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Low responsiveness to a hepatitis B virus vaccine in a Chinese population lacks association with ITGAL, CD58, TNFSF15, CCL15, TGFB3, and BCL6 gene variants
- Source :
- Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases. 64
- Publication Year :
- 2017
-
Abstract
- It is known that multiple genetic variants can affect immune responses to the hepatitis B virus (HBV) vaccine. A case-control study was undertaken to examine the possible association of low responsiveness to the HBV vaccine in a Chinese population with genetic polymorphisms in integrin subunit alpha L, CD58, tumor necrosis factor superfamily member 15, C-C motif chemokine ligand 15, transforming growth factor beta 3, and B-cell lymphoma 6 protein. The copy numbers of these six genes were detected in 129 low responders, 129 middle responders and 129 high responders to HBV vaccination. There were no significant differences in the copy numbers of these six genes between the groups. Thus, these findings indicated that the copy number variations of these genes may not be the reason for the low responsiveness to the HBV vaccine in a Chinese population.
- Subjects :
- 0301 basic medicine
Microbiology (medical)
Male
Tumor Necrosis Factor Ligand Superfamily Member 15
Hepatitis B virus
Hepatitis B vaccine
CD58
Gene Dosage
Biology
medicine.disease_cause
Microbiology
03 medical and health sciences
0302 clinical medicine
Immune system
Asian People
Genetics
medicine
Humans
Hepatitis B Vaccines
CCL15
Copy-number variation
Selection, Genetic
Molecular Biology
Gene
Ecology, Evolution, Behavior and Systematics
Genetic Variation
Macrophage Inflammatory Proteins
BCL6
CD58 Antigens
Hepatitis B
Virology
030104 developmental biology
Infectious Diseases
Chemokines, CC
Proto-Oncogene Proteins c-bcl-6
Female
Disease Susceptibility
030215 immunology
Subjects
Details
- ISSN :
- 15677257
- Volume :
- 64
- Database :
- OpenAIRE
- Journal :
- Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases
- Accession number :
- edsair.doi.dedup.....649c611c5d170ac0ce7b5085871e2534