A Functional Variant of CXCL16 Is Associated With Predisposition to Sepsis and MODS in Trauma Patients: Genetic Association Studies
Open Access
- 3 September 2021
- journal article
- research article
- Published by Frontiers Media SA in Frontiers in Genetics
- Vol. 12
Abstract
Purpose: CXC chemokines are mediators which mediate immune cells migration to sites of inflammation and injury. Chemokine C-X-C motif ligand 16 (CXCL16) plays an important role in the occurrence and development of sepsis through leukocyte chemotaxis, leukocyte adhesion and endotoxin clearance. In this study, we selected a set of tagging single nucleotide polymorphisms (tag SNPs) in the CXCL16 gene and investigated their clinical relevance to the development of sepsis and multiple organ dysfunction syndrome (MODS) in patients with major trauma in three independent Chinese Han populations.Methods: A total of 1,620 major trauma patients were enrolled in this study. Among these patients, 920 came from Chongqing in western China, 350 came from Zhejiang Province in eastern China, and 350 came from Guizhou Province in southwestern China. The improved multiplex ligation detection reaction (iMLDR) method was employed in the genotyping and genetic association analyses to determine the associations between CXCL16 haplotypes and sepsis morbidity rate and higher MOD scores in three cohorts.Results: Only CXCL16 T123V181 haplotype was associated with an increased risk for sepsis morbidity and higher MOD scores in the three cohorts (OR = 1.89,P= 0.001 for the Chongqing cohort; OR = 1.76,P= 0.004 for the Zhejiang cohort; OR = 1.55,P= 0.012 for the Guizhou cohort). The effect of T123V181 haplotype on the chemotaxis, migration and endotoxin clearance of immune cells were further observed. Protein modeling analysis showed that T123 and V181 might alter the structure of the CXCL16 active center. Thus it enhanced the chemotaxis and adhesion ability of immunocytes.Conclusion: We demonstrate the mechanism of CXCL16 T123V181 haplotype which regulates the sepsis morbidity rate and thus provide a new biomarker for early diagnosis of sepsis and MODS.Clinical Trial Registration: www.ClinicalTrials.gov, identifier NCT01713205 (https://www.clinicaltrials.gov/ct2/results?cond=&term=+NCT01713205&cntry=&state= &city=&dist=).Keywords
Funding Information
- Foundation for Innovative Research Groups of the National Natural Science Foundation of China
This publication has 54 references indexed in Scilit:
- Microbial Exposure During Early Life Has Persistent Effects on Natural Killer T Cell FunctionScience, 2012
- Identification of Haplotype Tag SNPs Within the Whole Myeloid Differentiation 2 Gene and Their Clinical Relevance in Patients With Major TraumaShock, 2012
- The CXCL16 A181V Mutation Selectively Inhibits Monocyte Adhesion to CXCR6 but Is Not Associated With Human Coronary Heart DiseaseArteriosclerosis, Thrombosis, and Vascular Biology, 2011
- STAT3 controls myeloid progenitor growth during emergency granulopoiesisBlood, 2010
- Genetic Polymorphisms and Posttraumatic ComplicationsComparative and Functional Genomics, 2010
- Clinical relevance of the interleukin 10 promoter polymorphisms in Chinese Han patients with major trauma: genetic association studiesCritical Care, 2009
- Regulation of CXCL16 expression and secretion by myeloid cells is not altered in rheumatoid arthritisAnnals of the Rheumatic Diseases, 2009
- Inhibition of CXCL16 Attenuates Inflammatory and Progressive Phases of Anti-Glomerular Basement Membrane Antibody-Associated GlomerulonephritisThe American Journal of Pathology, 2007
- CXCL16 Regulates Cell-Mediated Immunity toSalmonella entericaSerovar Enteritidis via Promotion of Gamma Interferon ProductionInfection and Immunity, 2006
- Genetic and Environmental Influences on Premature Death in Adult AdopteesNew England Journal of Medicine, 1988