The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.
The Peptide Vaccine of the Future
Open accessAbstract
The approach of peptide-based anticancer vaccination has proven the ability to induce cancer-specific immune responses in multiple studies for various cancer entities. However, clinical responses remain so far limited to single patients and broad clinical applicability was not achieved. Therefore, further efforts are required to improve peptide vaccination in order to integrate this low-side-effect therapy into the clinical routine of cancer therapy. To design clinically effective peptide vaccines in the future, different issues have to be addressed and optimized comprising antigen target selection as well as choice of optimal adjuvants and vaccination schedules. Furthermore, the combination of peptide-based vaccines with other immuno- and molecular targeted therapies as well as the development of predictive biomarkers could further improve efficacy. In this review, current approaches in the development of peptide-based vaccines and critical implications for optimal vaccine design are discussed.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Mutational landscape determines sensitivity to PD-1 blockade in non–small cell lung cancer
Rizvi, N. A., Hellmann, M. D., Snyder, A., Kvistborg, P., Makarov, V., Havel, J. J., Lee, W., Yuan, J., Wong, P., Ho, T. S., et al. (2015) · Science · doi:10.1126/science.aaa1348 · Cited by 7,802
Wherry, E. J. (2011) · Nature Immunology · doi:10.1038/ni.2035 · Cited by 4,062
Chimeric Antigen Receptor–Modified T Cells for Acute Lymphoid Leukemia
Grupp, S. A., Kalos, M., Barrett, D., Aplenc, R., Porter, D. L., Rheingold, S. R., Teachey, D. T., Chew, A., Hauck, B., Wright, J. F., et al. (2013) · New England Journal of Medicine · doi:10.1056/nejmoa1215134 · Cited by 3,509
An immunogenic personal neoantigen vaccine for patients with melanoma
Ott, P. A., Hu, Z., Keskin, D. B., Shukla, S. A., Sun, J., Bozym, D. J., Zhang, W., Luoma, A., Giobbie-Hurder, A., Peter, L., et al. (2017) · Nature · doi:10.1038/nature22991 · Cited by 2,936
Delves, P. J., & Roitt, I. M. (2000) · New England Journal of Medicine · doi:10.1056/nejm200007063430107 · Cited by 1,666
Loss of IFN-γ pathway genes in tumor cells as a mechanism of resistance to anti-CTLA-4 therapy
Gao, J., Shi, L. Z., Zhao, H., Chen, J., Xiong, L., He, Q., Chen, T., Roszik, J., Bernatchez, C., Woodman, S. E., et al. (2016) · Cell · doi:10.1016/j.cell.2016.08.069 · Cited by 1,300
Predicting immunogenic tumour mutations by combining mass spectrometry and exome sequencing
Yadav, M., Jhunjhunwala, S., Phung, Q. T., Lupardus, P., Tanguay, J., Bumbaca, S., Franci, C., Cheung, T. K., Fritsche, J., Weinschenk, T., et al. (2014) · Nature · doi:10.1038/nature14001 · Cited by 1,186
Quezada, S. A., Simpson, T. R., Peggs, K. S., Merghoub, T., Vider, J., Fan, X., Blasberg, R., Yagita, H., Muranski, P., Antony, P. A., et al. (2010) · Journal of Experimental Medicine · doi:10.1084/jem.20091918 · Cited by 898
Tracking T cells with tetramers: new tales from new tools
Klenerman, P., Cerundolo, V., & Dunbar, P. R. (2002) · Nature Reviews Immunology · doi:10.1038/nri777 · Cited by 190
Flagged first, then by citations
Research works printed but not linked: 143
- Kucerova, 2016, Spontaneous regression of tumour and the role of microbial infection - possibilities for cancer treatment, Anticancer Drugs, 27, 269, 10.1097/CAD.0000000000000337 · DOI
- Hoption Cann, 2003, Dr William Coley and tumour regression: a place in history or in the future, Postgrad. Med. J., 79, 672, 10.1093/postgradmedj/79.938.672 · DOI
- Coley, 1910, The treatment of inoperable sarcoma by bacterial toxins (the mixed toxins of the Streptococcus erysipelas and the Bacillus prodigiosus), Proc. R. Soc. Med., 3, 1
- Busch, 1866, Einfluss von Erysipel, Berliner Klin. Wschr., 3, 245
