In neonatal C57BL/6 mice, subcutaneous live BCG (10β΅ CFU, TICE strain) at postnatal day 1 raised 7-day survival to cecal-slurry polymicrobial sepsis to 82% versus 44% in saline controls (p<0.01); day-4 vaccination gave 65% versus 35%. Heat-inactivated BCG conferred no survival benefit, implicating live-microbe immunostimulation rather than passive antigen exposure .
BCG alone induced a modest cytokine response but blunted the septic response, lowering IL-6, KC, and M-CSF at 18 h post-sepsis (p<0.05). Flow cytometry showed expanded splenic LSK and GMP progenitors and CD11bβΊGr1βΊ MHCII-dim/- cells pre-sepsis; by 18 h post-sepsis these had declined in both groups but remained higher in vaccinated pups. Unexpectedly, CD11bβΊGr1βΊ cells from septic neonates (vaccinated or not) flipped from T-cell suppression to stimulating T-cell proliferation ex vivo, contradicting a prior monomicrobial-sepsis report .
scRNA-seq of 205,768 splenocytes (n=5β7/group, plus adult reference cohorts) identified M- and PMN-MDSC subsets via adult CLP reference animals. Sepsis alone upregulated 677 DEGs in PMN-MDSCs (525 up/152 down); BCG post-sepsis induced only 24 DEGs in PMN-MDSCs (mostly down) and 10 in M-MDSCs, suppressing neutrophil-degranulation and TLR4/MyD88-linked pathways and downregulating H1 linker histone genes across myeloid cells. RNA-velocity trajectories favored immature-to-mature neutrophil differentiation in vaccinated septic mice .
Strengths: rigorous litter-randomized design, live vs heat-inactivated BCG control isolating viability dependence, orthogonal functional (T-cell co-culture, Seahorse OCR/ECAR), flow, and transcriptomic readouts; public data (GEO GSE276868) support reproducibility .
Limitations and blind spots: (1) bacterial loads were not quantifiedβsurvival benefit could reflect inflammation tolerance rather than improved microbial clearance, a distinction the authors concede; (2) Gr1/CD11b sorting for functional assays conflates MDSCs with PMNs/monocytes, which the authors acknowledge ; (3) single-organ (spleen) sampling and only a 6/18-h post-sepsis window leave immune-memory duration and extramedullary compartments untested; (4) murine-to-human extrapolation is uncertain despite converging human BCG evidence (Guinea-Bissau RCTs) cited within the paper; (5) small pooled samples (3 pups/pool for Seahorse, n=4β7 per cytokine group) reduce statistical power and pooling risks pseudoreplication; (6) surprisingly, post-septic CD11bβΊGr1βΊ cells from naive mice also became T-cell stimulatory, weakening the causal claim that BCG-driven MDSC reprogramming is the survival mechanism. A related mouse study shows TET2-dependent trained-immunity memory can concurrently drive hematopoietic dysfunction, warning that myeloid-biased reprogramming may carry trade-offs not assessed here .
What would falsify the trained-immunity mechanism: a repeat experiment showing no survival benefit with BCG (already partially at risk given dose/timing sensitivity), depleting CD11bβΊGr1βΊ cells without abolishing protection, or demonstrating equal protection from heat-killed BCG in a larger cohort. Long-term epigenetic assessment of H1 histone changes in offspring would also be required to confirm durable training rather than transient priming.
This work extends the Brook et al. emergency-granulopoiesis framework by resolving which myeloid subsets are reprogrammed at single-cell resolution in neonates, and aligns mechanistically with human neonatal BCG data showing HSPC/monocyte reprogramming. Its translational value hinges on whether HI-BCG or nonviable alternatives can ever substituteβan avenue the null HI-BCG result makes unlikely, complicating use in high-risk settings.
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