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. 2020 Dec 29;24:704. doi: 10.1186/s13054-020-03336-0

Plasma levels of the active form of suPAR are associated with COVID-19 severity

Mingxiang Huang 1,#, Linlin Li 2,#, Jianshan Shen 1, Yao Wang 1, Rui Wang 1, Cai Yuan 3, Mingdong Huang 2,✉, Longguang Jiang 2,4,✉
PMCID: PMC7770382  PMID: 33372603

We read with great interest the recent study by Rovina et al., who found that the elevation of soluble urokinase plasminogen activator receptor (suPAR) plasma levels in coronavirus disease 2019 (COVID-19) patients, and suggested the suPAR can be an early predictor of severe respiratory failure [1]. There are three different suPAR forms (suPAR DI-III, suPAR DI, and suPAR DII-III) in circulation, in which suPAR DI-III is defined as the active form of suPAR by its capability of binding to uPA [2]. In addition, the uPA/uPAR system as a therapeutic target has been proposed to reduce mortality of COVID-19 [3]; therefore, further evaluation of the active form of suPAR plasma levels in different symptom types of COVID-19 patients and asymptomatic carriers could still provide important indications for required early admission and treatment.

In our study, we found that active suPAR levels in all COVID-19 patients were significantly higher than in healthy controls (5.51 ± 2.53 ng/mL vs 1.97 ± 0.78 ng/mL, p < 0.0001) using a ELISA assay modified from our previously reported method [4] where the active suPAR was captured by a uPAR ligand and measured using a polyclonal anti-uPAR antibody. Strikingly, the active suPAR levels in asymptomatic carriers (8.08 ± 4.81 ng/mL) are not only significantly higher than those in healthy controls (p < 0.0001) but also slightly higher than those in COVID-19 patients (p = 0.0278) (Table 1, Fig. 1a). Even though more data needs to be collected and the background of these patients are not clear, this is a significant research direction to pursue. If asymptomatic carriers could be identified and quarantined in an early stage, it will prevent them from increasing the disease transmission to an uncontrollable manner.

Table 1.

The active suPAR levels in plasma are associated correlated with high-sensitivity C-reaction protein (hs-CRP), neutrophil/leukocyte ratio, and lymphocyte counts

Patient type Number of samples Active suPAR (ng/mL) hs-CRP (mg/L) Neutrophil/leukocyte ratio (%) Lymphocyte (×109/L)
Moderate 57 4.57 ± 2.35 3.01 ± 3.67 59.98 ± 9.34 1.62 ± 0.60
Severe 30 5.97 ± 2.31 38.79 ± 57.81 64.60 ± 11.23 0.97 ± 0.35
Critical 21 6.68 ± 2.54 135.39 ± 93.88 87.49 ± 9.53 0.66 ± 0.37
Asymptomatic 9 8.08 ± 4.81 1.29 ± 1.14 65.78 ± 9.30 1.57 ± 0.49
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Fig. 1.

Fig. 1

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Level of plasma active suPAR in different classifications. a Active suPAR level in COVID-19 patients and asymptomatic carriers, compared with active suPAR level in healthy controls. b Level of active suPAR between three different COVID-19 classifications including moderate, severe, and critical

Patients involved three types of symptoms: moderate, severe, and critical in our study (Table 1). Our data show that active suPAR levels increase as the disease worsens (Fig. 1b). Moreover, correlation analyses demonstrated that active suPAR levels are positively correlated with high-sensitivity C-reaction protein (hs-CRP), neutrophil/leukocyte ratio, and lymphocyte counts (Table 1).

Therefore, taken together with the results from Rovina et al., these results demonstrated that the active suPAR as a COVID-19 prognostic biomarker may assist in the early triage of SARS-CoV-2-infected persons to prevent virus transmission. Further studies are needed to see whether the elevation of suPAR plasma levels in COVID-19 patients is due to the enhanced over-expression of uPAR or due to their increased shedding from the cell surface.

Acknowledgement

Not applicable.

