Diagnostic test using chimeric antibodies

The invention concerns the use of chimeric monoclonal antibodies or fragments thereof for diagnostic tests.
Since the development of the hybridoma technique for the production of monoclonal antibodies in clinical diagnosis they have been extensively used for immunological determinations. The monoclonal antibodies for this are usually produced in mouse cell lines and therefore, apart from the antigen-specific hypervariable region, only have mouse-specific regions. Such monoclonal antibodies from mice are used for immunological determinations e.g. RIA, IRMA, IEMA. In the diagnosis with the so-called "sandwich" assays e.g. the ELISA (enzyme-linked immunosorbent assay) a substance contained in human blood or serum is detected via two antibodies, one of which is immobilized on a solid phase and the second carries a label. Such a label is usually an enzyme label which can produce a color reaction for the detection.
However, in the past few years falsely increased test values have been identified with increasing frequency in certain patients when using such diagnostic detection methods. Such increased values occur when two circumstances coincide i.e.
a) a sandwich test concept which is based on a linking of two antibodies, i.e. an immobilized antibody on a wall and an antibody carrying a signal, by an antigen and
b) the occurrence of so-called heterophilic antibodies or of anti-mouse antibodies in the serum of the patient.
Human heterophilic antibodies are directed against IgG of different animal species, amongst others against mouse IgG, by which means as a rule the test antibodies are affected. Heterophilic antibodies, however, often show cross-reactions with IgG from the rat, cow, sheep, horse, guinea pig or monkeys, less often with IgG from the dog, cat or rabbit. The reason for this seem to be common epitopes in the F(ab').sub.2 fragment (Boscato and Stuart, Clin. Chem. 32 (1988), 1491-1495) or in the Fc part (Clark and Prince, Clin. Chem. 33 (1987), 414) of different IgG molecules.
Such heterophilic antibodies are widespread in humans and probably originate through the use of or injections of animal products. The development of anti-mouse antibodies in humans is also mainly attributable to this.
In the sandwich assays binding of the polyvalent heterophilic antibody or of the anti-mouse antibody to the monoclonal antibodies on the one hand causes a linking of the detection-antibody with the solid phase even in the absence of the antigen which thus produces a false test signal and on the other hand sterically hinders the correct antigen binding of the test antibodies.
It has therefore already been suggested that monoclonal antibodies from different species e.g. from mouse and rat be used in sandwich immunoassays in order to avoid such test interferences (Boscato and Stuart, Clin. Chem. 43, (1988) 27-33). The problem can, however, not be solved by this means since, as has already been mentioned, human heterophilic antibodies are directed against IgG of different animal species. Heterophilic antibodies of many patients react with mouse IgG as well as with rat IgG. Since monoclonal antibodies with a high efficiency can only be obtained at present from the mouse and rat this imposes limitations from the start.
Furthermore, Boscato and Stuart suggested saturating the antibodies of the patient by addition of non-immune IgG of those species from which the monoclonal test antibody is derived in order to avoid false measurement results when testing sera containing heterophilic antibodies. The preparation of such large amounts of mouse antibodies is, however, problematic, expensive and clearly does not lead to the desired result.
It was suggested by Kahn et al., J. Clin. Endocrin. Metabolism., 66 (1988), 526-533 that the heterophilic antibodies contained in the serum be removed by polyethylene glycol precipitation. This is also laborious and can only be used for antigen tests but not, however, for antibody tests. It was furthermore suggested in the same publication that the antibodies used diagnostically be iodinated so that they cannot be recognized any more by the human anti-mouse antibodies. This, however, also requires a lot of time and leads to a loss in activity of the antibodies.
A further suggestion i.e. to remove the heterophilic antibodies with an anti-human immunoglobulin or with protein A (Clin. Chem. 34 (1988), 261-264) is also too complicated for routine determinations and is again only suitable for antigen tests but not for antibody tests.
The object of the invention is therefore to eliminate the interfering effects of heterophilic antibodies in the serum of patients and to enable an undisturbed quantitative determination of substances, antigens as well as antibodies, in the serum of patients.
