Table 3.

Antileukocyte antibodies detected in plasma from TRALI and control donors

No. of casesTest results for total nNo. of cases with positive results
Antigranulocyte antibodies    
 TRALI donors (n = 104) 28 16 weakly positive3-150 4  
 Control donors (n = 24)  5 (no reaction) 3 weakly positive 2  
Anti–HLA class I antibodies    
 TRALI donors (n = 104) 28 1 moderately positive3-151 1  
 Control donors (n = 24)  5 (no reaction) 0 positive 
Anti–HLA class II antibodies (n = 75 TRALI donors) 20 5 moderately positive3-152 
No. of casesTest results for total nNo. of cases with positive results
Antigranulocyte antibodies    
 TRALI donors (n = 104) 28 16 weakly positive3-150 4  
 Control donors (n = 24)  5 (no reaction) 3 weakly positive 2  
Anti–HLA class I antibodies    
 TRALI donors (n = 104) 28 1 moderately positive3-151 1  
 Control donors (n = 24)  5 (no reaction) 0 positive 
Anti–HLA class II antibodies (n = 75 TRALI donors) 20 5 moderately positive3-152 

Antibody testing was performed as described in “Patients, materials, and methods.”

F3-150

All reactions were weak without definable specificity. Panel cells included cells positive for NA1, NA2, NB1, and NB2 antigens. Positive control antibodies included anti-NA1, anti-NA2, and anti-5b and gave strong reactions with appropriate control granulocytes.

F3-151

Moderate reactions with anti-A26 specificity defined. Positive controls gave moderate to strong reactions.

F3-152

Target cells included all serologically defined class II, DR types, except DR 12 and DR 14. Positive controls gave moderate to strong reactions. Of the 5 TRALI donors with positive reactions, 2 had strongly positive reactions with no definable specificity (both implicated plasmas were negative for antigranulocyte and anti-HLA class I antibodies) and 3 had weak or questionable reactions (all 3 implicated plasmas also tested nonspecifically weakly/questionably positive for antigranulocyte antibodies and were negative for anti-HLA class I antibodies).

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