Open Access

Plasma gelsolin as a biomarker of inflammation

Arthritis Research & Therapy200810:124

https://doi.org/10.1186/ar2547

Published: 3 December 2008

Abstract

The prognostic implications of declining plasma gelsolin levels have been documented after a diverse variety of acute insults. Because gelsolin concentrations fall prior to the development of complications, a pathophysiological role for gelsolin depletion has been postulated in delayed multiorgan failure. The original hypothesis about the function of circulating gelsolin was that it scavenged actin released from cells at the site of injury. Although extracellular actin may be the primary cause of gelsolin depletion, the biologic imperative for gelsolin could entail the modulation of several inflammatory mediators as much as the disposal of actin. Translational research is actively addressing whether replenishment of plasma gelsolin could provide an efficacious and well tolerated therapeutic intervention in selected seriously ill patients.

Osborn and colleagues demonstrate that patients with rheumatoid arthritis and knee effusions have plasma gelsolin levels lower than those in healthy volunteers [1]. Gelsolin was first identified as a cytoplasmic actin-regulatory protein essential for cell locomotion and phagocytosis. When a circulating isoform was subsequently discovered, its physiological significance was far from apparent.

For over two decades, researchers have struggled to define the raison d'être for actin-binding proteins in plasma, which under normal circumstances does not contain detectable actin. A straightforward hypothesis emerged that plasma gelsolin scavenges actin leaked into the circulation or interstitial space from injured tissue in order to abort subsequent damage instigated by extracellular actin filaments [2]. Hypogelsolinemia ensues after a wide spectrum of seemingly unrelated types of insults and precedes a second wave of injury that typically involves organs distant from the precipitating event [25]. The accumulated phenomenology has given way to plausible mechanisms, but rigorous science has yet to fully catch up with vigorous speculation.

Current dogma has expanded to now accommodate the convincing observations that plasma gelsolin can bind a variety of potentially inflammatory moieties, and can thereby modulate the exuberance of the host response to sepsis, malaria, burns, trauma, and other commonly encountered clinical conditions. Plasma gelsolin's primary function may be to protect seriously ill patients from their own overzealous inflammatory response. Identified ligands include platelet-activating factor, lysophosphatidic acid, and sphingosine 1 phosphate, as well as cell-wall constituents of Gram-negative and Gram-positive bacteria [68]. Actin exposed at the site of overwhelming injury may act as a sink to exhaust the supply of plasma gelsolin, in turn allowing redundant inflammatory cascades unfettered opportunity to wreak havoc upon multiple organ systems.

The lower the levels of plasma gelsolin, the less favorable the prognosis of acute illness becomes [25, 9]. Animal models further indicate that exogenous gelsolin administered during an identifiable window of opportunity can reduce injury and lower mortality [911]. More recently, evidence has begun to accumulate in chronic diseases. The current report by Osborn and colleagues provides data on patients with rheumatoid arthritis indicating that, at least in an acute-or-chronic circumstance, circulating gelsolin concentrations are depressed below the normal range [1]. Further, the authors document the presence of gelsolin–actin complexes in synovial fluid. The identification of gelsolin–actin complexes inside the joint space is strong presumptive evidence of the sequestration hypothesis, as long as the isoform associated with the complexes is plasma gelsolin.

Rheumatoid arthritis represents a chronic inflammatory state punctuated by episodes of acute synovitis. Kulakowska and colleagues have recently demonstrated that blood and cerebrospinal fluid gelsolin concentrations in patients with multiple sclerosis are lower than levels for patients with peripheral neurological disorders [12]. In their patients, intrathecal actin was not detectable. The participants were all considered to be in the early stages of relapsing–remitting multiple sclerosis. Whether the chronic disease or an acute flare is responsible for lowering gelsolin levels can be hard to dissect in the setting of waxing and waning illness. Both aspects of such disease entities can increase consumption as well as restrain production of plasma proteins such as gelsolin.

Translational research in this area is also being optimistically pursued. Inhalational use of recombinant human gelsolin potentates the bactericidal activity of cationic endogenous antimicrobial peptides and exogenous antibiotics. In fact, gelsolin was first investigated as an inhaled therapeutic agent to decrease the viscosity of airway secretions from patients with cystic fibrosis. Appropriately dosed infusions of recombinant human gelsolin can diminish evolving injury or reduce mortality rates in animal models of hyperoxia, burns, and sepsis [911]. A particular advantage of gelsolin therapy over previously failed immunomodulary therapies derives from its modulation of multiple proinflammatory pathways. Gelsolin also inhibits certain actions of bacterial endotoxin. Gelsolin repletion to physiological levels between the time of the initial insult and subsequent complications in patients identified by marked hypogelsolinemia as being at substantial risk for delayed multiorgan dysfunction could provide a directed and effective therapeutic intervention in critically ill patients.

Declarations

Acknowledgements

The author is indebted to Joann DiLullo for her indispensable assistance.

Authors’ Affiliations

(1)
Division of Vaccines/Infectious Diseases, Medical Communications Department, Merck Research Laboratories

References

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Copyright

© BioMed Central Ltd 2008

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