TY - JOUR
T1 - NK cells and their receptors in naive and rituximab-treated patients with anti-MAG polyneuropathy
AU - Benedetti, Luana
AU - Facco, Monica
AU - Franciotta, Diego
AU - Torre, Chiara Dalla
AU - Campagnolo, Marta
AU - Lucchetta, Marta
AU - Boscaro, Elisa
AU - Ermani, Mario
AU - Del Sette, Massimo
AU - Berno, Tamara
AU - Candiotto, Laura
AU - Zambello, Renato
AU - Briani, Chiara
PY - 2013/9/15
Y1 - 2013/9/15
N2 - Background: Natural killer (NK) cells can bridge innate and acquired immunity, and play a role in autoimmunity. A few studies evaluated the distribution of NK cells and the expression of their receptors in chronic immune-mediated demyelinating polyneuropathies. We investigated NK cell distribution and NK cell receptor expression in 20 naïve patients with anti-MAG polyneuropathy (MAG-PN). Methods: Using flow cytometry, we analysed NK cells and a series of NK cell receptors in the peripheral blood of patients with MAG-PN, and, as controls, in patients with chronic inflammatory demyelinating peripheral polyradiculoneuropathy (CIDP) and in healthy subjects. Six MAG-PN patients were also tested after rituximab treatment. Results: At baseline the percentage of NK cells did not differ among the groups. KIR2DL2 receptor expression in MAG-PN patients was higher, andCD94/NKG2A receptor expression in both MAG-PN and CIDP patients was lower than in healthy controls. These abnormalities did not correlate with any clinical or demographic variable. No modification was found after rituximab therapy. Conclusions: The data suggest that MAG-PN shows abnormalities in NK cell receptors that characterise other autoimmune diseases, and cannot help in differential diagnosiswith CIDP. The impairment of the relevant CD94/NKG2A inhibitory pathway, whichmight play a central role in the development and perpetuation of MAG-PN, warrants further functional investigations.
AB - Background: Natural killer (NK) cells can bridge innate and acquired immunity, and play a role in autoimmunity. A few studies evaluated the distribution of NK cells and the expression of their receptors in chronic immune-mediated demyelinating polyneuropathies. We investigated NK cell distribution and NK cell receptor expression in 20 naïve patients with anti-MAG polyneuropathy (MAG-PN). Methods: Using flow cytometry, we analysed NK cells and a series of NK cell receptors in the peripheral blood of patients with MAG-PN, and, as controls, in patients with chronic inflammatory demyelinating peripheral polyradiculoneuropathy (CIDP) and in healthy subjects. Six MAG-PN patients were also tested after rituximab treatment. Results: At baseline the percentage of NK cells did not differ among the groups. KIR2DL2 receptor expression in MAG-PN patients was higher, andCD94/NKG2A receptor expression in both MAG-PN and CIDP patients was lower than in healthy controls. These abnormalities did not correlate with any clinical or demographic variable. No modification was found after rituximab therapy. Conclusions: The data suggest that MAG-PN shows abnormalities in NK cell receptors that characterise other autoimmune diseases, and cannot help in differential diagnosiswith CIDP. The impairment of the relevant CD94/NKG2A inhibitory pathway, whichmight play a central role in the development and perpetuation of MAG-PN, warrants further functional investigations.
KW - Anti-MAG antibodies
KW - CD94/NKG2A
KW - IgM
KW - Monoclonal gammopathy
KW - Myelin associated glycoprotein
KW - Natural killer (NK) cells
KW - Rituximab
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U2 - 10.1016/j.jns.2013.05.015
DO - 10.1016/j.jns.2013.05.015
M3 - Article
C2 - 23764364
AN - SCOPUS:84882451220
SN - 0022-510X
VL - 331
SP - 86
EP - 89
JO - Journal of the Neurological Sciences
JF - Journal of the Neurological Sciences
IS - 1-2
ER -