TY - JOUR
T1 - Targeting natural killer cell reactivity by employing antibody to Nkp46
T2 - Implications for type 1 diabetes
AU - Yossef, Rami
AU - Gur, Chamutal
AU - Shemesh, Avishai
AU - Guttman, Ofer
AU - Hadad, Uzi
AU - Nedvetzki, Shlomo
AU - Miletić, Antonija
AU - Nalbandyan, Karen
AU - Cerwenka, Adelheid
AU - Jonjic, Stipan
AU - Mandelboim, Ofer
AU - Porgador, Angel
N1 - Publisher Copyright:
© 2015 Yossef et al.
PY - 2015/2/26
Y1 - 2015/2/26
N2 - Natural killer (NK) cells belong to the innate lymphoid cells. Their cytotoxic activity is regulated by the delicate balance between activating and inhibitory signals. NKp46 is a member of the primary activating receptors of NK cells. We previously reported that the NKp46 receptor is involved in the development of type 1 diabetes (T1D). Subsequently, we hypothesized that blocking this receptor could prevent or hinder disease development. To address this goal, we developed monoclonal antibodies for murine NKp46. One mAb, named NCR1.15, recognizes the mouse homologue protein of NKp46, named Ncr1, and was able to downregulate the surface expression of NKp46 on primary murine NK cells following antibody injection in vivo. Additionally, NCR1.15 treatments were able to down-regulate cytotoxic activity mediated by NKp46, but not by other NK receptors. To test our primary assumption, we examined T1D development in two models, non-obese diabetic mice and low-dose streptozotocin. Our results show a significantly lower incidence of diabetic mice in the NCR1.15-treated group compared to control groups. This study directly demonstrates the involvement of NKp46 in T1D development and suggests a novel treatment strategy for early insulitis.
AB - Natural killer (NK) cells belong to the innate lymphoid cells. Their cytotoxic activity is regulated by the delicate balance between activating and inhibitory signals. NKp46 is a member of the primary activating receptors of NK cells. We previously reported that the NKp46 receptor is involved in the development of type 1 diabetes (T1D). Subsequently, we hypothesized that blocking this receptor could prevent or hinder disease development. To address this goal, we developed monoclonal antibodies for murine NKp46. One mAb, named NCR1.15, recognizes the mouse homologue protein of NKp46, named Ncr1, and was able to downregulate the surface expression of NKp46 on primary murine NK cells following antibody injection in vivo. Additionally, NCR1.15 treatments were able to down-regulate cytotoxic activity mediated by NKp46, but not by other NK receptors. To test our primary assumption, we examined T1D development in two models, non-obese diabetic mice and low-dose streptozotocin. Our results show a significantly lower incidence of diabetic mice in the NCR1.15-treated group compared to control groups. This study directly demonstrates the involvement of NKp46 in T1D development and suggests a novel treatment strategy for early insulitis.
UR - http://www.scopus.com/inward/record.url?scp=84923785826&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0118936
DO - 10.1371/journal.pone.0118936
M3 - Article
C2 - 25719382
AN - SCOPUS:84923785826
SN - 1932-6203
VL - 10
JO - PLoS ONE
JF - PLoS ONE
IS - 2
M1 - e0118936
ER -