Proceedings of the National Academy of Sciences · 1996 · 63 citations · 19 references
Life SciencesImmunologyNeurologyAutoimmunityImmunogeneticsNeuroimmunologyHuman Leukocyte Antigen SystemMajor Histocompatibility ComplexMultiple SclerosisT Cell ActivationT Cell BiologyT Cell DifferentiationComplementarity-determining Region 3Complementarity-determining Region AnalysisMultiple Sclerosis ImmunopathogenesisMultiple Sclerosis ImmunopathologyPcr-based DetectionT Cell Receptor DiversityT Cell Repertoire FormationT-cell Receptor Gene Usage
We have used a PCR-based technology to study the V beta 5 and V beta 17 repertoire of T-cell populations in HLA-DR2 multiple sclerosis (MS) patients. We have found that the five MS DR2 patients studied present, at the moment of diagnosis and prior to any treatment, a marked expansion of a CD4+ T-cell population bearing V beta 5-J beta 1.4 beta chains. The sequences of the complementarity-determining region 3 of the expanded T cells are highly homologous. One shares structural features with that of the T cells infiltrating the central nervous system and of myelin basic protein-reactive T cells found in HLA-DR2 MS patients. An homologous sequence was not detectable in MS patients expressing DR alleles other than DR2. However, it is detectable but not expanded in healthy DR2 individuals. The possible mechanisms leading to its in vivo proliferation at the onset of MS are discussed.
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New diagnostic criteria for multiple sclerosis: Guidelines for research protocols
Charles M. Poser, Donald W. Paty, Labe C. Scheinberg et al. · Annals of Neurology · 1983 · 7.4K citations
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J Zhang, Silva Markovic‐Plese, B Lacet et al. · The Journal of Experimental Medicine · 1994 · 533 citations · Full text
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