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January 1, 1974JNCI Journal of the National Cancer Institute

Biologically Active Components from Mycobacterial Cell Walls. I. Isolation and Composition of Cell Wall Skeleton and Component P 3

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Authors

IAIchiro AzumaThe University of TokyoEREdgar RibiUniversity of Minnesota, DuluthTMThomas J. MeyerFrederick National Laboratory for Cancer Research

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Implication

Laboratory study reveals that combining mycobacterial cell wall skeleton with lipid component P3 restores full tumor regression activity, indicating a dual-component requirement for immunotherapy.

Key Points

  • To isolate and chemically characterize the specific fractions of the BCG mycobacterial cell wall responsible for tumor suppression and regression.
  • Digested BCG cell walls with proteolytic enzymes and extracted them with organic solvents to separate soluble free lipids from an insoluble cell wall skeleton (CWS-I).
  • Purified component P3 from wax D and cord factor fractions using microparticulate silica gel column chromatography under pressure elution.
  • Isolated CWS-I as a complex of 34% mycolic acid, 38.6% arabinogalactan (2.8:1 arabinose to galactose ratio), and 20.1% mucopeptide amino acids, which suppressed tumor growth but failed to regress established tumors.
  • Recombining chromatographically pure component P3 (containing trehalose and mycolic acids) with CWS-I restored tumor-regressing activity equal to that of intact BCG cell walls.

Cite This Study

Azuma et al. (1974) studied this question.

synapsesocial.com/papers/6a8a986b755d28965dfd74b9https://doi.org/10.1093/jnci/52.1.95
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