Volume 14 Supplement 1

Proceedings of the 8th Global Arthritis Research Network (GARN) Meeting and 1st Bio-Rheumatology International Congress (BRIC)

Open Access

Increased concentration of serum soluble LAG3 in systemic lupus erythematosus

  • Seri Yu1,
  • Keishi Fujio1,
  • Kazuyoshi Ishigaki1,
  • Hirofumi Shoda1,
  • Tomohisa Okamura1,
  • Tanita Noor1,
  • Shuji Sumitomo1 and
  • Kazuhiko Yamamoto1
Arthritis Research & Therapy201214(Suppl 1):P16

DOI: 10.1186/ar3617

Published: 29 February 2012


In systemic lupus erythematosus (SLE), type I interferon and plasmacytoid DCs (pDCs) are supposed to play important roles. However, there are few evidences for pDCs activation in SLE. Murine pDCs are reported to produce soluble LAG3 (sLAG3) upon activation and pDCs are responsible for most of sLAG3 in mice serum [1]. Therefore, serum sLAG3 concentration was examined in SLE and other autoimmune diseases.

Materials and methods

This study enrolled 45 SLE patients who met ACR criteiria. Disease activity was rated using a SLE disease activity index (SLEDAI). sLAG3 concentrations were measured by a quantitative sandwich enzyme immunoassay [2].


The ratio of sLAG3 concentration in SLE to control was 3.10+/-1.05, PM/DM to control was 1.04+/-0.08, and RA to control was 0.77+/-0.14. In addition, sLAG3 concentrations showed a significant correlation with SLEDAI. Interestingly, elevation of sLAG3 was observed even in patients with SLEDAI = 0. These results suggested that sLAG3 could be a specific and novel marker for SLE.


sLAG3 can be a novel marker for SLE. sLAG3 in sera of SLE patient may reflect the activation of pDCs. Because sLAG3 shows adjuvant effect when combined with active immunization [3], sLAG3 may contribute to the exacerbation of lupus. The association between elevated sLAG3, type I interferon signature and activation of pDCs should be investigated further.
Figure 1

sLAG3 concentrations in SLE and other autoimmune diseases measured by ELISA.

Authors’ Affiliations

Department of Allergy and Rheumatology, Graduate School of Medicine, The University of Tokyo


© Yu et al.; licensee BioMed Central Ltd. 2012

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.