Materials and Reagents

Disposable tips
1. 10 μL capacity (Thermo Fisher Scientific, QSP, catalog number: 104-Q, Rockford, US)
2. 200 μL capacity (Thermo Fisher Scientific, QSP, catalog number: TF140-200-Q, Rockford, US)
3. 1 mL capacity (Thermo Fisher Scientific, QSP, catalog number: 112NXL-Q, Rockford, US)
1.5 mL Microcentrifuge tube (Thermo Fisher Scientific, Invitrogen, catalog number: AM12400, Carlsbad, US)
100 mm culture dish (Corning, Falcon, catalog number: 353003, Glendale, US)
Amicon Ultra-15 centrifugal filter units, 10 kDa MWCO (Sigma, Millipore, catalog number: UFC901024, Darmstadt, Germany)
Carbonate bi-carbonate coating buffer (Medicago, catalog number: 09-8922-100, Uppsala, Sweden)
Bovine serum albumin (Sigma, catalog number: 90604-29-8, Saint Louis, US)
Tween-20 (Thermo Fisher Scientific, catalog number: BP337500, Carlsbad, US)
pcDNA3 expression vector (Thermo Fisher Scientific, Invitrogen™, catalog number: V79020, Carlsbad, US)
HEK293 cells (ATCC, catalog number: CRL-1573, Manassas, US)
Lipofectamine 2000 transfection reagent (Thermo Fisher Scientific, Invitrogen, catalog number: 11668027, Carlsbad, US)
Geneticin/G418 (Thermo Fisher Scientific, Gibco, catalog number: 11811023, Carlsbad, US)
Dulbecco’s Modified Eagle’s Medium (Life Sciences, Corning, catalog number: 10-017-CV, Glendale, US)
Fetal bovine serum (Thermo Fisher Scientific, Gibco, catalog number: 10099141, Carlsbad, US)
Commercial CD89 protein, human, recombinant (Sino Biological, catalog number: 10414-H08H, Beijing, China)
Human IgA1 standard, myeloma (Sigma, catalog number: 400109, Saint Louis, US)
PBS powder (Sigma, catalog number: P3813, Saint Louis, US)
3×FLAG peptide (Sigma, catalog number: F4799, Saint Louis, US)
ANTI-FLAG M2 affinity gel (Sigma, catalog number: A2220, Saint Louis, US)
Slide-A-Lyzer Dialysis Cassettes (Thermo Scientific, catalog number: 66380, Carlsbad, US)
Bio-Rad Protein Assay Dye Reagent (Bio-Rad, catalog number: #5000006, Hercules, US)
Primary antibodies and secondary antibodies
1. HRP-conjugated anti-DDDDK tag antibody [M2] (Abcam, catalog number: ab49763, Waltham, US)
2. HRP-conjugated anti-human IgA antibody [1H9] (Abcam, catalog number: ab7383, Waltham, US)
3. Recombinant anti-CD89 antibody (Abcam, catalog number: ab124717, Waltham, US)
ECL Western Blotting Substrate (Thermo Scientific, catalog number: 32209, Carlsbad, US)
Nunc MaxiSorp 96-Well plates (Thermo Fisher Scientific, catalog number: 44-2404-21, Glendale, US)
Immuno Clear Standard Modules (Thermo Scientific, catalog number: 468667, Carlsbad, US)
3,3′,5,5′-Tetramethylbenzidine (TMB) substrate set (BD, catalog number: 555214, Franklin Lakes, US)
Sulfuric acid (Thermo Scientific, catalog number: N600, Carlsbad, US)
Penicillin and streptomycin (Thermo Scientific, catalog number: 15140122, Carlsbad, US)
Cell culture mediums (see Recipes)
Growth medium
Selection medium
Cryopreservation medium
0.05 M carbonate sodium buffer (pH 9.6) (see Recipes)
0.01 M Phosphate Buffered Saline (PBS) buffer (see Recipes)
ELISA washing buffer (0.1% PBST buffer, pH 7.4) (see Recipes)
ELISA blocking buffer (1% BSA/PBST buffer) (see Recipes)
ELISA stop solution (1 M H₂SO₄) (see Recipes)