This object is achieved according to the present invention by the use of chimeric monoclonal antibodies which consist of human antibodies in which the variable regions are completely or partially replaced by the corresponding parts of a non-human monoclonal antibody of the desired specificity or by fragments thereof for diagnostic tests for the quantitative immunological determination of substances in blood or serum of patients.
A human antibody is preferably used as the chimetic antibody in which the variable regions (V.sub.H and V.sub.L) have been replaced by the corresponding regions of a non-human monoclonal antibody (e.g. from rat or preferably from mouse). Particularly preferred is the use of a monoclonal human antibody. A human antibody is likewise preferably used as a chimeric antibody in which the hypervariable regions from V.sub.H and V.sub.L have been partially--or particularly preferably--completely replaced by the corresponding regions of a non-human monoclonal antibody (e.g. rat and preferably mouse) (reshaped antibody). Such a preferred antibody thus contains the Fc part, the constant regions of the Fab part as well as the framework regions of the variable regions of a human antibody. The "framework regions" are understood as the four regions of each of the two heavy and of the two light chains of an antibody which surround the three hypervariable regions or are situated between them. The structure of such chimeric antibodies is described for example by Verhoeyen and Riechmann, in Bioessay, Vol. 8, 1988, pages 74 to 78. By the use of chimeric antibodies or fragments thereof according to the present invention the risk of an interaction of the test antibodies with heterophilic antibodies can be largely avoided. The use according to the present invention can be used for all determination procedures which use monoclonal antibodies, for example also for RIA, since also in this procedure there is a risk that test results may be distorted by heterophilic or anti-mouse antibodies. The invention is, however, particularly important and suitable for sandwich assays such as IRMA and IEMA.
Processes for the production of chimeric antibodies in which the variable regions have been replaced are described for example by Brhggemann et al., (1987), J. Exp. Med. 166, 1351-1361, Liu et al., (1987) Proc. Natl. Acad. Sci. USA 84 3439-3443, Whittle et al., Protein Engineering 1 (1987), 499-505, Nature 314 (1985) 452-454, J. Immunol. 137 (1986) 1066-1074, Gene 54 (1987) 33-40 and in WO86/01533 as well as in EP-A 0 239 400 and can be adapted by an expert according to the conditions needed for a special test. A slightly modified method for the preparation of a chimeric anti-TSH antibody (MAB<TSH>) is described in the Examples.
Processes for the production of chimeric antibodies in which only the hypervariable regions have been replaced (reshaped antibody) are described in Nature 321 (1986) 522-525 and Nature 332 (1988) 323-327. The preparation of fragments of antibodies can be carried out according to well-known methods, as described for example by Johnstone and Thorpe in Immunochemistry in Practice, Blackwell Scientific, 1982, pages 52 to 53.
In a preferred embodiment of the invention at least one monoclonal antibody or a fragment thereof is used in a diagnostic "sandwich-immunoassay". By this means a linking of both test antibodies can be avoided since at the most the non-chimeric antibody can be bound by heterophilic antibodies or by mouse antibodies, whereas, for the linking both test antibodies need to be bound. In certain cases, especially when relatively large amounts of heterophilic antibodies are present in a patient serum, it may be expedient to use only chimeric antibodies in immunological tests especially in order to avoid competing reactions.
In a preferred embodiment the diagnostic test in which chimeric monoclonal antibodies are used is an enzyme-linked immunosorbent assay (ELISA).
Even though the heterophilic antibodies usually bind to the Fc part of the monoclonal antibodies, in order to avoid any possible interaction it is preferable to use a chimeric antibody in which the variable or hypervariable regions of a human monoclonal antibody are replaced by the corresponding parts of a monoclonal mouse antibody of the desired specificity. By this means the interaction with human anti-mouse antibodies or heterophilic antibodies with cross-reactivity is avoided.
