Abstract
BackgroundTo address the clinical and virological significance of a high HTLV-1 proviral load (VL) in practical blood samples from asymptomatic and symptomatic carriers, we simultaneously examined VL and clonal expansion status using polymerase chain reaction (PCR) quantification (infected cell % of peripheral mononuclear cells) and Southern blotting hybridization (SBH) methods.ResultsThe present study disclosed extremely high VL with highly dense smears with or without oligoclonal bands in SBH. A high VL of 10% or more was observed in 16 (43.2%) of a total of 33 samples (one of 13 asymptomatic carriers, 8 of 12 symptomatic carriers, and 7 of 8 patients with lymphoma-type ATL without circulating ATL cells). In particular, an extremely high VL of 50% or more was limited to symptomatic carriers whose band findings always contained at least dense smears derived from polyclonally expanded cells infected with HTLV-1. Sequential samples revealed that the VL value was synchronized with the presence or absence of dense smears, and declined at the same time as disappearing dense smears. Dense smears transiently emerged at the active stage of the underlying disease. After disappearance of the smears, several clonal bands became visible and were persistently retained, explaining the process by which the clonality of HTLV-1-infected cells is established. The cases with only oligoclonal bands tended to maintain a stable VL of around 20% for a long time. Two of such cases developed ATL 4 and 3.5 years later, suggesting that a high VL with oligoclonal bands may be a predisposing risk to ATL.ConclusionThe main contributor to extremely high VL seems to be transient emergence of dense smears detected by the sensitivity level of SBH, corresponding to polyclonal expansion of HTLV-1-infected cells including abundant small clones. Major clones retained after disappearance of dense smears stably persist and acquire various malignant characteristics step by step.
Highlights
To address the clinical and virological significance of a high Human T-cell leukemia virus type-1 (HTLV-1) proviral load (VL) in practical blood samples from asymptomatic and symptomatic carriers, we simultaneously examined HTLV-1 proviral load (VL) and clonal expansion status using polymerase chain reaction (PCR) quantification and Southern blotting hybridization (SBH) methods
All 33 samples were divided into 3 groups; 13 asymptomatic healthy carriers, 12 symptomatic carriers with complications unrelated to HTLV-1 such as infectious diseases (Strongyloides, hepatic disorders due to HBV and HCV, chronic pneumonitis or bronchitis) and immune-disorders (CrowFukase syndrome, RA, and chronic eczema, and reactive unknown adenitis) and 8 patients with lymphoma-type adult T-cell leukemia (ATL)
The relationship between VL and band status is depicted in Figure 3, showing no-band or vague smears in all but one of the healthy carriers, either dense smears or a mixture of dense smears and oligoclonal bands in symptomatic carriers and mainly discrete clonal band in patients with lymphoma-type ATL
Summary
HTLV-1-infected individuals who are complicated by opportunistic infections, such as parasites, mycosis, viruses and some bacteria, and abnormal immunity due to aging are known to show an increased proviral load with polyclonal expansion [1113]. This condition associated with polyclonal expansion of the infected cells was considered to be the intermediate state prior to progression to ATL [14], but the pathological and clinical correlation between clonality and level of VL is not fully understood. We have had frequent opportunities to see unusual or indeterminate ATL patients or carriers with high VL with discrete band(s) in SBH, but no circulating ATL cells, especially among the elderly
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