US20100143954A1 - Galectin-3 Immunoassay - Google Patents

Galectin-3 Immunoassay Download PDF

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US20100143954A1
US20100143954A1 US12/608,821 US60882109A US2010143954A1 US 20100143954 A1 US20100143954 A1 US 20100143954A1 US 60882109 A US60882109 A US 60882109A US 2010143954 A1 US2010143954 A1 US 2010143954A1
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galectin
sample
seq
amino acids
concentration
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Pieter Muntendam
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BG Medicine Inc
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Publication of US20100143954A1 publication Critical patent/US20100143954A1/en
Assigned to BG MEDICINE, INC. reassignment BG MEDICINE, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: WANG, SHUNGUANG
Priority to US15/424,306 priority patent/US20170370944A1/en
Priority to US16/444,402 priority patent/US20200033367A1/en
Priority to US18/126,055 priority patent/US20240103018A1/en
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    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/577—Immunoassay; Biospecific binding assay; Materials therefor involving monoclonal antibodies binding reaction mechanisms characterised by the use of monoclonal antibodies; monoclonal antibodies per se are classified with their corresponding antigens
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
    • G01N33/6893—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids related to diseases not provided for elsewhere
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2851—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the lectin superfamily, e.g. CD23, CD72
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
    • G01N2333/435—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans
    • G01N2333/46—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans from vertebrates
    • G01N2333/47—Assays involving proteins of known structure or function as defined in the subgroups
    • G01N2333/4701—Details
    • G01N2333/4724—Lectins
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2800/00—Detection or diagnosis of diseases
    • G01N2800/32—Cardiovascular disorders
    • G01N2800/325—Heart failure or cardiac arrest, e.g. cardiomyopathy, congestive heart failure

Definitions

  • HF Heart failure
  • CHF congestive heart failure
  • HF ejection fraction
  • One or more of the following tests may also be used: radionuclide ventriculography, magnetic resonance imaging (MRI), a complete blood count, urinalysis, serum electrolytes, glycohemoglobin and blood lipids, tests of renal and hepatic function, tests of thyroid function, a chest radiograph, and a 12-lead electrocardiogram.
  • blood tests for biomarkers such as B-type natriuretic peptide (BNP)
  • BNP B-type natriuretic peptide
  • BNP B-type natriuretic peptide
  • Galectins constitute a family of proteins characterized by their galactose-specific binding. All share common amino acid sequence in regions of their structure known as the carbohydrate recognition domain or CRD.
  • CRD carbohydrate recognition domain
  • a second subgroup contains a single species, galectin-3, which comprises a single CRD linked to an N-terminal domain comprising repeats of short amino acid sequences such as PGA.
  • a third galectin subgroup contains galectins 4, 6, 8, 9, and 12, each of which comprises two CRDs joined by a linker of variable length. All of the galectins have significant amino acid sequence homology, and many appear in the human circulatory system.
  • galectin-3 Assays for galectin-3 exist, but none are suitable for routine clinical use. A suitable assay heretofore has eluded the art because of the complexity of galectin-3 as an analyte. It is difficult to specifically distinguish galectin-3 from other galectins in a sample, because galectin-3 shares a high degree of sequence similarity to the other 14 mammalian galectins, particularly in the conserved carbohydrate recognition domain (CRD). None of the other galectins has a known relation with HF. Another feature of galectin-3 that has hindered the development of a specific, reproducible detection assay is the propensity of galectin-3 to bind to various proteins, carbohydrates, nucleic acids and lipids. If an assay were developed that is industrially robust and sensitive and specific enough to quantitatively measure galectin-3 reproducibly in body fluids such as blood samples, the diagnosis and management of HF could be improved.
  • the present invention provides methods and kits for detecting the level of galectin-3 in a clinical sample. This permits improved management of the disease and provides diagnostic/prognostic information useful in its triage and management.
  • the invention relates to a kit for detecting the concentration of galectin-3 in a sample.
  • the kit includes two binding moieties, e.g., monoclonal antibodies, at least one of which is labeled with a detectable label.
  • the two binding moieties each bind respectively to spaced-apart epitopes on the N-terminal portion of galectin-3, which comprises the following 113 amino acid sequence:
  • the binding moieties respectively bind to an epitope defined by at least a portion of one of the following galectin-3 amino acid sequences: MADNFSLHDALS (amino acids 1-12 of SEQ ID NO:1), MADNFSLHDALSGS (amino acids 1-14 of SEQ ID NO:1), GNPNPQGWPGA (amino acids 15-25 of SEQ ID NO:1), WGNQPAGAGG (amino acids 26-35 of SEQ ID NO:1), YPGQAPPGAYPGQAPPGA (amino acids 45-62 of SEQ ID NO:1), YPGAPGAYPGAPAPGV (amino acids 63-78 of SEQ ID NO:1), YPGAPAPGVYPGPPSGPGA (amino acids 70-88 of SEQ ID NO:1), YPSSGQPSATGA (amino acids 89-100 of SEQ ID NO:1). While these depict linear epitopes, epitopes created by the secondary and tertiary structure of the N
  • the binding moieties used to detect galectin-3 are monoclonal antibodies, for example, M3/38, 9H3.2, and 87B5.
  • M3/38 detects a linear epitope (YPGQAPPGAYPGQAPPGA (amino acids 45-62 of SEQ ID NO:1)) on the N-terminus of galectin-3.
  • M3/38 was prepared from the supernatant of the rat hybridoma M3/38.1.2.8 HL.2, a clone of which can be found in the American Type Culture Collection with ATCC® number TIB-166.
  • 9H3.2 detects a linear epitope (MADNFSLHDALSGS (amino acids 1-14 of SEQ ID NO:1)) at the extreme N-terminus of galectin-3.
  • 9H3.2 is a mouse monoclonal IgG, affinity purified using protein A.
  • 9H3.2 is available from Millipore (Millipore, 290 Concord Road, Billerica, Mass. 01821, USA), catalog no.: MAB4033.
  • 87B5 detects a non-linear epitope comprising portions of GNPNPQGWPGA (amino acids 15-25 of SEQ ID NO:1) and YPGAPAPGVYPGPPSGPGAYPSSGQPSATGA (amino acids 70-100 of SEQ ID NO:1).