- Taefehshokr, 2020, Promising approaches in cancer immunotherapy, Immunobiology, 225, 151875, 10.1016/j.imbio.2019.11.010 · DOI
- Sahin, 2018, Personalized vaccines for cancer immunotherapy, Science, 359, 1355, 10.1126/science.aar7112 · DOI
- Roy, 2020, Breakthrough concepts in immune-oncology: cancer vaccines at the bedside, J. Leukoc. Biol., 108, 1455, 10.1002/JLB.5BT0420-585RR · DOI
- van Rooij, 2013, Tumor exome analysis reveals neoantigen-specific T-cell reactivity in an ipilimumab-responsive melanoma, J. Clin. Oncol., 31, e439, 10.1200/JCO.2012.47.7521 · DOI · Paper page
- Snyder, 2014, Genetic basis for clinical response to CTLA-4 blockade in melanoma, N. Engl. J. Med., 371, 2189, 10.1056/NEJMoa1406498 · DOI · Paper page
- Kloor, 2020, A Phase I/IIa trial of a frameshift peptide neoantigen-based vaccine for mismatch repair-deficient cancers, Clin. Cancer Res., 10.1158/1078-0432.CCR-19-3517 · DOI
- Fang, 2020, A pan-cancer clinical study of personalized neoantigen vaccine monotherapy in treating patients with various types of advanced solid tumors, Clin. Cancer Res., 26, 4511, 10.1158/1078-0432.CCR-19-2881 · DOI
- Nelde, 2017, HLA class I-restricted MYD88 L265P-derived peptides as specific targets for lymphoma immunotherapy, Oncoimmunology, 126, 2750
- Schenck, 2019, NeoPredPipe: high-throughput neoantigen prediction and recognition potential pipeline, BMC Bioinformatics, 20, 264, 10.1186/s12859-019-2876-4 · DOI
- Bjerregaard, 2017, MuPeXI: prediction of neo-epitopes from tumor sequencing data, Cancer Immunol. Immunother., 66, 1123, 10.1007/s00262-017-2001-3 · DOI
- Hundal, 2016, pVAC-Seq: a genome-guided in silico approach to identifying tumor neoantigens, Genome Med., 8, 11, 10.1186/s13073-016-0264-5 · DOI
- Bais, 2017, CloudNeo: a cloud pipeline for identifying patient-specific tumor neoantigens, Bioinformatics, 33, 3110, 10.1093/bioinformatics/btx375 · DOI
- Nielsen, 2010, MHC class II epitope predictive algorithms, Immunology, 130, 319, 10.1111/j.1365-2567.2010.03268.x · DOI
- Finn, 2018, Is it possible to develop cancer vaccines to neoantigens, what are the major challenges, and how can these be overcome? Neoantigens: nothing new in spite of the name, Cold Spring Harb. Perspect. Biol., 10, 10.1101/cshperspect.a028829 · DOI
- Bassani-Sternberg, 2016, Direct identification of clinically relevant neoepitopes presented on native human melanoma tissue by mass spectrometry, Nat. Commun., 7, 13404, 10.1038/ncomms13404 · DOI · Paper page
- Müller, 2017, “Hotspots” of antigen presentation revealed by human leukocyte antigen ligandomics for neoantigen prioritization, Front. Immunol., 8, 1367, 10.3389/fimmu.2017.01367 · DOI
- Pearson, 2016, MHC class I-associated peptides derive from selective regions of the human genome, J. Clin. Invest., 126, 4690, 10.1172/JCI88590 · DOI
- Laumont, 2016, Global proteogenomic analysis of human MHC class I-associated peptides derived from non-canonical reading frames, Nat. Commun., 7, 10238, 10.1038/ncomms10238 · DOI
- Erhard, 2018, Improved Ribo-seq enables identification of cryptic translation events, Nat. Methods, 15, 363, 10.1038/nmeth.4631 · DOI
- Parvizpour, 2019, In silico design of a triple-negative breast cancer vaccine by targeting cancer testis antigens, Bioimpacts, 9, 45, 10.15171/bi.2019.06 · DOI
- Safavi, 2019, In silico analysis of transmembrane protein 31 (TMEM31) antigen to design novel multiepitope peptide and DNA cancer vaccines against melanoma, Mol. Immunol., 112, 93, 10.1016/j.molimm.2019.04.030 · DOI
- Qazilbash, 2017, PR1 peptide vaccine induces specific immunity with clinical responses in myeloid malignancies, Leukemia, 31, 697, 10.1038/leu.2016.254 · DOI
- Rammensee, 1999, SYFPEITHI: database for MHC ligands and peptide motifs, Immunogenetics, 50, 213, 10.1007/s002510050595 · DOI
