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Immune profiling in M. tuberculosis infection enables stratification of patients with active disease

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What this work says

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

inferredcites →https://doi.org/10.1016/j.cell.2016.09.024openalex-snapshot

Genetic Adaptation and Neandertal Admixture Shaped the Immune System of Human Populations

inferredcites →https://doi.org/10.1016/j.celrep.2016.08.011openalex-snapshot

Standardized Whole-Blood Transcriptional Profiling Enables the Deconvolution of Complex Induced Immune Responses

inferredcites →https://doi.org/10.1016/j.chom.2015.12.003openalex-snapshot

Antigen Export Reduces Antigen Presentation and Limits T Cell Control of M. tuberculosis

inferredcites →https://doi.org/10.1016/j.clim.2017.09.019openalex-snapshot

Standardized whole blood stimulation improves immunomonitoring of induced immune responses in multi-center study

inferredcites →https://doi.org/10.1016/j.immuni.2014.03.002openalex-snapshot

Functional Analysis via Standardized Whole-Blood Stimulation Systems Defines the Boundaries of a Healthy Immune Response to Complex Stimuli

inferredcites →https://doi.org/10.1016/j.jinf.2016.11.010openalex-snapshot

Biomarkers for discrimination between latent tuberculosis infection and active tuberculosis disease

inferredcites →https://doi.org/10.1016/j.tube.2011.02.006openalex-snapshot

Discriminating between latent and active tuberculosis with multiple biomarker responses

inferredcites →https://doi.org/10.1016/s0140-6736(15)01316-1openalex-snapshot

A blood RNA signature for tuberculosis disease risk: a prospective cohort study

inferredcites →https://doi.org/10.1016/s2213-2600(16)00048-5openalex-snapshot

Genome-wide expression for diagnosis of pulmonary tuberculosis: a multicohort analysis

inferredcites →https://doi.org/10.1038/cti.2014.3openalex-snapshot

Clinical immune‐monitoring strategies for predicting infection risk in solid organ transplantation

inferredcites →https://doi.org/10.1038/ni1300openalex-snapshot

Systemic activation of dendritic cells by Toll-like receptor ligands or malaria infection impairs cross-presentation and antiviral immunity

inferredcites →https://doi.org/10.1038/s41564-019-0380-2openalex-snapshot

A systematic review of biomarkers to detect active tuberculosis

inferredcites →https://doi.org/10.1056/nejmoa1714021openalex-snapshot

Prevention of M. tuberculosis Infection with H4:IC31 Vaccine or BCG Revaccination

inferredcites →https://doi.org/10.1073/pnas.1714765115openalex-snapshot

Distinctive roles of age, sex, and genetics in shaping transcriptional variation of human immune responses to microbial challenges

inferredcites →https://doi.org/10.1128/jcm.02803-15openalex-snapshot

Interferon Gamma Release Assays for Latent Tuberculosis: What Are the Sources of Variability?

inferredcites →https://doi.org/10.1146/annurev-immunol-032712-095939openalex-snapshot

The Immune Response in Tuberculosis

inferredcites →https://doi.org/10.1164/rccm.201704-0817ocopenalex-snapshot

Optimization and Interpretation of Serial QuantiFERON Testing to Measure Acquisition of Mycobacterium tuberculosis Infection

inferredcites →https://doi.org/10.1183/09031936.00114810openalex-snapshot

Interferon-γ release assays for the diagnosis of active tuberculosis: a systematic review and meta-analysis

inferredcites →https://doi.org/10.1183/13993003.00153-2018openalex-snapshot

T-cell biomarkers for diagnosis of tuberculosis: candidate evaluation by a simple whole blood assay for clinical translation

inferredcites →https://doi.org/10.1186/1471-2466-9-21openalex-snapshot

Host markers in Quantiferon supernatants differentiate active TB from latent TB infection: preliminary report

inferredcites →https://doi.org/10.1371/journal.pmed.1002152openalex-snapshot

The Global Burden of Latent Tuberculosis Infection: A Re-estimation Using Mathematical Modelling

inferredcites →https://doi.org/10.3389/fimmu.2017.00796openalex-snapshot

Deconvolution of the Response to Bacillus Calmette–Guérin Reveals NF-κB-Induced Cytokines As Autocrine Mediators of Innate Immunity

What points at this work

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

inferred← citeshttps://doi.org/10.3389/fimmu.2022.1024224openalex-snapshot

Innate immune function during antineoplastic treatment is associated with 12-months survival in non-small cell lung cancer

inferred← citeshttps://doi.org/10.3389/fimmu.2022.897193openalex-snapshot

Tuberculosis alters immune-metabolic pathways resulting in perturbed IL-1 responses

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