The NK cell receptor repertoire: formation, adaptation and exploitation

2003 ◽  
Vol 15 (2) ◽  
pp. 233-237 ◽  
Author(s):  
Werner Held ◽  
Jérôme D Coudert ◽  
Jacques Zimmer
2010 ◽  
Vol 45 (6) ◽  
pp. 1022-1030 ◽  
Author(s):  
S Giebel ◽  
J Dziaczkowska ◽  
T Czerw ◽  
J Wojnar ◽  
M Krawczyk-Kulis ◽  
...  

2010 ◽  
Vol 41 (1) ◽  
pp. 258-258
Author(s):  
Adriana Monsiváis-Urenda ◽  
Daniel Noyola-Cherpitel ◽  
Alba Hernández-Salinas ◽  
Christian García-Sepúlveda ◽  
Neus Romo ◽  
...  

2010 ◽  
Vol 40 (5) ◽  
pp. 1418-1427 ◽  
Author(s):  
Adriana Monsiváis‐Urenda ◽  
Daniel Noyola‐Cherpitel ◽  
Alba Hernández‐Salinas ◽  
Christian García‐Sepúlveda ◽  
Neus Romo ◽  
...  

2017 ◽  
Vol 78 (3) ◽  
pp. 274-280 ◽  
Author(s):  
Guillermo Juárez-Vega ◽  
Velia Rangel-Ramírez ◽  
Adriana Monsiváis-Urenda ◽  
Perla Niño-Moreno ◽  
Christian Garcia-Sepúlveda ◽  
...  

Immunobiology ◽  
2020 ◽  
Vol 225 (3) ◽  
pp. 151909 ◽  
Author(s):  
Alma Celeste Ortega-Rodríguez ◽  
Laura Sherell Marín-Jáuregui ◽  
Elena Martínez-Shio ◽  
Berenice Hernández Castro ◽  
Roberto González-Amaro ◽  
...  

Author(s):  
Saeede Soleimanian ◽  
Ramin Yaghobi ◽  
Mohammad Hossein Karimi ◽  
Bita Geramizadeh ◽  
Jamshid Roozbeh

Natural killer (NK) cells are essential for controlling certain viral infections, including cytomegalovirus (CMV). In particular, the importance of NK cells in the context of CMV infection is underscored by the adaptive capabilities of these cells. Evidence suggests that some viruses can directly interfere with NK cell compartments and their activation and lead to shape-shifting the NK cell receptor repertoire. Still, it remains unknown whether the CMV can interact with NK cells without intermediaries. Here, we examined whether the direct effects of CMV lysate alter phenotypical properties of NK cells. To investigate this issue, NK cells were isolated from the blood of CMV seropositive healthy donors by negative magnetic separation. Isolated NK cells were cultured in the presence of CMV lysate and analyzed for the expression of NKG2A, NKG2C, and CD57 by FACS caliber. The results showed that NKG2C expression is significantly upregulated in the presence of CMV lysate compared to without stimulated group (mean increase, 6.65 %; 95% CI, 0.2582 to 13.02; p=0.043; R square: 0.38). Likewise, results have shown a significant decrease in the frequency of NKG2A+CD57- NK cell subsets (p=0.005; 95% CI, -13.49 to -3.151; R square: 0.5957) in the stimulated group compared to without stimulated ones. According to these results, CMV may drive a direct influence on NK cell receptor repertoire, including the expansion of NK cells expressing NKG2C receptor, which is needed for further studies.


Blood ◽  
2004 ◽  
Vol 104 (11) ◽  
pp. 5186-5186
Author(s):  
Michihiro Kobayashi ◽  
Hidefumi Hiramatsu ◽  
So-ichi Adachi ◽  
Tatsutoshi Nakahata

Abstract Interaction between killer immunoglobulin-like receptors (KIRs) and HLA class I ligands influence development of natural killer cell repertoire and response to allogeneic tissue. Recently several reports suggests donor/recipient KIR-ligand imcompatibility have great influence for outcome of allogeneic Hematopoietic Stem Cell transplantation (SCT). We examined recovery of the NK cell receptor after pediatric SCT to elucidate emergence of NKR repertoire and frequency after SCT is depend on whether donor or recipient type and effect of HLA disparity. [Patients and method] Nine patients receiving allogeneic SCT were examined. Expressions and frequency of KIR on NK cells were determined by flowcytometry using anti CD158a/h, 158b/j, 158e, 158i, 159a, 94, 56,and 3 antibodies. Donor and recipient KIR repertoire frequency prior to SCT were also examined. In cord blood transplantation, donor KIR repertoire was checked using residual thawed and infused cord blood. [Result] Among 9 patients, PBSCT were performed in 3 patients, CBT in 3, unrelated BMT in 3. HLA matched SCT was all 3 cases of unrelated BMT. KIR expression frequency was various in each patient. But in early phase, relatively both high percentage and absolute number of each KIR positive repertoire were observed, and then gradually decreased toward to 1 year after SCT. NK cell receptor repertoire reconstitution was generally well and rapid except for one patient who was treated with steroid pulse therapy for severe GVHD. KIR repertoire expression pattern at 1 year after SCT was similar to donor type compare to that of pre-SCT recipient. Donor/recipient HLA mismatch did not have obvious effect for NKR repertoire reconstitution. [Conclusion] NKR repertoire reconstitution after pediatric SCT depends on donor cell type.


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