Abbreviations

COVID-19

Coronavirus disease 2019

ELISA

Enzyme-linked immunosorbent assay

hs-CRP

High-sensitivity C-reaction protein

SARS-CoV-2

Severe acute respiratory syndrome coronavirus 2

suPAR

Soluble urokinase plasminogen activator receptor

uPA

Urokinase plasminogen activator

Authors’ contributions

All authors had full access to all of the data in the study and take responsibility for the integrity of the data. LJ has written the letter. The authors read and approved the final manuscript.

Funding

This study is financially supported by grants from the National Key R&D Program of China (2017YFE0103200), Natural Science Foundation of China (82070142, 31670739, 22077016), Natural Science Foundation of Fujian Province (2018J01897 and 2018J01729), and Fuzhou Municipal Science and Technology Program (2020-XG-021).

Availability of data and materials

The dataset supporting the conclusion of this article is available from the corresponding author upon reasonable request.

Ethics approval and consent to participate

The study was approved by the Ethics Committee of the Fuzhou pulmonary hospital of Fujian. All subjects provided informed written consent documents in accordance with the Declaration of Helsinki before enrollment.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Footnotes

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Mingxiang Huang and Linlin Li have contributed equally to this work

Contributor Information

Mingdong Huang, Email: hmd_lab@fzu.edu.cn.

Longguang Jiang, Email: jianglg@fzu.edu.cn.

References

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Crit Care. 2020 Dec 29;24:704.

Authors’ response

Jesper Eugen-Olsen 5, Salim Hayek 6, Jochen Reiser 7,✉, Evangelos J Giamarellos-Bourboulis 8,9,✉

The urokinase plasminogen activator receptor (uPAR) is an immune cell expressed GPI-linked receptor that may be cleaved from the cell surface generating soluble uPAR (suPAR). There are three forms of the suPAR molecule, the full length 3-domain protein (DIDIIDIII), and the cleaved forms (DIIDIII) and DI; only DIDIIDIII can bind uPA with high affinity generating soluble DIDIIDIII/uPA complexes [5]. Both the full length and DIIDIII molecules have been shown to carry independent prognostic value [6].

Huang et al. report that “active suPAR” increases with severity of COVID-19,” but surprisingly find that the level is even higher among some of the 9 included asymptomatic carriers. As part of our “International consortium on inflammation in COVID-19,” we have tested almost 1000 COVID-19 patients for suPAR. Among patients with no or mild symptoms of infection, we find average levels about 4 ng/ml, much lower than those that are hospitalized [7]. To further confirm this finding, we measured suPAR in the plasma of 11 patients with very mild symptoms. All were adults who provided written informed consent with molecular identification of SARS-CoV-2 by routine real-time PCR in the nasopharyngeal secretions sampled by a standard collection swab. Blood sampling was done within 15 min after swab collection; median suPAR was 2.0 ng/ml (range 1.70–5.21 ng/ml).

In the above studies of our group, but also in the vast majority of published studies so far, suPAR is measured by the suPARnostic® assays. These assays are using two monoclonal antibodies (developed into lateral flow quick tests, enzyme immunoassays, and turbidimetric assays on Roche, Abbott, and Siemens platforms) and are the only CE/IVD approved suPAR assays for clinical decision making on the market.

Why this difference between the suPARnostic® assays and the enzyme immunoassay is described by Huang et al.? Likely, because the suPARnostic® assays are developed based on prognostic value using combinations of antibodies on plasma from patients with known disease progression to identify antibodies that bind the suPAR molecules with the highest clinical value. On the contrary, the assay described by Haung et al. may capture only a subgroup of the prognostic relevant suPAR molecules.

In conclusion, our data using the suPARnostic® assays both in a large published cohort of patients [1, 7] and in a recent cohort of mild cases from Greece support that patients with asymptomatic or mild COVID-19 have lower levels of suPAR than severe cases.

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Data Availability Statement

    The dataset supporting the conclusion of this article is available from the corresponding author upon reasonable request.

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