In a previous study, we described the occurrence of T-cell receptor (T
CR)delta gene rearrangements in 9/100 acute myeloid leukemia (AML) cas
es. In this study, we further characterized these rearrangements by So
uthern Blot hybridization using a V delta 2 specific probe and polymer
ase chain reaction (PCR). Southern Blot analysis revealed that rearran
gements involved the V delta 2 gene segment in four patients. Interest
ingly the restriction fragments detected by the V delta 2 probe differ
ed markedly in size. PCR analysis revealed a complete V delta 2(Dn)J d
elta 1 gene rearrangement, an incomplete V delta 2D delta 3 rearrangem
ent and a large amplification product, which cannot be explained with
normal VDJ recombinatorial processes, in one case each. Furthermore al
though V delta 2 and J delta 1 were rearranged, no comigration of rear
ranged fragments was observed and no PCR product was obtained in one c
ase. Obtained results in AML differ from findings in acute lymphoblast
ic leukemia (ALL) of B-cell lineage, where a more homogeneous pattern
of rearrangements has been described. This heterogeneity might be rela
ted to the illegitimate occurrence of TCR delta gene rearrangements in
AML.