@article{EinseleBorghaeiOrlowskietal.2020,
  author    = {Einsele, Hermann and Borghaei, Hossein and Orlowski, Robert Z. and Subklewe, Marion and Roboz, Gail J. and Zugmaier, Gerhard and Kufer, Peter and Iskander, Karim and Kantarjian, Hagop M.},
  title     = {The BiTE (Bispecific T-Cell Engager) Platform: Development and Future Potential of a Targeted Immuno-Oncology Therapy Across Tumor Types},
  series = {Cancer},
  volume    = {126},
  journal   = {Cancer},
  number    = {14},
  doi       = {10.1002/cncr.32909},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-215426},
  pages     = {3192 -- 3201},
  year      = {2020},
  abstract  = {Immuno-oncology therapies engage the immune system to treat cancer. BiTE (bispecific T-cell engager) technology is a targeted immuno-oncology platform that connects patients' own T cells to malignant cells. The modular nature of BiTE technology facilitates the generation of molecules against tumor-specific antigens, allowing off-the-shelf immuno-oncotherapy. Blinatumomab was the first approved canonical BiTE molecule and targets CD19 surface antigens on B cells, making blinatumomab largely independent of genetic alterations or intracellular escape mechanisms. Additional BiTE molecules in development target other hematologic malignancies (eg, multiple myeloma, acute myeloid leukemia, and B-cell non-Hodgkin lymphoma) and solid tumors (eg, prostate cancer, glioblastoma, gastric cancer, and small-cell lung cancer). BiTE molecules with an extended half-life relative to the canonical BiTE molecules are also being developed. Advances in immuno-oncology made with BiTE technology could substantially improve the treatment of hematologic and solid tumors and offer enhanced activity in combination with other treatments.},
  language  = {en}
}
@article{HartungSeufertBergesetal.2012,
  author    = {Hartung, Andreas and Seufert, Florian and Berges, Carsten and Gessner, Viktoria H. and Holzgrabe, Ulrike},
  title     = {One-Pot Ugi/Aza-Michael Synthesis of Highly Substituted 2,5-Diketopiperazines with Anti-Proliferative Properties},
  series = {Molecules},
  volume    = {17},
  journal   = {Molecules},
  number    = {12},
  doi       = {10.3390/molecules171214685},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-130423},
  pages     = {14685-14699},
  year      = {2012},
  abstract  = {The well-known Ugi reaction of aldehydes with amines, carboxylic acids and isocyanides leads to the formation of acyclic alpha-acylaminocarboxamides. Replacement of the carboxylic acid derivatives with beta-acyl substituted acrylic acids gives access to highly substituted 2,5-diketopiperazines in one single reaction-step without additives or complex reaction procedures. The obtained diketopiperazines show anti-proliferative effects on activated T cells and represent therefore potential candidates for targeting unwanted T cell-mediated immune responses.},
  language  = {en}
}
@article{FujiKappEinsele2013,
  author    = {Fuji, Shigeo and Kapp, Markus and Einsele, Hermann},
  title     = {Monitoring of Pathogen-Specific T-Cell Immune Reconstitution after Allogeneic Hematopoietic Stem Cell Transplantation},
  series = {Frontiers in Immunology},
  volume    = {4},
  journal   = {Frontiers in Immunology},
  number    = {276},
  doi       = {10.3389/fimmu.2013.00276},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-129250},
  year      = {2013},
  abstract  = {The clinical outcome after allogeneic hematopoietic stem cell transplantation (HSCT) has been significantly improved during the last decades with regard to the reduction in organ failure, infection, and severe acute graft-versus-host disease. However, severe complications due to infectious diseases are still one of the major causes of morbidity and mortality after allogeneic HSCT, in particular in patients receiving haploidentical HSCT or cord blood transplant due to a slow and often incomplete immune reconstitution. In order to improve the immune control of pathogens without an increased risk of alloreactivity, adoptive immunotherapy using highly enriched pathogen-specificT cells offers a promising approach. In order to identify patients who are at high risk for infectious diseases, several monitoring assays have been developed with potential for the guidance of immunosuppressive drugs and adoptive immunotherapy in clinical practice. In this article, we aim to give a comprehensive overview regarding current developments of T-cell monitoring techniques focusing on T cells against viruses and fungi. In particular, we will focus on rather simple, fast, non-labor-intensive, cellular assays which could be integrated in routine clinical screening approaches.},
  language  = {en}
}