血液DNA病毒与自身免疫性疾病和COVID-19有关
Noah Sasa1,2,3,4, Shohei Kojima5, Rie Koide5
1Department of Statistical Genetics, Osaka University Graduate School of Medicine, Suita, Japan.
Nature genetics
|January 3, 2025
概括
这项研究揭示了人类病毒组中的特定病毒,如人类疹病毒6B (HHV-6B) 和anellovirus,与狼和类风湿性关节炎等自身免疫性疾病以及COVID-19等传染性疾病有关.
科学领域:
- 病毒学 病毒学
- 免疫学 免疫学 免疫学
- 遗传学 遗传学 是一个
背景情况:
- 了解病毒在自身免疫和传染病中的作用是有限的,特别是在人口规模上.
- 人类病毒对病原体的影响需要进一步调查.
研究的目的:
- 研究血液DNA病毒和自身免疫性疾病 (SLE,RA等) 之间的关联. 和COVID-19的情况.
- 为了确定与疾病风险和活动相关的特定病毒成分.
主要方法:
- 6,321名日本人的全基因组测序.
- 在内源性HHV-6 (eHHV-6) 和anellovirus的量化.
- 全基因组关联研究,长读测序,表位图绘制和单细胞RNA测序.
主要成果:
- 内源性HHV-6B (eHHV-6B) 阳性与SLE和肺膜蛋白酶 (PAP) 的风险增加相关.
- 高无病毒负载与SLE,RA和COVID-19有很强的相关性.
- eHHV-6B整合部位映射到染色体22q,在SLE患者中具有明显的免疫诱导.
结论:
- 人类病毒组,包括eHHV-6B和anellovirus,在自身免疫和传染病的发病过程中发挥着重要作用.
- 研究结果突出了这些疾病的潜在病毒生物标志物和治疗点.
更多相关视频
09:38Determining Immune System Suppression versus CNS Protection for Pharmacological Interventions in Autoimmune Demyelination
Published on: September 12, 2016
12.2K
06:03Author Spotlight: Advancing Immune Monitoring in Critical Care Patients Using Whole Blood Assays
Published on: September 20, 2024
1.2K
相关概念视频
Autoimmune Disorders
385
Autoimmune diseases are a group of disorders in which the body's immune system mistakenly attacks its own cells, tissues, and organs. This results from an overactive immune response against substances and tissues normally present in the body. Let's delve into the concept and mechanism of autoimmune diseases from an immune system point of view, explore different causes and examples of such diseases, and discuss potential solutions.
Concept and Mechanism of Autoimmune Diseases
The immune...
Concept and Mechanism of Autoimmune Diseases
The immune...
385
Immune Response Against Viral Pathogens
742
The immune system's response to viral infections is a complex and coordinated process involving natural killer (NK) cells, T cell-mediated responses, and antibody-mediated responses.
NK Cells
NK cells are a crucial part of our innate immune system, acting as the first line of defense against viral infections. These cells can recognize and kill infected cells without prior exposure to the virus, effectively slowing down the spread of infection. Additionally, NK cells produce proinflammatory...
NK Cells
NK cells are a crucial part of our innate immune system, acting as the first line of defense against viral infections. These cells can recognize and kill infected cells without prior exposure to the virus, effectively slowing down the spread of infection. Additionally, NK cells produce proinflammatory...
742
Viral Mutations
32.1K
A mutation is a change in the sequence of bases of DNA or RNA in a genome. Some mutations occur during replication of the genome due to errors made by the polymerase enzymes that replicate DNA or RNA. Unlike DNA polymerase, RNA polymerase is prone to errors because it is not capable of “proofreading” its work. Viruses with RNA-based genomes, like HIV, therefore accrue mutations faster than viruses with DNA-based genomes. Because mutation and recombination provide the raw material...
32.1K
Single Nucleotide Polymorphisms-SNPs
13.9K
A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
13.9K
Viral Recombination
23.2K
Cells are sometimes infected by more than one virus at once. When two viruses disassemble to expose their genomes for replication in the same cell, similar regions of their genomes can pair together and exchange sequences in a process called recombination. Alternatively, viruses with segmented genomes can swap segments in a process called reassortment.
23.2K
Genome-wide Association Studies-GWAS
12.4K
Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
GWAS does not require the identification of the target gene involved in...
12.4K
