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The prognostic value of the suPARnostic®ELISA in HIV-1 infected individuals is not affected by uPAR promoter polymorphisms
© Schneider et al; licensee BioMed Central Ltd. 2007
Received: 01 June 2007
Accepted: 16 November 2007
Published: 16 November 2007
High blood levels of soluble urokinase Plasminogen Activator Receptor (suPAR) are associated with poor outcomes in human immunodeficiency-1 (HIV-1) infected individuals. Research on the clinical value of suPAR in HIV-1 infection led to the development of the suPARnostic® assay for commercial use in 2006. The aim of this study was to: 1) Evaluate the prognostic value of the new suPARnostic® assay and 2) Determine whether polymorphisms in the active promoter of uPAR influences survival and/or suPAR values in HIV-1 patients who are antiretroviral therapy (ART) naive.
DNA samples were collected retrospectively from 145 Danes infected with HIV-1 with known seroconversion times. In addition, plasma was collected retrospectively from 81 of these participants for use in the suPAR analysis. Survival was analysed using Kaplan Meier analysis.
Survival was strongly correlated to suPAR levels (p < 0.001). Levels at or above 6 ng/ml were associated with death in 13 of 27 patients within a two-years period; whereas only one of 54 patients with suPAR levels below 6 ng/ml died during this period. We identified two common uPAR promoter polymorphisms: a G to A transition at -118 and an A to G transition at -465 comparative to the transcription start site. These promoter transitions influenced neither suPAR levels nor patient survival.
Plasma suPAR levels, as measured by the suPARnostic® assay, were strongly predictive of survival in ART-naïve HIV-1 infected patients. Furthermore, plasma suPAR levels were not influenced by uPAR promoter polymorphisms.
Patients with HIV infection receive regular clinical follow-up to assess the need for more invasive treatment regimens such as initiation of ART. Currently, this assessment relies on the evaluation of HIV RNA viral load and CD4 cell count; the former of which requires expensive, high technology laboratory facilities. Thus, there is a need for robust, reliable prognostic markers for HIV infection that can also be used in resource-limited settings. Inflammation increases HIV replication and CD4 T cell depletion  and markers of inflammation are potential candidates as prognostic markers for HIV. However, the plasma level of these markers should be independent of genetic polymorphisms in order to be reliable biomarkers.
An elevated level of suPAR is predictive of negative clinical outcome in a number of different diseases such as HIV-1, tuberculosis , pneumococcal bacteraemia , rheumatoid arthritis , multiple sclerosis  and certain forms of cancer [7, 8]. suPAR is an independent marker of survival in HIV-1 infection with a prognostic strength similar to that of CD4+ T-cell count and HIV-1 viral load [2, 9].
uPAR is a glycosylphosphatidylinositol (GPI)-linked 3-domain receptor expressed on monocytes, macrophages, activated T-lymphocytes, natural killer cells and neutrophils . uPAR interacts with several molecules including urokinase Plasminogen Activator (uPA), vitronectin and intracellular signalling molecules such as integrins (exp. CD11b/CD18) and a G-coupled receptor . uPAR is involved in several immune functions including cell adhesion and migration (for a review, see ). In vitro studies have shown a direct involvement of uPAR/uPA in the late stages of the HIV-1 lifecycle [13, 14].
The present study investigates whether plasma suPAR levels measured by the suPARnostic® assay are prognostic for HIV-1 disease progression and whether suPAR levels and survival are influenced by common genetic polymorphisms in the uPAR promoter region.