Equipment

-80°C freezer (e.g., Thermo Scientific Forma 900 Series)
Fixed volume single-channel pipettes (e.g., Thermo Fisher Scientific, catalog number: 4651140)
Refrigerated tabletop centrifuge (e.g., Thermo Sorvall Legend XTR refrigerated centrifuge)
Microplate absorbance reader (e.g.,Bio-Rad, catalog number: 1681130XTU)
CO₂ incubators (e.g., Thermo Fisher Scientific, catalog number: 51032875)
Liquid nitrogen tank (e.g., Thermo Scientific)
Gel imaging system (e.g., Biorad Gel Doc XRS+ Imaging System, catalog number: 1708265)

Procedure

Generation of stable cell lines for the expression of recombinant CD89
If using commercial CD89 from Sino Biological, skip sections A and B, and go directly to section C.
1. To generate recombinant soluble CD89 protein (rCD89), synthesize DNA that encodes human FcαRI/CD89 ectodomain (Met¹-Asn²²⁷ based on RefSeq accession: NP_001991.1) fused to a C-terminus 3×Flag of DYKDHD-G-DYKDHD-I-DYKDDDDK sequence.
2. Clone the cDNA fragment into pcDNA3 vector for expression using mammalian cells.
3. Transfect pcDNA3-rCD89-Flag plasmid into HEK293 cells cultured in growth medium using Lipofectamine 2000 in 6-well plates following the standard transfection protocol. The plasmid (2.5 μg, diluted in 100 μL of Opti-MEM medium) and Lipofectamine 2000 (7.5 μL, diluted in 100 μL of Opti-MEM medium) are mixed and incubated at room temperature for 15 min, then added to the well and mixed with the culture medium by gently pipetting.
4. After one day, dissociate the transfected cells by trypsin digestion and transfer the cells to 100 mm cell culture dishes with five-fold serial dilutions (five 100 mm dishes are used, with dilution ranges from 1:5 to 1:3125). Maintain the cells in 15 mL of selection medium.
5. Replace the selection medium every 3 days for 14 days until distinct cell clones are formed with an average of 100–500 cells per clone.
6. Isolate well-formed individual stable cell colonies under a microscope using a 20 μL pipette (by gently scratching and then catching the detached cell clones) and seed them in 96-well plates.
7. Maintain the cells in the selection medium for 5–7 days without changing the medium. Test the medium in each well for recombinant expression of rCD89-Flag by dot-blotting using HRP-conjugated anti-DDDDK tag antibody.
  1. Prepare a strip of nitrocellulose membrane and draw grids (1 cm × 1 cm) on it with a pencil.
  2. Spot 5 µL of medium samples onto the nitrocellulose membrane at the center of the grids. Minimize the area that the samples penetrate (usually less than 4 mm in diameter) by applying it slowly. Wait until the membrane is dry.
  3. Block the membrane with 5% dry milk in TBST and incubate for 1 h at room temperature.
  4. Pour off the block buffer, and keep the membrane always wet for the remainder of the procedure.
  5. Incubate the membrane with HRP-conjugated anti-DDDDK tag antibody (dilute at the ratio of 1:1,000 with 2% non-fat milk in TBST) for 1 h at room temperature.
  6. Wash the membrane three times with TBST.
  7. Incubate the membrane with ECL reagent and image with a chemiluminescence imaging system. The ECL reagent detects protein at the picogram level.
8. Select 2–3 stable cell clones with the highest recombinant protein expression and expend these individual clones to culture in 100 mm dishes.
9. Freeze down stable cell clones with cryopreservation medium (2 × 10⁷ cells/mL) using a cell freezing container (e.g., Nalgene 5100-0036), and then store the cell bank in a liquid nitrogen tank.
Expression and purification of recombinant CD89-Flag
1. Culture a high-yielding stable cell clone in 100 mm dishes with DMEM supplemented with 10% FBS and 500 μg/mL G418.
2. When the cells grow to ~90% confluency, change the medium to serum-free DMEM and culture for another 5 days to allow the production of rCD89-Flag protein in the culture medium.
3. Harvest the medium (~100 mL) and then concentrate the medium with Amicon Ultra-15 filters with a molecular weight cut-off of 10,000 Da. Spin the filters at 4,000 × g at room temperature until the sample was concentrated to less than 5 mL.