In a preferred embodiment of the invention a chimeric anti-TSH antibody or a fragment thereof is used for the detection of thyroid stimulating hormone (TSH) in patient serum using an ELISA test. For this two complete chimeric genes were reconstructed for the light and heavy chain from the cloned anti-TSH-MAB cDNAs with the aid of two mouse immunoglobulin genes as receptors and the constant regions of one human kappa and of one human gammal gene, these cDNAs were incorporated into an expression vector (Example 1) and expressed in a suitable host cell. The chimeric antibody was then isolated from the nutrient medium according to well known methods.
Thus according to the present invention falsely increased test results due to heterophilic antibodies or anti-mouse antibodies in the serum or blood of patients are successfully prevented in diagnostic immunoassays which use monoclonal antibodies from mice, above all in sandwich assays.
A further embodiment of the invention is thus a process for the diagnostic detection of substances in serum or blood of patients by binding of two monoclonal antibodies R.sub.1 and R.sub.2 directed against the substance, of which the first antibody R.sub.1 is capable of binding to a solid phase or is already bound and the second antibody R.sub.2 carries a label, binding of the antibody R.sub.1 to the solid phase if desired, separation of the complex formed of R.sub.1, substance and R.sub.2 which is bound to the solid phase and detection via the labelling of the antibody R.sub.2, whereby a chimeric monoclonal antibody or a fragment thereof is used at least for one of the antibodies R.sub.1 or R.sub.2.
The expression "capable of binding to a solid phase" also means, within the scope of the invention, inter alia that the antibody R.sub.1 can be fixed to the solid phase via an additional component such as e.g. a third antibody bound to the solid phase which is directed against the Fc part of R.sub.1, or a biotin molecule bound to R.sub.1 and streptavidin bound to the solid phase.
In this connection exemplary variants of the test method consist inter alia of
a) the use of an antibody bound to a solid phase against the Fc fragment of a human antibody which binds the Fc part of a chimeric human antibody directed against the antigen, and labelling of the complex via e.g. a peroxidase labelled second antibody which is likewise directed against the antigen;
b) the use of streptavidin bound to a solid phase, a biotinylated chimeric antibody directed against the antigen as well as a second labelled antibody which is likewise directed against the antigen;
c) the use of an antibody bound to a solid phase against the Fc.gamma. part of a mouse antibody, a mouse antibody capable of binding to it and which is directed against the antigen and of a labelled chimeric antibody directed against the antigen;
d) the use of streptavidin bound to a solid phase, a biotinylated mouse antibody directed against the antigen and of a labelled chimeric antibody which is likewise directed against the antigen;
e) the use of a chimeric antibody bound to a solid phase which is directed against the antigen and of a labelled mouse antibody which is likewise directed against the antigen; or
f) the use of a mouse antibody bound to a solid phase which is directed against the antigen and of a labelled chimeric antibody which is likewise directed against the antigen.
In the process according to the present invention the label of the one antibody can be a radioactive label as well as another type of label such as e.g. an enzymatic label. In accordance with the invention it is preferable to use an enzyme label which in turn is detected by a color reaction caused by the enzyme.
In this connection the labelling can also be indirect via a biotin bound to the respective antibody and a label bound to streptavidin, e.g. peroxidase. The wall of a reaction vessel can for example be used as the solid phase.
In all the variants mentioned instead of using whole antibodies it is also possible to use only certain fragments of these antibodies and an embodiment of the present invention.
In a preferred embodiment two chimeric monoclonal antibodies are used for the process according to the present invention. By this means a further increase in the reliability of the test results is achieved especially when high concentrations of heterophilic antibodies are present.
The process according to the present invention using chimeric monoclonal antibodies can also be used for diagnostic tests which are not based on the formation of a sandwich of antibodies and substance to be detected such as e.g. RIA since also in such tests there is a risk that the test results may be falsified by the presence of heterophilic antibodies, however it is of particular importance in sandwich immunoassays.
The production of monoclonal antibodies can be carried out according to the well known methods which have already been cited.
By means of the invention interferences in diagnostic tests caused by heterophilic antibodies or anti-mouse antibodies in the serum or blood of patients can be successfully avoided in a simple and effective manner. The necessity to add non-specific, non-immune IgG from the species from which the monoclonal antibodies were isolated or of a time-consuming precipitation of the heterophilic or anti-mouse antibodies as suggested by the state of the art can be avoided according to the present invention and even a significantly increased accuracy of the test results can be achieved.

