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Long-lived memory T lymphocyte responses against SARS coronavirus nucleocapsid protein in SARS-recovered patients

The nucleocapsid (N) protein is a structural component of severe acute respiratory syndrome (SARS) coronavirus (SARS-CoV) and can induce antibody responses in SARS patients during infection. However, it is not known whether SARS-CoV N protein can induce a long persistence of memory T-cell response i...

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Detalles Bibliográficos
Autores principales: Peng, Hui, Yang, Li-tao, Wang, Ling-yun, Li, Jian, Huang, Jun, Lu, Zhi-qiang, Koup, Richard A., Bailer, Robert T., Wu, Chang-you
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111820/
https://www.ncbi.nlm.nih.gov/pubmed/16690096
http://dx.doi.org/10.1016/j.virol.2006.03.036
Descripción
Sumario:The nucleocapsid (N) protein is a structural component of severe acute respiratory syndrome (SARS) coronavirus (SARS-CoV) and can induce antibody responses in SARS patients during infection. However, it is not known whether SARS-CoV N protein can induce a long persistence of memory T-cell response in human. In this study, we found that peripheral blood mononuclear cells (PBMCs) from fully recovered SARS individuals rapidly produced IFN-γ and IL-2 following stimulation with a pool of overlapping peptides that cover the entire N protein sequence. The N-specific IFN-γ(+)CD4(+) T cells were mainly composed of CD45RA(−)CCR7(+)CD62L(−) cells, whereas IFN-γ(+)CD8(+) memory T cells were mostly contained within CD45RA(+)CCR7(−)CD62L(−) cell population. Epitope mapping study indicated that a cluster of overlapping peptides located in the C-terminal region (amino acids [aa] 331 to 362) of N protein contained at least two different T-cell epitopes. The results indicated that human memory T-cell responses specific for SARS-CoV N protein could persist for 2 years in the absence of antigen, which would be a valuable for the design of effective vaccines against SARS-CoV and for basic studies of human T-cell memory.