  • 87B5 was prepared from the mouse-mouse hybridoma (X63-Ag8.653 ⁇ BALB/c mouse spleen cells) clone 87B5, and is an IgG2a that was affinity purified using Protein A.
  • 87B5 is available from Immuno-Biological Laboratories (IBL, 8201 Central Ave Nebr., Suite P, Minneapolis, Minn. 55432 USA)
  • the present invention relates to a method for detecting the level of human galectin-3 in a sample from a subject.
  • the method includes subjecting the sample to a double binding moiety sandwich assay.
  • at least one of the binding moieties is labeled with a detectable label and each of the binding moieties is specific for respective, non-overlapping epitopes on the N-terminal portion of galectin-3, such as those described above.
  • the detectable label is an enzyme or a fluorophore.
  • the sandwich assay may provide a quantitative result or a qualitative result, for example, a result indicative of the presence or absence of a galectin-3 concentration above a threshold.
  • the threshold may be in the range of, for example, 5-10 ng/ml, 10-15 ng/ml; 15-20 ng/ml; 20-25 ng/ml; 25-30 ng/ml; 30-35 ng/ml, or 35-40 ng/ml.
  • the method may include the additional step of comparing the result obtained in the assay to a data set relating the result to a galectin-3 concentration, e.g., a standard curve, to determine the concentration of galectin-3 in the sample, and then correlating the inferred concentration of galectin-3 with the risk that a subject is suffering from or at risk for developing HF, or to assess the stage or severity of the subject's HF.
  • a galectin-3 concentration e.g., a standard curve
  • the result also may be directly correlated with the risk that a subject is suffering from or at risk for developing HF, or to assess the stage or severity of the subject's HF.
  • the method may be repeated over time to obtain a trend.
  • Additional variables may be considered such as, but not limited to, a subject's height, weight, age, sex, levels of other biomarkers, etc., to determine a subject's risk for developing HF, or to assess the stage of the subject's HF or its severity.
  • the present invention relates to a method for detecting a risk of development or progression of heart failure in a subject, including determining whether the galectin-3 concentration in a sample from the subject exceeds a threshold in the range of 15-20 ng/ml.
  • FIG. 1 is a cartoon drawing of a double monoclonal sandwich assay of the type exploited by the invention.
  • FIG. 2 is an exemplary hypothetical standard curve relating signal to galectin-3 concentration useful in explaining the nature of the invention.
  • FIG. 3 is an exemplary second hypothetical standard curve relating signal to galectin-3 concentration useful in explaining the nature of the invention.
  • FIG. 4 is an exemplary survival probability curve for subjects with baseline galectin-3 level above and below a threshold value of 17.6 ng/ml in the acute decompensated HF study described in Example 2E.
  • FIG. 5 is an exemplary survival probability curve for subjects with baseline galectin-3 level above and below a threshold value of 17.6 ng/ml in the Chronic HF Study I described in Example 2F.
  • FIG. 6 is an exemplary survival probability curve for subjects with baseline galectin-3 level above and below a threshold value of 17.6 ng/ml in the Chronic HF Study II described in Example 2G.
  • quantify and “quantitate,” as used herein, refer to the process of measuring the amount of galectin-3, or the relative amount of galectin-3, in a sample versus a standard or another sample (e.g., in terms of its concentration, mass, moles, or volume in a sample).
  • HF heart failure
  • CHF congestive heart failure
  • Any structural or functional cardiac disorder can cause HF, with the majority of HF patients having impaired left ventricular (LV) myocardial function.
  • LV left ventricular
  • Symptoms of HF include dyspnea (shortness of breath), fatigue, and fluid retention.
  • AHA American Heart Association
  • Patients in stages A and B show clear risk factors but have not yet developed HF.
  • Patients in stages C and D currently exhibit or in the past have exhibited symptoms of HF.
  • Stage A patients are those with risk factors such as coronary artery disease, hypertension or diabetes mellitus who do not show impaired left ventricular (LV) function.
  • Stage B patients are asymptomatic, but have cardiac structural abnormalities or remodeling, such as impaired LV function, hypertrophy or geometric chamber distortion.
  • Stage C patients have cardiac abnormalities and are symptomatic.
  • Stage D patients have refractory HF in which they exhibit symptoms despite maximal medical treatment. They are typically recurrently hospitalized or unable to leave the hospital without specialized intervention.
  • Galectin-3 (GenBank Accession Nos.: NC — 000014.7 (gene) and NP — 002297.2 (protein)) is one of 15 mammalian beta galactoside-binding lectins, or “galectins,” characterized by their galactose-specific binding. Galectin-3 has variously been referred to in the literature as LGALS3, MAC-2 antigen, Carbohydrate binding protein (CBP)-35, laminin binding protein, galactose-specific lectin 3, mL-34, L-29, hL-31, epsilon BP, and IgE-binding protein.
  • CBP Carbohydrate binding protein
  • Galectin-3 is composed of a carboxyl-terminal carbohydrate recognition domain (CRD) and amino-terminal tandem repeats (Liu, F.-T. (2000) Role of galectin-3 in inflammation. In Lectins and Pathology . M. Caron and D. Seve, eds. Harwood Academic Publishers, Amsterdam, The Netherlands, p. 51; Liu, F.-T. et al. (1995) Am. J. Pathol. 147:1016). Galectin-3 normally distributes in epithelia of many organs and various inflammatory cells, including macrophages as well as dendritic cells and Kupfer cells (Flotte, T. J. et al. (1983) Am. J. Pathol. 111:112).
  • Galectin-3 has been shown to play a role in a variety of cellular process, including cell-cell adhesion, cell-matrix interactions, phagocytosis, cell cycle, apoptosis, angiogenesis and mRNA splicing. Galectin-3 has been shown to function through both intracellular and extracellular actions (Sano, H. et al. (2000) The Journal of Immunology, 165:2156-2164). It is a component of heterogeneous nuclear ribonuclear protein (hnRNP) (Laing, J. G. et al. (1998) Biochemistry 27:5329), a factor in pre-mRNA splicing (Dagher, S. F. et al. (1995) Proc. Natl.
  • hnRNP nuclear ribonuclear protein
  • Galectin-3 has been shown to act as a novel chemoattractant for monocytes and macrophages (Sano, H. et al. (2000) The Journal of Immunology, 2000, 165:2156-2164). Galectin-3 has been implicated in diseases and conditions such as cancer, inflammation, and heart failure. As disclosed in International Patent Publication No. WO2005/040817, quantitation of galectin-3 is particularly suitable for use in an assay to diagnose and detect the severity of HF and to predict outcome.
