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. 2020 Jul 23;7:15–22. doi: 10.1016/j.iotech.2020.07.002

Table 1.

Tumour antigens with potential for clinical application, including the antibody targets described in the manuscript, the technology used to identify these antibodies and (pre)clinical evaluation

Antigen Antibody identification Clinical evaluation References
Targets of allogeneic B-cell responses
 BCMA cDNA serum screen of patients with MM after allogeneic HCT and DLI Antibody–drug conjugate, CAR-T cells 35,36,63, 64, 65
 CML28 CML66 cDNA serum screen of patients with CML after allogeneic HCT and DLI 7,20,21,85
 RAFTK (PTK2B) cDNA serum screen of patients with CML after allogeneic HCT and DLI and western blot analysis of serum specifically for PTK2B 7,37
 NuSAP1 Protein array serum screen of patients with AML 26
 snRNP200 Screening of immortalized donor-derived memory B cells after allogeneic HCT for AML Tested in mouse models 33
 CD43s Screening of immortalized donor-derived memory B cells after allogeneic HCT for AML Tested in mouse models 34,61,68
Targets of autologous B-cell responses relevant for haematologic malignancies
 CD9 Screening of immortalized patient-derived memory B cells after adoptive T-cell transfer of tumour-reactive T cells for melanoma Preclinical evaluation 82, 83, 84,86, 87, 88, 89
 MUC1 Identified in serum of patients with many different types of tumours Vaccine, CAR-T cells 69, 70, 71, 72, 73, 74NCT04020575

AML, acute myeloid leukaemia; BCMA, B-cell maturation antigen; CAR, chimeric antigen receptor; CML, chronic myeloid leukaemia; DLI, donor lymphocyte infusion; HCT, haematopoietic cell transplantation; MM, multiple myeloma; MUC1, mucin 1; NuSAP1, nuclear and spindle-associated protein 1; RAFTK, related adhesion focal tyrosine kinase.