Chitinase-3-like Protein 1 Is Associated with Poor Virologic Control and Immune Activation in Children Living with HIV

被引:7
作者
Bernard, Isabelle [1 ]
Ransy, Doris G. G. [2 ]
Brophy, Jason [3 ,4 ]
Kakkar, Fatima [5 ]
Bitnun, Ari [6 ]
Samson, Lindy [3 ]
Read, Stanley [6 ]
Soudeyns, Hugo [2 ,7 ]
Hawkes, Michael T. T. [1 ,8 ,9 ,10 ,11 ]
机构
[1] Univ Alberta, Dept Pediat, Edmonton, AB T6G 2R3, Canada
[2] Ctr Rech CHU Sainte Justine, Unite immunopathol Virale, Montreal, PQ H3T 1C5, Canada
[3] Childrens Hosp Eastern Ontario, Div Infect Dis, Ottawa, ON K1H 8L1, Canada
[4] Univ Ottawa, Dept Pediat, Ottawa, ON K1N 6N5, Canada
[5] Univ Montreal, Dept Pediat, CHU Sainte Justine, Montreal, PQ H3T 1C5, Canada
[6] Univ Toronto, Hosp Sick Children, Dept Pediat, Div Infect Dis, Toronto, ON M5G 1X8, Canada
[7] Univ Montreal, Dept Microbiol Infectiol & Immunol, Montreal, PQ H3T 1J4, Canada
[8] Univ Alberta, Sch Publ Hlth, Edmonton, AB T6G 1C9, Canada
[9] Univ Alberta, Dept Med Microbiol & Immunol, Edmonton, AB T6G 1C9, Canada
[10] Stollery Sci Lab, Edmonton, AB T6G 1C9, Canada
[11] Women & Childrens Hlth Res Inst, Edmonton, AB T6G 1C9, Canada
来源
VIRUSES-BASEL | 2022年 / 14卷 / 12期
基金
加拿大健康研究院;
关键词
child; HIV; chitinase-3-like protein 1; inflammation; neutrophil; microbial translocation; LIPOPOLYSACCHARIDE-BINDING PROTEIN; INFECTED PATIENTS; SOLUBLE CD14; CHI3L1; NEUTROPHILS; MORTALITY; BIOMARKER; DISEASE;
D O I
10.3390/v14122602
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Perinatally infected children living with HIV (CLWH) face lifelong infection and associated inflammatory injury. Chitinase-like 3 protein-1 (CHI3L1) is expressed by activated neutrophils and may be a clinically informative marker of systemic inflammation in CLWH. We conducted a multi-centre, cross-sectional study of CLWH, enrolled in the Early Pediatric Initiation Canadian Child Cure Cohort Study (EPIC4). Plasma levels of CHI3L1, pro-inflammatory cytokines, and markers of microbial translocation were measured by enzyme-linked immunosorbent assays. Longitudinal clinical characteristics (viral load, neutrophil count, CD4+ and CD8+ T-lymphocyte counts, and antiretroviral (ARV) regimen) were abstracted from patient medical records. One-hundred-and-five (105) CLWH (median age 13 years, 62% female) were included in the study. Seventy-seven (81%) had viral suppression on combination antiviral therapy (cART). The median CHI3L1 level was 25 mu g/L (IQR 19-39). CHI3L1 was directly correlated with neutrophil count (rho = 0.22, p = 0.023) and inversely correlated with CD4/CD8 lymphocyte ratio (rho = -0.35, p = 0.00040). Children with detectable viral load had higher levels of CHI3L1 (40 mu g/L (interquartile range, IQR 33-44) versus 24 mu g/L (IQR 19-35), p = 0.0047). CHI3L1 levels were also correlated with markers of microbial translocation soluble CD14 (rho = 0.26, p = 0.010) and lipopolysaccharide-binding protein (rho = 0.23, p = 0.023). We did not detect differences in CHI3L1 between different cART regimens. High levels of neutrophil activation marker CHI3L1 are associated with poor virologic control, immune dysregulation, and microbial translocation in CLWH on cART.
引用
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页数:12
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