Table 3.

CD8 expansions in age-matched controls and multiple myeloma patients

Age-matched controlsPatients with MM3-150
No. subjects in study 27 22  
No. subjects showing CD8 expansions3-151 7  
Total no. CD8 expansions3-151 17 10  
Mean no. CD8 expansions per positive subject3-151 1.9 1.4  
No. subjects showing CD8 expansions predicted to be detectable by Southern blot3-152 1  
Total no. CD8 expansions predicted to be detectable by Southern blot3-152 
No. CD8 expansions predicted to be detectable by Southern blot per positive subject3-152 1.3 1  
Total no. CD8 expansions3-151,3-153 18 10 
Age-matched controlsPatients with MM3-150
No. subjects in study 27 22  
No. subjects showing CD8 expansions3-151 7  
Total no. CD8 expansions3-151 17 10  
Mean no. CD8 expansions per positive subject3-151 1.9 1.4  
No. subjects showing CD8 expansions predicted to be detectable by Southern blot3-152 1  
Total no. CD8 expansions predicted to be detectable by Southern blot3-152 
No. CD8 expansions predicted to be detectable by Southern blot per positive subject3-152 1.3 1  
Total no. CD8 expansions3-151,3-153 18 10 

Data were calculated as a function of total CD3+cells, except where noted otherwise.

MM indicates multiple myeloma.

F3-150

Reanalyzed data of 22 patients with MM from previous publication.5 

F3-151

After gating for CD8CD3+ T cells, expanded populations were those calculated as a function of total CD3+ cells and present at 3 SD or more above the mean percentage of Vβ+CD8 cells of the age-matched controls.

F3-152

A 4% to 5% monoclonal population can be detected with the Southern blot technique.8 The size of monoclonal Vβ+ populations (predicted to be detectable by Southern blot) was estimated by subtracting the mean values for the particular Vβ from the percentage of CD8CD3+ T cells, calculated as above. The mean values represent the percentage of polyclonal populations within individual TCRVβ subfamilies.

F3-153

Calculated as a function of total CD8 cells.

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