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Blood signatures for second stage human African trypanosomiasis: a transcriptomic approach
Julius Mulindwa1, Enock Matovu2, John Enyaru3
1Department of Biochemistry and Sports Sciences, College of Natural Sciences, Makerere University, P. O. Box 7062, Kampala, Uganda. mujuls@gmail.com.
BMC Medical Genomics
|February 1, 2020
Summary
Rhodesiense sleeping sickness triggers an innate immune response in early infection and anti-inflammatory pathways in late stages. This study identifies potential blood biomarkers for diagnosing late-stage disease.
Area of Science:
- Parasitology
- Immunology
- Neuroscience
Background:
- Rhodesiense sleeping sickness, caused by T. b. rhodesiense, is an acute, fatal disease if untreated.
- Understanding the host immune response is crucial for managing T. b. rhodesiense infections.
Purpose of the Study:
- To investigate the impact of T. b. rhodesiense infection on the patient's immune response.
- To differentiate immune responses in early (blood) and late (CSF) stages of the disease.
Main Methods:
- RNA sequencing (RNASeq) of blood and CSF samples from infected patients and healthy controls.
- Differential gene expression analysis using Tuxedo suite and DESeq2.
- Gene enrichment and pathway analysis using ToppCluster, DAVID, and InnateDB.
Main Results:
- Early infection showed enrichment of innate immune response genes in blood.
- Late infection (CSF) revealed enrichment of anti-inflammatory and neuro-degeneration pathways.
- Identified up-regulated genes (C1QC, MARCO, IGHD3-10) common to both blood and CSF.
Conclusions:
- The study elucidates host responses to T. b. rhodesiense in blood and CNS.
- Identified key immune pathways and potential biomarkers for diagnosing late-stage disease.
- Findings may aid in developing diagnostic tools and therapeutic strategies.
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