4. Assemble a 5 mL gravity column packed with 2 mL of anti-flag M2 antibody-conjugated affinity gel. Load the concentrated medium into the column.
5. Wash the gravity column three times with PBS (30 mL each time). Then elute the recombinant protein with 5 mL of 3× Flag peptides at 150 μg/mL in PBS.
6. Collect the elution buffer containing the rCD89 protein, and dialyze the purified protein against PBS buffer overnight at 4°C by using Slide-A-Lyzer Dialysis Cassettes with a molecular weight cut-off of 10,000 Da.
7. Measure the total protein concentration using Bio-Rad protein assay reagent, following the manufacturer’s instruction.
8. Store the recombinant protein at -80°C.
Detection of poly-IgA complexes in plasma by performing rCD89-directed ELISA
1. Plate Preparation
  1. Dilute rCD89 protein in carbonate sodium buffer (pH = 9.6) to a final concentration of 10 μg/mL. Immediately coat a 96-well ELISA microplate or strips with 100 μL of rCD89 protein per well. Seal the plate and incubate the reactions overnight at 4°C.
  2. Aspirate each well and then wash the wells with 300 μL of washing buffer. Repeat the process two more times for a total of three rounds of washes. After the last wash, remove any remaining wash buffer by aspiration, and then by inverting the plate to be patted against a stack of clean paper towels.
  3. Block the plate by adding 300 μL of blocking buffer to each well. Incubate the blocking reactions at 37°C for 1 h.
  4. Repeat aspirating and washing cycles as described in step C1b. The plates are now ready for measuring samples. However, avoid letting the empty wells to get air dried for a long time.
2. Prepare plasma samples and IgA standard
  1. Dilute the plasma samples 1:1,000 in blocking buffer (Plasma can be from freshly harvested samples, or from frozen stocks retrieved from -80°C storage. Based on our test results, 2–3 rounds of freeze-thaw cycles with storage at -80°C do not significantly change the reading of poly-IgA contents using the assay. If there is any precipitation from the freeze-thaw process, plasma samples should be centrifuged to remove the precipitates at 3000 x g at 4°C for 15 min).
  2. Dilute purified human IgA1 standard in blocking buffer in a concentration series ranging from 500 μg/mL to 7.8125 μg/mL.
3. Assay procedure
  1. Add 100 μL of diluted plasma samples or IgA1 standards in blocking buffer to each well. Cover the plate with an adhesive strip and incubate the reactions for 3 h at 37°C.
  2. Perform aspiration/washing cycles as described in step C1b above.
  3. Dilute the detection antibody (HRP-conjugated anti-human IgA antibody) 1:1,000 in blocking buffer. Add 100 μL of detection antibody solution to each well. Cover the plate with a new adhesive strip and incubate the reactions for 1 h at 37°C.
  4. Wash the wells three times as described in step C1b.
  5. Add 100 μL of TMB substrate solution to each well. Incubate the reactions for 25 min at room temperature. Avoid placing the plate under direct light.
  6. Add 100 μL of stop solution to each well.
  7. Measure the optical density of each well using a microplate reader under dual-wavelength set at 450/570 nm.

Data analysis

For testing plate-to-plate variability, in addition to the human IgA1 standard series, a sample standard is also included on each plate as the quality control. Only when the coefficient of variation of the quality control between different test plates is less than 10% the test optical density value is considered stable and reliable.
Concentrations of measured poly-IgA complexes in plasma for each sample are estimated by four-parameter logistic equation:
[y = (A - D) / [1 + (x/C) ^ B] + D
where y = optical density value, x = concentration, A = minimum asymptote, B = slope factor, C = concentration corresponding to the response midway between A and D, and D = maximum asymptote] (Figure 2) (Zhang et al., 2021)].

