PD-1/PD-L1 Control of Antigen-Specifically Activated CD4 T-Cells of Neonates

Int J Mol Sci. 2023 Mar 16;24(6):5662. doi: 10.3390/ijms24065662.

Abstract

Newborns are highly susceptible to infections; however, the underlying mechanisms that regulate the anti-microbial T-helper cells shortly after birth remain incompletely understood. To address neonatal antigen-specific human T-cell responses against bacteria, Staphylococcus aureus (S. aureus) was used as a model pathogen and comparatively analyzed in terms of the polyclonal staphylococcal enterotoxin B (SEB) superantigen responses. Here, we report that neonatal CD4 T-cells perform activation-induced events upon S. aureus/APC-encounter including the expression of CD40L and PD-1, as well as the production of Th1 cytokines, concomitant to T-cell proliferation. The application of a multiple regression analysis revealed that the proliferation of neonatal T-helper cells was determined by sex, IL-2 receptor expression and the impact of the PD-1/PD-L1 blockade. Indeed, the treatment of S. aureus-activated neonatal T-helper cells with PD-1 and PD-L1 blocking antibodies revealed the specific regulation of the immediate neonatal T-cell responses with respect to the proliferation and frequencies of IFNγ producers, which resembled in part the response of adults' memory T-cells. Intriguingly, the generation of multifunctional T-helper cells was regulated by the PD-1/PD-L1 axis exclusively in the neonatal CD4 T-cell lineage. Together, albeit missing memory T-cells in neonates, their unexperienced CD4 T-cells are well adapted to mount immediate and strong anti-bacterial responses that are tightly controlled by the PD-1/PD-L1 axis, thereby resembling the regulation of recalled memory T-cells of adults.

Keywords: CD4 T cell; PD-1/PD-L1; Staphylococcus aureus (S. aureus); T-helper cells; bacteria; immune checkpoint molecule; newborn; pediatric immunology; staphylococcus enterotoxin B (SEB).

MeSH terms

  • Adult
  • Antigens / metabolism
  • B7-H1 Antigen / metabolism
  • CD4-Positive T-Lymphocytes*
  • Humans
  • Infant, Newborn
  • Programmed Cell Death 1 Receptor* / metabolism
  • Staphylococcus aureus / metabolism
  • T-Lymphocytes, Helper-Inducer

Substances

  • Programmed Cell Death 1 Receptor
  • B7-H1 Antigen
  • Antigens