Patients and sample preparation
The seroconverter cohort consist of 145 HIV-1 infected Caucasians with documented time for seroconversion. DNA was isolated from these individuals using QIAamp Blood Mini Kit according to the manufacturer's protocol (QIAGEN, Valencia, Ca, USA) and stored at -20°C. The cohort comprised 122 males with a mean seroconvertion age of 32.0 years and 23 females who seroconverted at a mean age of 40.2 years. Seroconversion was defined as a seronegative and a seropositive HIV antibody test within a 12 months period. The time of seroconvertion is calculated as the midpoint in time between the last seronegative sample and the first seropositive sample. Patients were followed prospectively every 3–6 months. In this cross-sectional study, one plasma sample from each of the 81 patients taken before the introduction of ART on May 15th, 1996 was measured for suPAR (65 males, mean age 38.9 years and 16 females, mean age 44.4 years). Of these 81 patients, 61 patients had a CD4 count included in their medical records within three months of the blood sample date.
The AccuPrime PCR (Invitrogen, Carlsbad, Ca, USA) was performed according to the manufactures instructions using 3 μL DNA template and a primermix of 10 μM sense primer (uPARpr_s) 5'-ACTACGCCCGGCTAATTTTT-3' and antisense (uPARpr_as) 5'-CCCCCTCAATTAGACCCTGT-3' (Taq-Copenhagen, Copenhagen, Denmark). PCR-program 94°C for 2 minutes; 30*(94°C for 25 seconds; 55°C for 25 seconds and 68°C for 60 seconds). All PCR-products were run on a 2% volume agarose gel (SeaKem GTG agarose, BMA, Rockland, ME, USA) stained by ethidium bromide with a 100 bp ladder (New England Biolabs, Beverly, MA, USA).
DNA from 52 individuals was used for sequencing. Prior to sequencing the PCR product was purified using a PCR clean-up-system (Promega, Madison, WI, USA) according to the manufacturers protocol. Sequencing was carried out using 0,5 μL Terminator Ready Reaction Mix (BigDye Terminator v3.1 Cycle sequencing Kit, Applied Biosystems, Foster City, Ca, USA), 3 μL PCR-product, 3pmol Primer (either uPARpr_s or uPARpr_as), 4 μL 5× Sequencing buffer and sterile water to 20 μL. PCR-program: 96°C for 60 seconds; 25*(96°C for 10 seconds, 50°C for 5 seconds, 60°C for 4 minutes) followed by a sodium precipitation and sequencing on an ABI PRISM 3100 Genetic Analyzer (Applied Biosystems).
Restriction fragment length polymorphisms analysis (RFLP)
A hot start PCR was performed according to manufactures instructions (Qiagen), using 10 μL 10*PCR-buffer (including 15 mM MgCl2), 200 μM of each dNTP, 0,2 μM of each primer (uPARpr_s and uPARpr_as), 2.5 units HotStarTaq and 2 μl template DNA per reaction under a PCR-program of 95°C for 15 minutes; 35*(95°C for 30 seconds; 60°C for 30 seconds; 72°C for 1 minute); 72°C for 8 minutes.
Eci-1 restriction analysis was carried out using 1,5 units Eci-1 to 10 μL PCR-product with 1*NEBuffer2 and 100 μg/ml Bovine Serum Albumin (BSA) in a total of 15 μL pr. reaction and a control without Eci-1. MspA1 l restriction analysis was done using 2 units MspA1 l to 10 μL PCR-product with 1*NEBuffer4 and 100 μg/ml BSA in a total of 15 μL per reaction and a control without MspA1 l (New England Biolabs). Following incubation at 37°C for 2 hours, the RFLP product was analysed on 2% agarosegel (SeaKem GTG agarose, BMA) using ethidium bromide staining and a 100 bp ladder (New England Biolabs).