- Reynisson, 2020, NetMHCpan-4.1 and NetMHCIIpan-4.0: improved predictions of MHC antigen presentation by concurrent motif deconvolution and integration of MS MHC eluted ligand data, Nucleic Acids Res., 48, W449, 10.1093/nar/gkaa379 · DOI · Paper page
- Weinzierl, 2007, Distorted relation between mRNA copy number and corresponding major histocompatibility complex ligand density on the cell surface, Mol. Cell. Proteomics, 6, 102, 10.1074/mcp.M600310-MCP200 · DOI
- Fortier, 2008, The MHC class I peptide repertoire is molded by the transcriptome, J. Exp. Med., 205, 595, 10.1084/jem.20071985 · DOI
- Bassani-Sternberg, 2015, Mass spectrometry of human leukocyte antigen class I peptidomes reveals strong effects of protein abundance and turnover on antigen presentation, Mol. Cell. Proteomics, 14, 658, 10.1074/mcp.M114.042812 · DOI
- Shraibman, 2019, Identification of tumor antigens among the HLA peptidomes of glioblastoma tumors and plasma, Mol. Cell. Proteomics, 18, 1255, 10.1074/mcp.RA119.001524 · DOI
- Bilich, 2019, The HLA ligandome landscape of chronic myeloid leukemia delineates novel T-cell epitopes for immunotherapy, Blood, 133, 550, 10.1182/blood-2018-07-866830 · DOI
- Schuster, 2017, The immunopeptidomic landscape of ovarian carcinomas, Proc. Natl. Acad. Sci. U. S. A., 114, E9942
- Kowalewski, 2015, HLA ligandome analysis identifies the underlying specificities of spontaneous antileukemia immune responses in chronic lymphocytic leukemia (CLL), Proc. Natl. Acad. Sci. U. S. A., 112, E166, 10.1073/pnas.1416389112 · DOI
- Neidert, 2018, The natural HLA ligandome of glioblastoma stem-like cells: antigen discovery for T cell-based immunotherapy, Acta Neuropathol., 135, 923, 10.1007/s00401-018-1836-9 · DOI
- Reustle, 2020, Integrative -omics and HLA-ligandomics analysis to identify novel drug targets for ccRCC immunotherapy, Genome Med., 12, 32, 10.1186/s13073-020-00731-8 · DOI
- Teck, 2020, Cancer testis antigen Cyclin A1 harbors several HLA-A∗02:01-restricted T cell epitopes, which are presented and recognized in vivo, Cancer Immunol. Immunother., 69, 1217, 10.1007/s00262-020-02519-6 · DOI
- Bilich, 2020, Mass spectrometry-based identification of a B-cell maturation antigen-derived T-cell epitope for antigen-specific immunotherapy of multiple myeloma, Blood Cancer J., 10, 24, 10.1038/s41408-020-0288-3 · DOI
- Heidenreich, 2017, Mass spectrometry-based identification of a naturally presented receptor tyrosine kinase-like orphan receptor 1-derived epitope recognized by CD8+ cytotoxic T cells, Haematologica, 102, e460, 10.3324/haematol.2017.167312 · DOI
- Walz, 2015, The antigenic landscape of multiple myeloma: mass spectrometry (re)defines targets for T-cell-based immunotherapy, Blood, 126, 1203, 10.1182/blood-2015-04-640532 · DOI
- Freudenmann, 2018, Mapping the tumour human leukocyte antigen (HLA) ligandome by mass spectrometry, Immunology, 154, 331, 10.1111/imm.12936 · DOI
- Marcu, 2019, The HLA ligand atlas. A resource of natural HLA ligands presented on benign tissues, bioRxiv
- Marcu, 2020, The HLA Ligand Atlas: a novel immuno-oncology resource for T-cell antigen discovery, J. Clin. Oncol., 10.1200/JCO.2020.38.15_suppl.3128 · DOI
- 2013, The genotype-tissue expression (GTEx) project, Nat. Genet., 45, 580, 10.1038/ng.2653 · DOI · Paper page
- Uhlén, 2015, Proteomics. Tissue-based map of the human proteome, Science, 347, 1260419, 10.1126/science.1260419 · DOI · Paper page
- Melssen, 2017, Vaccines targeting helper T cells for cancer immunotherapy, Curr. Opin. Immunol., 47, 85, 10.1016/j.coi.2017.07.004 · DOI
- Bijker, 2007, CD8+ CTL priming by exact peptide epitopes in incomplete Freund’s adjuvant induces a vanishing CTL response, whereas long peptides induce sustained CTL reactivity, J. Immunol., 179, 5033, 10.4049/jimmunol.179.8.5033 · DOI
