Abstract
In a serum free, 2-mercaptoethanol supplemented culture medium muramyl dipeptide (MDP) is able to increase the number of plaque-forming cells (PFC) directed against syngeneic, bromelain-treated red blood cells (br-MRBC) and against an autoantigen, mouse albumin. The non-specific stimulation of anti-br-MRBC PFC by MDP, as by bacterial lipopolysaccharide (LPS), can be observed in spleen cell populations depleted of adherent and phagocytic cells, and in nu/nu spleen cell cultures. However, the kinetics of the induction of anti-br-MRBC PFC in murine spleen cell cultures in presence of LPS or of MDP are not identical. Moreover, MDP is able to stimulate C3H/He Orl (LPS low-responder strain) cells. Thus, the mechanisms of non-specific stimulation by MDP or by LPS could be different. Experiments done with thirteen structural analogues of MDP showed that there exists a good correlation between the adjuvant activity and the ability to induce anti-br-MRBC PFC.
MeSH Terms
Acetylmuramyl-Alanyl-Isoglutamine/immunology
Adjuvants, Immunologic
Animals
Autoantibodies/biosynthesis
Cells, Cultured
Epitopes
Glycopeptides/immunology
Hemolytic Plaque Technique
Isoantibodies/biosynthesis
Kinetics
Lipopolysaccharides/immunology
Mice
Mice, Nude
Spleen/cytology,immunology
Chemicals
Adjuvants, Immunologic
Autoantibodies
Epitopes
Glycopeptides
Isoantibodies
Lipopolysaccharides
Acetylmuramyl-Alanyl-Isoglutamine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Löwy I
Leclerc C
Chedid L
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27 references, click to expand
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