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Table 2 Putative neoepitopes encoding mutations found recurrently in hematological cancers

From: Isolation of T cell receptors targeting recurrent neoantigens in hematological malignancies

Protein

Mutation

Putative epitope

Peptide

HLA-Restriction

Predicted HLA binding affinity (nM)

Hematopoietic and Lymphoid Cancer Frequencies

CALR

K385Nfs*47

RPRTSCREA

CALR-REA

HLA-B*07:02

12

Essential thrombocythemia (31.1%), Myelofibrosis (27.3%)

SPARPRTSC

CALR-SPA

HLA-B*07:02

22

RMRRTRRKM

CALR-RMR

HLA-B*07:02

56

RPRTSCREAC

CALR-REAC

HLA-B*07:02

23

RMMRTKMRMR

CALRp2

HLA-A*03:01

41

KMRMRRMRR

CALRp7

HLA-A*03:01

35

RTRRKMRRK

CALRp15

HLA-A*03:01

54

FBXW7

R465C

TVCCMHLHEK

TVC

HLA-A*11:01

29

T-ALL (15.4%), Precursor T cell lymphoblastic lymphoma (15.6%)

STVCCMHLHEK

STV

HLA-A*11:01

65

HTSTVCCMHLH

HTS

HLA-A*11:01

495

R465H

STVHCMHLH

STVH

HLA-A*11:01

78

TVHCMHLHEK

TVH

HLA-A*11:01

43

P53

R248Q

SSCMGGMNQR

NQR

HLA-A*11:01

177

Mantle cell lymphoma (9.1%), B-ALL (6.9%), T-ALL (8.6%), Follicular lymphoma (18.5%), AML (7%), MDS (7.3%), CLL (10.9%), T cell lymphoma (18.6%), Burkitt’s lymphoma (18%), Diffuse large B cell lymphoma (12.6%)

R248W

SSCMGGMNWR

NWR

HLA-A*11:01

320

MyD88

L265P

RPIPIKYKAM

RPI

HLA-B*07:02

20

MGUS (46.8%), Waldenström’s macroglobulinaemia (86.3%), Diffuse large B cell lymphoma (14.4%)

SPGAHQKRPI

SPG

HLA-B*07:02

40

IDH2

R140Q

SPNGTIQNIL

SPN

HLA-B*07:02

72

AML (9.7%), Angioimmunoblastic T cell lymphoma (24.1%)

DNMT3A

R882H

VSNMSHLAR

VSN

HLA-A*11:01

61

AML (20.4%), MDS (9.1%), T cell lymphoma (25.7%),

STAT3

Y640F

QIQSVEPFTK

QIQ

HLA-A*11:01

60

T cell large granular lymphocytic leukaemia (34.3%), Adult T-cell leukemia/lymphoma (21.1%)

  1. The catalogue of somatic mutations in cancer (COSMIC) was used to identify mutations found recurrently in hematological cancers. The MHC binding algorithm NetMHC3.4 was utilized to identify putative neoepitopes encoding these mutations that were predicted to bind strongly to common European Caucasoid HLA class I alleles. T-ALL T cell acute lymphoblastic leukemia, B-ALL B cell acute lymphoblastic leukemia, AML acute myeloid leukemia, MDS myelodysplastic syndrome, CLL chronic lymphocytic leukemia, MGUS monoclonal gammopathy of undetermined significance