SuPAR measurements by Enzyme linked immunosorbent assay (ELISA)
SuPAR was measured using the suPARnostic® assay (ViroGates, Lyngby, Denmark) according to the manufactures instructions. Samples were labelled with a number and the technician was blinded to the identity of the patient sample. Briefly, a mastermix of 25 ul plasma and 225 ul assay buffer (containing HRP-labelled secondary antibody) was prepared and 100 ul was added in duplicates onto an ELISA plate (pre-coated from manufactures with catching antibody). After one hour of incubation, the plate was washed, substrate added for 20 minutes and reaction was stopped with 50 ul 0.5 M H2SO4. Plates were measured at 450 nM with reference 630 nM. One kit measured 39 samples in duplicates in less than two hours. The measured sample intra-assay variation was 3.0 % and inter-assay variation was 10.0 %. This is similar to the inter- and intra-assay variations described in the manufactures kit protocol (1.3 – 4.7% and 1.7 – 5.1%, respectively). The kit standard curve is validated to measure suPAR levels between 0.6 to 22.0 ng/ml with a detection limit (LLOD) of 0.1 ng/ml.
Comparisons were done using the nonparametric Mann-Whitney U test and Pearson Rank test. Heredity of Mentel was tested by the Hardy-Weinberg Equilibrium, and survival of the seroconverters was analyzed using Kaplain-Meier. For the survival analysis, patient follow-up was censored on May 15th, 1996 when HAART was introduced to the cohort. The level of significance was set to 0.05. Data were analyzed using the SPSS software, version 13.0.
Plasma suPAR measurements and HIV-1 disease progression
Allocation of patients according to suPAR below or above median
Low suPAR < 4.67 ng/mL (N = 40)
High suPAR ≥ 4.67 ng/mL (N = 41)
Low vs high P (Mann-Whitney U test)
Age at suPAR meas. (years)*
Time from seroconversion to suPAR meas. (years)*
Death within 2 years (Y/N)
Median (range) follow-up (years) from sample to 15th May 1996*
5.94 (0.21 – 13.63)
5.38 (0.35 – 10.68)
Death before 15th May 1996 (Y/N)
uPAR promoter restriction fragment length polymorphism assay
uPAR promoter transitions and HIV-1 disease progression
To investigate whether the uPAR promoter transitions influence HIV disease progression, the entire seroconverter cohort (N = 145) was analyzed for the promoter transitions using the RFLP assay. In this cohort, 130 (≈ 90%) were -118 G/G carriers and 15 (≈ 10%) patients were G/A heterozygotes while no homozygous A/A carriers were found. With regard to the -465A/G transition, 84 (≈ 58%) were A/A, 55 (≈ 38%) were A/G heterozygotes and 6 (≈ 4%) were G/G homozygotes. The mutations were in Hardy-Weinberg Equilibrium. No individuals were homozygotes for one of the transitions and heterozygote for the other transition, whereas a total of six individuals were heterozygotes for both transitions. By RFLP with MspA1 l and Eci-1 on PCR-products from these six individuals, fragments matching a restriction pattern of 709, 348, 184/177 and 85 bp were identified. This is consistent with one of the alleles not to be restricted by Eci-1, while the other allele additionally is restricted by MspA1 l, indicating that the two polymorphism are not travelling on the same allele and thereby are in genetic disequilibrium (see figure 4).
The aim of the current study was to evaluate the prognostic value of the newly available suPARnostic® assay in a cohort of HIV infected patients who were ART naïve. Furthermore, this study was designed to assess whether suPAR values, as measured by the new assay, are influenced by polymorphisms in the active region of the uPAR promoter.
We hypothesize that elevated plasma suPAR levels indicate a heightened inflammatory state. SuPAR correlates to C-reactive protein , which also predicts survival rates in HIV-1 infected individuals . Inflammation and immune activation are believed to be drivers of HIV replication and CD4 T-cell depletion [24, 25].
In agreement with the inflammation hypothesis, previous studies have shown a negative correlation between suPAR levels and CD4 T-cell counts and a positive correlation between suPAR and HIV viral load [2, 9] Likewise, we observed a negative correlation between suPAR levels and CD4 count in the present study, although it did not reach significance, which is likely due to the small number of patients included in the present study. In agreement with previous studies on suPAR and HIV-1, it appears that both suPAR levels and CD4 T-cell counts are independent predictors of mortality in HIV infection.
