SLE and Serum Complement: Causative, Concomitant or Coincidental?

Vaneet Sandhu1, Michele Quan2, *
1 Division of Rheumatology, Loma Linda University Medical Center, Loma Linda, CA, USA
2 Department of Internal Medicine, Arrowhead Regional Medical Center, Colton, CA, USA

Article Metrics

CrossRef Citations:
Total Statistics:

Full-Text HTML Views: 6794
Abstract HTML Views: 1553
PDF Downloads: 1544
ePub Downloads: 1043
Total Views/Downloads: 10934
Unique Statistics:

Full-Text HTML Views: 3278
Abstract HTML Views: 926
PDF Downloads: 772
ePub Downloads: 414
Total Views/Downloads: 5390

Creative Commons License
© 2017 Sandhu et al.

open-access license: This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International Public License (CC-BY 4.0), a copy of which is available at: ( This license permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

* Address correspondence to this author at the Department of Internal Medicine, Arrowhead Regional Medical Center, Colton, CA, USA, Tel: (909) 580-6343; E-mail:



Systemic Lupus Erythematosus (SLE) is an incurable autoimmune disorder with complement activation playing a key role in the pathogenesis of immune-mediated tissue injury. While quantifying complement to monitor SLE disease activity has been the standard of care since the 1950s, decreased complement levels are not consistently associated with flares.


We seek to clarify the SLE phenotype in which complement deficiency is causative, concomitant, or coincidental.


A PUBMED literature review was conducted using key words 'complement,' 'SLE,’ and ‘SLE flares’ in English-only journals from 1972-2017. Relevant clinical studies and review articles were found that examined the measurement of complement levels in SLE, and more specifically, interpretation of low serum complement levels regardless of disease activity.


Complement activation plays a key role in the pathophysiology of SLE and it is recommended to continue monitoring serum levels of C3 and C4 to assess for disease activity. However, it is important to note that decreased serum complement is not consistently associated with disease flares.

It is clinically important to find novel ways to assess disease activity in SLE. Increased serum levels of cell-bound complement activation products may more accurately reflect disease activity than conventional serum C3 and C4 monitoring.

Keywords: SLE, Systemic Lupus Erythematosus, SLE flares', Complement, CB-CAPS.