Abstract
Human cytomegalovirus (HCMV)-specific CD4(+) and CD8(+) T-cells were measured in the immunocompetent host as well as in 13 solid-organ transplant recipients (SOTR), and 12 young hematopoietic stem cell transplant recipients (HSCTR) by using a long-term (7-day) assay based on PBMC stimulation by HCMV-infected dendritic cells (iDC), and two short-term (24 h) assays, one for CD4(+) stimulation by infected cell lysate (iCL), and the other for CD8(+) stimulation by a pool of 34 epitopic peptides (pep-pool). In the immunocompetent, the number of T-cells activated by either iCL or the pep-pool was significantly reduced with respect to iDC. In both SOTR and HSCTR, the number of T-cells activated by iDC was comparable to that activated by iCL or the pep-pool. A significant correlation between iDC-activated T-cells and T-cells activated by either iCL or the pep-pool was observed. In conclusion, whenever a rapid result is needed, short-term assays may efficiently replace the iDC assay. (C) 2010 Elsevier Inc. All rights reserved.
| Lingua originale | Inglese |
|---|---|
| pagine (da-a) | 269-281 |
| Numero di pagine | 13 |
| Rivista | Clinical Immunology |
| Volume | 136 |
| DOI | |
| Stato di pubblicazione | Pubblicato - 2010 |
Keywords
- Human cytomegalovirus
- T-cell response
- Infected dendritic cells
- Immunocompromised patients
- Epitopic peptide pool
- Immunocompetent host
- Infected cell lysate
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