The current study was designed to determine the nucleotide sequence of two distinct T-cell-receptor delta chain (TCRδ) rearrangements which account for 95% of all rearranged alleles in common non-T, non-B lymphoid precursor acute lymphoblastic leukemia (LP-ALL). The results presented demonstrate that TCRS rearrangements in LP-ALL are incomplete, immature, and involve Vδ2 to Dδ3 or Dδ2 to Dδ3 joints. These rearrangements are found in most cases of ALL. These results are consistent with the hypothesis that these leukemias originate in multipotent lymphoid precursor cells. The remarkable diversity of the rearrangements detected by polymerase chain reaction, cloning and sequencing demonstrates the clonal specificity and potential for detection of leukemic residual disease. However, in some cases the number of nucleotide differences may not be sufficient for the discrimination of leukemic and non-leukemic cells carrying Vδ2-(D)-Dδ3 rearrangements. A novel inversional rearrangement was demonstrated in one leukemia. This novel inversional rearrangement potentially increases the degree of diversity of the junctional region which encodes the antigen binding domain of TCRδ.
|Original language||English (US)|
|Number of pages||9|
|State||Published - Oct 1992|