Nov 20 2019
The Allergy Explorer2 (ALEX2) is a quantitative in vitro diagnostic test for the measurement of allergen specific IgE (sIgE) and a semi-quantitative in vitro diagnostic test for the measurement of total IgE (tIgE) in human serum or plasma (exception EDTA-plasma). It is to be used by clinical chemistry laboratories, trained laboratory personnel and medical professionals for the purpose of supporting the clinical diagnosis of IgE mediated diseases, in conjunction with other clinical findings or diagnostic test results.
Allergic reactions are immediate type I hypersensitivity reactions and are mediated by antibodies belonging to the IgE class of immunoglobulins. After exposure to specific allergens, IgE–mediated release of histamine and other mediators from mast cells and basophils results in clinical manifestations such as asthma, allergic rhino-conjunctivitis, atopic eczema and gastrointestinal symptoms . Therefore, a detailed sensitization pattern to specific allergens assists in the evaluation of allergic patients [2-6].
All major type I allergen sources are covered by ALEX2. A complete list of ALEX2 allergen extracts and molecular allergens can be found at the bottom of this instruction. Link
For the correct use of ALEX2, it is necessary for the user to carefully read and follow these instructions for use. The manufacturer assumes no liability for any use of this test system which is not described in this document or for modifications by the user of the test system
ALEX2 is a solid-phase immunoassay. Allergens extracts or molecular allergens, which are coupled to nanoparticles, are deposited in a systematic fashion onto a solid phase forming a macroscopic array. First, the particle bound allergens react with specific IgE that is present in the patient’s sample. After incubation, non-specific IgE is washed off. The procedure continues by adding an enzyme labelled anti-human IgE detection antibody which forms a complex with the particle bound specific IgE. After a second washing step, substrate is added which is converted to an insoluble, coloured precipitate by the antibody-bound enzyme. Finally, the enzyme-substrate reaction is stopped by adding a blocking reagent. The amount of precipitate is proportional to the concentration of specific IgE in the patient sample. The lab test procedure is followed by image acquisition and analysis using the ImageXplorer device. The test results are analysed with MADx’s Raptor Analysis Software and reported in IgE response units (kUA/L). Total IgE results are also reported in IgE response units (kU/L).
The shipment of ALEX2 takes place at ambient temperature conditions. Nevertheless, the kit must be stored immediately upon delivery at 2-8°C. Stored correctly, ALEX2 and its components can be used until the indicated expiration date.
|Kit reagents are stable for 6 months after opening (at the indicated storage conditions).|
Dispose the used ALEX2 cartridge and unused kit components with laboratory chemical waste. Follow all national, state, and local regulations regarding disposal.
The meaning of the symbols stays the same, regardless of colour.
Warning (GHS pictogram)
Refer to safety data sheet for details
Indicates the manufacturer’s catalogue number so that the medical device can be identified.
Contains sufficient for <n> tests
Indicates the total number of IVD tests that can be performed with the IVD.
Do not use if package is damaged
Indicates a medical device that should not be used if the package has been damaged or opened.
Indicates the manufacturer’s batch code so that the batch or lot can be identified.
Consult instructions for use
Indicates the need for the user to consult the instructions for use.
Indicates the medical device manufacturer, as defined in EU Directives 90/385/ EEC, 93/42/EEC and 98/79/EC.
In vitro diagnostic medical device
Indicates a medical device that is intended to be used as an in vitro diagnostic medical device.
Do not re-use
Indicates a test that is intended for one use, or for use on a single patient during a single procedure.
Indicates the temperature limits to which the test (reagents) can be safely exposed to.
Indicates the date after which the test (reagents) is not to be used.