- Zwaveling, 2002, Established human papillomavirus type 16-expressing tumors are effectively eradicated following vaccination with long peptides, J. Immunol., 169, 350, 10.4049/jimmunol.169.1.350 · DOI
- Spitzer, 2017, Systemic immunity is required for effective cancer immunotherapy, Cell, 168, 487, 10.1016/j.cell.2016.12.022 · DOI · Paper page
- Hu, 2014, Immunologic hierarchy, class II MHC promiscuity, and epitope spreading of a melanoma helper peptide vaccine, Cancer Immunol. Immunother., 63, 779, 10.1007/s00262-014-1551-x · DOI
- Giuntoli, 2002, Direct costimulation of tumor-reactive CTL by helper T cells potentiate their proliferation, survival, and effector function, Clin. Cancer Res., 8, 922
- Bos, 2010, CD4+ T-cell help in the tumor milieu is required for recruitment and cytolytic function of CD8+ T lymphocytes, Cancer Res., 70, 8368, 10.1158/0008-5472.CAN-10-1322 · DOI
- Maslak, 2018, Phase 2 trial of a multivalent WT1 peptide vaccine (galinpepimut-S) in acute myeloid leukemia, Blood Adv., 2, 224, 10.1182/bloodadvances.2017014175 · DOI
- Rabu, 2019, Cancer vaccines: designing artificial synthetic long peptides to improve presentation of class I and class II T cell epitopes by dendritic cells, Oncoimmunology, 8, 10.1080/2162402X.2018.1560919 · DOI
- Sayem, 2015, Identification of glypican-3-derived long peptides activating both CD8+ and CD4+ T cells; prolonged overall survival in cancer patients with Th cell response, Oncoimmunology, 5
- Pedersen, 2016, Immunogenicity of HLA class I and II double restricted influenza a-derived peptides, PLoS One, 11, 10.1371/journal.pone.0145629 · DOI
- Ohtake, 2014, Identification of novel helper epitope peptides of survivin cancer-associated antigen applicable to developing helper/killer-hybrid epitope long peptide cancer vaccine, Immunol. Lett., 161, 20, 10.1016/j.imlet.2014.04.010 · DOI
- Daftarian, 2006, Eradication of established HPV 16-expressing tumors by a single administration of a vaccine composed of a liposome-encapsulated CTL-T helper fusion peptide in a water-in-oil emulsion, Vaccine, 24, 5235, 10.1016/j.vaccine.2006.03.079 · DOI
- Toes, 1996, Peptide vaccination can lead to enhanced tumor growth through specific T-cell tolerance induction, Proc. Natl. Acad. Sci. U. S. A., 93, 7855, 10.1073/pnas.93.15.7855 · DOI
- Aichele, 1995, T cell priming versus T cell tolerance induced by synthetic peptides, J. Exp. Med., 182, 261, 10.1084/jem.182.1.261 · DOI
- Kast, 1993, Strict peptide length is not required for the induction of cytotoxic T lymphocyte-mediated antiviral protection by peptide vaccination, Eur. J. Immunol., 23, 1189, 10.1002/eji.1830230534 · DOI
- Bijker, 2008, Superior induction of anti-tumor CTL immunity by extended peptide vaccines involves prolonged, DC-focused antigen presentation, Eur. J. Immunol., 38, 1033, 10.1002/eji.200737995 · DOI
- Southwood, 1998, Several common HLA-DR types share largely overlapping peptide binding repertoires, J. Immunol., 160, 3363, 10.4049/jimmunol.160.7.3363 · DOI
- Walter, 2012, Multipeptide immune response to cancer vaccine IMA901 after single-dose cyclophosphamide associates with longer patient survival, Nat. Med., 18, 1254, 10.1038/nm.2883 · DOI
- Hilf, 2019, Actively personalized vaccination trial for newly diagnosed glioblastoma, Nature, 565, 240, 10.1038/s41586-018-0810-y · DOI · Paper page
- Di Marco, 2017, Identification of immunogenic epitopes by MS/MS, Cancer J., 23, 102, 10.1097/PPO.0000000000000252 · DOI
- Peper, 2015, A combined approach of human leukocyte antigen ligandomics and immunogenicity analysis to improve peptide-based cancer immunotherapy, Cancer Immunol. Immunother., 64, 1295, 10.1007/s00262-015-1682-8 · DOI
- Mashishi, 2002, The ELISPOT assay: an easily transferable methods for measuring cellular responses and identifying T cell epitopes, Clin. Chem. Lab. Med., 40, 903, 10.1515/CCLM.2002.159 · DOI
