Neurology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Correspondence:
Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Correspondence are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Dasgupta, M. K.
Right arrow Articles by Dossetor, J. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Dasgupta, M. K.
Right arrow Articles by Dossetor, J. B.
NEUROLOGY 1982;32:1000
© 1982 American Academy of Neurology

Circulating immune complexes in multiple sclerosis

Relation with disease activity

Mrinal K. Dasgupta, Kenneth G. Warren, Kaivilayil V. Johny and John B. Dossetor

Division of Nephrology (Drs. Dasgupta, Johny and Dossetor) and Neurology (Dr. Warren), Department of Medicine, University of Alberta, Edmonton, Alberta, Canada.

Two hundred fifty-four MS patients were studied for circulating immune complexes (CIO by three different assays: Raji-RIA, Clq-PEG, and Conglutinin-BA. Thirty-five percent of the sera were positive by one or more of these tests; Raji-RIA had the highest sensitivity (29.4%). Incidence of CIC in acute relapse, progressive, remission, and stable state of MS was 33.3%, 30.2%, 26.1%, and 23.1%, respectively, by Raji-RIA, compared with 7.75% and 8.82% among normal and neurologic controls. The incidence of CIC in neurologic controls differed significantly from both acute relapse and progressive disease, and almost significantly from patients in remission. There was no significant difference between patients with stable MS and neurologic controls, and there was no association of CIC with HLA-B7.

Address correspondence and reprint requests to Dr. Dasgupta, Division of Nephrology, Department of Medicine, University of Alberta, Edmonton, T6G 2G3 Canada.

Accepted for publication January 20, 1982.

This research was supported by the Multiple Sclerosis Society of Canada; the G. and M. Muttart and the Richard E. Lee Foundations of Edmonton, Alberta; the Association of Canadian Travellers of Edmonton, Alberta; and the Friends of Multiple Sclerosis Research in Edmonton, Alberta.




This article has been cited by other articles:


Home page
NeurologyHome page
K.-M. Myhr, G. Raknes, H. Nyland, and C. Vedeler
Immunoglobulin G Fc-receptor (Fc{gamma}R) IIA and IIIB polymorphisms related to disability in MS
Neurology, June 1, 1999; 52(9): 1771 - 1771.
[Abstract] [Full Text] [PDF]


Home page
Arch NeurolHome page
R. A. Rudick, J. M. Bidlack, and D. W. Knutson
Multiple Sclerosis: Cerebrospinal Fluid Immune Complexes That Bind Clq
Arch Neurol, September 1, 1985; 42(9): 856 - 858.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1982 by AAN Enterprises, Inc.