HLA-A2 and B35 restricted hantaan virus nucleoprotein CD8+ T-cell epitope-specific immune response correlates with milder disease in hemorrhagic fever with renal syndrome

• Published in: PLoS neglected tropical diseases Vol. 7; no. 2; p. e2076
• Main Authors: Ma, Ying, Wang, Jiuping, Yuan, Bin, Wang, Meiliang, Zhang, Yun, Xu, Zhuwei, Zhang, Chunmei, Zhang, Yusi, Liu, Bei, Yi, Jing, Yang, Kun, Yang, Angang, Zhuang, Ran, Jin, Boquan
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 2013; Public Library of Science (PLoS)
• Subjects: Adult; Biology; CD8-Positive T-Lymphocytes - immunology; China; Disease control; Enzyme-Linked Immunospot Assay; Epitope Mapping; Epitopes, T-Lymphocyte - immunology; Female; Hantaan virus - immunology; Hemorrhagic Fever with Renal Syndrome - immunology; Hemorrhagic Fever with Renal Syndrome - pathology; HLA-A2 Antigen - immunology; HLA-B35 Antigen - immunology; Humans; Immune response; Immunology; Immunotherapy; Infections; Interferon-gamma - secretion; Male; Medicine; Middle Aged; Mortality; Nucleoproteins - immunology; Public health; T cell receptors; Tropical diseases; Vaccines; China; Asia; Epitope Mapping; Interferon-gamma; Hantaan virus; Nucleoproteins; Humans; Middle Aged; Male; Enzyme-Linked Immunospot Assay; Epitopes, T-Lymphocyte; CD8-Positive T-Lymphocytes; HLA-B35 Antigen; Hemorrhagic Fever with Renal Syndrome; HLA-A2 Antigen; China; Adult; Female
• ISSN: 1935-2735; 1935-2727; 1935-2735
• DOI: 10.1371/journal.pntd.0002076

Hantaan virus (HTNV) infection in humans is a serious public health concern in Asia. A potent T cell activation peptide vaccine from HTNV structure protein represents a promising immunotherapy for disease control. However, the T cell epitopes of the HTNV restricted by the HLA alleles and the role of epitope-specific T cell response after HTNV infection remain largely unexplored.
Five well-conserved novel CD8(+) T-cell epitopes of the HTNV nucleoprotein restricted by the most popular HLA alleles in Chinese Han population were defined with interferon-γ enzyme-linked immunospot assay in 37 patients infected with HTNV during hospitalization. Two epitopes aa129-aa137 and aa131-aa139 restricted by HLA-A2 and B35, respectively, were selected to evaluate the epitope-specific CD8(+) T-cell response. HLA-peptide pentamer complex staining showed that the frequency of single epitope-specific CD8(+) T cell could be detected in patients (95% confidence interval for aa129-aa137: 0.080%-0.208%; for aa131-aa139: 0.030%-0.094%). The frequency of epitope-specific pentamer(+) CD8(+) T-cell response was much higher in mild/moderate patients than in severe/critical ones at the acute stage of the disease. Moreover, the frequency of epitope-specific CD8(+) T cells at acute stage was inversely associated with the peak level of serum creatinine and was positively associated with the nadir platelet counts during the hospitalization. The intracellular cytokine staining and the proliferation assay showed that the effective epitope-specific CD8(+) T cells were characterized with the production of interferon-γ, expression of CD69 and the strong capacity of proliferation.
The novel HLA class I restricted HTNV nucleoprotein epitopes-specific CD8(+) T-cell responses would be closely related with the progression and the severity of the disease, which could provide the first step toward effective peptide vaccine development against HTNV infection in humans.