Targeting co-stimulatory receptors of the TNF superfamily for cancer immunotherapy

dc.contributor.authorMüller, Dafne
dc.date.accessioned2024-11-04T14:06:28Z
dc.date.available2024-11-04T14:06:28Z
dc.date.issued2022de
dc.date.updated2024-10-01T09:05:57Z
dc.description.abstractThe clinical approval of immune checkpoint inhibitors is an important advancement in the field of cancer immunotherapy. However, the percentage of beneficiaries is still limited and it is becoming clear that combination therapies are required to further enhance the treatment efficacy. The potential of strategies targeting the immunoregulatory network by “hitting the gas pedal” as opposed to “blocking the brakes” is being recognized and intensively investigated. Hence, next to immune checkpoint inhibitors, agonists of co-stimulatory receptors of the tumor necrosis factor superfamily (TNF-SF) are emerging as promising options to expand the immunomodulatory toolbox. In this review the development of different categories of recombinant antibody and ligand-based agonists of 4-1BB, OX40, and GITR is summarized and discussed in the context of the challenges presented by the structural and mechanistical features of the TNFR-SF. An overview of current formats, trends, and clinical studies is provided.en
dc.description.sponsorshipProjekt DEALde
dc.description.sponsorshipDeutsche Krebshilfede
dc.identifier.issn1179-190X
dc.identifier.issn1173-8804
dc.identifier.other1909015849
dc.identifier.urihttp://nbn-resolving.de/urn:nbn:de:bsz:93-opus-ds-151931de
dc.identifier.urihttp://elib.uni-stuttgart.de/handle/11682/15193
dc.identifier.urihttp://dx.doi.org/10.18419/opus-15174
dc.language.isoende
dc.relation.uridoi:10.1007/s40259-022-00573-3de
dc.rightsinfo:eu-repo/semantics/openAccessde
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/de
dc.subject.ddc570de
dc.subject.ddc610de
dc.titleTargeting co-stimulatory receptors of the TNF superfamily for cancer immunotherapyen
dc.typearticlede
ubs.fakultaetEnergie-, Verfahrens- und Biotechnikde
ubs.institutInstitut für Zellbiologie und Immunologiede
ubs.publikation.seiten21-33de
ubs.publikation.sourceBioDrugs 37 (2022), S. 21-33de
ubs.publikation.typZeitschriftenartikelde

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