Open AccessProtective effect of immunization with nonviral antigens against Friend leukemia virus in mice
Author(s) -
E. Nahon-Merlin,
F Lacour,
Charlotte Friend,
Roberto P. Revoltella
Publication year - 1979
Publication title -
proceedings of the national academy of sciences of the united states of america
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.76.4.2018
Subject(s) - immunogen , antibody , bovine serum albumin , virology , keyhole limpet hemocyanin , immunization , biology , adjuvant , virus , antigen , ovalbumin , murine leukemia virus , microbiology and biotechnology , immunology , monoclonal antibody
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 101.5 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.