Janus-faced myeloid-derived suppressor cell exosomes for the good and the bad in cancer and autoimmune disease

Myeloid-derived suppressor cells (MDSC) are a heterogeneous population of immature myeloid cells originally described to hamper immune responses in chronic infections. Meanwhile they are known to be a major obstacle in cancer immunotherapy. On the other hand, MDSC can interfere with allogeneic trans...

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Bibliographische Detailangaben
1. Verfasser: Zöller, Margot (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 02 February 2018
In: Frontiers in immunology
Year: 2018, Jahrgang: 9
ISSN:1664-3224
DOI:10.3389/fimmu.2018.00137
Online-Zugang:Verlag, kostenfrei, Volltext: http://dx.doi.org/10.3389/fimmu.2018.00137
Verlag, kostenfrei, Volltext: https://www.frontiersin.org/articles/10.3389/fimmu.2018.00137/full
Volltext
Verfasserangaben:Margot Zöller
Beschreibung
Zusammenfassung:Myeloid-derived suppressor cells (MDSC) are a heterogeneous population of immature myeloid cells originally described to hamper immune responses in chronic infections. Meanwhile they are known to be a major obstacle in cancer immunotherapy. On the other hand, MDSC can interfere with allogeneic transplant rejection and may dampen autoreactive T cell activity. Whether MDSC-Exosomes (Exo) can cope with the dangerous and potentially therapeutic activities of MDSC is not yet fully explored. After introducing MDSC and Exo, it will be discussed, whether a blockade of MDSC-Exo could foster the efficacy of immunotherapy in cancer and mitigate tumor progression supporting activities of MDSC. It also will be outlined, whether application of native or tailored MDSC-Exo might prohibit autoimmune disease progression. These considerations are based on the steadily increasing knowledge on Exo composition, their capacity to distribute throughout the organism combined with selectivity of targeting and the ease to tailor Exo and includes open questions that answers will facilitate optimizing protocols for a MDSC-Exo blockade in cancer as well as for strengthening their therapeutic efficacy in autoimmune disease.
Beschreibung:Gesehen am 12.04.2018
Beschreibung:Online Resource
ISSN:1664-3224
DOI:10.3389/fimmu.2018.00137