Figure 2. The standard curve for determining the plasma concentration of poly-IgA complex as measured by rCD89-directed ELISA. The y-axis values are readings of the optical density of the TMB reactions at 450 nm. The x-axis values are marked as the corresponding concentrations of the human IgA1 standards (μg/mL). The data series (the red dots) is obtained from measurements of the human IgA1 standards between 7.8125 and 500 μg/mL. The fitting curve is derived from the four-parameter logistic regression model, which is subsequently used to calculate the unit concentration of poly-IgA complex in patient samples.
In this protocol, the concentration unit of poly-IgA complex is indexed as U/mL that is equally converted from the μg/mL value of measured IgA. The reason for using U/mL here instead of μg/mL is to clarify the measured content being poly-IgA, as opposed to total IgA.

Recipes

Growth medium
Dulbecco’s Modified Eagle’s Medium (DMEM)
10% fetal bovine serum (FBS)
100 U/mL penicillin and streptomycin
Selection medium
Growth medium supplemented with G418 to 1 mg/mL.
Cryopreservation medium
Growth medium supplemented with DMSO to a final concentration of 10%.
0.05 M carbonate sodium buffer (pH 9.6)
1. Deposit one tablet in a beaker placed on a magnetic stirrer.
2. Add 50 mL of deionized water and stir the solution for a few min.
3. Adjust the water up to 100 mL, stir until full dissolution, and the buffer is ready to use.
0.01 M Phosphate Buffered Saline (PBS) buffer
1. Dissolve a 1 L bag of PBS powder in 500 mL of deionized water.
2. Adjust the water up to 1,000 mL, stir until full dissolution, and the buffer is ready to use.
ELISA washing buffer (0.1% PBST buffer, pH 7.4)
Reagent Final concentration Amount
0.01 M PBS buffer 0.01M 999 mL
Tween-20 n/a 1 mL
Total n/a 1,000 mL
ELISA blocking buffer (1% BSA/PBST buffer)
Reagent Final concentration Amount
Bovine serum albumin 1% 1g
0.1%PBST buffer 0.1% 100 mL
Total n/a 100 mL
* Dissolve BSA in PBST buffer by gently rocking the capped container.
ELISA stop solution (1 M H₂SO₄)
Reagent Final concentration Amount
98% concentrated sulfuric acid 1 M 27.8 mL
ddH₂O 0.1% 472.2 mL
Total n/a 500 mL

Acknowledgments

This study was supported by National Natural Science Foundation of China grants 81670649 and 81925006, the Capital Health Development Research Project of China grant 2018-2-4073, Beijing Science and Technology Plan Project of China grant D181100000118003, and CAMS Innovation Fund for Medical Sciences grant 2019-I2M-5-046 (to J. Lv). This protocol was adapted from procedures published in Zhang et al. (2021).

Competing interests

J. Jin reports having an ownership interest in Accubit Inc.; being an advisor to Shenzhen Lujing Biotechnology Corporation, Limited, which is developing this technology toward clinical application in diagnosis; having consultancy agreements with Alebund Pharmaceuticals, Mannin Research Inc., and Qbio Med, Inc.; and serving as a scientific advisor for, or member of, Scientific Reports. J. Jin, J. Lv, and H. Zhang report applying for a patent related to the methodology described in this protocol for measuring the level of poly-IgA complex in clinical samples. H. Zhang reports serving as a vice-director of the nephrology committee in the Beijing Society of Medicine, board committee member of nephrology in the Chinese Medical Doctor Association, board committee member of the Chinese Society of Nephrology, member of the International Society of Nephrology (ISN)–Advancing Clinical Trials committee and member of ISN Sister Renal Centers Global Outreach committee and having consultancy agreements with Calliditas, Janssen, Novartis, and OMEROS. X. Li is an employee of Shenzhen Lujing Biotechnology Corporation, Limited. All remaining authors have nothing to disclose.

