep44485openalex-extracted

Human Immunodeficiency Virus Type-1 Myeloid Derived Suppressor Cells Inhibit Cytomegalovirus Inflammation through Interleukin-27 and B7-H4

inferredcites →https://doi.org/10.1042/bj20020691openalex-extracted

Phagosome maturation: aging gracefully

inferredcites →https://doi.org/10.1054/tuld.1999.0212openalex-extracted

Antituberculosis activity of certain antifungal and antihelmintic drugs

inferredcites →https://doi.org/10.1073/pnas.1111825108openalex-extracted

Reciprocal seasonal variation in vitamin D status and tuberculosis notifications in Cape Town, South Africa

inferredcites →https://doi.org/10.1073/pnas.1113421108openalex-extracted

RETRACTED: Microtubule-associated protein 1 light chain 3 alpha (LC3)-associated phagocytosis is required for the efficient clearance of dead cells

inferredcites →https://doi.org/10.1073/pnas.1120251109openalex-extracted

Mycobacterium tuberculosis Eis protein initiates suppression of host immune responses by acetylation of DUSP16/MKP-7

inferredcites →https://doi.org/10.1073/pnas.1707792114openalex-extracted

Mycobacterium tuberculosis is protected from NADPH oxidase and LC3-associated phagocytosis by the LCP protein CpsA

inferredcites →https://doi.org/10.1073/pnas.96.25.14459openalex-extracted

Toll-like receptor-2 mediates mycobacteria-induced proinflammatory signaling in macrophages

inferredcites →https://doi.org/10.1074/jbc.m110.100818openalex-extracted

Activation of IL-27 p28 Gene Transcription by Interferon Regulatory Factor 8 in Cooperation with Interferon Regulatory Factor 1

inferredcites →https://doi.org/10.1080/15548627.2016.1241922openalex-extracted

MIR144* inhibits antimicrobial responses against Mycobacterium tuberculosis in human monocytes and macrophages by targeting the autophagy protein DRAM2

inferredcites →https://doi.org/10.1084/jem.20061440openalex-extracted

Regulation of IL-27 p28 gene expression in macrophages through MyD88- and interferon-γ–mediated pathways

inferredcites →https://doi.org/10.1084/jem.20141520openalex-extracted

Interleukin 27R regulates CD4+ T cell phenotype and impacts protective immunity during Mycobacterium tuberculosis infection

inferredcites →https://doi.org/10.1086/589774openalex-extracted

Interleukin‐12 and Interleukin‐27 Regulate Macrophage Control of Mycobacterium tuberculosis

inferredcites →https://doi.org/10.1093/ajcn/86.5.1376openalex-extracted

Serum 25-hydroxyvitamin D in a West African population of tuberculosis patients and unmatched healthy controls

inferredcites →https://doi.org/10.1093/infdis/167.6.1481openalex-extracted

T Cell Response to Mycobacterium tuberculosis

inferredcites →https://doi.org/10.1097/inf.0b013e31815b494copenalex-extracted

Susceptibility to Mycobacterial Infections in Children With X-Linked Chronic Granulomatous Disease

inferredcites →https://doi.org/10.1111/imm.13154openalex-extracted

Origin and ontogeny of lung macrophages: from mice to humans

inferredcites →https://doi.org/10.1126/science.1096158openalex-extracted

Regulation of Phagosome Maturation by Signals from Toll-Like Receptors

inferredcites →https://doi.org/10.1126/science.285.5428.732openalex-extracted

Host Defense Mechanisms Triggered by Microbial Lipoproteins Through Toll-Like Receptors

inferredcites →https://doi.org/10.1126/scitranslmed.3003045openalex-extracted

Vitamin D Is Required for IFN-γ–Mediated Antimicrobial Activity of Human Macrophages

inferredcites →https://doi.org/10.1128/iai.59.8.2737-2743.1991openalex-extracted

Human Mycobacterium tuberculosis-reactive CD4+ T-cell clones: heterogeneity in antigen recognition, cytokine production, and cytotoxicity for mononuclear phagocytes

inferredcites →https://doi.org/10.1128/iai.67.8.3980-3988.1999openalex-extracted

Early Emergence of CD8+T Cells Primed for Production of Type 1 Cytokines in the Lungs ofMycobacterium tuberculosis-Infected Mice

inferredcites →https://doi.org/10.1128/iai.68.3.1231-1234.2000openalex-extracted

Transient Loss of Resistance to Pulmonary Tuberculosis in p47phox−/−Mice

inferredcites →https://doi.org/10.1128/iai.73.10.6831-6837.2005openalex-extracted

Effect of Deletion or Overexpression of the 19-Kilodalton Lipoprotein Rv3763 on the Innate Response to Mycobacterium tuberculosis

inferredcites →https://doi.org/10.1128/iai.74.5.2686-2696.2006openalex-extracted

The Mycobacterial 38-Kilodalton Glycolipoprotein Antigen Activates the Mitogen-Activated Protein Kinase Pathway and Release of Proinflammatory Cytokines through Toll-Like Receptors 2 and 4 in Human Monocytes

inferredcites →https://doi.org/10.1146/annurev.immunol.19.1.683openalex-extracted

Interleukin-10 and the Interleukin-10 Receptor

inferredcites →https://doi.org/10.1146/annurev.immunol.22.012703.104758openalex-extracted

