Single-Cell Mapping of Progressive Fetal-to-Adult Transition in Human Naive T Cells

Whereas the human fetal immune system is poised to generate immune tolerance and suppress inflammation in utero, an adult-like immune system emerges to orchestrate anti-pathogen immune responses in post-natal life. It has been posited that cells of the adult immune system arise as a discrete ontological layer'' of hematopoietic stem-progenitor cells (HSPCs) and their progeny; evidence supporting this model in humans has, however, been inconclusive. Here, we combine bulk and single-cell transcriptional profiling of lymphoid cells, myeloid cells, and HSPCs from fetal, perinatal, and adult developmental stages to demonstrate that the fetal-to-adult transition occurs progressively along a continuum of maturity-with a substantial degree of inter-individual variation at the time of birth-rather than via a transition between discrete waves. These findings have important implications for the design of strategies for prophylaxis against infection in the newborn and for the use of umbilical cord blood (UCB) in the setting of transplantation.

Automated summary

The human fetal immune system is designed to generate immune tolerance and suppress inflammation in utero, while the adult immune system orchestrates anti-pathogen immune responses after birth. Cells of the adult immune system are posited to arise from a discrete layer of hematopoietic stem-progenitor cells and their progeny.