Ethics

The research was conducted in accordance with the principles of the Declaration of Helsinki and was approved by the local ethics committees.

References

Bakema, J. E. and van Egmond, M. (2011). The human immunoglobulin A Fc receptor FcαRI: a multifaceted regulator of mucosal immunity. Mucosal Immunol 4(6): 612-624.
Chen, A., Yang, S. S., Lin, T. J. and Ka, S. M. (2018). IgA nephropathy: clearance kinetics of IgA-containing immune complexes. Semin Immunopathol 40(6): 539-543.
Herr, A. B., Ballister, E. R. and Bjorkman, P. J. (2003). Insights into IgA-mediated immune responses from the crystal structures of human FcalphaRI and its complex with IgA1-Fc. Nature 423(6940): 614-620.
Hui, G. K., Wright, D. W., Vennard, O. L., Rayner, L. E., Pang, M., Yeo, S. C., Gor, J., Molyneux, K., Barratt, J. and Perkins, S. J. (2015). The solution structures of native and patient monomeric human IgA1 reveal asymmetric extended structures: implications for function and IgAN disease. Biochem J 471(2): 167-185.
Kanatsu, K., Doi, T., Sekita, K., Yoshida, H., Nagai, H. and Hamashima, Y. (1983). A comparative immunologic study of IgA nephropathy. Am J Kidney Dis 2(6): 618-625.
Lai, K. N., Tang, S. C., Schena, F. P., Novak, J., Tomino, Y., Fogo, A. B. and Glassock, R. J. (2016). IgA nephropathy. Nat Rev Dis Primers 2: 16001.
Magistroni, R., D'Agati, V. D., Appel, G. B. and Kiryluk, K. (2015). New developments in the genetics, pathogenesis, and therapy of IgA nephropathy. Kidney Int 88(5): 974-989.
Maliszewski, C. R., March, C. J., Schoenborn, M. A., Gimpel, S. and Shen, L. (1990). Expression cloning of a human Fc receptor for IgA. J Exp Med 172(6): 1665-1672.
Monteiro, R. C. and Van De Winkel, J. G. (2003). IgA Fc receptors.Annu Rev Immunol 21: 177-204.
Moroni, G., Belingheri, M., Frontini, G., Tamborini, F. and Messa, P. (2019). Immunoglobulin A Nephropathy. Recurrence After Renal Transplantation. Front Immunol 10: 1332.
Novak, J., Raskova Kafkova, L., Suzuki, H., Tomana, M., Matousovic, K., Brown, R., Hall, S., Sanders, J. T., Eison, T. M., Moldoveanu, Z., et al. (2011). IgA1 immune complexes from pediatric patients with IgA nephropathy activate cultured human mesangial cells. Nephrol Dial Transplant 26(11): 3451-3457.
Novak, J., Tomana, M., Matousovic, K., Brown, R., Hall, S., Novak, L., Julian, B. A., Wyatt, R. J. and Mestecky, J. (2005). IgA1-containing immune complexes in IgA nephropathy differentially affect proliferation of mesangial cells. Kidney Int 67(2): 504-513.
Reterink, T. J., van Zandbergen, G., van Egmond, M., Klar-Mohamad, N., Morton, C. H., van de Winkel, J. G. and Daha, M. R. (1997). Size-dependent effect of IgA on the IgA Fc receptor (CD89). Eur J Immunol 27(9): 2219-2224.
Zhang, X., Lv, J., Liu, P., Xie, X., Wang, M., Liu, D., Zhang, H. and Jin, J. (2021). Poly-IgA Complexes and Disease Severity in IgA Nephropathy. Clin J Am Soc Nephrol 16(11): 1652-1664.
Zhang, X., Xie, X., Shi, S., Liu, L., Lv, J. and Zhang, H. (2020). Plasma galactose-deficient immunoglobulin A1 and loss of kidney function in patients with immunoglobulin A vasculitis nephritis. Nephrol Dial Transplant 35(12): 2117-2123.