TY - JOUR
T1 - TCR Vβ usage by acetylcholine receptor-specific CD4+ T cells in myasthenia gravis
AU - Raju, Raghavanpillai
AU - Navaneetham, Duraiswamy
AU - Protti, Maria Pia
AU - Norton, Robert M.
AU - Hoppe, Bobbi L.
AU - Howard, James
AU - Conti-Fine, Bianca M.
PY - 1997/4
Y1 - 1997/4
N2 - In myasthenia gravis the muscle acetylcholine receptor (AChR) is the target of an autoimmune response. AChR epitopes recognized by CD4+ T cells in myasthenic patients have been identified. AChR-specific CD4+ cell lines can be propagated by stimulation of blood lymphocytes with synthetic or biosynthetic AChR sequences. We analysed, using a semi-quantitative PCR assay, the T cell receptor (TCR) Vβ usage of 16 anti-AChR polyclonal CD4+ T cell lines of known epitope specificity, propagated from myasthenic patients using pools of overlapping peptides corresponding to the sequence of an AChR subunit, or individual synthetic AChR sequences. Twelve lines had been propagated for less than 2 months, four lines for 3.5-5 months. Most lines had limited Vβ usage, but in most cases different Vβ regions were used for different epitopes in the same patient, and for the same epitope in different patients. In a few patients, the same Vβ regions were used for recognition of different epitopes. The Vβ4 and Vβ6 regions were used most frequently. These findings suggest that the potentially autoimmune T cells that survive clonal deletion have a limited TCR repertoire. Although the present data do allow conclusions on the role of a superantigen in triggering the anti-AChR autoimmune response, the finding that different Vβ regions were used in different patients does not support an important role of a superantigen in the maintenance of the CD4+ response in myasthenia gravis.
AB - In myasthenia gravis the muscle acetylcholine receptor (AChR) is the target of an autoimmune response. AChR epitopes recognized by CD4+ T cells in myasthenic patients have been identified. AChR-specific CD4+ cell lines can be propagated by stimulation of blood lymphocytes with synthetic or biosynthetic AChR sequences. We analysed, using a semi-quantitative PCR assay, the T cell receptor (TCR) Vβ usage of 16 anti-AChR polyclonal CD4+ T cell lines of known epitope specificity, propagated from myasthenic patients using pools of overlapping peptides corresponding to the sequence of an AChR subunit, or individual synthetic AChR sequences. Twelve lines had been propagated for less than 2 months, four lines for 3.5-5 months. Most lines had limited Vβ usage, but in most cases different Vβ regions were used for different epitopes in the same patient, and for the same epitope in different patients. In a few patients, the same Vβ regions were used for recognition of different epitopes. The Vβ4 and Vβ6 regions were used most frequently. These findings suggest that the potentially autoimmune T cells that survive clonal deletion have a limited TCR repertoire. Although the present data do allow conclusions on the role of a superantigen in triggering the anti-AChR autoimmune response, the finding that different Vβ regions were used in different patients does not support an important role of a superantigen in the maintenance of the CD4+ response in myasthenia gravis.
KW - autoimmunity
KW - myasthenia gravis
KW - PCR
KW - preferential TCR Vβ usage
KW - T cell epitopes
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U2 - 10.1006/jaut.1996.0120
DO - 10.1006/jaut.1996.0120
M3 - Article
C2 - 9185882
AN - SCOPUS:0031128368
VL - 10
SP - 203
EP - 217
JO - Journal of Autoimmunity
JF - Journal of Autoimmunity
SN - 0896-8411
IS - 2
ER -