The following Examples in conjunction with the Figures elucidate the invention further.
FIG. 1 shows the DNA and amino acid sequence of the kappa chain of a monoclonal antibody against TSH;
FIG. 2 shows the DNA and amino acid sequence of the gamma chain of a monoclonal antibody against TSH;
FIG. 3 shows the DNA and amino acid sequence of the kappa chain of a chimeric monoclonal antibody against TSH;
FIG. 4 shows the DNA and amino acid sequence of the gamma chain of a chimeric monoclonal antibody against TSH;
FIG. 5 shows the vector p11196. Vector p11196 was constructed on the basis of the pUC vectors (C. Yanisch-Perron et al., Gene 33, (1985), 103-119) (nucleotide position 630 to 2675 of pUC18). The NotI fragment (.rect-hollow.) carries the functional rearranged V region of a K gene of the mouse. An EcoRV cleavage site was introduced at the beginning of the V region and a XhoI cleavage site at the end of the J region by mutagenesis (nucleotide position 6 or 312 respectively).
FIG. 6 shows the vector p11197. Vector p11197 was constructed on the basis of the pUC vectors (C. Yanisch-Perron et al., Gene 33, (1985), 103-119) (nucleotide position 630 to 2675 of pUC18). The NotI fragment (.rect-hollow.) carries the VDJ region of a functional rearranged .gamma..sub.1 gene of the mouse.
FIG. 7 shows the vector p10195. Vector p10195 was constructed on the basis of pSV2 neo (R.C. Mulligan and P. Berg (1981), Proc. Nat. Acad. Sci. USA 78, 2072-2076). A DNA fragment containing the K enhancer of the mouse (.rect-hollow.) as well as a DNA fragment containing the constant region of a human K gene () were cloned between its EcoRI and BamHI cleavage sites. This resulted in the loss of the BamHI cleavage site.
FIG. 8 shows the vector p11201. Vector p11201 was constructed on the basis of pSV2gpt (R.C. Mulligan and P. Berg (1981), Proc. Nat. Acad. Sci. USA 78, 2072-2076). A DNA fragment containing the enhancer of the heavy immunoglobulin chains of the mouse (.rect-hollow.) as well as a DNA fragment containing the constant region of a human .gamma..sub.1 gene () were cloned between its EcoRI and BamHI cleavage sites. In this process the EcoRI cleavage site from pSV2gpt was converted into a NotI cleavage site.
FIG. 9 and 10 show the cloning steps of the kappa and gamma chain construction;
FIG. 11 shows a comparison of the standard curves for a TSH monoclonal antibody, curve 2 (FIG. 1 and 2) and for a chimeric anti-TSH antibody, curve 1 (FIG. 3 and 4, Example 1). OD: optical density, absorbance.

EXAMPLE 1
Production of a chimeric antibody against TSH (chimeric monoclonal antibody, chimeric anti-TSH MAB)
a) Construction of vector p11196 (FIG. 5)
A 1.8 Kb long XbaI fragment from the K gene of the anti-idiotypic MAB A2044 (F. Sablitzky et al., (1985), EMBO J. 4, 345-350) was filled up at the ends with the Klenow fragment of DBA-Polymerase I, provided with NotI linkers (5'GCGGCCGC3') and cloned in pUC18 which had been cleaved with DraII/PvuII (Yanisch-Perron, C, G. Vieira and G. Messing, Gene 33 (1985) 103-119) and whose ends had likewise been filled up and provided with NotI linkers (T. Maniatis, E. F. Fritsch and J. Sambrook (1982), Molecular Cloning--A Laboratory Manual; Cold Spring Harbor Laboratory).
b) Construction of vector p11197 (FIG. 6)
A 1 Kb long EcoRI/HindIII fragment from the .gamma.l gene of the anti-idiotypic MAB A2044 (F. Sablitzky et al., (1985), EMBO J. 4, 345-350) was filled up at the ends, provided with NotI linkers and cloned in the vector pUC18 (Yanisch-Perron, C, G. Vieira and G. Messing, Gene 33 (1985) 103-119) which had been cleaved with DraII/PvuII and treated in the same way.