- Freer, 2013, Intracellular cytokine detection by fluorescence-activated flow cytometry: basic principles and recent advances, Methods, 61, 30, 10.1016/j.ymeth.2013.03.035 · DOI
- Yoshimura, 2016, A phase 2 randomized controlled trial of personalized peptide vaccine immunotherapy with low-dose dexamethasone versus dexamethasone alone in chemotherapy-naive castration-resistant prostate cancer, Eur. Urol., 70, 35, 10.1016/j.eururo.2015.12.050 · DOI
- Shima, 2019, Randomized phase II trial of survivin 2B peptide vaccination for patients with HLA-A24-positive pancreatic adenocarcinoma, Cancer Sci., 110, 2378, 10.1111/cas.14106 · DOI
- Ravandi, 2018, Evaluating measurable residual disease in acute myeloid leukemia, Blood Adv., 2, 1356, 10.1182/bloodadvances.2018016378 · DOI
- Bilich, 2017, Definition and characterization of a peptide warehouse for the patient-individualized peptide vaccination study (iVAC-L-CLL01) after first line therapy of CLL, Blood, 130, 5346
- Slansky, 2020, Peptide mimotopes alter T cell function in cancer and autoimmunity, Semin. Immunol., 47, 101395, 10.1016/j.smim.2020.101395 · DOI
- Candia, 2016, On peptides and altered peptide ligands: from origin, mode of action and design to clinical application (immunotherapy), Int. Arch. Allergy Immunol., 170, 211, 10.1159/000448756 · DOI
- Li, 2013, Immune responses induced in HHD mice by multiepitope HIV vaccine based on cryptic epitope modification, Mol. Biol. Rep., 40, 2781, 10.1007/s11033-012-2202-y · DOI
- Sun, 2018, A modified HLA-A∗0201-restricted CTL epitope from human oncoprotein (hPEBP4) induces more efficient antitumor responses, Cell Mol. Immunol., 15, 768, 10.1038/cmi.2017.155 · DOI
- Zaremba, 1997, Identification of an enhancer agonist cytotoxic T lymphocyte peptide from human carcinoembryonic antigen, Cancer Res., 57, 4570
- Gladney, 2012, Heteroclitic peptides enhance human immunodeficiency virus-specific CD8+ T cell responses, Vaccine, 30, 6997, 10.1016/j.vaccine.2012.09.067 · DOI
- Salazar, 2000, Agonist peptide from a cytotoxic T-lymphocyte epitope of human carcinoembryonic antigen stimulates production of TC1-type cytokines and increases tyrosine phosphorylation more efficiently than cognate peptide, Int. J. Cancer, 85, 829, 10.1002/(SICI)1097-0215(20000315)85:6<829::AID-IJC16>3.0.CO;2-K · DOI
- Adegoke, 2015, Heteroclitic peptides increase proliferation and reduce evidence of human immunodeficiency virus-specific CD8+ T cell dysfunction, Viral Immunol., 28, 455, 10.1089/vim.2015.0036 · DOI
- Zom, 2016, TLR2 ligand-synthetic long peptide conjugates effectively stimulate tumor-draining lymph node T cells of cervical cancer patients, Oncotarget, 7, 67087, 10.18632/oncotarget.11512 · DOI
- Deres, 1989, In vivo priming of virus-specific cytotoxic T lymphocytes with synthetic lipopeptide vaccine, Nature, 342, 561, 10.1038/342561a0 · DOI
- Rauen, 2014, Enhanced cross-presentation and improved CD8+ T cell responses after mannosylation of synthetic long peptides in mice, PLoS One, 9, e103755, 10.1371/journal.pone.0103755 · DOI
- Vermaelen, 2019, Vaccine strategies to improve anticancer cellular immune responses, Front. Immunol., 10, 8, 10.3389/fimmu.2019.00008 · DOI
- Delves, 2000, The immune system. Second of two parts, N. Engl. J. Med., 343, 108, 10.1056/NEJM200007133430207 · DOI
- He, 2018, Peptide delivery systems for cancer vaccines, Adv. Ther., 1, 1800060, 10.1002/adtp.201800060 · DOI
- Aucouturier, 2002, Montanide ISA 720 and 51: a new generation of water in oil emulsions as adjuvants for human vaccines, Expert Rev. Vaccines, 1, 111, 10.1586/14760584.1.1.111 · DOI
- Varypataki, 2017, Efficient eradication of established tumors in mice with cationic liposome-based synthetic long-peptide vaccines, Cancer Immunol. Res., 5, 222, 10.1158/2326-6066.CIR-16-0283 · DOI
