Neonatal T cells unleash innate powers to combat congenital cytomegalovirus infection Editorial


Author: Grassmann, S.
Title: Neonatal T cells unleash innate powers to combat congenital cytomegalovirus infection
Abstract: Approximately 1 in 200 newborns worldwide are affected by congenital cytomegalovirus (CMV). Most of these cases are asymptomatic due to successful control of the infection by the newborn's immune system. In this issue of the JCI, Semmes et al. characterized the cellular immune response in cord blood of neonates with CMV infection. The authors found that conventional T cells with NK-like features expanded during congenital CMV infection. To exert their antiviral function, these cells relied on Fc receptors, recognizing virus-infected cells bound by IgG. Thereby, the fetal and maternal immune system can optimally cooperate to control CMV infection: maternal IgG crossing the placenta opsonizes virus-infected cells subsequently lysed by neonatal NK-like T cells. This finding suggests that innate-like programming of conventional T cells may have evolved to combat congenital CMV infection, offering insights that could inform the development of future therapies. Copyright: © 2025, Grassmann et al.
Keywords: review; nonhuman; t lymphocyte; t-lymphocytes; immune system; immunology; fetal blood; fetus blood; cellular immunity; immunoglobulin g; infant, newborn; newborn; natural killer cell; umbilical cord blood; killer cells, natural; pregnancy; fc receptor; innate immunity; immunity, innate; drug therapy; cytomegalovirus infection; cytomegalovirus; placenta; antiviral activity; receptors, fc; cytomegalovirus infections; humans; human; female; special situation for pharmacovigilance; congenital cytomegalovirus infection
Journal Title: Journal of Clinical Investigation
Volume: 135
Issue: 1
ISSN: 0021-9738
Publisher: American Society for Clinical Investigation  
Date Published: 2025-01-02
Start Page: e187789
Language: English
DOI: 10.1172/jci187789
PUBMED: 39744950
PROVIDER: scopus
PMCID: PMC11684798
DOI/URL:
Notes: Editorial -- Source: Scopus
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