1988
DOI: 10.1128/jvi.62.7.2490-2497.1988
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Cell-mediated immunity induced in mice after vaccination with a protease activation mutant, TR-2, of Sendai virus

Abstract: Our previous study has shown that, although a trypsin-resistant mutant of Sendai virus, TR-2, replicates only in a single cycle in mouse lung with a negligible lesion, the animal acquires a strong immunity against lethal infection with wild-type Sendai virus, suggesting that TR-2 could be used as a new type of live vaccine (M.

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Cited by 10 publications
(2 citation statements)
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“…In addition, a maximum murine CTL response to Sendai virus was observed at about 12 p.i. (27). In contrast, maximum direct CTL responses in horses against equine herpesvirus were detected by 2 and 3 weeks p.i.…”
Section: Discussionmentioning
confidence: 82%
“…In addition, a maximum murine CTL response to Sendai virus was observed at about 12 p.i. (27). In contrast, maximum direct CTL responses in horses against equine herpesvirus were detected by 2 and 3 weeks p.i.…”
Section: Discussionmentioning
confidence: 82%
“…Sendai virus, a member of the family paramyxoviridae, is a common causative agent for pneumonia in mice and often causes outbreaks of the disease in laboratory mice (11). To protect mice from Sendai virus infection, several experiments including our own vaccination experiment using a trypsin-resistant mutant have been conducted (2,3,10,26,42,43,47). However, detailed mechanism of the protection is yet to be elucidated.…”
mentioning
confidence: 99%