Each component (reagent) is stable until the date stated on each individual component’s label. It is not recommended to pool any reagents from different kit lots. For a list of allergen extracts and molecular allergens immobilized on the ALEX2 array, please contact firstname.lastname@example.org.
|ALEX2 kit components
|ALEX2 Cartridge||2 Blister á 10 ALEX2 for 20 analyses in total. Calibration via master curve - deposited in barcode of each array.||Ready for use. Store at 2-8°C until expiry date.|
|ALEX2 Sample Diluent||1 bottle á 9 mL||Ready for use. Store at 2-8°C until expiry date. Allow reagent to reach room temperature before use. Opened reagent is stable for 6 months at 2-8°C, includes CCD inhibitor.|
|ALEX2 Washing Solution||2 bottles á 50 mL||Ready for use. Store at 2-8°C until expiry date. Allow reagent to reach room temperature before use. Opened reagent is stable for 6 months at 2-8°C.|
|ALEX2 Detection Antibody||1 bottle á 11 mL||Ready for use. Store at 2-8°C until expiry date. Allow reagent to reach room temperature before use. Opened reagent is stable for 6 months at 2-8°C.|
|ALEX2 Substrate Solution||1 bottle á 11 mL||Ready for use. Store at 2-8°C until expiry date. Allow reagent to reach room temperature before use. Opened reagent is stable for 6 months at 2-8°C.|
|ALEX2 Stop Solution||1 bottle á 2.4 mL||Ready for use. Store at 2-8°C until expiry date. Allow stop solution to reach room temperature before use. Opened reagent is stable for 6 months at 2-8°C. May appear as a turbid solution after prolonged storage. This has no effect on results.|
Maintenance services according to manufacturer’s instructions.
Do not touch the array surface. Any surface defects caused by blunt or sharp objects can interfere with the correct readout of the results. Do not acquire ALEX2 images before array is completely dry (dry at room temperature).
Preparation of samples: Serum or plasma (heparin, citrate, no EDTA) samples from capillary or venous blood can be used. Blood samples can be collected using standard procedures. Store samples at 2–8°C for up to one week. Keep serum and plasma samples at -20°C for prolonged storage. Shipment of serum/plasma samples at room temperature is applicable. Always allow samples to reach room temperature before use.
Incubation chamber: Close lid for all assay steps to prevent drop in humidity.
Parameters of Procedure
It is not recommended to run more assays than can be pipetted in 8 min. All incubations are performed at room temperature, 20-26°C.
|All reagents are to be used at room temperature (20-26°C). The assay must not be performed in direct sunlight.|
Prepare incubation chamber
Open incubation chamber and place paper towels on bottom part. Soak paper towels with purified water until no dry parts of the paper towels are visible.
1. Sample incubation/CCD inhibition
Take out the needed number of ALEX2 cartridges and place them into the array holder(s). Add 400 μL of ALEX2 sample diluent to each cartridge. Add 100 μL patient sample to the cartridges. Ensure that the resulting solution is spread evenly. Place the cartridges onto the lab rocker and start the serum incubation with 8 rpm for 2 hours. Close incubation chamber before starting the lab rocker. After 2 hours, discharge the patient samples into a collection container. Carefully wipe off droplets from the cartridge using a paper towel.
|Avoid touching the array surface with the paper towel! Avoid any carry over or cross-contamination of patient samples between individual ALEX2 cartridges!|
Optional or positive Hom s LF (CCD marker): with the standard CCD antibody inhibition protocol (as described in paragraph 2: sample incubation/CCD inhibition) the CCD inhibition efficiency is 85%. If a higher rate of inhibition efficiency is required, prepare a 1 mL sample tube, add 400 μL sample diluent and 100 μL serum. Incubate for 30 minutes (non-shaking) and then proceed with the usual assay procedure.
Note: The extra CCD inhibition step leads in many cases to an inhibition rate for CCD antibodies of above 95%.
1a. Washing I
Add 500 μL ALEX2 Washing Solution to each cartridge and incubate on the lab rocker (at 8 rpm) for 5 minutes. Discharge the washing solution into a collection container and vigorously tap the cartridges on a stack of dry paper towels.