  • galectin-3 comprises an atypical N-terminal domain, comprising the amino acid sequence:
  • the sequences of the N-terminus of galectin-3 are dissimilar to sequences of other mammalian galectins but comprise multiple repeats of the type PGAYPG(X) 1-4 (SEQ ID NO:2), with intervening proline-, glycine-, and tyrosine-rich regions.
  • the existence of repeated sequences in the N-terminal domain decreases the number of different potential epitopes specific to galectin-3, complicating the development of a detection assay.
  • N-terminal epitopes can reliably distinguish galectin-3 from other mammalian galectins.
  • N-terminal epitopes include, but are not limited to, MADNFSLHDALS (amino acids 1-12 of SEQ ID NO:1), MADNFSLHDALSGS (amino acids 1-14 of SEQ ID NO:1), GNPNPQGWPGA (amino acids 15-25 of SEQ ID NO:1), WGNQPAGAGG (amino acids 26-35 of SEQ ID NO:1), YPGQAPPGAYPGQAPPGA (amino acids 45-62 of SEQ ID NO:1), YPGAPGAYPGAPAPGV (amino acids 63-78 of SEQ ID NO:1), YPGAPAPGVYPGPPSGPGA (amino acids 70-88 of SEQ ID NO:1), YPSSGQPSATGA (amino acids 89-100 of SEQ ID NO:1), where the letters represent
  • the concentration of galectin-3 may be quantitated in a bodily fluid sample using a pair of binding moieties that bind specifically to N-terminal portions of galectin-3.
  • a “binding moiety” refers to a molecule that binds or interacts selectively or preferentially with a polypeptide or peptide.
  • binding moieties include, but are not limited to, proteins, such as antibodies, galectin binding protein (GBP) interaction fusion protein, peptide aptamers, avimers, Fabs, sFvs, Adnectins and Affibody® ligands; nucleic acids, such as DNA and RNA (including nucleotide aptamers), and lipids, such as membrane lipids.
  • proteins such as antibodies, galectin binding protein (GBP) interaction fusion protein, peptide aptamers, avimers, Fabs, sFvs, Adnectins and Affibody® ligands
  • nucleic acids such as DNA and RNA (including nucleotide aptamers)
  • lipids such as membrane lipids.
  • the methods and compositions of the present invention can be used to detect the concentration of galectin-3 in a clinical sample, such as serum, for the diagnosis of HF.
  • the test sample used in the detection of galectin-3 can be any body fluid or tissue sample, including, but not limited to, whole blood, serum, plasma, or lymph, and less preferably urine, gastric juices, bile, saliva, sweat, and spinal fluids, stool, or muscle biopsy.
  • the sample is a blood sample.
  • the sample is a plasma sample. Serum samples may also be used.
  • the body fluids may be either processed (e.g., serum) or unprocessed. Methods of obtaining a body fluid from a subject are known to those skilled in the art.
  • galectin-3 is detected and quantified using a “sandwich” assay.
  • binding moieties such as monoclonal antibodies that specifically bind to non-overlapping sites (“epitopes”) on the N-terminus of galectin-3 are used. See FIG. 1 .
  • one binding moiety is immobilized on a solid surface where it binds with and captures galectin-3. This first binding moiety is therefore also referred to herein as the capture binding moiety.
  • a second binding moiety is detectably labeled, for example, with a fluorophore, enzyme, or colored particle, such that binding of the second binding moiety to the galectin-3-complex indicates that galectin-3 has been captured.
  • the intensity of the signal is proportional to the concentration of galectin-3 in the sample.
  • the second binding moiety is therefore also referred to herein as the detection binding moiety or label binding moiety.
  • a binding moiety can be any type of molecule, as long as it specifically binds to a portion of the N-terminus of galectin-3.
  • the binding moieties used are monoclonal anti-galectin-3 antibodies, i.e., monoclonals raised against or otherwise selected to bind to separate portions of the N-terminal 113 amino acids of galectin-3.
  • Such assay procedures can be referred to as two-site immunometric assay methods, “sandwich” methods or (when antibodies are the binders) “sandwich immunoassays.”
  • the capture and detection antibodies can be contacted with the test sample simultaneously or sequentially. Sequential methods, sometimes referred to as the “forward” method, can be accomplished by incubating the capture antibody with the sample, and adding the labeled detection antibody at a predetermined time thereafter.
  • the labeled detection antibody can be incubated with the sample first and then the sample can be exposed to the capture antibody (sometimes referred to as the “reverse” method). After any necessary incubation(s), which may be of short duration, the label is detected and may also be measured.
  • Such assays may be implemented in many specific formats known to those of skill in the art, including through use of various high throughput clinical laboratory analyzers or with point of care or home testing devices.
  • a lateral flow device may be used in the sandwich format, wherein the presence of galectin-3 above a baseline sensitivity level in a biological sample will permit formation of a sandwich interaction upstream of or at the capture zone in the lateral flow assay.
  • the capture zone as used herein may contain capture binding moieties such as antibody molecules, suitable for capturing galectin-3, or immobilized avidin or the like for capture of a biotinylated complex. See, for example, U.S. Pat. No. 6,319,676.
  • the device may also incorporate a luminescent label suitable for capture in the capture zone, the concentration of galectin 3 being proportional to the intensity of the signal at the capture site. Suitable labels include fluorescent labels immobilized on polystyrene microspheres. Colored particles also may be used.
  • assay formats that may be used in the methods of the invention include, but are not limited to, flow-through devices. See, for example, U.S. Pat. No. 4,632,901.
  • one binding moiety for example, an antibody
  • This membrane is then overlaid on an absorbent layer that acts as a reservoir to pump sample volume through the device.
  • the remaining protein-binding sites on the membrane are blocked to minimize non-specific interactions.
  • a biological sample is added to the membrane and filters through, allowing any analyte specific to the antibody in the sample to bind to the immobilized antibody.
  • a labeled secondary antibody may be added or released that reacts with captured marker to complete the sandwich.
  • the secondary antibody can be mixed with the sample and added in a single step. If galectin-3 is present, a colored spot develops on the surface of the membrane.
