Abstract
Parasite-specific CD4+ T cells have been shown to transfer protection against Leishmania major in susceptible BALB/c mice. An epitope-tagged expression library was used to identify the antigen recognized by a protective CD4+ T cell clone. The expression library allowed recombinant proteins made in bacteria to be captured by macrophages for presentation to T cells restricted to major histocompatibility complex class II. A conserved 36-kilodalton member of the tryptophan-aspartic acid repeat family of proteins was identified that was expressed in both stages of the parasite life cycle. A 24-kilodalton portion of this antigen protected susceptible mice when administered as a vaccine with interleukin-12 before infection.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Amino Acid Sequence
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Animals
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Antigens, Protozoan / chemistry
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Antigens, Protozoan / genetics
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Antigens, Protozoan / immunology*
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Cloning, Molecular
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Histocompatibility Antigens Class II / immunology
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Immunodominant Epitopes
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Interleukin-12 / administration & dosage
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Interleukin-4 / immunology
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Leishmania major / genetics
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Leishmania major / immunology*
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Leishmaniasis, Cutaneous / prevention & control*
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Mice
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Mice, Inbred BALB C
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Molecular Sequence Data
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Protozoan Proteins / chemistry
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Protozoan Proteins / genetics
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Protozoan Proteins / immunology*
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Protozoan Vaccines / immunology
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Th1 Cells / immunology*
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Vaccines, Synthetic / immunology
Substances
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Antigens, Protozoan
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Histocompatibility Antigens Class II
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Immunodominant Epitopes
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Protozoan Proteins
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Protozoan Vaccines
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Vaccines, Synthetic
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LACK antigen, Leishmania
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Interleukin-12
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Interleukin-4
Associated data
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GENBANK/U27568
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GENBANK/U27569