Selected publications pre PRIMA
Gjølberg, T.T., Wik, J.A., Johannessen, H. et al. Antibody blockade of Jagged1 attenuates choroidal neovascularization. Nat Commun 14, 3109 (2023). https://doi.org/10.1038/s41467-023-38563-w
Philippon, C., Tao, S.A., Clement, D., et al. Allelic Variation of KIR and HLA Tunes the Cytolytic Payload and Determines Functional Hierarchy of NK Cell Repertoires. Blood Adv 2023; bloodadvances.2023009827. https://doi.org/10.1182/bloodadvances.2023009827
Hermansen, J.U., Yin, Y., Urban, A. et al. A tumor microenvironment model of chronic lymphocytic leukemia enables drug sensitivity testing to guide precision medicine. Cell Death Discov. 9, 125 (2023). https://doi.org/10.1038/s41420-023-01426-w
Mukadam, A.S., et al. Cytosolic antibody receptor TRIM21 is required for effective tau immunotherapy in mouse models. Science379,1336-1341(2023). https://doi.org/10.1126/science.abn1366
Casey, N.P, Klee, C.H., Fåne, A., et al. Efficient chimeric antigen receptor (CAR) targeting of a central epitope of CD22. Journal of Biological Chemistry, 104883 (2023) https://doi.org/10.1016/j.jbc.2023.104883
Fernández-Quintero, M-L-, Ljungars, A., Waibl, F., et al. Assessing developability early in the discovery process for novel biologics, mAbs, 15:1 (2023). https://doi.org/10.1080/19420862.2023.2171248
Foss S, Jonsson A, Bottermann M et al. Potent TRIM21 and complement-dependent intracellular antiviral immunity requires the IgG3 hinge. Sci. Immunol.7,eabj1640 (2022). https://doi.org/10.1126/sciimmunol.abj1640
Pataskar, A., Champagne, J., Nagel, R. et al. Tryptophan depletion results in tryptophan-to-phenylalanine substitutants. Nature 603, 721–727 (2022). https://doi.org/10.1038/s41586-022-04499-2
Ali, M., Giannakopoulou, E., Li, Y. et al. T cells targeted to TdT kill leukemic lymphoblasts while sparing normal lymphocytes. Nat Biotechnol 40, 488–498 (2022). https://doi.org/10.1038/s41587-021-01089-x
Cichocki, F., Bjordahl, R., Goodridge, J.P. et al. Quadruple gene-engineered natural killer cells enable multi-antigen targeting for durable antitumor activity against multiple myeloma. Nat Commun 13, 7341 (2022). https://doi.org/10.1038/s41467-022-35127-2
Bollineni, R.C., Tran, T.T, Lund-Johansen, F., et al. Chasing neoantigens; invite naïve T cells to the party. Current Opinion in Immunology, Volume 75, 102172 (2022). https://doi.org/10.1016/j.coi.2022.102172
Haroun-Izquierdo A, Vincenti M, Netskar H, et alAdaptive single-KIR+NKG2C+ NK cells expanded from select superdonors show potent missing-self reactivity and efficiently control HLA-mismatched acute myeloid leukemia. Journal for ImmunoTherapy of Cancer 2022;10:e005577. https://doi.org/10.1136/jitc-2022-005577
Robert, P.A., Akbar, R., Frank, R. et al. Unconstrained generation of synthetic antibody–antigen structures to guide machine learning methodology for antibody specificity prediction. Nat Comput Sci 2, 845–865 (2022). https://doi.org/10.1038/s43588-022-00372-4
Salomé B., Sfakianos JP, Ranti D., et al. NKG2A and HLA-E define an alternative immune checkpoint axis in bladder cancer. Cancer Cell, 40(9) (2022). https://doi.org/10.1016/j.ccell.2022.08.005
Grevys, A., Frick, R., Mester, S.,et al. Antibody variable sequences have a pronounced effect on cellular transport and plasma half-life. iScience, Volume 25, Issue 2 (2022). https://doi.org/10.1016/j.isci.2022.103746
Rye, I.H., Huse, K., Josefsson, S.E., Kildal, W., et al. Breast cancer metastasis: immune profiling of lymph nodes reveals exhaustion of effector T cells and immunosuppression. Mol Oncol, 16: 88-103 (2022). https://doi.org/10.1002/1878-0261.13047
Giliberto, M., Thimiri Govinda Raj, D.B., Cremaschi, A., et al. Ex vivo drug sensitivity screening in multiple myeloma identifies drug combinations that act synergistically. Mol Oncol, 16: 1241-1258 (2022). https://doi.org/10.1002/1878-0261.13191
Shapiro RM, Birch GC, Hu G. et al. Expansion, persistence, and efficacy of donor memory-like NK cells infused for posttransplant relapse. J Clin Invest. 2022;132(11):e154334 (2022). https://doi.org/10.1172/JCI154334
Skånland SS, Inngjerdingen M, Bendiksen H, et al. Functional testing of relapsed chronic lymphocytic leukemia guides precision medicine and maps response and resistance mechanisms. An index case. Haematologica 2022;107(8):1994-1998; https://doi.org/10.3324/haematol.2021.280393.