  • ELISA Enzyme-Linked Immunosorbent Assay
  • an antibody e.g., anti-galectin-3
  • a solid phase i.e., a microtiter plate
  • antigen e.g., galectin-3
  • a labeled antibody e.g., enzyme linked
  • enzymes that can be linked to the antibody are alkaline phosphatase, horseradish peroxidase, luciferase, urease, and ⁇ -galactosidase.
  • the enzyme-linked antibody reacts with a substrate to generate a colored reaction product that can be measured.
  • This measurement can be used to derive the concentration of galectin-3 present in a sample, for example, by comparing the measurement to a galectin-3 standard curve.
  • Galectin-3 concentration in a sample from a subject may be determined to be above or below a threshold.
  • the threshold may be in the range of, for example, 5-10 ng/ml, 10-15 ng/ml; 15-20 ng/ml; 20-25 ng/ml; 25-30 ng/ml; 30-35 ng/ml, or 35-40 ng/ml.
  • any of the immunoassays described herein suitable for use with the kits and methods of the present invention can also use any binding moiety in the place of an antibody.
  • anti-galectin-3 antibodies preferably monoclonal antibodies, are used as binding moieties.
  • a monoclonal antibody refers to an antibody that is derived from a single clone, including any eukaryotic, prokaryotic, or phage clone.
  • the monoclonal antibody may comprise, or consist of, two proteins, i.e., heavy and light chains.
  • the monoclonal antibody can be prepared using one of a wide variety of techniques known in the art including the use of hybridoma, recombinant, and phage display technologies, or a combination thereof.
  • Anti-galectin-3 monoclonal antibodies may be prepared using any known methodology, including the seminal hybridoma methods, such as those described by Kohler and Milstein (1975), Nature. 256:495.
  • a hybridoma method a mouse, hamster, or other appropriate host animal is immunized with an immunizing agent to elicit lymphocytes that produce or are capable of producing antibodies that will specifically bind to the immunizing agent.
  • the lymphocytes may be immunized in vitro.
  • the immunizing agent will typically include at least a portion of the galectin-3 polypeptide or a fusion protein thereof.
  • synthetic polypeptide or recombinant polypeptide comprising any galectin-3 N-terminal epitopes may be used as an immunizing agent.
  • N-terminal epitopes include, but are not limited to, MADNFSLHDALS (amino acids 1-12 of SEQ ID NO:1), MADNFSLHDALSGS (amino acids 1-14 of SEQ ID NO:1), GNPNPQGWPGA (amino acids 15-25 of SEQ ID NO:1), WGNQPAGAGG (amino acids 26-35 of SEQ ID NO:1), YPGQAPPGAYPGQAPPGA (amino acids 45-62 of SEQ ID NO:1), YPGAPGAYPGAPAPGV (amino acids 63-78 of SEQ ID NO:1), YPGAPAPGVYPGPPSGPGA (amino acids 70-88 of SEQ ID NO:1), YPSSGQPSATGA (amino acids 89-100 of SEQ ID NO:1).
  • MADNFSLHDALS amino acids 1-12 of SEQ ID NO:1
  • MADNFSLHDALSGS amino acids 1-14 of SEQ ID NO:1
  • GNPNPQGWPGA amino
  • a fusion protein may be made by fusing a polypeptide to a carrier protein, for example, keyhole limpet hemocyanin (KLH, EMD Biosciences, San Diego, Calif.), BSA (EMD Biosciences, San Diego, Calif.), or ovalbumin (Pierce, Rockford, Ill.).
  • KLH keyhole limpet hemocyanin
  • BSA EMD Biosciences, San Diego, Calif.
  • ovalbumin Pierford, Ill.
  • the immunizing agent may be administered to a mammal with or without adjuvant according to any of a variety of standard methods.
  • the immunizing agent may be administered only once, but is preferably administered more than once according to standard boosting schedules.
  • PBLs peripheral blood lymphocytes
  • spleen cells or lymph node cells are used if non-human mammalian sources are desired.
  • the lymphocytes are then fused with an immortalized cell line using a suitable fusing agent, such as polyethylene glycol, to form a hybridoma cell population which is screened for species having appropriate specificity and affinity to epitopes on the N-terminal portion of galectin-3 (Goding, (1986) Monoclonal Antibodies: Principles and Practice, Academic Press, pp. 59-103).
  • Immortalized cell lines are usually transformed mammalian cells, particularly myeloma cells of rodent, bovine and human origin.
  • rat or mouse myeloma cell lines are employed.
  • the hybridoma cells may be cultured in a suitable culture medium that preferably contains one or more substances that inhibit the growth or survival of the unfused, immortalized cells.
  • a suitable culture medium that preferably contains one or more substances that inhibit the growth or survival of the unfused, immortalized cells.
  • the culture medium for the hybridomas typically will include hypoxanthine, aminopterin, and thymidine (“HAT medium”), which substances prevent the growth of HGPRT-deficient cells.
  • Preferred immortalized cell lines are those that fuse efficiently, support stable high level expression of antibody by the selected antibody-producing cells, and are sensitive to a medium such as HAT medium. More preferred immortalized cell lines are murine myeloma lines, which can be obtained, for instance, from the Salk Institute Cell Distribution Center, San Diego, Calif. and the American Type Culture Collection, Manassas, Va. Human myeloma and mouse-human heteromyeloma cell lines also have been described for the production of human monoclonal antibodies (Kozbor, J. (1984) Immunol., 133:3001; Brodeur et al., Monoclonal Antibody Production Techniques and Applications, Marcel Dekker, Inc., New York, (1987) pp. 51-63).
  • the culture medium in which the hybridoma cells are cultured can then be assayed for the presence of monoclonal antibodies directed against the N-terminus of galectin-3, e.g., by screening with a labeled galectin-3 N-terminal polypeptide.
  • the binding specificity of monoclonal antibodies produced by the hybridoma cells is determined by immunoprecipitation or by an in vitro binding assay, such as radioimmunoassay (RIA) or enzyme-linked immunoabsorbent assay (ELISA).
  • RIA radioimmunoassay
  • ELISA enzyme-linked immunoabsorbent assay
  • the binding affinity of the monoclonal antibody can, for example, be determined by the Scatchard analysis of Munson and Pollard (1980), Anal. Biochem., 107:220.
  • Various analysis protocols to determine binding specificity are available commercially as kits or as a service.
