4.8 Review

Human NK cells: from surface receptors to the therapy of leukemias and solid tumors

Journal

FRONTIERS IN IMMUNOLOGY
Volume 5, Issue -, Pages 1-8

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2014.00087

Keywords

NK cells; killer Ig-like receptors; alloreactive NK cells; activating NK receptors; hematopoietic stem cell; transplantation; acute leukemias; tumor microenvironment

Categories

Funding

  1. Associazione Italiana Ricerca sul Cancro (AIRC) [10225]
  2. Special Program Molecular Clinical Oncology 5 x 1000 project [9962]
  3. MFAG project [6384]
  4. Ministero dell'Istruzione, Universita e Ricerca (MIUR): MIUR-FIRB project [RBLA039LSF-001]
  5. Ministero della Salute: RF2006-Ricerca Oncologica-Project of Integrated Program [RO strategici 3/07, RO strategici 8/07]
  6. Ricerca Finalizzata [RF-IG-20081200689, RF-2010-2316319, RF-2010-2316606]
  7. MIUR-PRIN project [2009T4TC33_004]
  8. International Leibniz Research Cluster (ILRC) Network project ImmunoMemory - Senatsausschuss Wettbewerb (SAW)
  9. Fondazione Italiana per la Ricerca sul Cancro (FIRC)

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Natural Killer (NK) cells are major effector cells of the innate immunity. The discovery, over two decades ago, of major histocompatibility complex-class l-specific inhibitory NK receptors and subsequently of activating receptors, recognizing ligands expressed by tumor or virus-infected cells, paved the way to our understanding of the mechanisms of selective recognition and killing of tumor cells. Although NK cells can efficiently kill tumor cells of different histotypes in vitro, their activity may be limited in vivo by their inefficient trafficking to tumor lesions and by the inhibition of their function induced by tumor cells themselves and by the tumor microenvironment. On the other hand, the important role of NK cells has been clearly demonstrated in the therapy of high risk leukemias in the haploidentical hematopoietic stem cell (HSC) transplantation setting. NK cells derived from donor HSC kill leukemic cells residual after the conditioning regimen, thus preventing leukemia relapses. In addition, they also kill residual dendritic cells and T lymphocytes, thus preventing both GvH disease and graft rejection.

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