CD4 + CD25 hi CD127 - Treg and CD4 + CD45R0 + CD49b + LAG3 + Tr1 cells in bone marrow and peripheral blood samples from children with neuroblastoma

Metastatic spread in the bone marrow (BM) at diagnosis is the worst prognostic factor for neuroblastoma (NB) patients. Here, we analyzed the presence of two immunosuppressive cell subsets, CD4 CD25 CD127 regulatory T (Treg) cells and CD4 CD45R0 CD49b LAG3 type 1 regulatory (Tr1) cells, in BM and per...

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Veröffentlicht in:Oncoimmunology 2016-12, Vol.5 (12), p.e1249553
Hauptverfasser: Morandi, Fabio, Pozzi, Sarah, Barco, Sebastiano, Cangemi, Giuliana, Amoroso, Loredana, Carlini, Barbara, Pistoia, Vito, Corrias, Maria Valeria
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Sprache:eng
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Zusammenfassung:Metastatic spread in the bone marrow (BM) at diagnosis is the worst prognostic factor for neuroblastoma (NB) patients. Here, we analyzed the presence of two immunosuppressive cell subsets, CD4 CD25 CD127 regulatory T (Treg) cells and CD4 CD45R0 CD49b LAG3 type 1 regulatory (Tr1) cells, in BM and peripheral blood (PB) samples from NB patients and controls. Frequency of both regulatory cell subsets was lower in BM and PB samples from NB patients than in respective healthy controls. No correlation was found between the frequency of Treg and Tr1 cells and prognostic factors at diagnosis, such as age and stage. Only amplification correlated to a higher number of Treg in BM and of Tr1 in PB. These findings suggested an altered trafficking of regulatory T cells in NB, but delineated a limited role of these subsets in BM microenvironment and/or periphery in NB. These observations should be considered designing immunotherapeutic approaches for metastatic NB.
ISSN:2162-4011
2162-402X
2162-402X
DOI:10.1080/2162402X.2016.1249553