c) Oligonucleotide directed mutageneses
In the DNA sequence of FIG. 1 an EcoRV cleavage site was inserted at position 1 with the aid of the oligonucleotide I and a XhoI cleavage site was inserted at position 325 (oligonucleotide II). The nucleotides 1 to 9 of the oligonucleotide I are homologous to the leader peptide region of the kappa chain of the anti-TSH MAB which is not included in FIG. 1. FIG. 1 shows the mature kappa chain of the MAB. In the DNA sequence of FIG. 2 a PvuII cleavage site was inserted at position 7 (oligonucleotide III) and a PstI cleavage site at position 344 (oligonucleotide IV). In the sequence of the VJ region of the K gene of MAB A2044 in p11196 (F. Sablitzky et al., (1985), EMBO J. 4, 345-350) an EcoRV cleavage site was inserted at position 1 (oligonucleotide V) and a XhoI cleavage site at position 310 (oligonucleotide VI) (FIG. 5). All mutageneses were carried out according to the "gapped-duplex" method of Inouye et al., (Synth. Appl. DNA RNA; (1987), Ed. S. A. Narang; Academic Press; 181-206) starting from plasmid DNA.
Oligonucleotides used:
I: 5'ACCAACGGTGATATCGTGATGACCCAG3'
II: 5'GGCACCAAGCTCGAGATCAAACGG3'
III: 5'ATGAGCAGCTGCAAGAGTCAGGAC3'
IV: 5'GTCACCGTCTCTGCAGCCAAAACG3'
V: 5'GATATCGTGCTAACTCAGTCTCCA3'
VI: 5'GCTGCTGGGACCAAGCTCGAGCTG3'
d) Construction of vector p10195 (FIG. 7)
A 2 Kb EcoRI/-Asp700 fragment (Asp700 converted by linker in BamHI) which contains the enhancer region (Nature 307 (1984) 80-82) of the K gene of MAB A2044 was cloned in the plasmid pSV2neo (R. C. Mulligan, P. Berg (1981), Proc. Nat. Acad. Sci. USA 78, 2072-2076) which had been cleaved with EcoRI and BamHI, a 2.8 Kb EcoRI fragment (also filled up) from pC1 (H.-G. Klobeck et al., (1984), Nucl. Acids Res. 12, 6995-7006) which contains the constant region of a human K gene was cloned. A XbaI cleavage site located upstream of the mouse K enhancer of the resulting plasmid was converted into a NotI cleavage site by insertion of a linker (FIG. 7).
e) Construction of vector p11201 (FIG. 8)
A 7 Kb HindIII fragment which contained the constant regions of a human .gamma.l gene (.gamma.1-10) (N. Takahashi et al., (1982), Cell 29, 671-679) was cloned in the plasmid pSV2gpt (R. C. Mulligan, P. Berg (1981), Proc. Nat. Acad. Sci. USA 78, 2072-2076) which had been cleaved with EcoRI and BamHI. (This original HindIII fragment was converted into an EcoRI-BamHI fragment by filling up the HindIII ends and intermediate cloning in the Asp718 cleavage site of pUC19 (C. Yanisch-Perron et al., (1985), Gene 3, 103-119) which was also filled up). A 1.6 Kb HindIII-EcoRI fragment containing the enhancer region (Cell 41 (1985) 885-897) of the .gamma.l gene of MAB A2044 (F. Sablitzky et al., (1985), EMBO J. 4, 345-350) was inserted in the same orientation into the EcoRI cleavage site of the resulting plamid. In this process the HindIII cleavage site was converted into a NotI cleavage site as well as adapted to the EcoRI cleavage site with the aid of an adaptor (5'AATTGCGGGCCGC3' hybridized with 5'AGCTGCGGCCGC3') (FIG. 8).
