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. 2022 Jan 21;11:e70393. doi: 10.7554/eLife.70393

Author response table 1.

Present manuscript: Baseline signature associated with risk Moncunill et al. 2020 STM: Protective signature
PBMC sampling timepoint Baseline 1 month post-third vaccination
PBMC stimulation Vehicle (DMSO); stimulated on site before cryopreservation of cell pellets for subsequent RNA extraction. 24-hour antigen (CSP) stimulation adjusted by vehicle (DMSO); PBMC were cryopreserved before stimulation
Background correction N/A Yes, subtraction of expression in vehicle-stimulated PBMC (thus the observed response is specific to antigen stimulation, i.e. recall response)
Presence of monocyte-related BTMs Yes, of the 45 BTMs, 7 were monocyte-related: M81, M118.1, M11.0, M118.0, S4, M73, M4.15 Yes, of the 24 BTMs, 3 were monocyte-related: M81, M118.1, M11.0
Gene expression measurement RNA-seq Microarray
Hypothesis: Stabilin-1high immunosuppressive monocytes circulating at baseline may inhibit protective RTS,S-induced T-cell responses [supported by (18)] or another RTS,S-induced protective adaptive response. Protected individuals may have monocytes that are qualitatively superior in mediating, e.g., Fc receptor/antibody-dependent responses (reflected by an altered transcriptional profile), resulting in improved control of infection.