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Volume 217, Issue 1, Pages 95-101 (10 December 2009)


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Serum anti-GAGA4 IgM antibodies differentiate relapsing remitting and secondary progressive multiple sclerosis from primary progressive multiple sclerosis and other neurological diseases

Johannes Brettschneidera1, Troy D. Jaskowskib1, Hayrettin Tumania, Sana Abdula, Dee Husebyec, Haniah Serajc, Harry R. Hilld, Ella Firee, Larissa Spectore, Jennifer Yardene, Nir Dotane, John W. RosefCorresponding Author Informationemail address

Received 17 May 2009; received in revised form 26 July 2009; accepted 28 July 2009. published online 02 November 2009.

Abstract 

The serum level of IgM antibodies against Glc(α1,4)Glc(α) (GAGA4) is higher in relapsing remitting multiple sclerosis (RRMS) compared to other neurological disease (OND) patients and healthy controls (HC). Detecting the level of anti-GAGA4 antibody by enzyme immunoassay and total IgM, we confirmed that anti-GAGA4 IgM can differentiate RRMS from OND patients and HC. Moreover, secondary progressive MS (SPMS) and RRMS patients have similar levels of anti-GAGA4 demonstrating the biomarker's presence throughout the disease. Interestingly, the anti-GAGA4 assay may also differentiate between primary progressive MS (PPMS) and RRMS/SPMS patients, since nearly all PPMS patients were negative for the assay.

a Department of Neurology, University of Ulm, Ulm, Germany

b Immunology, Research & Development, ARUP Institute for Clinical and Experimental Pathology, Salt Lake City, UT, USA

c Department of Neurology, University of Utah, Salt Lake City, UT, USA

d Departments of Pathology, Pediatrics and Medicine, University of Utah, Salt Lake City, UT, USA

e Glycominds Ltd., Lod, Israel

f Neurovirology Research Laboratory VASLCHCS and the Department of Neurology, University of Utah, Salt Lake City, UT, USA

Corresponding Author InformationCorresponding author. Neurovirology Research Laboratory VASLCHCS and the Department of Neurology, University of Utah, Salt Lake City, UT, 84112, USA. Tel.: +1 801 584 1292; fax: +1 801 584 5654.

1 The authors contributed equally to the study and appear in alphabetical order.

PII: S0165-5728(09)00301-4

doi:10.1016/j.jneuroim.2009.07.017


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