To further explore the combined prognostic value of suPAR and CD4, we plotted patients who died within a two-year follow-up period in a CD4/suPAR graph. Patients with a low CD4 count (defined as below 200) and high suPAR levels (defined as above 6 ng/ml) had high two-year mortality while those with low CD4 and low suPAR levels were still alive after two years. Thus, suPAR and CD4 both added clinical value on the risk of mortality in this cohort of non-ART-treated HIV-1 patients.
A cut-off limit for suPAR has yet to be defined. In this study, only 1 of 54 patients with plasma suPAR levels below 6 ng/ml died within two years following blood sampling, while 13 of 27 patients with suPAR at or above 6 ng/ml died in the same period (figure 3). We focused the analysis of suPARs prognostic value to a two-year period of the following two reasons: 1) Disease progression biomarkers, including CD4 and viral load are measured at regular intervals (3 – 6 months) to monitor the state of the patient. Similarly, other biomarkers, such as suPAR, should provide useful and immediate prognostic clinical information 2) Due to the small number of patients included in the present study, the numbers were too small for meaningful statistical analysis following this period. Hence, larger studies are needed to confirm whether 6 ng/ml is a relevant cut-of suPAR and longitudinal studies should address the dynamics of suPAR in relation to HIV disease progression.
Two common mutations were defined in this study: a G to A transition at -118 and an A to G transition at -465 upstream of the transcription start site. Neither of these mutations had any influence on survival nor suPAR plasma levels. Previous studies have shown that in vitro regulation of the PEA3/etc site at -247 to -241 could influence the promoter activity [18, 22], however these studies did not analyze plasma suPAR levels.
This is the first paper that applies the suPARnostic® assay to non-ART HIV disease progression. A resent South African study employed the suPARnostic® assay to individuals initiating ART . In 293 HIV infected initiating ART with a median CD4 count of 47 cells per ul and followed for 4 months, pre-treatment CD4 and suPAR levels were predictors of mortality (39 died) during the 4 month treatment period. In multivariate analysis, only suPAR levels remained significantly associated with survival (RH per log suPAR increase 10.0, 95%CI 2.8 – 35.7) .
This study confirms that the suPAR level measured using the suPARnostic® assay is an independent prognostic marker of mortality in HIV-1 patients who are not on ART treatment. Moreover, these results suggest that patients with suPAR levels at or above 6 ng/ml should be considered for initiation of ART, in particular in cases with CD4 between 350 and 200 cells per ul. Finally, this study found that the value of suPAR levels as a biomarker for survival in HIV patients is not affected by uPAR promoter polymorphisms.
- Rodriguez B, Sethi AK, Cheruvu VK, Mackay W, Bosch RJ, Kitahata M, Boswell SL, Mathews WC, Bangsberg DR, Martin J, Whalen CC, Sieg S, Yadavalli S, Deeks SG, Lederman MM: Predictive value of plasma HIV RNA level on rate of CD4 T-cell decline in untreated HIV infection. JAMA. 2006, 296: 1498-1506. 10.1001/jama.296.12.1498.View ArticlePubMedGoogle Scholar
