Table 1

Characteristics of isolated CD4+CD25+ T-cell clones

CloneClone derived fromGenomic location of dominant integration site, hg 18*Proviral load composed of dominant integration site, %
Asymptomatic carrier 1 Chromosome 6: 84613188 98.95 
Asymptomatic carrier 1 Chromosome 1: 184745603 99.95 
HAM/TSP patient 1 Chromosome 16: 52158560 99.9 
HAM/TSP patient 1 Chromosome X: 114257179 99.9 
HAM/TSP patient 1 Chromosome 10: 2277787 100 
HAM/TSP patient 1 Chromosome 13: 74997821 98.88 
HAM/TSP patient 2 Chromosome 10: 80828281 99.96 
HAM/TSP patient 2 Chromosome 5: 1997980 99.9 
HAM/TSP patient 2 Chromosome 4: 70601874 95.2 
10 HAM/TSP patient 2 Chromosome X: 129048967 100 
11 HAM/TSP patient 2 Chromosome 14: 45274700 100 
12 HAM/TSP patient 3 Chromosome 4: 107219655 99.9 
13 HAM/TSP patient 3 Chromosome 12: 40920384 100 
14 HAM/TSP patient 4 Chromosome 5: 50609660 98.4 
15 HAM/TSP patient 4 Chromosome 3: 76576960 99.9 
16 HAM/TSP patient 4 Chromosome 19: 32974427 100 
17 HAM/TSP patient 4 Chromosome 19: 38521388 100 
18 HAM/TSP patient 4 Chromosome 14: 80728657 95.5 
19 HAM/TSP patient 4 Chromosome 4: 169472575 100 
20 HAM/TSP patient 5 Chromosome 3:75952018 100 
21 Polymyositis patient 1 Chromosome 2: 214080658 99.95 
22 Polymyositis patient 1 Chromosome 6: 167451858 99.9 
23 Polymyositis patient 1 Chromosome 22: 31885379 100 
24 Polymyositis patient 1 Chromosome 3: 32582626 98.6 
25 ATLL patient 1 Chromosome 22: 42654531 99.89 
26 ATLL patient 2 Chromosome 4: 9905297 99.8 
27 Asymptomatic carrier 2 Chromosome 8: 87708389 52 
27 Asymptomatic carrier 2 Chromosome 9: 11420980 42 
CloneClone derived fromGenomic location of dominant integration site, hg 18*Proviral load composed of dominant integration site, %
Asymptomatic carrier 1 Chromosome 6: 84613188 98.95 
Asymptomatic carrier 1 Chromosome 1: 184745603 99.95 
HAM/TSP patient 1 Chromosome 16: 52158560 99.9 
HAM/TSP patient 1 Chromosome X: 114257179 99.9 
HAM/TSP patient 1 Chromosome 10: 2277787 100 
HAM/TSP patient 1 Chromosome 13: 74997821 98.88 
HAM/TSP patient 2 Chromosome 10: 80828281 99.96 
HAM/TSP patient 2 Chromosome 5: 1997980 99.9 
HAM/TSP patient 2 Chromosome 4: 70601874 95.2 
10 HAM/TSP patient 2 Chromosome X: 129048967 100 
11 HAM/TSP patient 2 Chromosome 14: 45274700 100 
12 HAM/TSP patient 3 Chromosome 4: 107219655 99.9 
13 HAM/TSP patient 3 Chromosome 12: 40920384 100 
14 HAM/TSP patient 4 Chromosome 5: 50609660 98.4 
15 HAM/TSP patient 4 Chromosome 3: 76576960 99.9 
16 HAM/TSP patient 4 Chromosome 19: 32974427 100 
17 HAM/TSP patient 4 Chromosome 19: 38521388 100 
18 HAM/TSP patient 4 Chromosome 14: 80728657 95.5 
19 HAM/TSP patient 4 Chromosome 4: 169472575 100 
20 HAM/TSP patient 5 Chromosome 3:75952018 100 
21 Polymyositis patient 1 Chromosome 2: 214080658 99.95 
22 Polymyositis patient 1 Chromosome 6: 167451858 99.9 
23 Polymyositis patient 1 Chromosome 22: 31885379 100 
24 Polymyositis patient 1 Chromosome 3: 32582626 98.6 
25 ATLL patient 1 Chromosome 22: 42654531 99.89 
26 ATLL patient 2 Chromosome 4: 9905297 99.8 
27 Asymptomatic carrier 2 Chromosome 8: 87708389 52 
27 Asymptomatic carrier 2 Chromosome 9: 11420980 42 

hg 18 indicates human genome build 18 (NCBI build 36).

*

This column shows the genomic location of the dominant integration site by chromosome and position using hg18 assembly as reference.

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