Discovery and Biology of IL-23 and IL-27: Related but Functionally Distinct Regulators of Inflammation

inferredcites →https://doi.org/10.1165/rcmb.2010-0319ocopenalex-extracted

IL-10 Blocks Phagosome Maturation in Mycobacterium tuberculosis– Infected Human Macrophages

inferredcites →https://doi.org/10.1165/rcmb.2015-0147leopenalex-extracted

Flow Cytometry Reveals Similarities Between Lung Macrophages in Humans and Mice

inferredcites →https://doi.org/10.1186/1478-811x-12-16openalex-extracted

IL-12 and IL-27 regulate the phagolysosomal pathway in mycobacteria-infected human macrophages

inferredcites →https://doi.org/10.1186/s12890-017-0517-0openalex-extracted

TLR4-NOX2 axis regulates the phagocytosis and killing of Mycobacterium tuberculosis by macrophages

inferredcites →https://doi.org/10.1242/jcs.050443openalex-extracted

Direct recruitment of H+-ATPase from lysosomes for phagosomal acidification

inferredcites →https://doi.org/10.1242/jcs.222984openalex-extracted

LC3-associated phagocytosis at a glance

inferredcites →https://doi.org/10.1371/journal.ppat.1001230openalex-extracted

Mycobacterium tuberculosis Eis Regulates Autophagy, Inflammation, and Cell Death through Redox-dependent Signaling

inferredcites →https://doi.org/10.1371/journal.ppat.1002689openalex-extracted

Vitamin D Inhibits Human Immunodeficiency Virus Type 1 and Mycobacterium tuberculosis Infection in Macrophages through the Induction of Autophagy

inferredcites →https://doi.org/10.3389/fimmu.2021.647019openalex-extracted

Monocytic-Myeloid Derived Suppressor Cells of HIV-Infected Individuals With Viral Suppression Exhibit Suppressed Innate Immunity to Mycobacterium tuberculosis

inferredcites →https://doi.org/10.3945/jn.108.094979openalex-extracted

Hypovitaminosis D Is Common among Pulmonary Tuberculosis Patients in Tanzania but Is Not Explained by the Acute Phase Response

inferredcites →https://doi.org/10.4049/jimmunol.0802217openalex-extracted

NADPH Oxidase 2 Interaction with TLR2 Is Required for Efficient Innate Immune Responses to Mycobacteria via Cathelicidin Expression

inferredcites →https://doi.org/10.4049/jimmunol.148.1.189openalex-extracted

T lymphocytes mediating protection and cellular cytolysis during the course of Mycobacterium tuberculosis infection. Evidence for different kinetics and recognition of a wide spectrum of protein antigens

inferredcites →https://doi.org/10.4049/jimmunol.150.5.1886openalex-extracted

Macrophage activation: lipoarabinomannan from avirulent and virulent strains of Mycobacterium tuberculosis differentially induces the early genes c-fos, KC, JE, and tumor necrosis factor-alpha

inferredcites →https://doi.org/10.4049/jimmunol.160.9.4490openalex-extracted

Induction of In Vitro Human Macrophage Anti- Mycobacterium tuberculosis Activity: Requirement for IFN-γ and Primed Lymphocytes

inferredcites →https://doi.org/10.4049/jimmunol.162.9.5407openalex-extracted

Mice Deficient in CD4 T Cells Have Only Transiently Diminished Levels of IFN-γ, Yet Succumb to Tuberculosis

inferredcites →https://doi.org/10.4049/jimmunol.169.6.3155openalex-extracted

Toll-Like Receptor 4 Expression Is Required to Control Chronic Mycobacterium tuberculosis Infection in Mice

inferredcites →https://doi.org/10.4049/jimmunol.172.1.567openalex-extracted

Signal Transducer and Activator of Transcription 3 Is the Dominant Mediator of the Anti-Inflammatory Effects of IL-10 in Human Macrophages

inferredcites →https://doi.org/10.4049/jimmunol.173.5.3392openalex-extracted

IL-6 and IL-10 Induction from Dendritic Cells in Response to Mycobacterium tuberculosis Is Predominantly Dependent on TLR2-Mediated Recognition

inferredcites →https://doi.org/10.4049/jimmunol.174.6.3534openalex-extracted

The IL-27 Receptor Chain WSX-1 Differentially Regulates Antibacterial Immunity and Survival during Experimental Tuberculosis

inferredcites →https://doi.org/10.4049/jimmunol.177.11.7880openalex-extracted

General Nature of the STAT3-Activated Anti-Inflammatory Response

inferredcites →https://doi.org/10.4049/jimmunol.178.11.7190openalex-extracted

IFN-γ- and TNF-Independent Vitamin D-Inducible Human Suppression of Mycobacteria: The Role of Cathelicidin LL-37

inferredcites →https://doi.org/10.4049/jimmunol.178.12.7607openalex-extracted

IL-27 Synthesis Induced by TLR Ligation Critically Depends on IFN Regulatory Factor 3

inferredcites →https://doi.org/10.4049/jimmunol.179.4.2060openalex-extracted

Cutting Edge: Vitamin D-Mediated Human Antimicrobial Activity against Mycobacterium tuberculosis Is Dependent on the Induction of Cathelicidin

inferredcites →https://doi.org/10.4049/jimmunol.181.10.7115openalex-extracted

IL-15 Links TLR2/1-Induced Macrophage Differentiation to the Vitamin D-Dependent Antimicrobial Pathway

inferredcites →https://doi.org/10.4161/15548627.2014.981791openalex-extracted

IFNG-mediated immune responses enhance autophagy againstMycobacterium tuberculosisantigens in patients with active tuberculosis

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1007/s12265-025-10656-5openalex-snapshot

Recent Insights Into Targeting Interleukin-27 in Coronary Artery Disease

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