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用非病毒抗原免疫对小鼠中Friend白血病病毒的保护作用。

Protective effect of immunization with nonviral antigens against Friend leukemia virus in mice.

作者信息

Nahon-Merlin E, Lacour F, Friend C, Revoltella R

出版信息

Proc Natl Acad Sci U S A. 1979 Apr;76(4):2018-21. doi: 10.1073/pnas.76.4.2018.

Abstract

DBA/2 mice immunized with poly(A).poly(U) complexed with methylated bovine serum albumin and emulsified in Freund's complete adjuvant were protected against challenge with Friend leukemia virus. There was no correlation between the level of antibody to the immunogen in the prechallenge serum and induced resistance to the virus. Although prechallenge sera of mice given the same amount of the duplex in a single inoculum bound 9.7% of poly(A).poly([(3)H]U) input, as compared to 45.3% bound by the prechallenge sera of mice given the immunogen in divided doses, both groups of mice were equally resistant to infection. Immunization with two other nonviral agents, bovine serum albumin fraction V or dinitrophenylated keyhole limpet hemocyanin, induced the same level of protection. A sparing effect of approximately 10(1.5) in infectivity was afforded the immunized mice. Immunization with either poly(A).poly(U) alone or with the carrier methylated bovine serum albumin was ineffective. In addition to antibodies to the respective immunogens, the prechallenge sera of the immunized mice also contained antibody to Friend leukemia virus gp71. The presence of such viral antibodies was not always related to resistance to infection by Friend virus. Some immunized mice that survived infection did not have gp71 antibody in their serum before challenge, and mice immunized with poly(A).poly(U) alone were susceptible to infection, although their prechallenge sera contained antibody to gp71. The mechanism involved in the induction of resistance to infection is not known. The effect may be mediated through a modification of the expression of both endogenous and exogenous type C viruses and affect immunological mechanisms controlling cellular responses.

摘要

用与甲基化牛血清白蛋白复合并在弗氏完全佐剂中乳化的聚(A)·聚(U)免疫的DBA/2小鼠可免受Friend白血病病毒攻击。攻击前血清中针对免疫原的抗体水平与诱导的抗病毒能力之间没有相关性。尽管单次接种相同量双链体的小鼠攻击前血清结合了9.7%输入的聚(A)·聚([³H]U),而分剂量给予免疫原的小鼠攻击前血清结合了45.3%,但两组小鼠对感染的抵抗力相同。用另外两种非病毒剂,即牛血清白蛋白V组分或二硝基苯基化的钥孔戚血蓝蛋白免疫,诱导出相同水平的保护作用。对免疫小鼠的感染性有大约10¹·⁵的节约效应。单独用聚(A)·聚(U)或与载体甲基化牛血清白蛋白一起免疫均无效。除了针对各自免疫原的抗体外,免疫小鼠的攻击前血清还含有针对Friend白血病病毒gp71的抗体。此类病毒抗体的存在并不总是与对Friend病毒感染的抵抗力相关。一些在感染中存活的免疫小鼠在攻击前血清中没有gp71抗体,而单独用聚(A)·聚(U)免疫的小鼠易受感染,尽管它们的攻击前血清含有针对gp71的抗体。诱导抗感染的机制尚不清楚。这种效应可能是通过对内源性和外源性C型病毒表达的修饰介导的,并影响控制细胞反应的免疫机制。

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