Repeat this step 2 more times.
2. Add detection antibody
Add 500 μL of ALEX2 Detection Antibody to each cartridge.
|Make sure that the complete array surface is covered by the ALEX2 Detection Antibody solution.|
Place the cartridges into the incubation chamber on the lab rocker and incubate at 8 rpm for 30 minutes. Discharge the detection antibody solution into a collection container. Carefully wipe off remaining droplets from the cartridges using a paper towel.
2a. Washing II
Add 500 μL ALEX2 Washing Solution to each cartridge and incubate on the lab rocker at 8 rpm for 5 minutes. Discharge the washing solution into a collection container and vigorously tap the cartridges on a stack of dry paper towels.
Repeat this step 4 more times.
3+4. Add substrate solution and stop substrate reaction
Add 500 μL of ALEX2 Substrate Solution to each cartridge. Start a timer with filling the first cartridge and proceed with the filling of the remaining cartridges. Make sure that the complete array surface is covered by the substrate solution and incubate the arrays for 8 minutes without shaking (lab rocker at 0 rpm and in horizontal position).
After exactly 8 minutes, add 100 μL of the ALEX2 Stop Solution to all cartridges, starting with the first cartridge to assure that all arrays are incubated for the same time with the Substrate solution. Carefully agitate to evenly distribute the stop solution in the array cartridges, after the stop solution was pipetted onto all arrays. Afterwards discharge substrate/stop solution from the cartridges and wipe off any remaining droplets from the cartridges using a paper towel.
|Do NOT SHAKE during substrate incubation!!|
4a. Washing III
Add 500 μL ALEX2 Washing Solution to each cartridge and incubate on the lab rocker at 8 rpm for 30 seconds. Discharge the washing solution into a collection container and vigorously tap the cartridges on a stack of dry paper towels.
5. Image analysis
After finishing the assay procedure, air dry the arrays at room temperature until they are completely dry (can take up to 45 min).
|The complete drying is essential for the sensitivity of the test. Only completely dried arrays provide an optimal signal to noise ratio.|
Finally, the dried arrays are scanned with the ImageXplorer and analysed with Raptor software (see details in the Raptor software handbook). The Raptor software is only verified in combination with the ImageXplorer instrument, therefore MADx does not take any responsibilities for results, which have been obtained with any other image capture device (like scanners).
Systematic variations in signal levels between lots are normalized by heterologous calibration against an IgE reference curve. A curve fit is calculated, and the resulting equation applied to transform arbitrary intensity units into quantitative units. Curve parameters for each lot are adjusted by in-house reference testing against a serum preparation tested on ImmunoCAP (Thermo Fisher Scientific) for specific IgE against several allergens. The ALEX2 results are therefore indirectly traceable against the WHO reference preparation 11/234 for total IgE. Lot specific calibration parameters are encoded in the barcode. ALEX2 sIgE test results are expressed as kUA/L. Total IgE results are semi-quantitative and calculated from an anti-IgE measurement with lot-specific calibration factors encoded in the ALEX2 barcode.
Specific IgE: 0.3-50 kUA/L quantitative
Total IgE: 20-2500 kU/L semi-quantitative
Record keeping for each assay
According to good laboratory practice it is recommended to record the lot numbers of all reagents used.
According to good laboratory practice it is recommended that quality control samples are included within defined intervals.
For the image analysis of processed arrays, the ImageXplorer is to be used. ALEX2 images are automatically analysed using MADx’s Raptor analysis software and a report is generated summarising the results for the user.
ALEX2 is a quantitative method for specific IgE and semi-quantitative method for total IgE. Allergen specific IgE antibodies are expressed as IgE response units (kUA/L), total IgE results as kU/L. MADx’s Raptor analysis software automatically calculates and reports sIgE results (quantitatively) and tIgE results (semi- quantitatively).
A definitive clinical diagnosis should only be made in conjunction with all available clinical findings by medical professionals and shall not be based on results of a single diagnostic method only.
