A method to screen T lymphocyte epitopes after oral immunisation of humans: application to cholera toxin B subunit

The response to oral immunisation of humans with classical biotype cholera toxin B subunit was studied to identify immunodominant T lymphocyte determinants. The in vitro proliferative response to pools of 12-mer peptides and larger peptides used individually was analysed by a novel statistical appro...

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Published inVaccine Vol. 13; no. 9; pp. 817 - 820
Main Authors Castello-Branco, Luiz R.R., Griffin, George E., Dougan, Gordon, Lewis, David J.M.
Format Journal Article
LanguageEnglish
Published Oxford Elsevier Ltd 01.06.1995
Elsevier
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ISSN0264-410X
1873-2518
DOI10.1016/0264-410X(94)00036-M

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Abstract The response to oral immunisation of humans with classical biotype cholera toxin B subunit was studied to identify immunodominant T lymphocyte determinants. The in vitro proliferative response to pools of 12-mer peptides and larger peptides used individually was analysed by a novel statistical approach, and identified an immunodominant region in residues 70–79 in immunised subjects, when either pools or individual peptides were employed. In contrast, a patient infected with El Tor biotype had a dominant response to residues 40–60. The statistical software employed in this study may enable efficient screening of antigens for immunodominant T lymphocyte determinants when blood precursor frequencies are low following immunisation, and may therefore be of special relevance to mucosal vaccines.
AbstractList The response to oral immunisation of humans with classical biotype cholera toxin B subunit was studied to identify immunodominant T lymphocyte determinants. The in vitro proliferative response to pools of 12-mer peptides and larger peptides used individually was analysed by a novel statistical approach, and identified an immunodominant region in residues 70-79 in immunised subjects, when either pools or individual peptides were employed. In contrast, a patient infected with El Tor biotype had a dominant response to residues 40-60. The statistical software employed in this study may enable efficient screening of antigens for immunodominant T lymphocyte determinants when blood precursor frequencies are low following immunisation, and may therefore be of special relevance to mucosal vaccines.
The response to oral immunisation of humans with classical biotype cholera toxin B subunit was studied to identify immunodominant T lymphocyte determinants. The in vitro proliferative response to pools of 12-mer peptides and larger peptides used individually was analysed by a novel statistical approach, and identified an immunodominant region in residues 70–79 in immunised subjects, when either pools or individual peptides were employed. In contrast, a patient infected with El Tor biotype had a dominant response to residues 40–60. The statistical software employed in this study may enable efficient screening of antigens for immunodominant T lymphocyte determinants when blood precursor frequencies are low following immunisation, and may therefore be of special relevance to mucosal vaccines.
The response to oral immunisation of humans with classical biotype cholera toxin B subunit was studied to identify immunodominant T lymphocyte determinants. The in vitro proliferative response to pools of 12-mer peptides and larger peptides used individually was analysed by a novel statistical approach, and identified an immunodominant region in residues 70-79 in immunised subjects, when either pools or individual peptides were employed. In contrast, a patient infected with El Tor biotype had a dominant response to residues 40-60. The statistical software employed in this study may enable efficient screening of antigens for immunodominant T lymphocyte determinants when blood precursor frequencies are low following immunisation, and may therefore be of special relevance to mucosal vaccines.The response to oral immunisation of humans with classical biotype cholera toxin B subunit was studied to identify immunodominant T lymphocyte determinants. The in vitro proliferative response to pools of 12-mer peptides and larger peptides used individually was analysed by a novel statistical approach, and identified an immunodominant region in residues 70-79 in immunised subjects, when either pools or individual peptides were employed. In contrast, a patient infected with El Tor biotype had a dominant response to residues 40-60. The statistical software employed in this study may enable efficient screening of antigens for immunodominant T lymphocyte determinants when blood precursor frequencies are low following immunisation, and may therefore be of special relevance to mucosal vaccines.
Author Dougan, Gordon
Griffin, George E.
Lewis, David J.M.
Castello-Branco, Luiz R.R.
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Issue 9
Keywords peptide
vaccine
T lymphocyte
epitope
cholera
Human
Immunization
Antigenic determinant
Vibrio cholerae
Oral administration
Subunit
Infection
Toxin
Antigenicity
T-Lymphocyte
Bacteriosis
Bacteria
Vibrionaceae
Cholera
Recognition
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SubjectTerms Administration, Oral
Bacteriology
Biological and medical sciences
Cell Division - immunology
cholera
Cholera - immunology
Cholera - therapy
Cholera Toxin - administration & dosage
Cholera Toxin - immunology
Cholera Toxin - therapeutic use
epitope
Fundamental and applied biological sciences. Psychology
Humans
Immunodominant Epitopes - immunology
Microbiology
peptide
T lymphocyte
T-Lymphocytes - cytology
T-Lymphocytes - immunology
vaccine
Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies
Title A method to screen T lymphocyte epitopes after oral immunisation of humans: application to cholera toxin B subunit
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https://www.ncbi.nlm.nih.gov/pubmed/7483803
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