Int J Cancer. 1996 Mar 28;66(1):18-23. Unique Identifier : AIDSLINE
To examine the relationship between human T-lymphotrophic virus type I
(HTLV-I) proviral DNA and its expression in the lymph nodes, HTLV-I DNA
and tax/rex mRDA were directly amplified by polymerase chain reaction in
situ hybridization (PCR/ISH), and reverse transcription (RT)-PCR/ISH
[RT-PCR/ISH]. We studied 24 lymph nodes from patients with adult T-cell
leukemia/lymphoma (ATLL), incipient ATLL (I-ATLL), and HTLV-I associated
lymphadenitis dermatopathic type (HAL-D) and enlarged paracortical type
(HAL-EP). In ATLL, 40-60% of the nucleated cells were positive for for
HTLV-I proviral DNA by PCR/ISH, while in I-ATLL and HAL, respectively
5-20% and less than 1-5% of cells were positive. The number of mRNA
expressing cells was smaller than that of the proviral DNA-positive
cells. The mRNA-expressing cells varied in number among the ATLL and
I-ATLL cases, while they were only rarely observed in HAL-D and HAL-EP.
These results show that HTLV-I infection and activation might increase
with malignant transformation of the target T helper cells.
Adult Aged DNA, Viral/*ANALYSIS Female Gene Expression Regulation,
Neoplastic Gene Expression Regulation, Viral Human HTLV-I/*GENETICS
HTLV-I Infections/*DIAGNOSIS/GENETICS In Situ Hybridization/*METHODS
Leukemia, T-Cell/*MICROBIOLOGY Lymph Nodes/*MICROBIOLOGY Male Middle
Age Polymerase Chain Reaction/*METHODS RNA, Viral/*ANALYSIS JOURNAL
ARTICLE