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Enhanced expression of mir-181b in b cells of cll improves the anti-tumor cytotoxic t cell response

Authors :
Di Marco, M.
Veschi, S.
Lanuti, P.
Ramassone, A.
Pacillo, S.
Pagotto, S.
Pepe, F.
George-William, J. N.
Curcio, C.
Marchisio, M.
Miscia, S.
Innocenti, Idanna
Autore, Francesco
Vannata, B.
Di Gregorio, P.
Di Gioacchino, M.
Valentinuzzi, S.
Iezzi, Martina
Mariani-Costantini, R.
Larocca, Luigi Maria
Laurenti, Luca
Veronese, A.
Visone, R.
Innocenti I.
Autore F.
Iezzi M.
Larocca L. M. (ORCID:0000-0003-1739-4758)
Laurenti L. (ORCID:0000-0002-8327-1396)
Di Marco, M.
Veschi, S.
Lanuti, P.
Ramassone, A.
Pacillo, S.
Pagotto, S.
Pepe, F.
George-William, J. N.
Curcio, C.
Marchisio, M.
Miscia, S.
Innocenti, Idanna
Autore, Francesco
Vannata, B.
Di Gregorio, P.
Di Gioacchino, M.
Valentinuzzi, S.
Iezzi, Martina
Mariani-Costantini, R.
Larocca, Luigi Maria
Laurenti, Luca
Veronese, A.
Visone, R.
Innocenti I.
Autore F.
Iezzi M.
Larocca L. M. (ORCID:0000-0003-1739-4758)
Laurenti L. (ORCID:0000-0002-8327-1396)
Publication Year :
2021

Abstract

The clinical progression of B cell chronic lymphocytic leukemia (CLL) is associated with immune cell dysfunction and a strong decrease of miR-181b-5p (miR-181b), promoting the death of CLL cells. Here we investigated whether the reduction of miR-181b impairs the immune response in CLL. We demonstrate that activated CD4+ T cells increase miR-181b expression in CLL through CD40– CD40L signaling, which enhances the maturation and activity of cytotoxic T cells and, consequently, the apoptotic response of CLL cells. The cytotoxic response is facilitated by a depletion of the anti-inflammatory cytokine interleukin 10, targeted by miR-181b. In vivo experiments in NOD.Cg-Prkdcscid Il2rgtm1Wjl/SzJ mice confirmed that miR-181b promotes the apoptotic death of CLL cells only when functional T cells are restored. Overall, our findings suggest that the reinstatement of miR-181b in CLL cells could be an exploitable adjuvant therapeutic option for the treatment of CLL.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1289307330
Document Type :
Electronic Resource