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. 1996 Nov 12;93(23):13102–13107. doi: 10.1073/pnas.93.23.13102

Table 1.

Specificity and dose-dependency of the LTβR–Fc chimeric fusion protein

Mouse* Tg LTβR–Fc, μg/ml Relative inhibition of cytokine cytotoxicity§
Body, g Spleen, g Thymus, g Peyer’s patches
LTαβ LTα TNF n cm2
1610.20 + 0.05 1.1 <1 <1 19.5 0.093 0.128 11 0.35
1610.30 + 0.10 1.6 <1 <1 20.3 0.084 0.097 8 0.31
1610.1 + 0.50 6.7 <1 <1 19.8 0.078 0.121 10 0.15
1610.3 + 0.50 5.8 <1 <1 17.1 0.055 0.089 7 0.16
1610.10 + 1.25 18.3 <1 <1 17.8 0.055 0.084 5 0.09
1610.2 + 1.30 19.2 <1 <1 14.5 0.049 0.113 5 0.07
*

Mice were 6-week-old female littermates born from heterozygous parents. 

Expression of the LTβR–Fc transgene was determined by Southern blot analysis. 

Concentration of the soluble LTβR–Fc fusion protein in the sera was determined by ELISA. 

§

Determined by the ability of 1% sera to inhibit either LTαβ-, LTα-, or TNF-mediated killing of WEHI-164 cells; 10 ng/ml of purified murine LTβR–Fc fusion protein in 1% NMS was able to inhibit LTαβ-killing by 19.2-fold. 

Similar values were observed with age- and sex-matched nontransgenic mice.