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Detecting specific cytotoxic T lymphocytes against SARS-coronavirus with DimerX HLA-A2:Ig fusion protein.

Identifieur interne : 005824 ( Main/Merge ); précédent : 005823; suivant : 005825

Detecting specific cytotoxic T lymphocytes against SARS-coronavirus with DimerX HLA-A2:Ig fusion protein.

Auteurs : Yue-Dan Wang [République populaire de Chine] ; Wei Feng Chen

Source :

RBID : pubmed:15451471

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English descriptors

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

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pubmed:15451471

Le document en format XML

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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>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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<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>
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