f) Assembly of the expression plasmid for the light chain of the chimeric antibody
The DNA of FIG. 1 was cleaved by EcoRV and XhoI at the cleavage sites introduced by mutagenesis. The 323 bp fragment corresponding to the V region was cloned in the vector p11196 which had also been similarly cleaved with EcoRV and XhoI. The resulting vector p11223 was cleaved with NotI; the 1.8 Kb fragment corresponding to the immunoglobulin part was isolated and cloned in the vector p10195, which had been cleaved with NotI (FIG. 9). The resulting vector p11225, DSM 5094 was purified by CsCl density gradient centrifugation (T. Maniatis et al., (1982), Molecular Cloning--A Laboratory Manual; Cold Spring Harbor Laboratory).
g) Assembly of the expression plasmid for the heavy chain of the chimeric antibody
The cDNA of FIG. 2 was cleaved by PvuII and PstI at the cleavage sites introduced by mutagenesis. As a result of an internal PstI cleavage site two fragments corresponding to the V region are formed of 231 bp and 103 bp. Both fragments were cloned in their original orientation in the vector p11197 which had also been cleaved with PvuII and PstI. The resulting vector p11221 was cleaved with NotI. The 1 Kb large NotI fragment corresponding to the immunoglobulin part was cloned in the NotI cleavage site of vector p11201 (FIG. 10). The resulting vector p11224, DSM 5093 was purified by CsCl density gradient centrifugation (T. Maniatis et al., (1982), Molecular Cloning--A Laboratory Manual; Cold Spring Harbor Laboratory).
h) Transfection of mammalian cells with the expression plasmids
Vector p11224, DSM 5093 as well as vector p11225, DSM 5094 were linearized at their single PvuI cleavage site (in the bacterial amp.sup.R gene). Sp2/0 Ag14 cells (ATCC CRL1581) were cultured on RPMI medium (G. E. Moore, R. E. Gerner & H. A. Franklin (1967) Culture of Normal Human Leucocytes. J.A.M.A. 199, 519-526) which was supplemented with 10% foetal calf serum, 20 mmol/1 glutamine, 1 mmol/1 Na pyruvate, 20 .mu.g/ml 8-azaguanine and amino acids (MEM amino acids, for composition see R. G. Ham, (1963) Exp. Cell. Res. 29, 515-526). Cells which grew exponentially (approx. 5.times.10.sup.5 /ml) were resuspended to 1.25.times.10.sup.6 /ml in 1.times. HeBS buffer (G. Chu et al., (1987), Nucl. Acids Res. 15, 1311-1326). Linearized vector p11224 and p11225, DSM 5094 were each added in a concentration of 12.5 .mu.g/ml. Cells and DNA were preincubated for 10 minutes at 0.degree. C. and 800 .mu.l aliquots were subsequently subjected to a single electrical impulse of 230 V (Bio Rad Gene Pulser) and then incubated for a further 10 minutes at 0.degree. C.
Afterwards the cells (as described, however without 8-azaguanine) were plated in RPMI on cloning plates.
24 hours after the transfection they were selected with G418 (Geneticin Gibco, 1 mg/ml) or G418 and additionally mycophenolic acid (in three increasing steps from 250 ng/ml to 500 ng/ml to 2 .mu.g/ml). Using both methods of selection clones were obtained that contained vector p11224, DSM 5093 as well as vector p11225, DSM 5094 and actively expressed chimeric anti-TSH MAB (ECACC 88091403). The amino acid and DNA sequence of the kappa and gamma chain of the chimeric anti-TSH MAB are shown in FIG. 3 and 4.
The hybridoma cell line which produces the chimeric anti-TSH MAB is deposited at the European Collection of Animal Cell Culture, Porton Down, GB under the number ECACC 88091403.