  • Monoclonal antibodies also may be made by recombinant DNA methods, such as those described in U.S. Pat. No. 4,816,567.
  • DNA encoding suitable monoclonal antibodies can be isolated and sequenced using conventional procedures (e.g., by using oligonucleotide probes that are capable of binding specifically to genes encoding the heavy and light chains of murine antibodies).
  • the hybridoma cells serve as a preferred source of such DNA.
  • the DNA may be placed into expression vectors, which are then transfected into host cells such as simian COS cells, Chinese hamster ovary (CHO) cells, or myeloma cells that do not otherwise produce immunoglobulin protein, to obtain the synthesis of monoclonal antibodies in the recombinant host cells.
  • host cells such as simian COS cells, Chinese hamster ovary (CHO) cells, or myeloma cells that do not otherwise produce immunoglobulin protein, to obtain the synthesis of monoclonal antibodies in the recombinant host cells.
  • the DNA also may be modified, for example, by substituting the coding sequence for human heavy and light chain constant domains in place of the homologous murine sequences (U.S. Pat. No. 4,816,567; Morrison et al., (1984) Proc. Natl. Acad. Sci.
  • non-immunoglobulin polypeptide can be substituted for the constant domains of an antibody of the invention, or can be substituted for the variable domains of one antigen-combining site of an antibody of the invention to create a chimeric bivalent antibody.
  • the antibodies may be monovalent antibodies.
  • Methods for preparing monovalent antibodies are well known in the art. For example, one method involves recombinant expression of immunoglobulin light chain and modified heavy chain.
  • the heavy chain is truncated generally at any point in the Fc region so as to prevent heavy chain crosslinking.
  • the relevant cysteine residues are substituted with another amino acid residue or are deleted so as to prevent crosslinking.
  • In vitro methods are also suitable for preparing monovalent antibodies. Digestion of antibodies to produce fragments thereof, particularly, Fab fragments, can be accomplished using routine techniques known in the art.
  • Antibodies can also be produced using phage display libraries (Hoogenboom and Winter (1991), J. Mol. Biol. 227:381; Marks et al. (1991), J. Mol. Biol., 222:581). The techniques of Cole et al. and Boerner et al. are also available for the preparation of monoclonal antibodies (Cole et al. (1985), Monoclonal Antibodies and Cancer Therapy, Alan R. Liss, p. 77 and Boerner et al. (1991), J. Immunol., 147(1):86-95). Similarly, antibodies can be made by introducing of immunoglobulin loci into transgenic animals, e.g., mice in which the endogenous immunoglobulin genes have been partially or completely inactivated.
  • the antibodies may also be affinity matured using known selection and/or mutagenesis methods as described above.
  • Preferred affinity matured antibodies have an affinity which is five times, more preferably 10 times, even more preferably 20 or 30 times greater than the starting antibody from which the matured antibody is prepared.
  • the antibodies used to detect galectin-3 are monoclonal antibodies, for example, M3/38, 9H3.2, and 87B5.
  • M3/38 detects a linear epitope (YPGQAPPGAYPGQAPPGA (amino acids 45-62 of SEQ ID NO:1)) on the N-terminus of galectin-3.
  • M3/38 was prepared from the supernatant of the rat hybridoma M3/38.1.2.8 HL.2, a clone of which can be found in the American Type Culture Collection with ATCC® number TIB-166.
  • 9H3.2 detects a linear epitope (MADNFSLHDALSGS (amino acids 1-14 of SEQ ID NO:1) at the extreme N-terminus of galectin-3.
  • MADNFSLHDALSGS amino acids 1-14 of SEQ ID NO:1
  • 9H3.2 is a mouse monoclonal IgG, affinity purified using protein A.
  • 9H3.2 is available from Millipore (Millipore, 290 Concord Road, Billerica, Mass. 01821, USA), catalog no.: MAB4033.
  • 87B5 detects a non-linear epitope comprising portions of GNPNPQGWPGA (amino acids 15-25 of SEQ ID NO:1) and YPGAPAPGVYPGPPSGPGAYPSSGQPSATGA (amino acids 70-100 of SEQ ID NO:1).
  • 87B5 was prepared from the mouse-mouse hybridoma (X63-Ag8.653 ⁇ BALB/c mouse spleen cells) clone 87B5, and is an IgG2a that was affinity purified using Protein A.
  • 87B5 is available from Immuno-Biological Laboratories (IBL, 8201 Central Ave Nebr., Suite P, Minneapolis, Minn. 55432 USA).
  • the capture binding moiety is the anti-galectin-3 monoclonal antibody, M3/38 and the labeled detection binding moiety is a second anti-galectin-3 monoclonal antibody, 87B5.
  • the given designations for these antibodies are not limiting.
  • the capture antibody is 9H3.2 and the labeled detection binding moiety is M3/38.
  • Other antibodies which recognize the epitopes described above also may be used.
  • binding moieties may be used with the methods and kits of the present invention.
  • binding moieties include, but are not limited to, proteins, peptide aptamers, avimers, Adnectins and Affibody® ligands; nucleic acids, such as DNA and RNA (including nucleotide aptamers), and lipids, such as membrane lipids.
  • Nucleotide aptamers are small peptides or small nucleotide sequences that bind with high affinity to a target of choice. Nucleotide aptamers are produced by a selection process called Systematic Evolution of Ligands by Exponential Enrichment (SELEX), also referred to as in vitro selection or in vitro evolution. In this procedure, a target molecule is exposed to a large, randomly generated oligonucleotide library. The unbound oligonucleotides are separated out of the mixture by any number of methods, usually affinity chromatography. The oligonucleotides that remain bound are eluted and amplified.
  • SELEX Systematic Evolution of Ligands by Exponential Enrichment
  • the target molecule is then exposed to the newly-synthesized oligonucleotides, and the selection process is repeated for several rounds with increasingly stringent conditions to separate out unbound sequences.
  • the resulting oligonucleotides are then sequenced to determine their identity. See U.S. patent application Ser. No. 07/536,428; U.S. Pat. No. 5,475,096; and U.S. Pat. No. 5,270,163.
  • Peptide aptamers typically consist of a short variable peptide domain.
  • Peptide aptamers comprise a variable peptide loop attached at both ends to a protein scaffold. This double structural constraint greatly increases the binding affinity of the peptide aptamer to levels comparable to an antibody's (nanomolar range).