- Zhou, 2020, Engineering ApoE3-incorporated biomimetic nanoparticle for efficient vaccine delivery to dendritic cells via macropinocytosis to enhance cancer immunotherapy, Biomaterials, 235, 119795, 10.1016/j.biomaterials.2020.119795 · DOI
- Mach, 2000, Differences in dendritic cells stimulated in vivo by tumors engineered to secrete granulocyte-macrophage colony-stimulating factor or Flt3-ligand, Cancer Res., 60, 3239
- Rausch, 2019, Results of a phase 1/2 study in metastatic renal cell carcinoma patients treated with a patient-specific adjuvant multi-peptide vaccine after resection of metastases, Eur. Urol. Focus, 5, 604, 10.1016/j.euf.2017.09.009 · DOI
- Hoeller, 2016, Systematic review of the use of granulocyte–macrophage colony-stimulating factor in patients with advanced melanoma, Cancer Immunol. Immunother., 65, 1015, 10.1007/s00262-016-1860-3 · DOI
- Krutzik, 2005, TLR activation triggers the rapid differentiation of monocytes into macrophages and dendritic cells, Nat. Med., 11, 653, 10.1038/nm1246 · DOI
- Ribi, 1979, Peptides as requirement for immunotherapy of the Guinea-pig line-10 tumor with endotoxins, Cancer Immunol. Immunother., 7, 43, 10.1007/BF00205409 · DOI
- Beutler, 2003, Innate immune sensing and its roots: the story of endotoxin, Nat. Rev. Immunol., 3, 169, 10.1038/nri1004 · DOI
- Qureshi, 1982, Purification and structural determination of nontoxic lipid A obtained from the lipopolysaccharide of Salmonella typhimurium, J. Biol. Chem., 257, 11808, 10.1016/S0021-9258(18)33836-5 · DOI
- Rastakhiz, 2019, Preparation of nanoliposomes linked to HER2/neu-derived (P5) peptide containing MPL adjuvant as vaccine against breast cancer, J. Cell Biochem., 10.1002/jcb.27090 · DOI
- Smith, 2018, Trial Watch: toll-like receptor agonists in cancer immunotherapy, Oncoimmunology, 7, 10.1080/2162402X.2018.1526250 · DOI
- Gouttefangeas, 2018, Personalized cancer vaccines: adjuvants are important, too, Cancer Immunol. Immunother., 67, 1911, 10.1007/s00262-018-2158-4 · DOI
- Sabbatini, 2012, Phase I trial of overlapping long peptides from a tumor self-antigen and poly-ICLC shows rapid induction of integrated immune response in ovarian cancer patients, Clin. Cancer Res., 18, 6497, 10.1158/1078-0432.CCR-12-2189 · DOI
- Rammensee, 2019, A new synthetic toll-like receptor 1/2 ligand is an efficient adjuvant for peptide vaccination in a human volunteer, J. Immunother. Cancer, 7, 307, 10.1186/s40425-019-0796-5 · DOI
- van Montfoort, 2009, Antigen storage compartments in mature dendritic cells facilitate prolonged cytotoxic T lymphocyte cross-priming capacity, Proc. Natl. Acad. Sci. U. S. A., 106, 6730, 10.1073/pnas.0900969106 · DOI
- Krekorian, 2019, Imaging of T-cells and their responses during anti-cancer immunotherapy, Theranostics, 9, 7924, 10.7150/thno.37924 · DOI
- Haen, 2020, Towards new horizons: characterization, classification and implications of the tumour antigenic repertoire, Nat. Rev. Clin. Oncol., 17, 595, 10.1038/s41571-020-0387-x · DOI
- Britten, 2013, The regulatory landscape for actively personalized cancer immunotherapies, Nat. Biotechnol., 31, 880, 10.1038/nbt.2708 · DOI
- Seol, 2019, A pilot prospective study of refractory solid tumor patients for NGS-based targeted anticancer therapy, Transl Oncol., 12, 301, 10.1016/j.tranon.2018.10.011 · DOI
- Parakh, 2017, Evolution of anti-HER2 therapies for cancer treatment, Cancer Treat. Rev., 59, 1, 10.1016/j.ctrv.2017.06.005 · DOI
- Narita, 2019, A randomized, double-blind, phase III trial of personalized peptide vaccination for recurrent glioblastoma, Neuro Oncol., 21, 348, 10.1093/neuonc/noy200 · DOI
- Rabsteyn, 2019, Abstract B124: personalized peptide vaccination based on patient-individual tumor-specific variants induces T-cell responses in pediatric patients, 10.1158/2326-6074.CRICIMTEATIAACR18-B124 · DOI
- Bui, 2006, Predicting population coverage of T-cell epitope-based diagnostics and vaccines, BMC Bioinformatics, 7, 153, 10.1186/1471-2105-7-153 · DOI