Akbar, R., Bashour, H., Rawat, P., et al. Progress and challenges for the machine learning-based design of fit-for-purpose monoclonal antibodies, mAbs, 14:1, (2022) https://doi.org/10.1080/19420862.2021.2008790
Minton AR, Smith LD, Bryant DJ, Strefford JC, Forconi F, Stevenson FK, et al. B-cell receptor dependent phagocytosis and presentation of particulate antigen by chronic lymphocytic leukemia cells. Explor Target Antitumor Ther. 2022;3:37–49. https://doi.org/10.37349/etat.2022.00070
Imbery, JF, Heinzelbecker, J, Jebsen, JK, McGowan, M, Myklebust, C, Bottini, N, et al. T-helper cell regulation of CD45 phosphatase activity by galectin-1 and CD43 governs chronic lymphocytic leukaemia proliferation. Br J Haematol. 2022; 198: 556– 573. https://doi.org/10.1111/bjh.18285
Sandvei, M.S., Jacobsen, G.W., Stien, M.H., et al. A national intercalated medical student research program – student perceptions, satisfaction, and factors associated with pursuing a PhD, Medical Education Online, 27:1 (2022) https://doi.org/10.1080/10872981.2022.2122105
Bartok, O., Pataskar, A., Nagel, R. et al. Anti-tumour immunity induces aberrant peptide presentation in melanoma. Nature 590, 332–337 (2021). https://doi.org/10.1038/s41586-020-03054-1
Lund-Johansen, F., Tran, T. & Mehta, A. Towards reproducibility in large-scale analysis of protein–protein interactions. Nat Methods 18, 720–721 (2021). https://doi.org/10.1038/s41592-021-01202-7
Woan, KV, et al. Harnessing features of adaptive NK cells to generate iPSC-derived NK cells for enhanced immunotherapy. Cell Stem Cell (2021). https://doi.org/10.1016/j.stem.2021.08.013
Luca, BA, Steen, CB, et al. Atlas of clinically distinct cell states and ecosystems across human solid tumors. Cell 184, 5482-5496 e5428 (2021). https://doi.org/10.1016/j.cell.2021.09.014
Steen, CB, Luca, B.A., Esfahani, M.S., et al. The landscape of tumor cell states and ecosystems in diffuse large B cell lymphoma. Cancer Cell 39, 1422-1437 e1410 (2021). https://doi.org/10.1016/j.ccell.2021.08.011
Ask, EH, Tschan-Plessl, A., Gjerdingen, T.J., et al. A systemic protein deviation score linked to PD-1+CD8+T cell expansion that predicts overall survival in diffuse large B cell lymphoma. Med 1, 180-195 (2021). https://doi.org/10.1016/j.medj.2020.10.006
Szodoray, P., Andersen, T.K., Heinzelbecker, J., et al. Integration of T helper and BCR signals governs enhanced plasma cell differentiation of memory B cells by regulation of CD45 phosphatase activity. Cell Reports, 36 (6), (2021). https://doi.org/10.1016/j.celrep.2021.109525
Bern, M, Nilsen J., Ferrarese, M., et al. An engineered human albumin enhances half-life and transmucosal delivery when fused to protein-based biologics. Sci Transl Med 12 (2020). https://doi.org/10.1126/scitranslmed.abb0580
Wise, J.F., Nakken, S., Steen, C.B. et al. Mutational dynamics and immune evasion in diffuse large B-cell lymphoma explored in a relapse-enriched patient series. Blood Adv 2020; 4 (9): 1859–1866. https://doi.org/10.1182/bloodadvances.2019001325
