Detecting specific cytotoxic T lymphocytes against SARS-coronavirus with DimerX HLA-A2:Ig fusion protein.
Identifieur interne : 002D58 ( PubMed/Checkpoint ); précédent : 002D57; suivant : 002D59Detecting specific cytotoxic T lymphocytes against SARS-coronavirus with DimerX HLA-A2:Ig fusion protein.
Auteurs : Yue-Dan Wang [République populaire de Chine] ; Wei Feng ChenSource :
- Clinical immunology (Orlando, Fla.) [ 1521-6616 ] ; 2004.
Descripteurs français
- KwdFr :
- Acide iotalamique (analogues et dérivés), Animaux, Antigène HLA-A2 (immunologie), Cytométrie en flux, Déterminants antigéniques des lymphocytes T (immunologie), Humains, Immunoglobulines (immunologie), Interféron gamma (immunologie), Lymphocytes T cytotoxiques (immunologie), Méglumine, Protéines de fusion virale, Syndrome respiratoire aigu sévère (immunologie), Virus du SRAS (immunologie).
- MESH :
- analogues et dérivés : Acide iotalamique.
- immunologie : Antigène HLA-A2, Déterminants antigéniques des lymphocytes T, Immunoglobulines, Interféron gamma, Lymphocytes T cytotoxiques, Syndrome respiratoire aigu sévère, Virus du SRAS.
- Animaux, Cytométrie en flux, Humains, Méglumine, Protéines de fusion virale.
English descriptors
- KwdEn :
- Animals, Epitopes, T-Lymphocyte (immunology), Flow Cytometry, HLA-A2 Antigen (immunology), Humans, Immunoglobulins (immunology), Interferon-gamma (immunology), Iothalamic Acid (analogs & derivatives), Meglumine, SARS Virus (immunology), Severe Acute Respiratory Syndrome (immunology), T-Lymphocytes, Cytotoxic (immunology), Viral Fusion Proteins.
- MESH :
- chemical , analogs & derivatives : Iothalamic Acid.
- chemical , immunology : Epitopes, T-Lymphocyte, HLA-A2 Antigen, Immunoglobulins, Interferon-gamma.
- immunology : SARS Virus, Severe Acute Respiratory Syndrome, T-Lymphocytes, Cytotoxic.
- Animals, Flow Cytometry, Humans, Meglumine, Viral Fusion Proteins.
Abstract
To assess specific cytotoxic T lymphocytes (CTLs) against Severe acute respiratory syndrome (SARS)-coronavirus, a modified DimerX flow cytometry assay was performed with peripheral blood mononuclear cell (PBMC) from HLA-A2+ SARS-recovered donors at different time points post disease. CD8+DimerX-S1203+ CTLs were detected in the PBMC from these donors up to 3 months after recovery. The percentages of CD8+DimerX-S1203+ cells paralleled the numbers of interferon-gamma-positive spots in an ELISPOT assay using the same antigenic peptide. In conclusion, DimerX-based flow cytometry staining may prove to be a real-time method to screen for CTL directed at epitopes from a newly identified virus.
DOI: 10.1016/j.clim.2004.07.004
PubMed: 15451471
Affiliations:
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<affiliation wicri:level="1"><nlm:affiliation>Department of Immunology, School of Basic Medical Sciences, Peking University Health Science Center, Beijing 100083, China. wangyuedan@hotmail.com</nlm:affiliation>
<country xml:lang="fr">République populaire de Chine</country>
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<author><name sortKey="Chen, Wei Feng" sort="Chen, Wei Feng" uniqKey="Chen W" first="Wei Feng" last="Chen">Wei Feng Chen</name>
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<term>Humans</term>
<term>Immunoglobulins (immunology)</term>
<term>Interferon-gamma (immunology)</term>
<term>Iothalamic Acid (analogs & derivatives)</term>
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<term>Antigène HLA-A2 (immunologie)</term>
<term>Cytométrie en flux</term>
<term>Déterminants antigéniques des lymphocytes T (immunologie)</term>
<term>Humains</term>
<term>Immunoglobulines (immunologie)</term>
<term>Interféron gamma (immunologie)</term>
<term>Lymphocytes T cytotoxiques (immunologie)</term>
<term>Méglumine</term>
<term>Protéines de fusion virale</term>
<term>Syndrome respiratoire aigu sévère (immunologie)</term>
<term>Virus du SRAS (immunologie)</term>
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<term>HLA-A2 Antigen</term>
<term>Immunoglobulins</term>
<term>Interferon-gamma</term>
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<term>Déterminants antigéniques des lymphocytes T</term>
<term>Immunoglobulines</term>
<term>Interféron gamma</term>
<term>Lymphocytes T cytotoxiques</term>
<term>Syndrome respiratoire aigu sévère</term>
<term>Virus du SRAS</term>
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<term>T-Lymphocytes, Cytotoxic</term>
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<term>Meglumine</term>
<term>Viral Fusion Proteins</term>
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<front><div type="abstract" xml:lang="en">To assess specific cytotoxic T lymphocytes (CTLs) against Severe acute respiratory syndrome (SARS)-coronavirus, a modified DimerX flow cytometry assay was performed with peripheral blood mononuclear cell (PBMC) from HLA-A2+ SARS-recovered donors at different time points post disease. CD8+DimerX-S1203+ CTLs were detected in the PBMC from these donors up to 3 months after recovery. The percentages of CD8+DimerX-S1203+ cells paralleled the numbers of interferon-gamma-positive spots in an ELISPOT assay using the same antigenic peptide. In conclusion, DimerX-based flow cytometry staining may prove to be a real-time method to screen for CTL directed at epitopes from a newly identified virus.</div>
</front>
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<Abstract><AbstractText>To assess specific cytotoxic T lymphocytes (CTLs) against Severe acute respiratory syndrome (SARS)-coronavirus, a modified DimerX flow cytometry assay was performed with peripheral blood mononuclear cell (PBMC) from HLA-A2+ SARS-recovered donors at different time points post disease. CD8+DimerX-S1203+ CTLs were detected in the PBMC from these donors up to 3 months after recovery. The percentages of CD8+DimerX-S1203+ cells paralleled the numbers of interferon-gamma-positive spots in an ELISPOT assay using the same antigenic peptide. In conclusion, DimerX-based flow cytometry staining may prove to be a real-time method to screen for CTL directed at epitopes from a newly identified virus.</AbstractText>
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