Table 1.
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.