Majzner RG, Rietberg SP, Sotillo E, et al. Tuning the Antigen Density Requirement for CAR T-cell Activity. Cancer Discov. 2020 May;10(5):702-723. https://doi.org/10.1158/2159-8290.CD-19-094
Shaw, A., Hoffecker, I.T., Smyrlaki, I. et al. Binding to nanopatterned antigens is dominated by the spatial tolerance of antibodies. Nature Nanotech 14, 184–190 (2019). https://doi.org/10.1038/s41565-018-0336-3
Saetersmoen, M.L., Hammer, Q., Valamehr, B. et al. Off-the-shelf cell therapy with induced pluripotent stem cell-derived natural killer cells. Semin Immunopathol 41, 59–68 (2019). https://doi.org/10.1007/s00281-018-0721-x
Ali, M., Foldvari, Z., Giannakopoulou, E. et al. Induction of neoantigen-reactive T cells from healthy donors. Nat Protoc 14, 1926–1943 (2019). https://doi.org/10.1038/s41596-019-0170-6
Sikorski, K., Mehta, A., Inngjerdingen, M. et al. A high-throughput pipeline for validation of antibodies. Nat Methods 15, 909–912 (2018). https://doi.org/10.1038/s41592-018-0179-8
Bjorklund, A. T. et al. Complete Remission with Reduction of High-Risk Clones following Haploidentical NK-Cell Therapy against MDS and AML. Clin Cancer Res 24, 1834-1844, (2018). https://doi.org/10.1158/1078-0432.CCR-17-3196
Haapaniemi, E., Botla, S., Persson, J., et al. CRISPR-Cas9 genome editing induces a p53-mediated DNA damage response. Nat Med 24, 927-930 (2018). https://doi.org/10.1038/s41591-018-0049-z
Grevys, A., Nilsen, J., Sand, K.M., et al. A human endothelial cell-based recycling assay for screening of FcRn targeted molecules. Nat Commun 9, 621 (2018). https://doi.org/10.1038/s41467-018-03061-x
Wang, D., Fløisand, Y., Myklebust, C. et al. Autologous bone marrow Th cells can support multiple myeloma cell proliferation in vitro and in xenografted mice. Leukemia 31, 2114–2121 (2017). https://doi.org/10.1038/leu.2017.69
Olweus, J. Manufacture of CAR-T cells in the body. Nat Biotechnol 35, 520–521 (2017). https://doi.org/10.1038/nbt.3898
Karpanen, T & Olweus, J. The Potential of Donor T-Cell Repertoires in Neoantigen-Targeted Cancer Immunotherapy. Front Immunol 8, 1718 (2017). https://doi.org/10.3389/fimmu.2017.01718
Stronen, E., Toebes, M., Kelderman, S., et al. Targeting of cancer neoantigens with donor-derived T cell receptor repertoires. Science 352, 1337-1341 (2016). https://doi.org/10.1126/science.aaf2288
Lund-Johansen, F., de la Rosa Carrillo, D., Mehta, A. et al. MetaMass, a tool for meta-analysis of subcellular proteomics data. Nat Methods 13, 837–840 (2016). https://doi.org/10.1038/nmeth.3967
Mensali, N., et al. Targeting B-cell neoplasia with T-cell receptors recognizing a CD20-derived peptide on patient-specific HLA. Oncoimmunology 5, e1138199, (2016). https://doi.org/10.1080/2162402X.2016.1138199
Kumari, S., et al. Alloreactive cytotoxic T cells provide means to decipher the immunopeptidome and reveal a plethora of tumor-associated self-epitopes. Proc Natl Acad Sci U S A 111, 403-408 (2014). https://doi.org/10.1073/pnas.1306549111