In certain areas of application (e.g. food allergy), circulating IgE antibodies may remain undetectable although a clinical manifestation of food allergy against a certain allergen may be present, because these antibodies may be specific to allergens that are modified during industrial processing, cooking or digestion and hence do not exist in the original food for which the patient is tested.
Negative venom results only indicate undetectable levels of venom specific IgE antibodies (e.g. due to long term non-exposure) and do not preclude the existence of clinical hypersensitivity to insect stings.
The close association between allergen specific IgE antibody levels and allergic disease is well known and is described thoroughly in literature . Each sensitized patient will show an individual IgE profile when tested with ALEX2. The IgE response with samples from healthy non-allergic individuals will be below 0.3 kUA/L for single molecular allergens and for allergen extracts when tested with ALEX2. Good laboratory practice recommends that each laboratory establishes its own range of expected values.
The lot-to-lot variation was determined on 3 cartridge lots in three sperate runs. Multi-sensitized samples were included in the study. The study comprised 319 allergen per sample combinations covering 191 individual allergens at 3 different levels (> 10 kUA/L, 1-10 kUA/L and 0.3-1 kUA/L .
|Concentration - kUA/L||Intra CV%||Inter CV%||Total CV%|
|≥0.3 - <1.0||18.4||26.1||24.7|
|≥1 - <10||11.6||12.7||12.1|
In the repeatability study, multi-sensitized samples were tested 10 times by the same operator on different days. The study comprised 319 allergen per sample combinations covering 165 individual allergens at 3 different levels (>10 kUA/L, 1-10 kUA/L and 0.3 - 1 kUA/L) .
|Concentration - kUA/L||Total CV%|
|≥0.3 - <1.0||25.6|
|≥1 - <10||13.8|
The Limit of Detection was determined in accordance with CLSI guideline EP17-A  for representative allergen components and was below 0.3 kUA/L for all allergen components and all allergen extracts.
There is no detectable cross-reactivity with other human Immunoglobulins (IgA, IgG1, IgG2, IgG3, IgG4 and IgM) at normal physiological concentrations.
There is no detectable interference with bilirubin, cholesterol/triglycerides and haemoglobin at normal physiological concentrations.
Neither is there an interference with tIgE which was tested in concentrations of up to 3000 kU/L.
The herein presented performance data were obtained using the procedure outlined in this Instructions for Use. Any change or modification in the procedure may affect the results and Macro Array Diagnostics disclaims all warranties expressed (including the implied warranty of merchantability and fitness for use) in such an event. Consequently, Macro Array Diagnostics and its authorized distributors shall not be liable for damages indirect or consequential in such an event.
