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Distinct Mitochondria-Mediated T-Cell Apoptosis Responses in Children and Adults With Coronavirus Disease 2019

Yang Yang, Liangjian Kuang, Linhai Li, Yongjian Wu, Bei Zhong, Xi Huang

2021The Journal of Infectious Diseases34 citationsDOIOpen Access PDF

Abstract

BACKGROUND: Lymphopenia is a key feature for adult patients with coronavirus disease 2019 (COVID-19), although it is rarely observed in children. The underlying mechanism remains unclear. METHODS: Immunohistochemical and flow cytometric analyses were used to compare the apoptotic rate of T cells from COVID-19 adults and children and apoptotic responses of adult and child T cells to COVID-19 pooled plasma. Biological properties of caspases and reactive oxygen species were assessed in T cells treated by COVID-19 pooled plasma. RESULTS: Mitochondria apoptosis of peripheral T cells were identified in COVID-19 adult patient samples but not in the children. Furthermore, increased tumor necrosis factor-α and interleukin-6 in COVID-19 plasma induced mitochondria apoptosis and caused deoxyribonucleic acid damage by elevating reactive oxygen species levels of the adult T cells. However, the child T cells showed tolerance to mitochondrial apoptosis due to mitochondria autophagy. Activation of autophagy could decrease apoptotic sensitivity of the adult T cells to plasma from COVID-19 patients. CONCLUSIONS: Our results indicated that the mitochondrial apoptosis pathway was activated in T cells of COVID-19 adult patients specifically, which may shed light on the pathophysiological difference between adults and children infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2 ).

Topics & Concepts

ApoptosisMitochondrionReactive oxygen speciesAutophagyTumor necrosis factor alphaCaspaseIntrinsic apoptosisImmunologyProgrammed cell deathBiologyCoronavirusCoronavirus disease 2019 (COVID-19)DiseaseMedicineCancer researchCell biologyPathologyBiochemistryInfectious disease (medical specialty)COVID-19 Clinical Research StudiesLong-Term Effects of COVID-19Cell death mechanisms and regulation