Hyperinflammatory syndrome, natural killer cell function, and genetic polymorphisms in the pathogenesis of severe dengue
Background Severe dengue, characterized by shock and organ dysfunction, is driven by an excessive host immune response. We investigated the role of hyperinflammation in dengue pathogenesis. Methods Patients recruited into an observational study were divided into 3 plasma leak severity grades. Hyper...
প্রধান লেখক: | , , , , , , , , , , , |
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বিন্যাস: | Journal article |
ভাষা: | English |
প্রকাশিত: |
Oxford University Press
2022
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_version_ | 1826309127690780672 |
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author | Vuong, NL Cheung, K-W Periaswamy, B Vi, TT Duyen, HTL Leong, YS Binte Hamis, ZN Gregorova, M Ooi, EE Sessions, O Rivino, L Yacoub, S |
author_facet | Vuong, NL Cheung, K-W Periaswamy, B Vi, TT Duyen, HTL Leong, YS Binte Hamis, ZN Gregorova, M Ooi, EE Sessions, O Rivino, L Yacoub, S |
author_sort | Vuong, NL |
collection | OXFORD |
description | Background
Severe dengue, characterized by shock and organ dysfunction, is driven by an excessive host immune response. We investigated the role of hyperinflammation in dengue pathogenesis.
Methods
Patients recruited into an observational study were divided into 3 plasma leak severity grades. Hyperinflammatory biomarkers were measured at 4 time points. Frequencies, activation, and cytotoxic potential of natural killer (NK) cells were analyzed by flow cytometry. RNA was extracted from sorted CD56+ NK cells and libraries were prepared using SMART-Seq and sequenced using HiSeq3000 (Illumina).
Results
Sixty-nine patients were included (grade 0, 42 patients; grade 1, 19 patients; grade 2, 8 patients). Patients with grade 2 leakage had higher biomarkers than grade 0, including higher peak ferritin levels (83.3% vs 45.2%) and H-scores (median, 148.5 vs 105.5). NK cells from grade 2 patients exhibited decreased expression of perforin and granzyme B and activation markers. RNA sequencing revealed 3 single-nucleotide polymorphisms in NK cell functional genes associated with more severe leakage—NK cell lectin-like receptor K1 gene (KLRK1) and perforin 1 (PRF1).
Conclusions
Features of hyperinflammation are associated with dengue severity, including higher biomarkers, impaired NK cell function, and polymorphisms in NK cell cytolytic function genes (KLRK1 and PRF1). Trials of immunomodulatory therapy in these patients is now warranted.
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first_indexed | 2024-03-07T07:29:34Z |
format | Journal article |
id | oxford-uuid:e09cf3ea-3c39-40d4-a897-848b51f40caf |
institution | University of Oxford |
language | English |
last_indexed | 2024-03-07T07:29:34Z |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | dspace |
spelling | oxford-uuid:e09cf3ea-3c39-40d4-a897-848b51f40caf2022-12-13T07:59:23ZHyperinflammatory syndrome, natural killer cell function, and genetic polymorphisms in the pathogenesis of severe dengueJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:e09cf3ea-3c39-40d4-a897-848b51f40cafEnglishSymplectic ElementsOxford University Press2022Vuong, NLCheung, K-WPeriaswamy, BVi, TTDuyen, HTLLeong, YSBinte Hamis, ZNGregorova, MOoi, EESessions, ORivino, LYacoub, SBackground Severe dengue, characterized by shock and organ dysfunction, is driven by an excessive host immune response. We investigated the role of hyperinflammation in dengue pathogenesis. Methods Patients recruited into an observational study were divided into 3 plasma leak severity grades. Hyperinflammatory biomarkers were measured at 4 time points. Frequencies, activation, and cytotoxic potential of natural killer (NK) cells were analyzed by flow cytometry. RNA was extracted from sorted CD56+ NK cells and libraries were prepared using SMART-Seq and sequenced using HiSeq3000 (Illumina). Results Sixty-nine patients were included (grade 0, 42 patients; grade 1, 19 patients; grade 2, 8 patients). Patients with grade 2 leakage had higher biomarkers than grade 0, including higher peak ferritin levels (83.3% vs 45.2%) and H-scores (median, 148.5 vs 105.5). NK cells from grade 2 patients exhibited decreased expression of perforin and granzyme B and activation markers. RNA sequencing revealed 3 single-nucleotide polymorphisms in NK cell functional genes associated with more severe leakage—NK cell lectin-like receptor K1 gene (KLRK1) and perforin 1 (PRF1). Conclusions Features of hyperinflammation are associated with dengue severity, including higher biomarkers, impaired NK cell function, and polymorphisms in NK cell cytolytic function genes (KLRK1 and PRF1). Trials of immunomodulatory therapy in these patients is now warranted. |
spellingShingle | Vuong, NL Cheung, K-W Periaswamy, B Vi, TT Duyen, HTL Leong, YS Binte Hamis, ZN Gregorova, M Ooi, EE Sessions, O Rivino, L Yacoub, S Hyperinflammatory syndrome, natural killer cell function, and genetic polymorphisms in the pathogenesis of severe dengue |
title | Hyperinflammatory syndrome, natural killer cell function, and genetic polymorphisms in the pathogenesis of severe dengue |
title_full | Hyperinflammatory syndrome, natural killer cell function, and genetic polymorphisms in the pathogenesis of severe dengue |
title_fullStr | Hyperinflammatory syndrome, natural killer cell function, and genetic polymorphisms in the pathogenesis of severe dengue |
title_full_unstemmed | Hyperinflammatory syndrome, natural killer cell function, and genetic polymorphisms in the pathogenesis of severe dengue |
title_short | Hyperinflammatory syndrome, natural killer cell function, and genetic polymorphisms in the pathogenesis of severe dengue |
title_sort | hyperinflammatory syndrome natural killer cell function and genetic polymorphisms in the pathogenesis of severe dengue |
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