Abstract

IT is generally accepted that the presence of killed mycobacteria in complete Freund's adjuvant is necessary to induce a typical delayed hypersensitivity to soluble antigens1 and attempts have been made to isolate the active component. The preparations obtained initially were of a peptidoglycolipidic nature2. Hydrosoluble adjuvants containing an arabinogalactan and the wall peptidoglycan have been isolated3–5. We have shown previously that the purified cell wall peptidoglycan of several Gram-negative bacteria exhibit the same adjuvant effect as mycobacteria for the induction of delayed hypersensitivity6,7 and that the disaccharide peptide monomer (β-1,4-N-acetylglucosaminyl-N-acetylmuramyl-L- diaminopimelic acid (L)-D-Ala) was still active8. Similar findings have been made independently with the peptidoglycan of mycobacteria9,10, the subunit structure of which is only slightly different: N-acetylmuramic acid is replaced by N-glycolylmuramic acid and both Glu and diaminopimelic acid residues have amide substituents. The present study was undertaken to determine to what chemical structure of the peptidoglycan adjuvant activity was related.

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