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Human T-cell clones recognize a major M. leprae protein antigen expressed in E. coli
Leprosy is a chronic infectious disease caused by Mycobacterium leprae . As with other intracellular parasites, protective immunity is dependent on T cells and cell-mediated immunity 1 . In animal models, immunization with killed armadillo-derived M. leprae elicits strong T-cell responses, delayed-t...
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Published in: | Nature (London) 1986-01, Vol.319 (6048), p.63-66 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Leprosy is a chronic infectious disease caused by
Mycobacterium leprae
. As with other intracellular parasites, protective immunity is dependent on T cells and cell-mediated immunity
1
. In animal models, immunization with killed armadillo-derived
M. leprae
elicits strong T-cell responses, delayed-type hypersensitivity and protection against viable challenge
2–5
. We have recently shown that killed
M. leprae
can induce delayed-type hypersensitivity in healthy human volunteers
6
. Identification of the M. leprae antigens that are recognized by T cells and may be involved in protection has been hampered by the inability to cultivate the organism
in vitro
and by difficulties in antigen purification from limited quantities of armadillo-derived bacillus. Because genes for the major protein antigens of
M. leprae
as seen by mouse monoclonal antibodies have been isolated
7,8
, it has become possible to test whether these individual antigens are recognized by T cells. We screened crude λ gtll phage lysates of
Escherichia coli
containing individual
M. leprae
antigens using
M. leprae
-specific T-cell clones isolated from
M. leprae
-vaccinated volunteers. Using this method, we find that nearly half of the
M. leprae
-specific T-cell clones are stimulated to proliferate by lysates containing an epitope of a
M. leprae
protein of relative molecular mass 18,000 (18K). |
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ISSN: | 0028-0836 1476-4687 |
DOI: | 10.1038/319063a0 |