Memory T cell responses targeting the SARS coronavirus persist up to 11 years post-infection.
Identifieur interne : 000F94 ( Main/Exploration ); précédent : 000F93; suivant : 000F95Memory T cell responses targeting the SARS coronavirus persist up to 11 years post-infection.
Auteurs : Oi-Wing Ng [Singapour] ; Adeline Chia [Singapour] ; Anthony T. Tan [Singapour] ; Ramesh S. Jadi [Singapour] ; Hoe Nam Leong [Singapour] ; Antonio Bertoletti [Singapour] ; Yee-Joo Tan [Singapour]Source :
- Vaccine [ 1873-2518 ] ; 2016.
Descripteurs français
- KwdFr :
- Antigènes d'histocompatibilité de classe I (immunologie), Coronavirus du syndrome respiratoire du Moyen-Orient, Déterminants antigéniques des lymphocytes T (immunologie), Humains, Immunité cellulaire, Lymphocytes T CD8+ (immunologie), Mémoire immunologique, Protéines de la matrice virale (immunologie), Protéines nucléocapside (immunologie), Réactions croisées, Syndrome respiratoire aigu sévère (), Syndrome respiratoire aigu sévère (immunologie), Virus du SRAS.
- MESH :
- immunologie : Antigènes d'histocompatibilité de classe I, Déterminants antigéniques des lymphocytes T, Lymphocytes T CD8+, Protéines de la matrice virale, Protéines nucléocapside, Syndrome respiratoire aigu sévère.
- Coronavirus du syndrome respiratoire du Moyen-Orient, Humains, Immunité cellulaire, Mémoire immunologique, Réactions croisées, Syndrome respiratoire aigu sévère, Virus du SRAS.
English descriptors
- KwdEn :
- CD8-Positive T-Lymphocytes (immunology), Cross Reactions, Epitopes, T-Lymphocyte (immunology), Histocompatibility Antigens Class I (immunology), Humans, Immunity, Cellular, Immunologic Memory, Middle East Respiratory Syndrome Coronavirus, Nucleocapsid Proteins (immunology), SARS Virus, Severe Acute Respiratory Syndrome (immunology), Severe Acute Respiratory Syndrome (prevention & control), Viral Matrix Proteins (immunology).
- MESH :
- chemical , immunology : Epitopes, T-Lymphocyte, Histocompatibility Antigens Class I, Nucleocapsid Proteins, Viral Matrix Proteins.
- immunology : CD8-Positive T-Lymphocytes, Severe Acute Respiratory Syndrome.
- prevention & control : Severe Acute Respiratory Syndrome.
- Cross Reactions, Humans, Immunity, Cellular, Immunologic Memory, Middle East Respiratory Syndrome Coronavirus, SARS Virus.
Abstract
Severe acute respiratory syndrome (SARS) is a highly contagious infectious disease which first emerged in late 2002, caused by a then novel human coronavirus, SARS coronavirus (SARS-CoV). The virus is believed to have originated from bats and transmitted to human through intermediate animals such as civet cats. The re-emergence of SARS-CoV remains a valid concern due to the continual persistence of zoonotic SARS-CoVs and SARS-like CoVs (SL-CoVs) in bat reservoirs. In this study, the screening for the presence of SARS-specific T cells in a cohort of three SARS-recovered individuals at 9 and 11 years post-infection was carried out, and all memory T cell responses detected target the SARS-CoV structural proteins. Two CD8(+) T cell responses targeting the SARS-CoV membrane (M) and nucleocapsid (N) proteins were characterized by determining their HLA restriction and minimal T cell epitope regions. Furthermore, these responses were found to persist up to 11 years post-infection. An absence of cross-reactivity of these CD8(+) T cell responses against the newly-emerged Middle East respiratory syndrome coronavirus (MERS-CoV) was also demonstrated. The knowledge of the persistence of SARS-specific celullar immunity targeting the viral structural proteins in SARS-recovered individuals is important in the design and development of SARS vaccines, which are currently unavailable.
DOI: 10.1016/j.vaccine.2016.02.063
PubMed: 26954467
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Severe acute respiratory syndrome (SARS) is a highly contagious infectious disease which first emerged in late 2002, caused by a then novel human coronavirus, SARS coronavirus (SARS-CoV). The virus is believed to have originated from bats and transmitted to human through intermediate animals such as civet cats. The re-emergence of SARS-CoV remains a valid concern due to the continual persistence of zoonotic SARS-CoVs and SARS-like CoVs (SL-CoVs) in bat reservoirs. In this study, the screening for the presence of SARS-specific T cells in a cohort of three SARS-recovered individuals at 9 and 11 years post-infection was carried out, and all memory T cell responses detected target the SARS-CoV structural proteins. Two CD8(+) T cell responses targeting the SARS-CoV membrane (M) and nucleocapsid (N) proteins were characterized by determining their HLA restriction and minimal T cell epitope regions. Furthermore, these responses were found to persist up to 11 years post-infection. An absence of cross-reactivity of these CD8(+) T cell responses against the newly-emerged Middle East respiratory syndrome coronavirus (MERS-CoV) was also demonstrated. The knowledge of the persistence of SARS-specific celullar immunity targeting the viral structural proteins in SARS-recovered individuals is important in the design and development of SARS vaccines, which are currently unavailable.</div>
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<name sortKey="Jadi, Ramesh S" sort="Jadi, Ramesh S" uniqKey="Jadi R" first="Ramesh S" last="Jadi">Ramesh S. Jadi</name>
<name sortKey="Leong, Hoe Nam" sort="Leong, Hoe Nam" uniqKey="Leong H" first="Hoe Nam" last="Leong">Hoe Nam Leong</name>
<name sortKey="Tan, Anthony T" sort="Tan, Anthony T" uniqKey="Tan A" first="Anthony T" last="Tan">Anthony T. Tan</name>
<name sortKey="Tan, Yee Joo" sort="Tan, Yee Joo" uniqKey="Tan Y" first="Yee-Joo" last="Tan">Yee-Joo Tan</name>
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