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Immunological significance of Mycobacterium leprae cell walls.
Author(s) -
Johanne Melancon-Kaplan,
S W Hunter,
Michael McNeil,
C Stewart,
Robert L. Modlin,
Thomas H. Rea,
J Convit,
Padmini Salgame,
V Mehra,
Barry R. Bloom
Publication year - 1988
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.85.6.1917
Subject(s) - mycobacterium leprae , peptidoglycan , arabinogalactan , cell wall , antigen , microbiology and biotechnology , mycobacterium , biology , immune system , proteolysis , chemistry , biochemistry , bacteria , immunology , leprosy , enzyme , genetics
Cell walls of Mycobacterium leprae, prepared by differential solvent extraction, were shown to contain arabinogalactan, mycolates, and peptidoglycan. In addition, amino acid analysis revealed the unexpected presence of large amounts of protein that retained potent immunological reactivity. Purified cell walls stimulated proliferation of T cells from tuberculoid, but not from lepromatous leprosy, patients and elicited delayed-type hypersensitivity skin reactions in guinea pigs and patients sensitized to M. leprae. Analysis of the precursor frequency of antigen-reactive human peripheral T cells revealed that as many cells (approximately equal to 1/6000) proliferate to antigen contained in cell walls as to intact M. leprae. Sequential removal of mycolates and arabinogalactan resulted in a large peptidoglycan-protein complex that retained all the immunological activity. This immunological reactivity and the inherent protein were destroyed by proteolysis. Thus, cell wall protein is a major contributor to cell-mediated immune reactivity to this pathogenic mycobacterium.

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