Skip to main content
. 2022 Sep 30;13:989464. doi: 10.3389/fmicb.2022.989464

Table 2.

Summary table containing the technique and major conclusions of the articles discussed in this section.

Technique Major conclusions References
Seq-Well Genetic profile of macrophages exposed to M. tuberculosis Gierahn et al., 2017
10x Chromium Single-cell landscape of M. tuberculosis-infected macaques lungs during TB and latency Esaulova et al., 2021
CITE-Seq Differential abundance and function of TH17 subset between progressors and non-progressors donors Nathan et al., 2021
10x Chromium Identification of latent individuals with high risk to develop active TB disease based on monocytes immune cells Bossel Ben-Moshe et al., 2019
10x Chromium Identification of NK cell subset depleted, and monocytes and B cells increase during TB Cai et al., 2020
CITE-Seq Understanding of the roles that different host cell populations play during the course of an infection Pisu et al., 2021
Seq-Well S3 Transcriptional landscape of inflammatory skin disease, leprosy Hughes et al., 2020
10x Chromium Primary suppressive landscape in the L-LEP patients Mi et al., 2022
Seq-Well Single-cell profiling of tuberculosis lung granulomas Gideon et al., 2020
Seq-Well Integration of scRNA-seq with spatial sequencing, to delineate the cellular and molecular structure of the organized granuloma in leprosy Ma et al., 2021
In situ sequencing Different immune landscapes of M. tuberculosis granulomas depending on the time after infection Carow et al., 2019