Mature CD8+ T lymphocyte response to viral infection during fetal life

Abstract

Immunization of newborns against viral infections may be hampered by ineffective CD8 + T cell responses. To characterize the function of CD8 + T lymphocytes in early life, we studied newborns with congenital human cytomegalovirus (HCMV) infection. We demonstrate that HCMV infection in utero leads to the expansion and the differentiation of mature HCMV-specific CD8 + T cells, which have similar characteristics to those detected in adults. High frequencies of HCMV-specific CD8 + T cells were detected by ex vivo tetramer staining as early as after 28 weeks of gestation. During the acute phase of infection, these cells had an early differentiation phenotype (CD28 -CD27 + CD45RO + , perforin low ), and they acquired a late differentiation phenotype (CD28 -CD27 -CD45RA + , perforin high ) during the course of the infection. The differentiated cells showed potent perforin-dependent cytolytic activity and produced antiviral cytokines. The finding of a mature and functional CD8 + T cell response to HCMV suggests that the machinery required to prime such responses is in place during fetal life and could be used to immunize newborns against viral pathogens.