Chronic lymphocytic leukemia (CLL) is characterized by the expansion of malignant CD5(+) B lymphocytes in blood, bone marrow and lymphoid organs. CD1d-restricted invariant Natural Killer T (iNKT) cells are innate-like T lymphocytes strongly implicated in tumor surveillance. We investigated the impact of iNKT cells in the natural history of the disease both in Eμ;-Tcl1 (Tcl1) CLL mouse model and 68 CLL patients. We found that Tcl1-CLL cells express CD1d and iNKT cells critically delay the disease onset, but become functionally impaired upon disease progression. In patients, disease progression correlates also with high CD1d expression on CLL cells and impaired iNKT cells. Conversely, disease stability correlates with negative/low CD1d expression on CLL cells and normal iNKT cells, suggesting an indirect leukemia control. iNKT cells indeed hinder CLL survival in vitro by restraining CD1d-expressing Nurse Like Cells, a relevant pro-leukemia macrophage population. Finally, multivariate analysis identifies iNKT cell frequency as independent predictor of disease progression. Together, these results support iNKT cell contribution to CLL immune-surveillance and highlight iNKT cell frequency as prognostic marker for disease progression.

Invariant NKT cells contribute to chronic lymphocytic leukemia surveillance and prognosis / Gorini, Francesca; Azzimonti, Laura; Delfanti, Gloria; Scarfò, Lydia; Scielzo, Cristina; Bertilaccio, Maria Teresa; Ranghetti, Pamela; Gulino, Alessandro; Doglioni, Claudio; DI NAPOLI, Arianna; Capri, Miriam; Franceschi, Claudio; Caligaris Cappio, Federico; Ghia, Paolo; Bellone, Matteo; Dellabona, Paolo; Casorati, Giulia; de Lalla, Claudia. - In: BLOOD. - ISSN 0006-4971. - 129:26(2017), pp. 3440-3451. [10.1182/blood-2016-11-751065]

Invariant NKT cells contribute to chronic lymphocytic leukemia surveillance and prognosis

DI NAPOLI, Arianna;
2017

Abstract

Chronic lymphocytic leukemia (CLL) is characterized by the expansion of malignant CD5(+) B lymphocytes in blood, bone marrow and lymphoid organs. CD1d-restricted invariant Natural Killer T (iNKT) cells are innate-like T lymphocytes strongly implicated in tumor surveillance. We investigated the impact of iNKT cells in the natural history of the disease both in Eμ;-Tcl1 (Tcl1) CLL mouse model and 68 CLL patients. We found that Tcl1-CLL cells express CD1d and iNKT cells critically delay the disease onset, but become functionally impaired upon disease progression. In patients, disease progression correlates also with high CD1d expression on CLL cells and impaired iNKT cells. Conversely, disease stability correlates with negative/low CD1d expression on CLL cells and normal iNKT cells, suggesting an indirect leukemia control. iNKT cells indeed hinder CLL survival in vitro by restraining CD1d-expressing Nurse Like Cells, a relevant pro-leukemia macrophage population. Finally, multivariate analysis identifies iNKT cell frequency as independent predictor of disease progression. Together, these results support iNKT cell contribution to CLL immune-surveillance and highlight iNKT cell frequency as prognostic marker for disease progression.
2017
invariant nk-t; cll; killer t-cells; b-cells; disease progression
01 Pubblicazione su rivista::01a Articolo in rivista
Invariant NKT cells contribute to chronic lymphocytic leukemia surveillance and prognosis / Gorini, Francesca; Azzimonti, Laura; Delfanti, Gloria; Scarfò, Lydia; Scielzo, Cristina; Bertilaccio, Maria Teresa; Ranghetti, Pamela; Gulino, Alessandro; Doglioni, Claudio; DI NAPOLI, Arianna; Capri, Miriam; Franceschi, Claudio; Caligaris Cappio, Federico; Ghia, Paolo; Bellone, Matteo; Dellabona, Paolo; Casorati, Giulia; de Lalla, Claudia. - In: BLOOD. - ISSN 0006-4971. - 129:26(2017), pp. 3440-3451. [10.1182/blood-2016-11-751065]
File allegati a questo prodotto
File Dimensione Formato  
Gorini_Invariant-NKT_2017.pdf

accesso aperto

Tipologia: Versione editoriale (versione pubblicata con il layout dell'editore)
Licenza: Tutti i diritti riservati (All rights reserved)
Dimensione 2.65 MB
Formato Adobe PDF
2.65 MB Adobe PDF

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/954186
Citazioni
  • ???jsp.display-item.citation.pmc??? 26
  • Scopus 58
  • ???jsp.display-item.citation.isi??? 57
social impact