The following chimeric MAB's can be prepared in an analogous way:
______________________________________starting with thecDNA of a MAB (mouse)from cell lines chimeric MAB______________________________________ECACC 84122006 against follicle stimulating hormone (FSH)ECACC 84122001 against luteinizing hormone (LH)ECACC 85121701 against testosterone______________________________________
EXAMPLE 2
Function test for the chimeric anti-TSH MAB in a double-MAB sandwich test
a) Anti-TSH MAB
A MAB was used as the anti-TSH MAB whose amino acid sequences of the kappa and gamma chains are shown in FIG. 1 and 2.
b) Preparation of a peroxidase conjugate of a TSH-binding mouse antibody which is complementary to the anti-TSH MAB (FIG. 1 and 2).
The IgG fraction of the monoclonal anti-TSH antibody, ECACC 87122202, was purified from ascites fluid by ammonium sulphate precipitation and chromatography on a DEAE ion exchanger according to A. Johnstone and R. Thorpe, Immunochemistry in Practice, Blackwell Scientific, 1982, pages 44 to 45. 90 mg Fab fragments were prepared from 200 mg IgG according to the method of Johnstone and Thorpe ibid. pages 52 to 53. 50 mg of the Fab fragments was reacted with S-acetyl-thio-succinic acid anhydride and coupled with 50 mg prepolymerized maleinimido-hexanoyl peroxidase according to the method described in DE-A-38 25 735, Example 8.2. A conjugate pool was obtained with a molecular weight from 2 to 3 million by AcA 22 chromatography. Yield 31 mg protein with 13500 U peroxidase (POD) activity.
c) Procedure for the function test
1. Reference ELISA (enzyme-linked immunosorbent assay) with anti-TSH MABs
Step 1:
The wells of a microtitre plate were coated (two hours, 25.degree. C.) with 5 .mu.g/ml polyclonal sheep (anti-mouse Fc.gamma.) IgG (immunosorbed) by spontaneous adsorption and recoated with 1% crotein C in 50 mM HEPES buffer/150 mM NaCl, pH 7.0 (30 minutes at 25.degree. C.) to saturate the remaining adsorption sites.
Step 2
0.2 ml anti-TSH MAB (Example 2a) at a concentration of 50 ng IgG/ml dissolved in RPMI cell culture medium was pipetted into each of the emptied wells and incubated for 60 minutes at room temperature. Buffer without MAB-IgG was used for controls.
Step 3:
After washing three times with buffer A, 40 .mu.l TSH standard solution or patient serum (with interfering factors, diluted 1+1 in buffer B) together with 200 .mu.l buffer B were pipetted into each well and incubated for 60 minutes at room temperature.
The TSH standard solutions were prepared by supplementing bovine serum with a solution of TSH. The resulting TSH concentrations of the various supplemented standard solutions were assigned by measurement with a commercial TSH test (Enzymun-Test.sup.R TSH, Boehringer Mannheim GmbH, Order No. 736 082).
Step 4:
After washing twice with buffer A each well was filled with 0.2 ml enzyme-conjugate solution (Example 2b) with 100 mU/ml POD activity (dilution of the conjugate concentrate from b) in buffer C). The conjugate was incubated for 60 minutes at room temperature.
Step 5:
After washing three times with buffer C each well was filled with 0.2 ml ABTS.RTM. substrate (2,2'-azino-di-[3-ethylbenzthiazoline sulphonate] 1.9 mmol/1 ABTS.RTM., 100 mmol/1 phosphate citrate buffer, pH 4.4, sodium perborate 3.2 mmol/1) and incubated for 60 minutes at room temperature.
The absorbance values of the resulting dye solutions in the wells were measured at 405 nm with a photometer suitable for microtitre plates.
Buffer A:
16 mmol/1 potassium phosphate buffer, pH 6.9
0.2% bovine serum albumin
0.15 mol/1 NaCl
0.1% bovine IgG
Buffer B:
Buffer A with the addition of 0.1% sheep IgG.
Buffer C:
36 mmol/1 potassium phosphate buffer, pH 6.9
0.2% bovine serum albumin
0.15 mol/1 NaCl
2% Dextran T500
0.01% phenol
(concentrations are the final concentrations in the test)
ELISA test with chimeric anti-TSH MAB (Example 1)
The test procedure with the chimeric MAB follows exactly the steps of the reference test c)1. with the following specific changes:
In step 1, polyclonal sheep(anti-human Fc.gamma.) IgG (immunosorbed) was coated. In step 2, a dilution of cell culture supernatant with 50 ng chimeric anti-TSH MAB/ml was pipetted.
