| 초록 |
In hepatitis C Virus (HCV) high-risk groups, HCV-specific
T cell responses have been detected in seronegative,
aviremic
persons who have no evidence of HCV infection. Herein,
we investigated functional profiles of HCV-specific T-cell
responses in seronegative, aviremic patients of a HCV
high-risk group. Seventy seven hemodialysis patients with
chronic renal disease were analyzed by IFN-γ ELISpot
assays, and eight of 71 (11.3%) seronegative, aviremic
patients
displayed HCV-specific T-cell responses. Their HCV-
specific memory T cells were characterized by assessing
cytokine
polyfunctionality, known to provide antiviral protection. By
intracellular staining of IFN-γ, TNF-α, IL-2 and MIP-1β,
we
identified two distinct populations in the seronegative,
aviremic patients: polyfunctional responders and TNF-α-
predominant
responders. In further analysis, occult HCV infection was
excluded as a cause of the HCV-specific T cell
response via secondary nested RT-PCR of HCV RNA in
peripheral blood mononuclear cell samples. HCV-specific
T
cells targeted multiple epitopes including non-structural
proteins in a single patient, demonstrating that their T cells
had been primed by HCV proteins synthesized within the
host. We conclude that HCV-specific memory T cells of
seronegative, aviremic patients arise from authentic HCV
replication in the host, but not from current occult HCV
infection. By functional pattern of HCVspecific T cells,
there are two distinct populations in these patients:
polyfunctional
responders and TNF-α-predominant responders. |