Table 1.

Cytokine profile of human CD4+ T lymphocytes following CD3/CD28 or CD3/CD46 stimulation



Activation condition
Cytokines, pg/mL
CD3
CD3/CD28
CD3/CD46
IL-1α*  —   30 ± 1.5   20 ± 1.0  
IL-1β*  —   —   —  
IL-2*  —   500 ± 100   —  
IL-4*  —   50 ± 2.0   —  
IL-6*  —   —   —  
IL-7*  —   —   —  
IL-8*  30 ± 3.0   100 ± 15   350 ± 65  
IL-10*  —   250 ± 50   1800 ± 300 
IL-12†   —   —   —  
IL-15†   40 ± 2   70 ± 2   20 ± 2.0  
TNF-α*  50 ± 8.0   200 ± 30   600 ± 100 
IFN-γ*  80 ± 14   200 ± 40   900 ± 150 
GM-CSF*  100 ± 10   300 ± 40   2200 ± 400 
Soluble CD40L (CD154)†
 

 
80 ± 5
 
1300 ± 190
 


Activation condition
Cytokines, pg/mL
CD3
CD3/CD28
CD3/CD46
IL-1α*  —   30 ± 1.5   20 ± 1.0  
IL-1β*  —   —   —  
IL-2*  —   500 ± 100   —  
IL-4*  —   50 ± 2.0   —  
IL-6*  —   —   —  
IL-7*  —   —   —  
IL-8*  30 ± 3.0   100 ± 15   350 ± 65  
IL-10*  —   250 ± 50   1800 ± 300 
IL-12†   —   —   —  
IL-15†   40 ± 2   70 ± 2   20 ± 2.0  
TNF-α*  50 ± 8.0   200 ± 30   600 ± 100 
IFN-γ*  80 ± 14   200 ± 40   900 ± 150 
GM-CSF*  100 ± 10   300 ± 40   2200 ± 400 
Soluble CD40L (CD154)†
 

 
80 ± 5
 
1300 ± 190
 

Purified peripheral T cells (CD4+/CD45RA+) were activated with the indicated antibodies, supernatants were collected at day 3, and secreted cytokines were measured using the *ProteoPlexTM 16-Well Human Cytokine Array (Novagen, Madison, WI) or †ELISA. The expression of IL-10, TNF-α, IFN-γ, and GM-CSF was also confirmed by ELISA (not shown). Activation conditions were performed in triplicate. Data are the mean ± SD of 5 independent experiments using 5 different donors.

— indicates not detectable (cytokine content < 5 pg/mL)

The observed level of statistical difference in cytokine production between CD3/CD28- and CD3/CD46-activated cells was P < .001 by the paired Student t test in all cases

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