Allergen extracts: Aca m, Aca s, Ach d, Ail a, All c, All s, Ama r, Amb a, Ana o, Api m, Ara h, Art v, Ave s, Ber e, Bos d meat, Bos d milk, Bro p, Cam d, Can f ♂ urine, Can s, Cap a, Cap h epithelia, Cap h milk, Car c, Car i, Car p, Che a, Che q, Chi spp., Cic a, Cit s, Cla h, Clu h, Cor a pollen, Cuc p, Cup s, Cyn d, Dau c, Dol spp., Ecu c milk, Equ c meat, Fag e, Fic c, Fic b, Fra e, Gad m, Gal d meat, Gal d white, Gal d yolk, Hel a, Hom g, Hor v, Jug r, Jun a, Len c, Lit s, Loc m, Lol spp., Lup a, Mac i, Man i, Mel g, Mor r, Mus a, Myt e, Ori v, Ory c meat, Ory s, Ost e, Ovi a epithelia, Ovi a meat, Ovi a milk, Pan b, Pan m, Pap s, Par j, Pas n, Pec spp., Pen ch, Per a, Per a, Pers a, Pet c, Phr c, Pim a, Pis s, Pla l, Pol d, Pop n, Pru du, Pru spp., Pyr c, Raj c, Rud spp., Sac c, Sal k, Sal s, Sco s, Sec c flour, Sec c pollen, Ses i, Sin a, Sol spp., Sola l, Sola t, Sus d epithel, Sus d meat, Ten m, Thu a, Tri fo, Tri s, Tyr p, Ulm c, Urt d, Vac m, Ves v, Zea m flour
Purified natural components: nAct d 1, nAct d 10, nAct d 2, nAct d 5, nApi m 1, nAra h 1, nAra h 3, nAra h 6, nBer e 1, nBos d 4, nBos d 5, nBos d 6, nBos d 8, nCan f 3, nCor a 11, nCor a 14, nCor a 9, nCup a 1, nEqu c 3, nFag e 2, nFel d 2, nGad m 1, nGad m 2 + 3, nGal d 1, nGal d 2, nGal d 3, nGal d 4, nGal d 5, nGly m 6, nGly m 8, nJug r 1, nJug r 2, nJug r 4, nJug r 6, nLol p 1, nMac i 2S Albumin, nMal d 2, nMus m 1, nOle e 1, nPap s 2S Albumin, nPen m 1, nPho d 2, nPis v 2, nPis v 3, nSes i 1, nSin a 1, nSola l 6, nTri a aA_TI, nVit v 1
recombinant components: rPru p 3, rAln g 1, rAln g 4, rAlt a 1, rAlt a 6, rAmb a 1, rAmb a 4, rAna o 2, rAna o 3, rAni s 1, rAni s 3, rApi g 1, rApi g 2, rApi g 6, rApi m 10, rAra h 15, rAra h 2, rAra h 8, rAra h 9, rArg r 1, rArt v 1.0101, rArt v 3.0201, rAsp f 1, rAsp f 3, rAsp f 4, rAsp f 6, Rat n, rBet v 1, rBet v 2, rBet v 6, rBla g 1, rBla g 2, rBla g 4, rBla g 5, rBla g 9, rBlo t 10, rBlo t 21, rBlo t 5, rBos d 2, rCan f 1, rCan f 2, rCan f 4, rCan f 6, rCan f Fel d 1 like, rCan s 3, rCav p 1, rChe a 1, rCla h 8, rClu h 1, rCor a 1.0103, rCor a 1.0401, rCor a 12(RUO), rCor a 8, rCra c 6, rCry j 1, rCuc m 2, rCyn d 1, rCyp c 1, rDau c 1, rDer f 1, rDer f 2, rDer p 1, rDer p 10, rDer p 11, rDer p 2, rDer p 20, rDer p 21, rDer p 23, rDer p 5, rDer p 7, rEqu c 1, rEqu c 4, rFag s 1, rFel d 1, rFel d 4, rFel d 7, rFra a 1 + 3, rFra e 1, rGly d 2, rGly m 4, rGly m 5, rHev b 1, rHev b 11, rHev b 3, rHev b 5, rHev b 6.02, rHev b 8, rHom s LF, rJug r 3, rLep d 2, rMal d 1, rMal d 3, rMala s 11, rMala s 5, rMala s 6, rMer a 1, rMes a 1 (RUO), rOle e 7 (RUO), rOle e 9, rOry c 1, rOry c 2, rOry c 3, rPar j 2, rPen m 2, rPen m 3, rPen m 4, rPer a 7, rPhl p 1, rPhl p 12, rPhl p 2, rPhl p 5.0101, rPhl p 6, rPhl p 7, rPhod s 1, rPis v 1, rPis v 4 (RUO), rPla a 1, rPla a 3, rPla l 1, rPol d 5, rPru p 7(RUO), rRaj c Parvalbumin, rSal k 1, rSal s 1, rSco s 1, rSus d 1, rThu a 1, rTri a 14, rTri a 19, rTyr p 2, rVes v 1, rVes v 5, rXip g 1, rZea m 14