Human CD8+ T-Cell Responses Against the 4 Dengue Virus Serotypes Are Associated With Distinct Patterns of Protein Targets
D Weiskopf, C Cerpas, MA Angelo… - The Journal of …, 2015 - academic.oup.com
The Journal of infectious diseases, 2015•academic.oup.com
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 …
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 …
Abstract
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 γ–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 γ 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.
Oxford University Press