Single nucleotide polymorphisms/haplotypes associated with multiple rubella-specific immune response outcomes post-MMR immunization in healthy children

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• 作者：Inna G. Ovsyannikova ; Hannah M. Salk ; Beth R. Larrabee ; V. Shane Pankratz…
• 关键词：Rubella vaccine ; Single nucleotide polymorphisms (SNPs) ; Genetic association ; Neutralizing antibodies ; Cytokines ; Rubella ; Rubella vaccine ; Rubella virus ; Measles ; mumps ; rubella vaccine ; Single nucleotide polymorphism ; Genetic association studies ; Antibodies ; Neutralizing ; Cytokines
• 刊名：Immunogenetics
• 出版年：2015
• 出版时间：October 2015
• 年：2015
• 卷：67
• 期：10
• 页码：547-561
• 全文大小：991 KB
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• 作者单位：Inna G. Ovsyannikova (1)
  Hannah M. Salk (1)
  Beth R. Larrabee (2)
  V. Shane Pankratz (2)
  Gregory A. Poland (1)
  
  1. Mayo Clinic Vaccine Research Group, Mayo Clinic, Guggenheim 611C, 200 1st Street S.W., Rochester, Minnesota, 55905, USA
  2. Department of Health Sciences Research, Mayo Clinic, Rochester, MN, 55905, USA
  
• 刊物类别：Biomedical and Life Sciences
• 刊物主题：Biomedicine
  Immunology
  Allergology
  Cell Biology
  
• 出版者：Springer Berlin / Heidelberg
• ISSN：1432-1211

文摘

The observed heterogeneity in rubella-specific immune response phenotypes post-MMR vaccination is thought to be explained, in part, by inter-individual genetic variation. In this study, single nucleotide polymorphisms (SNPs) and multiple haplotypes in several candidate genes were analyzed for associations with more than one rubella-specific immune response outcome, including secreted IFN-γ, secreted IL-6, and neutralizing antibody titers. Overall, we identified 23 SNPs in 10 different genes that were significantly associated with at least two rubella-specific immune responses. Of these SNPs, we detected eight in the PVRL3 gene, five in the PVRL1 gene, one in the TRIM22 gene, two in the IL10RB gene, two in the TLR4 gene, and five in other genes (PVR, ADAR, ZFP57, MX1, and BTN2A1/BTN3A3). The PVRL3 gene haplotype GACGGGGGCAGCAAAAAGAAGAGGAAAGAACAA was significantly associated with both higher IFN-γ secretion (t-statistic 4.43, p-lt;-.0001) and higher neutralizing antibody titers (t-statistic 3.14, p--.002). Our results suggest that there is evidence of multigenic associations among identified gene SNPs and that polymorphisms in these candidate genes contribute to the overall observed differences between individuals in response to live rubella virus vaccine. These results will aid our understanding of mechanisms behind rubella-specific immune response to MMR vaccine and influence the development of vaccines in the future. Keywords Rubella vaccine Single nucleotide polymorphisms (SNPs) Genetic association Neutralizing antibodies Cytokines