  • the variable loop length is typically 10 to 20 amino acids, and the scaffold may be any protein that is soluble and compact, such as the bacterial protein thioredoxin A.
  • a variable loop can be inserted within the reducing active site of thioredoxin A, which is a -Cys-Gly-Pro-Cys- loop in the wild protein, the two cysteine lateral chains being able to form a disulfide bridge.
  • Peptide aptamer selection can be made using different systems, such as the yeast two-hybrid system. For further discussion of peptide aptamers, see International Patent Publication No. WO2007/117657.
  • An avimer is a short peptide sequence that contains multiple regions of low affinity to a target. The presence of multiple unique regions of low affinity act together to produce a high affinity binding moiety. Small size and high disulfide density contribute to the low immunogenicity of avimers.
  • a highly diverse pool of monomers is created by synthetic recombination. This pool of monomers can be screened against a target protein using phage display or another preferred screening method. Once candidates are found, another monomer is added and the new library of dimers is screened against the target. After iteration, a trimer with very high binding affinity for its target protein is isolated (see Silverman et al. (2005), Nature Biotechnology 23, 1556-1561).
  • Adnectin consists of a backbone of the natural amino acid sequence of a certain domain of human fibronectin and one to three targeting loops which contain randomized sequence. Adnectins are screened and isolated based on ability to specifically recognize a therapeutic target of interest (see, for example, U.S. Pat. No. 6,818,418).
  • Affibody® ligands are small peptides comprised of a “scaffold” domain and a variable domain.
  • the “scaffold” domain comprises a non-cysteine three-helix bundle domain, a structure based on staphylococcal protein A.
  • the variable domain contains randomly-generated sequences which can be screened against a target of interest. Libraries of Affibody® ligands are constructed, and the libraries can be screened to find candidates with high binding affinity to a protein of interest. See Nygren, P.- ⁇ . (2008) FEBS Journal 275, 2668-2676.
  • galectin-3 binding partners that bind to the N-terminus of galectin-3 can be isolated or produced recombinantly and used as binding moieties. Galectin-3 binding partners or fragments thereof can be used as either capture or detection binding moieties, depending upon the particular constraints of the assay. Examples of galectin-3 binding partners include, but are not limited to mycolic acids and lipopolysaccharides (Barboni et al. (2005) FEBS Letters 579:6749-6755). Additionally, circulating galectin-3 triggers an auto-immune response resulting in the generation of auto-antibodies against galectin-3 in serum under both normal and pathological conditions (Jensen-Jarolim et al.
  • the capture binding moiety provides a means of separation from the remainder of the test mixture. Accordingly, as is understood in the art, the capture binding moiety can be introduced to the assay in an already immobilized or insoluble form, that is, a form which enables separation of the complex from the remainder of the test solution. Alternatively, immobilization may be done by capture of an immune complex comprising galectin-3 subsequent to introduction of a soluble form of the capture binding moiety to the sample.
  • immobilized capture binding moieties are binding moieties covalently or noncovalently attached to a solid phase such as a magnetic particle, a latex particle, a microtiter plate well, a membrane, a chip, a bead, a cuvette, an array, or other reaction vessel or holder.
  • a soluble capture binding moiety is a binding moiety which has been chemically modified with a ligand, e.g., a hapten, biotin, or the like, and which acts as a hook to permit selective capture of complex including galectin-3.
  • These methods can employ bifunctional linking agents, for example, or the solid phase can be derivatized with a reactive group, such as an epoxide or an imidizole, that will bind the molecule on contact.
  • a reactive group such as an epoxide or an imidizole
  • Biospecific capture reagents against different target proteins can be mixed in the same place, or they can be attached to solid phases in different physical or addressable locations.
  • the label used can be selected from any of those known conventionally in the art.
  • Preferred labels are those that permit more precise quantitation.
  • labels include but are not limited to a fluorescent moiety, an enzyme, an electrochemically active species, a radioactive isotope, a chemiluminescent molecule, a latex or gold particle, a detectable ligand (e.g., detectable by secondary binding of a labeled binding partner for the ligand), etc.
  • the label is an enzyme or a fluorescent molecule.
  • Methods for affixing the label to the binding moiety are well known in the art, and include covalent and non-covalent linkage.
  • a binding moiety can be labeled with a fluorescent compound.
  • a fluorescent compound When the fluorescently labeled binding moiety is exposed to light of the proper wavelength, its presence can then be detected by the fluorescence emitted.
  • fluorescent labeling compounds are Cy3 and Cy5 (water-soluble fluorescent dyes of the cyanine dye family-“Cy” dyes), fluorescein isothiocyanate, rhodamine, phycoerytherin, phycocyanin, allophycocyanin, o-phthalaldehyde and fluorescamine.
  • the detection binding moiety is detectably labeled by linking the binding moiety to an enzyme.
  • the enzyme when exposed to its substrate, will react with the substrate in such a manner as to produce a chemical moiety which can be detected, for example, by spectrophotometric, fluorometric or visual means.
  • Enzymes which can be used to detectably label the binding moieties of the present invention include, but are not limited to, malate dehydrogenase, staphylococcal nuclease, delta-V-steroid isomerase, yeast alcohol dehydrogenase, alpha-glycerophosphate dehydrogenase, triose phosphate isomerase, horseradish peroxidase, alkaline phosphatase, asparaginase, glucose oxidase, beta-galactosidase, ribonuclease, urease, catalase, glucose-VI-phosphate dehydrogenase, glucoamylase and acetylcholinesterase.
  • Detection may also be accomplished using a radioactively labeled binding moiety. It is then possible to detect the binding moiety through the use of radioimmune assays.
  • the radioactive isotope can be detected by such means as the use of a gamma counter or a scintillation counter or by audoradiography.
  • Isotopes which are particularly useful for the purpose of the present invention are 3 H, 131 I, 35 S, 14 C, and preferably 125 I.
  • a binding moiety also can be detectably labeled by coupling it to a chemiluminescent compound.
  • the presence of the chemiluminescent-binding moiety is then determined by detecting the presence of luminescence that arises during the course of a chemical reaction.
  • particularly useful chemiluminescent labeling compounds are luminol, luciferin, isoluminol, theromatic acridinium ester, imidazole, acridinium salt and oxalate ester.
