Lenalidomide enhances MOR202-dependent macrophage-mediated effector functions via the vitamin D pathway.
Leukemia
; 32(11): 2445-2458, 2018 11.
Article
en En
| MEDLINE
| ID: mdl-29654274
ABSTRACT
Macrophages are key mediators of the therapeutic effects exerted by monoclonal antibodies, such as the anti-CD38 antibody MOR202, currently introduced in multiple myeloma (MM) therapy. Therefore, it is important to understand how antibody-mediated effector functions of myeloma-associated macrophages (MAMs) are regulated. Here, we focused on the effects of vitamin D, a known regulator of macrophage effector functions. Consequently, it was the aim of this study to assess whether modulation of the vitamin D pathway alters the tumoricidal activity of MAMs. Here, we demonstrate that MAMs display a defective vitamin D pathway with reduced expression level of CYP27B1 and limited tumoricidal activity which can be restored by the IMiD lenalidomide in vitro. Furthermore, our data indicate that the vitamin D pathway of MAMs from MM patients does recover during an IMiD-containing therapy shown by an improved MOR202-mediated cytotoxic activity of these MAMs against primary MM cells ex vivo. Here, the ex vivo cytotoxic activity could be further enhanced by vitamin D supplementation. These data suggest that vitamin D holds a key role for the effector functions of MAMs and that vitamin D supplementation in IMiD combination trials could further increase the therapeutic efficacy of anti-CD38 antibodies such as MOR202, which remains to be investigated in clinical studies.
Texto completo:
1
Bases de datos:
MEDLINE
Asunto principal:
Vitamina D
/
Lenalidomida
/
Macrófagos
/
Anticuerpos Monoclonales
/
Mieloma Múltiple
Idioma:
En
Revista:
Leukemia
Año:
2018
Tipo del documento:
Article
País de afiliación:
Alemania