Table 1.
T cell disease | JAK mutation | STAT mutation | Other mutations/fusions | Reference(s) |
---|---|---|---|---|
Extranodal NKTCL | JAK1: Y652D JAK3: C565DEL, A572V, A573V, V722I | STAT3: S614R, D66IY, A703T, STAT5B: N642H, Y665F | 20, 22, 23 | |
Hepatosplenic γδTCL | STAT3: Y640F, D661Y STAT5B: N642H, Y665F, E679K | 23 | ||
CTCL, including Sézary syndrome | JAK1: Y654F, L710VJAK3: Y123H, A573V, S989I | STAT3: I498Y, Y640F STAT5B: N642H, Q706L | 26, 30, 58 | |
HTLV-1 ATLL | JAK3: L156P, R172Q, E183G | 34,64 | ||
PTCL-NOS | JAK3: L1073F | STAT5B: Q743H | IL-7RQ445* | 95 |
ETP-ALL | JAK1: S512L, A634D, V658F, R724H/Q, V782M, L783F, R879S/C/H JAK2: R683S/G/Q, I682F, R867Q, D873N, P933R JAK3: V715ITYK2: V15A, G36D, S47N, R274H, R425H, V731I, E957D, R1027H | IL-7R, TEL-JAK2 | 31,35,37, 65, 69, 70 | |
AITL | JAK2: V617F, G511S | 614,661 | 32 | |
NK, LGL leukemia | JAK1: Y652DJAK3: C365del, A572V, A573V, V722I, L1073F | STAT3: S614R, G618R, Y640F, N647I, D661Y/VHI, STAT5B: N642H, Y665F | 13–15, 59 | |
ALK-negative ALCL | JAK1: G1097D/S/V, Y640F, L910P | STAT3: S614R, G618R, Y640F, N647I, D661H/Y, lins, A662V | NFB2-ROS1, NFB2-TYK2, PABPC4-TYK2, lead to constitutive pSTAT3 activation | 16–18, Chen etal. 2016a |
T-PLL | JAK1: L653F, Y658FJAK3: Q503H, Q507P/H, M511I, A572V, A573V, R629D, 630del, L653F, R657Q/W, V658F, V674F/A, V678L, V722I, Y824D, L857P | STAT5B: N642H, R659C, Y665H, Q706L | IL-2RG: M270 del, K315E | 25–27 |
EATL | STAT5B: N642H | 23 |
J. Chen, Y. Zhang, M. Petrus, W. Xiao, A. Nicolae, et al., submitted manuscript.
Abbreviations: AITL, angioimmunoblastic T cell lymphoma; ALCL, anaplastic large cell lymphoma; ALL, acute lymphoblastic leukemia; ATLL, adult T cell leukemia/lymphoma; CTCL, cutaneous T cell lymphoma; EATL, enteropathy-associated T cell lymphoma; ETP, acute lymphoblastic leukemia; γδTCL, γδ T cell lymphoma; HTLV-1, human T cell lymphotropic virus 1; LGL, large granulocytic leukemia; NKTCL, natural killer cell lymphoma; PTCL-NOS, peripheral T cell lymphoma not otherwise specified; T-PLL, T cell prolymphocytic leukemia.