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. 2018 Oct 18;2(20):2704–2712. doi: 10.1182/bloodadvances.2018022723

Table 2.

The patients with STAT3 mutations

Cohort UPN Cause of PRCA STAT3 mutation
Allele-specific PCR Amplicon (% PB or BM MNCs) Amplicon (% CD8+ T)
Nagano/Kanazawa 47 Idiopathic Y640F, D661Y Y640F (2.9), D661Y (7.3) Y640F (6), D661Y (13.7)
166 Idiopathic G618R (7.8), D698H (2) NT
182 CD, SjS R152W (48.9) NT
243 Idiopathic D661V (1.9)
245 Thymoma Y640F Y640F (2.2) Y640F (15.8)
399 Idiopathic S614R (9.1), Y640F (2.3) NT
3 T-LGLL Y640F, D661Y Y640F (5.6), D661Y (1.1) NT
8 T-LGLL D661Y D661Y (0.96)* NT
13 T-LGLL D661Y D661Y (0.57)* NT
37 T-LGLL Y640F Y640F (3.1) NT
170 T-LGLL D661Y D661Y (1.2) S614R (1.5), D661Y (1.2)
192 T-LGLL D661H (4.8) NT
194 T-LGLL Y640F (1.1)
291 T-LGLL D661Y D661Y (2.5) D661Y (3)
293 T-LGLL Y640F (2.5)
Akita 452 Thymoma F174V (1.9), S614R (8) NT
453 Idiopathic Y640F D170G (6.4), Y640F (1.5) NT
455 T-LGLL S614R (25.9) NT

—, not detected; CD, Crohn's disease; NT, not tested; PB, peripheral blood; SjS, Sjögren syndrome; UPN, unique patient number.

*

The percentage of STAT3-mutated DNA, as determined by an allele-specific quantitative PCR.

CD8+ T cells were sorted from BM MNCs.