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. Author manuscript; available in PMC: 2009 Jan 2.
Published in final edited form as: Curr Immunol Rev. 2007 Aug;3(3):151–159. doi: 10.2174/157339507781483496

Table 1.

Potential Impact of Populations/Processes Either Differentially Represented in or Unique to the Neonate

Cell Subset/Process Potential Consequences
Developmental specific epigenetic patterns at the Th2 and Th1 locus Rapid development of robust Th2 function (mouse); persistence of low level Th2 function in Th1 cells (human); typically reduced Th1 responses (human)
↑ homeostatically proliferating cells Natural memory population; both Th1 and Th2 rapid effector activity; may provide mature levels of protection against cross-reactive exogenous antigens (human, mouse)
↑ fetal origin cells Robust cytokine production; variable Th1/Th2 ratios, depending on antigen concentration (mouse) or unknown conditions (human)
↑ RTE Variable IL-2, IL-4 production and proliferation
↑ cells with forbidden TCR May contribute to early life autoimmunity but also to responses against cross-reacting infectious agents
↓ Treg activity/numbers May modulate the development of either Th1 or Th2 function
↑ TCR with no N region Promiscuous reactivity, beneficial in infections; Low affinity or reduced reactivity to self-antigens, protective against autoimmunity