Altered mitochondrial respiration in peripheral blood mononuclear cells of post-acute sequelae of SARS-CoV-2 infection

被引:4
作者
Dirajlal-Fargo, Sahera [1 ,2 ]
Maison, David P. [3 ]
Durieux, Jared C. [1 ]
Andrukhiv, Anastasia [3 ]
Funderburg, Nicholas [4 ]
Ailstock, Kate [4 ]
Gerschenson, Mariana [3 ,6 ]
Mccomsey, Grace A. [1 ,5 ]
机构
[1] Case Western Reserve Univ, Cleveland, OH 44106 USA
[2] Ann & Robert H Lurie Childrens Hosp, Chicago, IL USA
[3] Univ Hawaii Manoa, John A Burns Sch Med, Dept Cell & Mol Biol, Honolulu, HI 96822 USA
[4] Ohio State Univ, Sch Hlth & Rehabil Sci, Div Med Lab Sci, Columbus, OH USA
[5] Case Western Reserve Univ, Univ Hosp Cleveland, Pediat & Med, 11100 Euclid Ave,Lakeside 1400F, Cleveland, OH 44106 USA
[6] Univ Hawaii Manoa, John A Burns Sch Med, Cell & Mol Biol, 651 Ilalo St,BSB 211B, Honolulu, HI 96813 USA
基金
美国国家卫生研究院;
关键词
COVID; Long COVID; Mitochondria; PASC; COVID-19; SYMPTOMS;
D O I
10.1016/j.mito.2024.101849
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Peripheral blood mononuclear cells (PBMC) mitochondrial respiration was measured ex vivo from participants without a history of COVID (n = 19), with a history of COVID and full recovery (n = 20), and with PASC (n = 20). Mean mitochondrial basal respiration, ATP-linked respiration, maximal respiration, spare respiration capacity, ATP-linked respiration, and non-mitochondrial respiration were highest in COVID + PASC+ (p <= 0.04). Every unit increase in non-mitochondrial respiration, ATP-linked respiration, basal respiration, spare respiration capacity, and maximal respiration increased the predicted odds of PASC between 1 % and 6 %. Mitochondrial dysfunction in PBMCs may be contributing to the etiology of PASC.
引用
收藏
页数:8
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