The concentration of chimeric anti-TSH MAB was determined with a human Fc.gamma.-specific microtitre ELISA.
FIG. 11 shows a comparison of the standard curves for the test with anti-TSH MAB (Example 2cl) (curve 2) and the test with chimeric anti-TSH MAB (Example 2c2) (curve 1). The course of the calibration curves is, within the limits of error, identical. It follows from this that the TSH binding site in the chimeric MAB is unchanged and that the Fc.gamma. part of the chimeric MAB responds in the same way as that of human IgG.
As a control a microtitre plate coated according to Example 2cl with sheep(anti-mouse Fc.gamma.) IgG was used in the test according to Example 2c2. As expected the resulting absorbances for the standard samples were not different from the blank values.
Table 1 shows the measured values for three different patient sera (PS 71, PS 92, PS 99) which were known to yield falsely increased values in the mouse double-MAB immune test. The sample PS 107, a normal human serum with <0.5 .mu.U TSH/ml and without interfering factors, was also tested as a control.
The resulting absorbances in both test systems for the serum samples were converted on the respective standard curve to .mu.U TSH/ml sample.
As a control that in the test system with chimeric anti-TSH MAB a defined amount of TSH was correctly recovered in human sera with interfering factors, each of the sera was supplemented with 20 .mu.U TSH/ml and also measured.
TABLE 1______________________________________Results of function tests with anti-TSH MAB and chimericanti-TSH MAB______________________________________1. Test system using a coating of sheep (anti-mouse Fc.gamma.) Absorbance Anti-TSH MAB .DELTA. A.sub.405Sample (Example 2cl) (against blank) .mu.U TSH/ml______________________________________PS 71 + 0.585 19.2 - 0.015PS 92 + 0.268 8.0 - 0.008PS 99 + 0.550 17.6 - 0.022Normal serum + 0.015 <0.5107 - 0.005______________________________________2. Test system using a coating of sheep (anti-human Fc.gamma.) Chimeric Ab- Anti-TSH MAB sorbance .mu.U/Sample (Example 2c2) .DELTA. A.sub.405 TSH/ml______________________________________PS 71 + 0.00 0.5 - 0.00PS 92 + 0.045 1.2 - 0.00PS 99 + 0.015 <1.0 - 0.01PS 71 + 20 .mu.U TSH/ml + 0.603 19.4PS 92 + 20 .mu.U TSH/ml + 0.678 22.1PS 99 + 20 .mu.U TSH/ml + 0.641 20.8zero standard + + 0.622 20.220 .mu.U TSH/ml______________________________________
The TSH concentrations of the patient sera were measured with an Enzymun TSH test kit (Boehringer Mannheim GmbH, order no, 7 36082). This test is not interfered with by anti-mouse IgG interfering factors since it contains a conjugate of a Fab fragment of a polyclonal anti-TSH antibody from sheep and peroxidase instead of a conjugate of a Fab fragment of an anti-TSH antibody from mouse and peroxidase.
Values found: PS 71 (0.52 .mu.U/ml), PS 92 (2.2 .mu.U/ml), PS 99 (0.9 .mu.U/ml).
From the values in the Table it is obvious that the test system according to Example 1c1 finds apparent TSH contents in the patient sera with interfering factors which are falsely grossly increased. By use of the chimeric anti-TSH MABs in a test system which is in all other respects completely analogous (Example 2c2) this interference is completely eliminated. Genuinely increased TSH-contents are correctly recovered within the limits of error.

Number	Date	Country
2007336	Jul 1990	CAX
0266663	May 1988	EPX
0274394	Jul 1988	EPX
0323806	Jul 1989	EPX
WO8601533	Mar 1986	WOX
9007861	Jul 1990	WOX

	Number	Date	Country
Parent	948073	Sep 1992
Parent	459481	Jan 1990

Diagnostic test using chimeric antibodies

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