J. A. Hutchinson and E. K. Geissler, Now or never? The case for cell-based immunosuppression in kidney transplantation, Kidney Int, vol.87, pp.1116-1124, 2015.

J. A. Hutchinson, P. Riquelme, and E. K. Geissler, Human regulatory macrophages, Methods Mol Biol, vol.677, pp.181-192, 2011.
URL : https://hal.archives-ouvertes.fr/inserm-02154878

J. A. Hutchinson, P. Riquelme, and B. Sawitzki, Cutting edge: immunological consequences and trafficking of human regulatory macrophages administered to renal transplant recipients, J Immunol, vol.187, pp.2072-2078, 2011.

N. Ahrens, P. Riquelme, and C. Bach, Donor-specific anti-HLA antibodies present in pooled human serum do not prevent development of human Mreg_UKR from monocytes in culture, Transplantation, vol.101, pp.188-190, 2017.

J. A. Hutchinson, Macrophages in transplantation, Transplantation, vol.99, pp.898-899, 2015.

F. O. Martinez, S. Gordon, and M. Locati, Transcriptional profiling of the human monocyte-to-macrophage differentiation and polarization: new molecules and patterns of gene expression, J Immunol, vol.177, pp.7303-7311, 2006.

D. H. Munn, E. Shafizadeh, and J. T. Attwood, Inhibition of T cell proliferation by macrophage tryptophan catabolism, J Exp Med, vol.189, pp.1363-1372, 1999.

M. Sironi, F. O. Martinez, D. 'ambrosio, and D. , Differential regulation of chemokine production by Fcgamma receptor engagement in human monocytes: association of CCL1 with a distinct form of M2 monocyte activation (M2b, Type 2), J Leukoc Biol, vol.80, pp.342-349, 2006.

J. Kzhyshkowska, G. Workman, and M. Cardo-vila, Novel function of alternatively activated macrophages: stabilin-1-mediated clearance of SPARC, J Immunol, vol.176, pp.5825-5832, 2006.

B. R. Rosborough, D. Raïch-regué, and H. R. Turnquist, Regulatory myeloid cells in transplantation, Transplantation, vol.97, pp.367-379, 2014.

J. A. Hutchinson, P. Riquelme, and J. Wundt, Could treatment with neohepatocytes benefit patients with decompensated chronic liver disease?, Am J Hematol, vol.82, pp.947-948, 2007.

C. M. Soref, Y. P. Di, and L. Hayden, Characterization of a novel airway epithelial cell-specific short chain alcohol dehydrogenase/reductase gene whose expression is up-regulated by retinoids and is involved in the metabolism of retinol, J Biol Chem, vol.276, pp.24194-24202, 2001.

R. J. Jones, S. Dickerson, and P. M. Bhende, Epstein-Barr virus lytic infection induces retinoic acid-responsive genes through induction of a retinolmetabolizing enzyme, DHRS9, J Biol Chem, vol.282, pp.8317-8324, 2007.

M. Lidén and U. Eriksson, Understanding retinol metabolism: structure and function of retinol dehydrogenases, J Biol Chem, vol.281, pp.13001-13004, 2006.

A. Moreau, E. Varey, and L. Bouchet-delbos, Cell therapy using tolerogenic dendritic cells in transplantation, Transplant Res, vol.1, p.13, 2012.
URL : https://hal.archives-ouvertes.fr/inserm-00796724

C. Macedo, H. R. Turnquist, and M. Castillo-rama, Rapamycin augments human DC IL-12p70 and IL-27 secretion to promote allogeneic Type 1 polarization modulated by NK cells, Am J Transplant, vol.13, pp.2322-2333, 2013.
DOI : 10.1111/ajt.12351
URL : https://onlinelibrary.wiley.com/doi/pdf/10.1111/ajt.12351

C. Macedo, H. Turquist, and D. Metes, Immunoregulatory properties of rapamycin-conditioned monocyte-derived dendritic cells and their role in transplantation, Transplant Res, vol.1, p.16, 2012.

G. Amodio, M. Comi, and D. Tomasoni, HLA-G expression levels influence the tolerogenic activity of human DC-10, Haematologica, vol.100, pp.548-557, 2015.

G. Amodio and S. Gregori, Human tolerogenic DC-10: perspectives for clinical applications, Transplant Res, vol.1, p.14, 2012.
DOI : 10.1186/2047-1440-1-14
URL : https://transplantationresearch.biomedcentral.com/track/pdf/10.1186/2047-1440-1-14

S. Gregori, D. Tomasoni, and V. Pacciani, Differentiation of type 1T regulatory cells (Tr1) by tolerogenic DC-10 requires the IL-10-dependent ILT4/ HLA-G pathway, Blood, vol.116, pp.935-944, 2010.

N. Obermajer, R. Muthuswamy, and J. Lesnock, Positive feedback between PGE2 and COX2 redirects the differentiation of human dendritic cells toward stable myeloid-derived suppressor cells, Blood, vol.118, pp.5498-5505, 2011.

N. Obermajer and P. Kalinski, Generation of myeloid-derived suppressor cells using prostaglandin E2, Transplant Res, vol.1, p.15, 2012.

J. Xue, S. V. Schmidt, and J. Sander, Transcriptome-based network analysis reveals a spectrum model of human macrophage activation, Immunity, vol.40, pp.274-288, 2014.

X. Pares, J. Farres, and N. Kedishvili, Medium-and short-chain dehydrogenase/reductase gene and protein families: Medium-chain and short-chain dehydrogenases/reductases in retinoid metabolism, Cell Mol Life Sci, vol.65, pp.3936-3949, 2008.

I. Szatmari, A. Pap, and R. Ruhl, PPARgamma controls CD1d expression by turning on retinoic acid synthesis in developing human dendritic cells, J Exp Med, vol.203, pp.2351-2362, 2006.

P. Riquelme, S. Tomiuk, and A. Kammler, IFN-?-induced iNOS expression in mouse regulatory macrophages prolongs allograft survival in fully immunocompetent recipients, Mol Ther, vol.21, pp.409-422, 2013.

L. Carretero-iglesia, L. Bouchet-delbos, and C. Louvet, Comparative study of the immunoregulatory capacity of in vitro generated tolerogenic dendritic cells, suppressor macrophages, and myeloid-derived suppressor cells, Transplantation, vol.100, pp.2079-2089, 2016.
URL : https://hal.archives-ouvertes.fr/inserm-02150814

H. R. Turnquist and A. W. Thomson, Identity crisis. Transplantation, vol.100, pp.258-259, 2016.

P. Riquelme, Regulatory myeloid cells for tolerance-inducing therapy: finding their own identity, Transplantation, vol.100, pp.2022-2023, 2016.

M. Raverdeau and K. H. Mills, Modulation of Tcell and innate immune responses by retinoic acid, J Immunol, vol.192, pp.2953-2958, 2014.