Presence of Effector CD8 super(+) T Cells in Hepatitis C Virus-Exposed Healthy Seronegative Donors

CTL responses against multiple hepatitis C virus (HCV) epitopes were detected in 7 of 29 (24.1%) healthy family members (HFM) persistently exposed to chronically HCV-infected patients (HCV-HFM). These precursor CTL were at very low or undetectable frequencies, as determined by limiting dilution anal...

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Veröffentlicht in:The Journal of immunology (1950) 1999-06, Vol.162 (11), p.6681-6689
Hauptverfasser: Scognamiglio, P, Accapezzato, D, Casciaro, MA, Cacciani, A, Artini, M, Bruno, G, Chircu, M L, Sidney, J, Southwood, S, Abrignani, S, Sette, A, Barnaba, V
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Sprache:eng
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Zusammenfassung:CTL responses against multiple hepatitis C virus (HCV) epitopes were detected in 7 of 29 (24.1%) healthy family members (HFM) persistently exposed to chronically HCV-infected patients (HCV-HFM). These precursor CTL were at very low or undetectable frequencies, as determined by limiting dilution analysis. However, when HCV-specific effector CD8 super(+) T cells, freshly isolated from PBMC of HCV-HFM, were assessed by a sensitive enzyme-linked immunospot assay, their frequencies were severalfold higher than those of precursor CTL. These results indicate that the two assays detect two functionally distinct T cell populations and that the effector cells are not assayed by the super(51)Cr-release assay. Furthermore, the combination of cell depletion and enzyme-linked immunospot analyses showed that the effector cells were confined into a CD8 super(+) CD45RO super(+) CD28 super(-) population. The persistence of effector CD8 super(+) T cells specific for both the structural and nonstructural viral proteins in uninfected HCV-HFM, suggest that: 1) an immunological memory is established upon a subclinical infection without any evidence of hepatitis, in a large cohort of HCV-exposed individuals; 2) because these cells required neither restimulation nor the addition of particular cytokines in vitro for differentiating in effectors, they should be capable of prompt HCV-specific effector function in vivo, possibly providing antiviral protection; and 3) the maintenance of effector T cell responses may be sustained by persisting low-level stimulation induced by inapparent infections.
ISSN:0022-1767