- Sidenius N, Sier CF, Ullum H, Pedersen BK, Lepri AC, Blasi F, Eugen-Olsen J: Serum level of soluble urokinase-type plasminogen activator receptor is a strong and independent predictor of survival in human immunodeficiency virus infection. Blood. 2000, 96: 4091-4095.PubMedGoogle Scholar
- Eugen-Olsen J, Gustafson P, Sidenius N, Fischer TK, Parner J, Aaby P, Gomes VF, Lisse I: The serum level of soluble urokinase receptor is elevated in tuberculosis patients and predicts mortality during treatment: a community study from Guinea-Bissau. Int J Tuberc Lung Dis. 2002, 6: 686-692.PubMedGoogle Scholar
- Wittenhagen P, Kronborg G, Weis N, Nielsen H, Obel N, Pedersen SS, Eugen-Olsen J: The plasma level of soluble urokinase receptor is elevated in patients with Streptococcus pneumoniae bacteraemia and predicts mortality. Clin Microbiol Infect. 2004, 10: 409-415. 10.1111/j.1469-0691.2004.00850.x.View ArticlePubMedGoogle Scholar
- Slot O, Brunner N, Locht H, Oxholm P, Stephens RW: Soluble urokinase plasminogen activator receptor in plasma of patients with inflammatory rheumatic disorders: increased concentrations in rheumatoid arthritis. Ann Rheum Dis. 1999, 58: 488-492.View ArticlePubMedPubMed CentralGoogle Scholar
- Balabanov R, Lisak D, Beaumont T, Lisak RP, Dore-Duffy P: Expression of urokinase plasminogen activator receptor on monocytes from patients with relapsing-remitting multiple sclerosis: effect of glatiramer acetate (copolymer 1). Clin Diagn Lab Immunol. 2001, 8: 1196-1203. 10.1128/CDLI.8.6.1196-1203.2001.PubMedPubMed CentralGoogle Scholar
- Stephens RW, Nielsen HJ, Christensen IJ, Thorlacius-Ussing O, Sorensen S, Dano K, Brunner N: Plasma urokinase receptor levels in patients with colorectal cancer: relationship to prognosis. J Natl Cancer Inst. 1999, 91: 869-874. 10.1093/jnci/91.10.869.View ArticlePubMedGoogle Scholar
- Sier CF, Stephens R, Bizik J, Mariani A, Bassan M, Pedersen N, Frigerio L, Ferrari A, Dano K, Brunner N, Blasi F: The level of urokinase-type plasminogen activator receptor is increased in serum of ovarian cancer patients. Cancer Res. 1998, 58: 1843-1849.PubMedGoogle Scholar
- Ostrowski SR, Piironen T, Hoyer-Hansen G, Gerstoft J, Pedersen BK, Ullum H: High plasma levels of intact and cleaved soluble urokinase receptor reflect immune activation and are independent predictors of mortality in HIV-1-infected patients. J Acquir Immune Defic Syndr. 2005, 39: 23-31. 10.1097/01.qai.0000157950.02076.a6.View ArticlePubMedGoogle Scholar
- Plesner T, Behrendt N, Ploug M: Structure, function and expression on blood and bone marrow cells of the urokinase-type plasminogen activator receptor, uPAR. Stem Cells. 1997, 15: 398-408.View ArticlePubMedGoogle Scholar
- Resnati M, Pallavicini I, Wang JM, Oppenheim J, Serhan CN, Romano M, Blasi F: The fibrinolytic receptor for urokinase activates the G protein-coupled chemotactic receptor FPRL1/LXA4R. Proc Natl Acad Sci U S A. 2002, 99: 1359-1364. 10.1073/pnas.022652999.View ArticlePubMedPubMed CentralGoogle Scholar
- Blasi F, Carmeliet P: uPAR: a versatile signalling orchestrator. Nat Rev Mol Cell Biol. 2002, 3: 932-943. 10.1038/nrm977.View ArticlePubMedGoogle Scholar
- Wada M, Wada NA, Shirono H, Taniguchi K, Tsuchie H, Koga J: Amino-terminal fragment of urokinase-type plasminogen activator inhibits HIV-1 replication. Biochem Biophys Res Commun. 2001, 284: 346-351. 10.1006/bbrc.2001.4965.View ArticlePubMedGoogle Scholar
