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Priority Paper Evaluation

Broad-spectrum immunosuppression by classless monocytes in non-Hodgkin’s lymphoma

    &
    Maher K Gandhi

    Clinical Immunohaematology Laboratory, Queensland Institute of Medical Research, 300 Herston Road, Herston, Queensland, 4006, Australia

    Department of Haematology, Princess Alexandra Hospital, Brisbane, Queensland, 4102, Australia

    Published Online:https://doi.org/10.2217/imt.11.56

    Evaluation of: Lin Y, Gustafson MP, Bulur PA, Gastineau DA, Witzig TE, Dietz AB: Immunosuppressive CD14+HLA-DRlow/- monocytes in B-cell non-Hodgkin’s lymphoma. Blood 117, 872–881 (2011). The mechanisms of systemic immunosuppression in B-cell non-Hodgkin’s lymphoma (NHL) are poorly characterized. Lin and colleagues collected blood from 40 NHL patients prior to therapy. Monocytes from NHL patients suppressed T-cell proliferation, were unresponsive to Toll-like receptor stimulation by CpG and resistant to maturing into CD83+ dendritic cells. This suppression was mediated in part through arginine metabolism, as exogenous arginine supplementation reversed this, and NHL patients had elevated arginase I in their plasma. These cells had decreased HLA-DR and TNF-α receptor II (CD120b) expression compared with controls. Patients with increased ratios of CD14+HLA-DRlow/- monocytes had more advanced disease and suppressed immune functions, indicating that CD14+HLA-DRlow/- monocytes are a pivotal and profoundly effective contributor to systemic immunosuppression in NHL.

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