Demonstration of frequent occurrence of clonal T cells in the peripheral blood but not in the skin of patients with small plaque parapsoriasis

Citation
Jm. Muche et al., Demonstration of frequent occurrence of clonal T cells in the peripheral blood but not in the skin of patients with small plaque parapsoriasis, BLOOD, 94(4), 1999, pp. 1409-1417
Citations number
44
Categorie Soggetti
Hematology,"Cardiovascular & Hematology Research
Journal title
BLOOD
ISSN journal
00064971 → ACNP
Volume
94
Issue
4
Year of publication
1999
Pages
1409 - 1417
Database
ISI
SICI code
0006-4971(19990815)94:4<1409:DOFOOC>2.0.ZU;2-4
Abstract
Clinical, immunohistological, and molecular biological data suggest the chr onic dermatosis small plaque parapsoriasis (SPP) to be a precursor of mycos is fungoides (MF), However, most data are contradictory and confusing due t o inexact definition of SPP. Recently, clonal T cells were detected in skin and blood samples of early MF. Because demonstration of identical T-cell c lones in skin and blood of SPP patients would indicate a close relationship of SPP to MF, we investigated the clonality of skin and blood specimens fr om 14 well-defined SPP patients. By a polymerase chain reaction (PCR) ampli fying T-cell receptor gamma rearrangements and subsequent high-resolution e lectrophoresis, clonal T cells were detected in 9 of 14 initial and 32 of 4 9 follow-up blood samples, but in 0 of 14 initial skin specimens. Even a do ne-specific PCR showing the persistence of the initial blood T-cell clone i n 20 of 20 follow-up samples, failed to detect the T-cell clone in the skin . In 2 patients, the clonal T cells were shown to be CD4(+). For the first time, the majority of SPP patients was shown to carry a T-cell clone in the peripheral blood. Although a relation between circulating clonal i cells a nd SPP cannot directly be proven by the applied techniques, our results ind icate blood T-cell clonality to be a characteristic feature of SPP and CTCL because analysis of multiple controls and clinical workup of our SPP patie nts excluded other factors simulating or causing a clonal T-cell proliferat ion. A sufficient cutaneous antitumor response but also an extracutaneous o rigin of the T-cell clones might explain the failure to detect skin infiltr ating clonal T cells. (C) 1999 by The American Society of Hematology.