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. 2003 Feb;77(3):1727–1737. doi: 10.1128/JVI.77.3.1727-1737.2003

TABLE 2.

IL-6 and TNF-α in culture media of LCMV/WE-infected cells

Cells Infectiona Virus titer, 106 PFU/ml IL-6, pg/ml (mean ± SD) TNF-α, pg/ml (mean ± SD)
HepG2 Mock NDc <4 <5
LPS ND <4 <5
WE 1.1 <4 <5
WE-UV ND <4 <5
WE + LPS 1.3 <4 <5
hNHepsb Mock ND 414 ± 39 <5
WE 1.2 397 ± 56 <5
WE-UV ND 430 ± 39 <5
WE + LPS 1.5 427 ± 49 <5
Human MDM Mock ND <4 <5
LPS ND 7,241 ± 340 38,080 ± 2,365
WE 0.1 <4 <5
WE-UV ND <4 <5
WE + LPS 0.08 7,086 ± 296 40,980 ± 2,963
a

PHA (GIBCO-BRL) and LPS from Escherichia coli 055:B55 (Sigma, St. Louis, Mo.) gave very similar results and were added to maintenance culture medium after virus adsorption to final concentrations of 5 μg/ml and 100 ng/ml, respectively. LCMV-WE was inactivated by UV light (WE-UV) as described in Materials and Methods.

b

Results with hNHep were very similar to results with human PBMC.

c

ND, not determined.