  • Galectin-3 may exist in a sample in a plurality of different forms characterized by detectably different masses. These forms can result from pre-translational modifications, post-translational modifications or both.
  • Pre-translational modified forms include allelic variants, splice variants, and RNA-editing forms.
  • Post-translationally modified forms include forms resulting from, among other things, proteolytic cleavage (e.g., fragments of a parent protein), complexation, glycosylation, phosphorylation, lipidation, oxidation, methylation, cystinylation, sulphonation and acetylation. Modified forms of galectin-3, as long as they retain the relevant N-terminal epitopes, may be detected according to the methods of the present invention.
  • the galectin-3 assay of the invention can be used to identify subjects at risk for developing or to identify subjects suffering from HF.
  • patients or other subjects with an identified risk of developing HF may be monitored for changes in galectin-3 levels quantitated from a body fluid over time using an immunoassay of the invention.
  • a subject with an identified risk to develop HF may monitor his or her galectin-3 levels over time, for example, monthly, quarterly, bi-yearly, yearly, every 2 years, or every 5 years.
  • galectin-3 may be used as a diagnostic marker to determine the presence, stage or severity of HF in a subject or to predict his or her prognosis by measuring the concentration of galectin-3 in a sample and comparing this result to data correlating galectin-3 concentration with severity or stage of HF disease of human subjects.
  • Methods of diagnosis and/or predicting prognosis described herein may be combined with other methods for diagnosis and/or predicting prognosis commonly used in the art, such as echocardiograms with Doppler analysis, radionuclide ventriculography, magnetic resonance imaging (MRI), a complete blood count, urinalysis, serum electrolytes, glycohemoglobin and blood lipids, tests of renal and hepatic function, tests of thyroid function, a chest radiograph, a 12-lead electrocardiogram, blood tests for biomarkers such as BNP, etc.
  • echocardiograms with Doppler analysis radionuclide ventriculography, magnetic resonance imaging (MRI), a complete blood count, urinalysis, serum electrolytes, glycohemoglobin and blood lipids, tests of renal and hepatic function, tests of thyroid function, a chest radiograph, a 12-lead electrocardiogram, blood tests for biomarkers such as BNP, etc.
  • MRI magnetic resonance imaging
  • the methods and kits of the present invention are also suitable for use in detecting other conditions characterized by an increased or decreased concentration of galectin-3.
  • the expression of this galectin-3 is up-regulated during inflammation (Flotte et al. (1983) Am. J. Pathol. 111:112.), cell proliferation (Agrwal, et al. (1999) J. Biol. Chem. 264:17236) and cell differentiation (Nangia-Makker et al. (1993). Cancer Res. 53:1) and through transactivation by viral proteins (Hsu, D. et al. (1996) Am. J. Pathol. 148:1661). Its expression is also affected by neoplastic transformation.
  • galectin-3 upregulation is found in certain types of lymphomas (Hsu, D. et al. (1996) Am. J. Pathol. 148:1661), and thyroid carcinoma (Fernadez, P. L. et al. (1997) J. Pathol. 181:80), while galectin-3 is down-regulated in other types of malignancies such as colon (Lotz, M. M. et al. (1993) Proc. Natl. Acad. Sci. USA 90:3466), breast (Castronovo, V., F. A. et al. (1996) J. Pathol. 179:43.), ovarian (Van den Brüle, F. A. et al. (1994) Eur. J.
  • Galectin-3 plays a role in many other diseases, conditions and disorders, including autoimmune disorders and vascular complications in diabetes and hypertension. Galectin-3 has been detected in tissues affected by inflammatory diseases. For example, galectin-3 was detected in the tears of patients with inflammatory ocular diseases (Hrdlickova-Cela et al. (2001), Br J Opthalmol, 85:1336-40). Increased galectin-3 levels have also been noted in human atherosclerotic lesions (Ohshima et al. (2003), Arthritis Rheum, 48:2788-95; Nachtigal et al. (1998), Am J Pathol, 152:1199-208).
  • the invention also provides a kit for quantitating galectin-3 useful in detecting an increased risk of HF, diagnosing presence of HF, determining severity of HF, or predicting prognosis of a subject with HF.
  • the kit may comprise one or more binding moieties for quantitating the level of galectin-3 in a bodily fluid.
  • a kit can comprise capture and detection binding moieties that specifically recognize epitopes on the N-terminus of galectin-3.
  • the capture and detection binding moieties may comprise an antibody that is immunospecific for galectin-3.
  • the kit comprises two anti-galectin-3 monoclonal antibodies, e.g., M3/38, 9H3.2, or 87B5.
  • Capture binding moieties present in a kit may be pre-attached to a solid surface, for example, but not limited to, a plastic or glass container or slide.
  • a kit may further comprise containers for mixing the sample with the binding moieties. Such containers may be suitable for use with a detection apparatus capable of detecting the signal produced by the detection binding moiety.
  • the kit may further comprise one or more reagents (e.g., a different antibody) for measuring the level of a second marker indicative of the same disease.
  • a kit of the invention may additionally comprise one or more of the following: (1) instructions for using the kit for determining the level of galectin-3; (2) a labeled binding partner to any antibody present in the kit; (3) a solid phase (such as a reagent strip) upon which any such antibody is immobilized; and (4) a label or insert indicating regulatory approval for diagnostic, prognostic, or therapeutic use or any combination thereof. If a labeled binding partner to the antibody is not provided, the antibody itself can be labeled with a detectable marker, e.g., a chemiluminescent, enzymatic, fluorescent, or radioactive moiety.
  • a detectable marker e.g., a chemiluminescent, enzymatic, fluorescent, or radioactive moiety.
  • the human galectin-3 ELISA is an enzyme-linked immunosorbent assay for the quantitative detection of human galectin-3 in EDTA plasma.
  • Human galectin-3 present in the sample or standard bound to antibodies adsorbed to the microwells. Following incubation unbound material was removed during a wash step. HRP conjugated to anti-human galectin-3 antibody was added and bound to the galectin-3 captured by the coating antibody. Following incubation unbound HRP-conjugate was removed during a wash step, and substrate solution reactive with HRP was added to the wells. A colored product was formed in proportion to the amount of human galectin-3 present in the sample or standard. The reaction was terminated by addition of acid and absorbance was measured at 450 nm.
