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Changes of CD8+CD28- Tregs and Gamma-Delta-T-cells in a Neonate with Intrauterine Cytomegalovirus Infection: A Case Report.
Chen, Xian; Jin, Zhenchao; Zhou, Ping; Xie, Tingyan; Jiang, Fan; Tang, Quan.
Afiliación
  • Chen X; Department of Laboratory Medicine, Shenzhen Baoan Women's and Children's Hospital, Shenzhen, China.
  • Jin Z; Department of Neonatology, Shenzhen Baoan Women's and Children's Hospital, Shenzhen, China.
  • Zhou P; Department of Neonatology, Shenzhen Baoan Women's and Children's Hospital, Shenzhen, China.
  • Xie T; Research Laboratory, Shenzhen Baoan Women's and Children's Hospital, Shenzhen, China.
  • Jiang F; Department of Laboratory Medicine, Shenzhen Baoan Women's and Children's Hospital, Shenzhen, China.
  • Tang Q; Research Laboratory, Shenzhen Baoan Women's and Children's Hospital, Shenzhen, China. tangquan1987@126.com.
BMC Pediatr ; 24(1): 587, 2024 Sep 16.
Article en En | MEDLINE | ID: mdl-39285316
ABSTRACT

BACKGROUND:

Congenital cytomegalovirus (cCMV) infection can lead to a range of adverse outcomes. The majority of cCMV neonates with clinical symptoms are infected postnatally; however, established cases of intrauterine infection are uncommon, resulting in a paucity of reports on clinical findings and lymphocytes expression in CMV-infected neonates. CASE PRESENTATION We followed a neonate with cCMV infection from the onset of hospitalization to several months of follow-up. This infant was intrauterine CMV-positive in the amniotic fluid of the mother at 21 weeks' gestation and received intravenous ganciclovir infusion and sequential oral valganciclovir after birth. The typical clinical signs manifested in the nervous system, liver, and peripheral blood and were documented during the hospitalizaion period and up to the follow-up visit. Flow cytometry was employed to examine the expression of T cells, their subsets, and the associated cytokines in peripheral blood samples at various time points. The flow data for the cCMV neonate were compared with those of the controls at each time point. Following treatment, clinical symptoms improved and the infant became CMV negative. However, developmental delays occurred later in life. The proportion of CD8+CD28- Tregs in the peripheral blood of the neonate with congenital CMV infection was higher than that in the controls at the three time points. The expression levels of perforin and granzyme B secreted by γδ T cells (Vδ1 and Vδ2 T cells), increased during the course of hospitalization until follow-up and were higher than those in the controls at the three time points.

CONCLUSIONS:

Despite the alleviation of clinical symptoms, developmental delay in later life remains inevitable in this intrauterine cCMV neonate. CD8+CD28- Tregs and Vδ1 and Vδ2 T cells secreting perforin and granzyme B may be involved in congenital CMV infection, although this hypothesis requires validation in a larger study. This report may contribute to our understanding of the effect of current treatment and the immune status of intrauterine cCMV-infected neonates.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Linfocitos T Reguladores / Infecciones por Citomegalovirus Límite: Female / Humans / Male / Newborn / Pregnancy Idioma: En Revista: BMC Pediatr Asunto de la revista: PEDIATRIA Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Linfocitos T Reguladores / Infecciones por Citomegalovirus Límite: Female / Humans / Male / Newborn / Pregnancy Idioma: En Revista: BMC Pediatr Asunto de la revista: PEDIATRIA Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido