A Genetic Model Reveals Biological Features of Neonatal CD4 Helper Cells Undergone Homeostasis in Mice.

CD4 ⁺ T cells are essential for regulating effective immune response to pathogens and immune balance. Recent studies have demonstrated the unique features of T cells in neonate mice, such as more sensitive to antigen response and preference toward T helper 2 (Th2) response and regulatory T cells (Tregs) differentiation. However, the biological characteristics of neonatal age-derived CD4 ⁺ T cells following homeostasis remain unclear. Here we utilized a lineage tracing model of TCR δ ^CreER R26 ^ZsGreen to mark neonatal- and adult-derived CD4 ⁺ T cells followed by a combination analysis of activation, proliferation, survival, and differentiation. Our results showed that neonatal CD4 ⁺ T cells had higher capacity of activation, proliferation, apoptosis, and differentiation toward Th2 and T helper 17 (Th17) lineages, accompanied by a reduced potential for T helper 1 (Th1), T helper 9 (Th9), and Treg lineages. In contrast, tracked neonatal CD4 ⁺ T cells exhibited similar characters of above-mentioned of tracked adult cells in adult mice. Therefore, our data support a natural requirement for CD4 ⁺ T cells to acquire fully-equipped functional potentials of adult cells.
Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
(Copyright © 2021 Lei, Zhang, Yang, Su, Liu, Yang, Wang, Zou, Wang, Jiao, Zhang, Zheng, Zhang, Zhang, Shi, Zhou, Sun and Zhang.)