4.7 Article

Human CD8+ T-Cell Responses Against the 4 Dengue Virus Serotypes Are Associated With Distinct Patterns of Protein Targets

期刊

JOURNAL OF INFECTIOUS DISEASES
卷 212, 期 11, 页码 1743-1751

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jiv289

关键词

dengue virus; serotype specific; CD8(+) T cells; Nicaragua; Sri Lanka; Brazil

资金

  1. National Institutes of Health [HHSN272200900042C, HHSN27220140045C]
  2. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico [458713/2014 7]
  3. Brazilian Ministry of Science, Technology, and Innovation
  4. Fundo Nacional de Saude, Brazilian Ministry of Health [777588/2012]

向作者/读者索取更多资源

Background. All 4 dengue virus (DENV) serotypes are now simultaneously circulating worldwide and responsible for up to 400 million human infections each year. Previous studies of CD8(+) T-cell responses in HLA-transgenic mice and human vaccinees demonstrated that the hierarchy of immunodominance among structural versus nonstructural proteins differs as a function of the infecting serotype. This led to the hypothesis that there are intrinsic differences in the serotype-specific reactivity of CD8+ T-cell responses. Methods. We tested this hypothesis by analyzing serotype-specific CD8(+) T-cell reactivity in naturally infected human donors from Sri Lanka and Nicaragua, using ex vivo interferon.-specific enzyme-linked immunosorbent spot assays. Results. Remarkably similar and clear serotype-specific patterns of immunodominance in both cohorts were identified. Pooling of epitopes that accounted for 90% of the interferon. response in both cohorts resulted in a global epitope pool. Its reactivity was confirmed in naturally infected donors from Brazil, demonstrating its global applicability. Conclusions. This study provides new insight into differential serotype-specific immunogenicity of DENV proteins. It further provides a potentially valuable tool for future investigations of CD8+ T-cell responses in the typically small sample volumes available from patients with acute fever and children without requiring prior knowledge of either infecting DENV serotype or HLA type.

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