Table 1.

The membrane proximal domain of NKp46 recognizes the HA of different viruses


Virus

HA type

NKp44-Ig

NKp46-Ig

NKp46D2-Ig

NKp46D1-Ig

NKp30-Ig

CD99-Ig
Uninfected   —   7   3   4   2   2   0  
SV   HA-NA   350   77   95   8   7   0.5  
Beijing   H1N1   128   44   77   7   4   0  
X-127   H1N1   220   107   160   5   6   1  
New Caledonia   H1N1   518   315   420   5   10   0  
Sydney   H3N2   120   58   100   10   8   1  
Moscow   H3N2   24   20   50   8   8   0  
Yamanashi
 
B strain
 
117
 
37
 
51
 
8
 
12
 
0
 

Virus

HA type

NKp44-Ig

NKp46-Ig

NKp46D2-Ig

NKp46D1-Ig

NKp30-Ig

CD99-Ig
Uninfected   —   7   3   4   2   2   0  
SV   HA-NA   350   77   95   8   7   0.5  
Beijing   H1N1   128   44   77   7   4   0  
X-127   H1N1   220   107   160   5   6   1  
New Caledonia   H1N1   518   315   420   5   10   0  
Sydney   H3N2   120   58   100   10   8   1  
Moscow   H3N2   24   20   50   8   8   0  
Yamanashi
 
B strain
 
117
 
37
 
51
 
8
 
12
 
0
 

721.221 cells were incubated overnight with or without influenza viruses that express different types of HA. Cells (50 000/well) were washed and stained with the various Ig fusion proteins (5 μg/well) followed by PE-conjugated goat antihuman Fc. The level of infection was determined by staining with human sera derived from individuals immunized with a trivalent influenza vaccine. Median fluorescence intensity (MFI) numbers were rounded to the nearest whole number after subtracting background staining (of PE-conjugated goat antihuman Fc). These results represent one experiment of 15 performed. — indicates no infection.

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