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Use of low toxicity adjuvants and killed virus to induce protective immunity against the Friend murine leukaemia retrovirus-induced disease.

Abstract
Low toxic and synthetic adjuvants were investigated in the induction of protective immunity against Friend murine retrovirus-induced erythroleukaemia by immunization with inactivated Friend murine leukaemia helper virus (F-MuLV). 6-O-(2-tetradecyl-hexadecanoyl)-N-acetylmuramyl-L-alanyl-D-isoglutamine (B30-MDP) showed a significant enhancement of the protective immunity against Friend virus-induced erythroleukaemia not only in H-2a/b mice known to make good immune responses to F-MuLV envelope, but also in H-2a/a mice which are usually unable to respond to F-MuLV envelope protein. Another analogue of N-acetylmuramyl-D-isoglutamine (MDP), N alpha-acetylmuramyl-L-alanyl-D-isoglutaminyl-N epsilon-stearoyl-L-lysine [MDP-Lys(L18)], which has been shown to enhance non-specific protective activity against bacterial and viral infections, however, showed no adjuvant activity in the present system. A combined adjuvant of the synthesized mycobacterial cord factor, trehalose dimycolate (TDM) and detoxified bacterial endotoxin, monophosphoryl lipid A from Salmonella minnesota, gave good protection which was comparable to complete Freund's adjuvant in both H-2a/b and H-2a/a mice.
AuthorsC Ishihara, M Miyazawa, J Nishio, I Azuma, B Chesebro
JournalVaccine (Vaccine) Vol. 10 Issue 5 Pg. 353-6 ( 1992) ISSN: 0264-410X [Print] Netherlands
PMID1574922 (Publication Type: Journal Article)
Chemical References
  • Adjuvants, Immunologic
  • Vaccines, Inactivated
  • Viral Vaccines
Topics
  • Adjuvants, Immunologic (pharmacology)
  • Animals
  • Friend murine leukemia virus (immunology)
  • Immunization
  • Leukemia, Experimental (prevention & control)
  • Mice
  • Vaccines, Inactivated (immunology)
  • Viral Vaccines (immunology)

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