病毒学
细胞毒性T细胞
生物
病毒
异源的
抗原
甲型流感病毒
质粒
正粘病毒科
DNA
核蛋白
免疫学
基因
体外
遗传学
作者
Jeffrey B. Ulmer,John Donnelly,Suezanne E. Parker,Gary Rhodes,Philip L. Felgner,Varavani Dwarki,Stanislaw H. Gromkowski,R. Randall Deck,Corrille M. DeWitt,Arthur Friedman,L A Hawe,Karen Leander,Douglas Martinez,Helen C. Perry,John W. Shiver,Donna L. Montgomery,Margaret A. Liu
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1993-03-19
卷期号:259 (5102): 1745-1749
被引量:2342
标识
DOI:10.1126/science.8456302
摘要
Cytotoxic T lymphocytes (CTLs) specific for conserved viral antigens can respond to different strains of virus, in contrast to antibodies, which are generally strain-specific. The generation of such CTLs in vivo usually requires endogenous expression of the antigen, as occurs in the case of virus infection. To generate a viral antigen for presentation to the immune system without the limitations of direct peptide delivery or viral vectors, plasmid DNA encoding influenza A nucleoprotein was injected into the quadriceps of BALB/c mice. This resulted in the generation of nucleoprotein-specific CTLs and protection from a subsequent challenge with a heterologous strain of influenza A virus, as measured by decreased viral lung titers, inhibition of mass loss, and increased survival.
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