- Alfano M, Sidenius N, Panzeri B, Blasi F, Poli G: Urokinase-urokinase receptor interaction mediates an inhibitory signal for HIV-1 replication. Proc Natl Acad Sci U S A. 2002, 99: 8862-8867. 10.1073/pnas.142078099.View ArticlePubMedPubMed CentralGoogle Scholar
- Casey JR, Petranka JG, Kottra J, Fleenor DE, Rosse WF: The structure of the urokinase-type plasminogen activator receptor gene. Blood. 1994, 84: 1151-1156.PubMedGoogle Scholar
- Wang Y, Dang J, Johnson LK, Selhamer JJ, Doe WF: Structure of the human urokinase receptor gene and its similarity to CD59 and the Ly-6 family. Eur J Biochem. 1995, 227: 116-122. 10.1111/j.1432-1033.1995.tb20366.x.View ArticlePubMedGoogle Scholar
- Soravia E, Grebe A, De LP, Helin K, Suh TT, Degen JL, Blasi F: A conserved TATA-less proximal promoter drives basal transcription from the urokinase-type plasminogen activator receptor gene. Blood. 1995, 86: 624-635.PubMedGoogle Scholar
- Dang J, Boyd D, Wang H, Allgayer H, Doe WF, Wang Y: A region between -141 and -61 bp containing a proximal AP-1 is essential for constitutive expression of urokinase-type plasminogen activator receptor. Eur J Biochem. 1999, 264: 92-99. 10.1046/j.1432-1327.1999.00583.x.View ArticlePubMedGoogle Scholar
- Wang Y, Dang J, Wang H, Allgayer H, Murrell GA, Boyd D: Identification of a novel nuclear factor-kappaB sequence involved in expression of urokinase-type plasminogen activator receptor. Eur J Biochem. 2000, 267: 3248-3254. 10.1046/j.1432-1327.2000.01350.x.View ArticlePubMedGoogle Scholar
- Lengyel E, Wang H, Stepp E, Juarez J, Wang Y, Doe W, Pfarr CM, Boyd D: Requirement of an upstream AP-1 motif for the constitutive and phorbol ester-inducible expression of the urokinase-type plasminogen activator receptor gene. J Biol Chem. 1996, 271: 23176-23184. 10.1074/jbc.271.18.10672.View ArticlePubMedGoogle Scholar
- Allgayer H, Wang H, Gallick GE, Crabtree A, Mazar A, Jones T, Kraker AJ, Boyd DD: Transcriptional induction of the urokinase receptor gene by a constitutively active Src. Requirement of an upstream motif (-152/-135) bound with Sp1. J Biol Chem. 1999, 274: 18428-18437. 10.1074/jbc.274.26.18428.View ArticlePubMedGoogle Scholar
- Hapke S, Gawaz M, Dehne K, Kohler J, Marshall JF, Graeff H, Schmitt M, Reuning U, Lengyel E: beta(3)A-integrin downregulates the urokinase-type plasminogen activator receptor (u-PAR) through a PEA3/ets transcriptional silencing element in the u-PAR promoter. Mol Cell Biol. 2001, 21: 2118-2132. 10.1128/MCB.21.6.2118-2132.2001.View ArticlePubMedPubMed CentralGoogle Scholar
- Lau B, Sharrett AR, Kingsley LA, Post W, Palella FJ, Visscher B, Gange SJ: C-reactive protein is a marker for human immunodeficiency virus disease progression. Arch Intern Med. 2006, 166: 64-70. 10.1001/archinte.166.1.64.View ArticlePubMedGoogle Scholar
- Decrion AZ, Dichamp I, Varin A, Herbein G: HIV and inflammation. Curr HIV Res. 2005, 3: 243-259. 10.2174/1570162054368057.View ArticlePubMedGoogle Scholar
- McCune JM: The dynamics of CD4+ T-cell depletion in HIV disease. Nature. 2001, 410: 974-979. 10.1038/35073648.View ArticlePubMedGoogle Scholar
- Lawn SD, Myer L, Bangani N, Vogt M, Wood R: Plasma levels of soluble urokinase-type plasminogen activator receptor (suPAR) and early mortality risk among patients enrolling for antiretroviral treatment in South Africa. BMC Infect Dis. 2007, 7:41.: 41-10.1186/1471-2334-7-41.View ArticleGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2334/7/134/prepub
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