- Vita, 2015, The immune epitope database (IEDB) 3.0, Nucleic Acids Res., 43, D405, 10.1093/nar/gku938 · DOI
- Wick, 2018, GAPVAC-101: first-in-human trial of a highly personalized peptide vaccination approach for patients with newly diagnosed glioblastoma, J. Clin. Oncol., 36, 2000, 10.1200/JCO.2018.36.15_suppl.2000 · DOI
- Le Dieu, 2009, Peripheral blood T cells in acute myeloid leukemia (AML) patients at diagnosis have abnormal phenotype and genotype and form defective immune synapses with AML blasts, Blood, 114, 3909, 10.1182/blood-2009-02-206946 · DOI
- Nakata, 2018, Wilms tumour 1 peptide vaccine as a cure-oriented post-chemotherapy strategy for patients with acute myeloid leukaemia at high risk of relapse, Br. J. Haematol., 182, 287, 10.1111/bjh.14768 · DOI
- Brown, 2020, Prospective, randomized, single-blinded, multi-center phase II trial of two HER2 peptide vaccines, GP2 and AE37, in breast cancer patients to prevent recurrence, Breast Cancer Res. Treat., 181, 391, 10.1007/s10549-020-05638-x · DOI
- Ahmad, 2004, Escape from immunotherapy: possible mechanisms that influence tumor regression/progression, Cancer Immunol. Immunother., 53, 844, 10.1007/s00262-004-0540-x · DOI
- Ramsay, 2008, Chronic lymphocytic leukemia T cells show impaired immunological synapse formation that can be reversed with an immunomodulating drug, J. Clin. Invest., 118, 2427
- Duan, 2020, Turning cold into hot: firing up the tumor microenvironment, Trends Cancer, 6, 605, 10.1016/j.trecan.2020.02.022 · DOI · Paper page
- Khleif, 2015, Strategies and designs for combination immune therapy, J. Transl. Med., 13, K7, 10.1186/1479-5876-13-S1-K7 · DOI
- MacKay, 2018, Combination of a T cell activating immunotherapy with immune modulators alters the tumor microenvironment and promotes more effective tumor control in preclinical models, Cancer Res., 78, 1761, 10.1158/1538-7445.AM2018-1761 · DOI
- Sharabi, 2015, Stereotactic radiation therapy augments antigen-specific PD-1–mediated antitumor immune responses via cross-presentation of tumor antigen, Cancer Immunol. Res., 3, 345, 10.1158/2326-6066.CIR-14-0196 · DOI
- Ali, 2016, Vaccines combined with immune checkpoint antibodies promote cytotoxic T-cell activity and tumor eradication, Cancer Immunol. Res., 4, 95, 10.1158/2326-6066.CIR-14-0126 · DOI
- Rini, 2016, IMA901, a multipeptide cancer vaccine, plus sunitinib versus sunitinib alone, as first-line therapy for advanced or metastatic renal cell carcinoma (IMPRINT): a multicentre, open-label, randomised, controlled, phase 3 trial, Lancet Oncol., 17, 1599, 10.1016/S1470-2045(16)30408-9 · DOI
- Shi, 2008, Bortezomib down-regulates the cell-surface expression of HLA class I and enhances natural killer cell-mediated lysis of myeloma, Blood, 111, 1309, 10.1182/blood-2007-03-078535 · DOI
- Kowalewski, 2016, Carfilzomib alters the HLA-presented peptidome of myeloma cells and impairs presentation of peptides with aromatic C-termini, Blood Cancer J., 6, 10.1038/bcj.2016.14 · DOI
- Shraibman, 2016, HLA peptides derived from tumor antigens induced by inhibition of DNA methylation for development of drug-facilitated immunotherapy, Mol. Cell. Proteomics, 15, 3058, 10.1074/mcp.M116.060350 · DOI
- Nelde, 2018, HLA ligandome analysis of primary chronic lymphocytic leukemia (CLL) cells under lenalidomide treatment confirms the suitability of lenalidomide for combination with T-cell-based immunotherapy, Oncoimmunology, 128, 3234
- Chong, 2020, Integrated proteogenomic deep sequencing and analytics accurately identify non-canonical peptides in tumor immunopeptidomes, Nat. Commun., 11, 1293, 10.1038/s41467-020-14968-9 · DOI
- Bassani-Sternberg, 2010, Soluble plasma HLA peptidome as a potential source for cancer biomarkers, Proc. Natl. Acad. Sci. U. S. A., 107, 18769, 10.1073/pnas.1008501107 · DOI
