1887

Abstract

Summary

Leukocytes, subjected once to interferon (IFN) induction by HVJ (Sendai virus), were studied for their capability to produce IFN after a second similar stimulus. Substantial amounts of IFN (about 30000 IU/ml) were recovered. Experiments using cycloheximide or actinomycin D and kinetic studies showed that this IFN originated mainly in IFN which resided within the cell as a result of the first induction and was released after the second stimulation. Increasing amounts of HVJ used for the second stimulus resulted in proportionally increased yields of IFN, reaching a plateau at the same dose of HVJ (1000 HAU/ml) as that which gave optimal yields after the first stimulation. Evidence is presented that the capacity of HVJ to trigger the production of a second IFN harvest is closely associated with its infectivity.

Keyword(s): HVJ , IFN (HuIFN-α) and induction
Loading

Article metrics loading...

/content/journal/jgv/10.1099/0022-1317-67-4-809
1986-04-01
2024-12-03
Loading full text...

Full text loading...

/deliver/fulltext/jgv/67/4/JV0670040809.html?itemId=/content/journal/jgv/10.1099/0022-1317-67-4-809&mimeType=html&fmt=ahah

References

  1. Mogensen K. E., Cantell K. 1977; Production and preparation of human leukocyte interferon. Pharmacology and Therapeutics C1:369–381
    [Google Scholar]
  2. Sugita K., Maru M., Sano K. 1974; A sensitive plaque assay for Sendai virus in an established line of monkey kidney cells. Japanese Journal of Microbiology 18262–264
    [Google Scholar]
/content/journal/jgv/10.1099/0022-1317-67-4-809
Loading
/content/journal/jgv/10.1099/0022-1317-67-4-809
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error