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Dominant T-cell clones of unknown significance in patients with idiopathic sensory neuropathies.

Authors :
Gherardi RK
Farcet JP
Créange A
Claudepierre P
Malapert D
Authier FJ
Delfau-Larue MH
Source :
Neurology [Neurology] 1998 Aug; Vol. 51 (2), pp. 384-9.
Publication Year :
1998

Abstract

Objective: To determine whether idiopathic sensory neuropathies could be associated with circulating dominant T-cell clones, a T-cell equivalent to monoclonal gammopathy of unknown significance.<br />Background: A number of predominantly sensory neuropathies remain of unknown etiology. Circulating dominant T-cell clones may be observed in the elderly, in autoimmune disorders, and in chronic viral infections.<br />Methods: Twenty patients with chronic sensory or predominantly sensory neuropathies considered idiopathic after intensive investigation were evaluated for the presence of dominant T-cell clones in blood using PCR amplification of the variable region of the T-cell receptor gamma-chain gene. They were classified as chronic idiopathic axonal polyneuropathy (CIAP) or sensory neuronopathy, i.e., chronic idiopathic ataxic neuropathy (CIAN), according to clinical and electrophysiologic criteria.<br />Results: Occurrence of clonal expansions of T cells was strikingly high in patients with idiopathic sensory neuropathies (16/20, 80%), with a similar proportion in CIAP (12/15, 80%) and CIAN (4/5, 80%), as compared with elderly normal controls (2/10, 20%), elderly controls with degenerative neurologic diseases (2/10, 20%), and elderly patients with idiopathic chronic inflammatory demyelinating polyneuropathy (2/10, 20%) (all p < 0.005).<br />Conclusion: Both CIAN and CIAP are associated with dominant T-cell clones of unknown significance that cannot simply be attributed to the age of patients. Relevance of T-cell clones to the pathogenesis of idiopathic sensory neuropathies remains to be determined.

Details

Language :
English
ISSN :
0028-3878
Volume :
51
Issue :
2
Database :
MEDLINE
Journal :
Neurology
Publication Type :
Academic Journal
Accession number :
9710007
Full Text :
https://doi.org/10.1212/wnl.51.2.384