- Shraibman, 2018, Identification of tumor antigens among the HLA peptidomes of glioblastoma tumors and plasma, Mol. Cell. Proteomics, 17, 2132, 10.1074/mcp.RA118.000792 · DOI
- Ritz, 2017, Purification of soluble HLA class I complexes from human serum or plasma deliver high quality immuno peptidomes required for biomarker discovery, Proteomics, 17, 10.1002/pmic.201600364 · DOI
- Noguchi, 2010, Assessment of immunological biomarkers in patients with advanced cancer treated by personalized peptide vaccination, Cancer Biol. Ther., 10, 1266, 10.4161/cbt.10.12.13448 · DOI
- Kanekiyo, 2018, IgG response to MHC class I epitope peptides is a quantitative predictive biomarker in the early course of treatment of colorectal cancer using therapeutic peptides, Oncol. Rep., 39, 2385
- Kitahara, 2016, Prediction of the efficacy of immunotherapy by measuring the integrity of cell-free DNA in plasma in colorectal cancer, Cancer Sci., 107, 1825, 10.1111/cas.13085 · DOI
- Kijima, 2017, MicroRNA-6826 and-6875 in plasma are valuable non-invasive biomarkers that predict the efficacy of vaccine treatment against metastatic colorectal cancer, Oncol. Rep., 37, 23, 10.3892/or.2016.5267 · DOI
- Suekane, 2020, Identification of biomarkers for personalized peptide vaccination in 2,588 cancer patients, Int. J. Oncol., 56, 1479
- Shindo, 2017, Predictive biomarkers for the efficacy of peptide vaccine treatment: based on the results of a phase II study on advanced pancreatic cancer, J. Exp. Clin. Cancer Res., 36, 36, 10.1186/s13046-017-0509-1 · DOI
- Murciano-Goroff, 2020, The future of cancer immunotherapy: microenvironment-targeting combinations, Cell Res., 30, 507, 10.1038/s41422-020-0337-2 · DOI
- Pelster, 2019, Combined targeted therapy and immunotherapy in melanoma: a review of the impact on the tumor microenvironment and outcomes of early clinical trials, Ther. Adv. Med. Oncol., 10.1177/1758835919830826 · DOI
- Yoshida, 2011, Characteristics of severe adverse events after peptide vaccination for advanced cancer patients: analysis of 500 cases, Oncol. Rep., 25, 57
- Feyerabend, 2009, Novel multi-peptide vaccination in Hla-A2+ hormone sensitive patients with biochemical relapse of prostate cancer, Prostate, 69, 917, 10.1002/pros.20941 · DOI
Cited by
Sorted by citations
Sittplangkoon, C., Alameh, M.-G., Weissman, D., Lin, P. J. C., Tam, Y. K., Prompetchara, E., & Palaga, T. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.983000 · Cited by 79
“Although tumor antigen-derived peptide immunogens for cancer therapeutic vaccines are traditionally used, there are various limitations, including the manufacturing cost and the need for strong adjuvants to induce anti-tumor immunity (4).”
Background
Metadata
- Authors
- Nelde, A., Rammensee, H.-G., & Walz, J. S.
- Affiliations
- Universitätsklinikum Tübingen (DE)
- German Cancer Research Center (DE)
- Corresponding author
- Walz, Juliane S.
- Venue
- Molecular & Cellular Proteomics
- Publisher
- Elsevier BV
- Published
- 2021
- Volume
- 20
- Pages
- 100022
- ISSN
- 1535-9476 (ISSN-L)
- PMC
- PMC7950068
- OpenAlex
- W3113006303
- Cited by
- 205
- References
- 9
- Citations by year
- 2026: 21 · 2025: 37 · 2024: 50 · 2023: 37 · 2022: 43 · 2021: 17
- FWCI
- 2.30
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Molecular & Cellular Proteomics (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › vaccines and immunoinformatics approaches
- Physical Sciences › Chemistry › Organic Chemistry › Chemical Synthesis and Analysis
- Keywords
- peptide vaccine, cancer immunotherapy, antigen selection, adjuvants, vaccination schedule, predictive biomarkers, combination therapy, vaccine design
- MeSH terms
- Adjuvants, Immunologic, Antigens, Humans, Neoplasms, Biomarkers, Cancer Vaccines, Vaccines, Subunit
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review