  • a standard curve was prepared from 7 human galectin-3 standard dilutions and human galectin-3 sample concentration determined.
  • Plasma was removed from the clot or cells as soon as possible after clotting and separation of the blood sample. Samples containing a visible precipitate were clarified prior to use in the assay. Grossly hemolyzed or lipemic specimens were not used. Samples were aliquoted and stored frozen at ⁇ 20° C. to avoid loss of bioactive human galectin-3. Prior to assay, frozen samples were brought to room temperature slowly and mixed gently.
  • Wash Buffer (1 ⁇ ) was prepared by mixing 50 ml of Wash Buffer Concentrate (20 ⁇ , PBS with 1% Tween 20) into a clean 1000 ml graduated cylinder. The final volume was brought to 1000 ml with deionized water and the solution was gently mixed. The pH of the final solution was adjusted to 7.4. Wash Buffer (1 ⁇ ) was transferred to a clean wash bottle.
  • Assay Buffer was prepared by adding 5 ml of Assay Buffer Concentrate (20 ⁇ , PBS with 1% Tween 20 and 10% BSA) into a clean 100 ml graduated cylinder. The final volume was brought to 100 ml with deionized water and the solution was gently mixed.
  • a concentrated HRP-Conjugate solution was diluted 1:100 ratio in Assay Buffer (1 ⁇ ) in a clean plastic tube.
  • Human galectin-3 standard was diluted to 60 ng/ml by addition of distilled water, and the mixture was gently swirled to ensure complete and homogeneous solubilization. The reconstituted standard was allowed to sit for 10 minutes prior to dilutions being made.
  • Lyophilized human galectin-3 was reconstituted in distilled water to the following volumes: High Control (180 ⁇ l, 56-84 ng/ml), Medium Control (200 ⁇ l, 32-48 ng/ml), and Low Control (130 ⁇ l, 3.4-5.8 ng/ml). Vials were swirled to ensure quantitative solubilization of contents. The reconstituted controls were allowed to sit for 10 minutes.
  • Microwell strips were washed twice with approximately 400 ⁇ l Wash Buffer per well with thorough aspiration of microwell contents between washes. The Wash Buffer was allowed to sit in the wells for about 10-15 seconds before aspiration.
  • the wells were emptied and the microwell strips were tapped on absorbent paper to remove excess Wash Buffer. The microwell strips were not allowed to dry.
  • Sample Diluent 100 ⁇ l of Sample Diluent were added in duplicate to the blank wells. 80 ⁇ l of Sample Diluent was added to the sample wells. 20 ⁇ l of each sample was added in duplicate to the sample wells. Wells were covered with an adhesive film and incubated at room temperature (18 to 25° C.) for 1 hour on a microplate shaker set at 200 rpm. The adhesive film was removed and the wells emptied. The microwell strips were washed 3 times as above.
  • TMB Substrate Solution tetramethyl-benzidine
  • the enzyme reaction was stopped by quickly pipetting 100 ⁇ l of Stop Solution (1M Phosphoric acid) into each well.
  • the absorbance of each microwell was read on a spectro-photometer using 450 nm as the primary wave length (optionally 620 nm as the reference wave length; 610 nm to 650 nm is acceptable).
  • the plate reader was blanked according to the manufacturer's instructions by using the blank wells. The absorbance of both the samples and the standards was determined. The average absorbance values for each set of duplicate standards and samples were calculated.
  • a standard curve was created by plotting the mean absorbance for each standard concentration on the ordinate against the human galectin-3 concentration on the abscissa. A best fit curve was drawn through the points of the graph. See FIG. 2 .
  • the concentration of circulating human galectin-3 may be determined for each sample, by finding the mean absorbance value on the ordinate and extending a horizontal line to the standard curve. At the point of intersection, a vertical line was extended to the abscissa and the corresponding human galectin-3 concentration was read.
  • the limit of detection (LoD) of human galectin-3 defined as the analyte concentration resulting in an absorbance significantly higher than that of the dilution medium (mean plus 3 standard deviations) was determined to be 0.09 ng/ml (mean of 12 independent assays).
  • Intra-assay reproducibility was evaluated in 4 independent experiments. Each assay was carried out with 6 replicates of 8 plasma samples containing different concentrations of human galectin-3. Two standard curves were run on each plate. Data below show the mean human galectin-3 concentration and the coefficient of variation for each sample (see Table 3). The calculated overall intra-assay coefficient of variation was 4.2%.
  • Inter-assay reproducibility (assay to assay reproducibility within one laboratory) was evaluated in 4 independent experiments. Each assay was carried out with 6 replicates of 8 plasma samples containing different concentrations of human galectin-3. Two standard curves were run on each plate. Data below show the mean human galectin-3 concentration and the coefficient of variation calculated on 24 determinations of each sample. The calculated overall inter-assay coefficient of variation was 4.0%.
  • the spike recovery was evaluated by spiking 3 levels of human galectin-3 into 3 individual plasma samples. Recoveries were determined in 4 independent experiments with 2 replicates each. The unspiked plasma samples were used as blank in these experiments. The overall mean recovery was 101% (see Table 5).
  • Table 7 shows the components of an exemplary kit for the detection of galectin-3.
  • One anti-galectin-3 antibody, M3/38 was coated onto the surface of the wells in a microtiter plate and served as the capture antibody to bind galectin-3 molecules in samples, while the other anti-galectin-3 antibody, a horseradish peroxidase (HRP)-labeled anti-galectin-3 antibody (87B5) was provided in solution and functions as the detection antibody for detecting galectin-3 molecules bound to the capture antibody. While M3/38 and 87B5 were used in this example, use of these specific antibodies is not required with the kits and methods of the present invention.
  • HRP horseradish peroxidase
  • Galectin-3 controls (C1 and C2) were comprised of a protein matrix spiked with recombinant human galectin-3.
  • the kit of Example 2A was used in a microtiter plate-based ELISA assay to quantitate galectin-3 levels. Included in the kit were two monoclonal antibodies against galectin-3. In the assay, described in greater detail in the following paragraph, standards and quality control materials were introduced into the wells and incubated for 60 minutes. During this incubation, the galectin-3 present in the standards was bound to the capture antibody coated onto the well surface. A subsequent wash step removed all unbound material introduced with the sample including unbound galectin-3. The detection antibody was then introduced into the well and incubated for 60 minutes. During this time, an antibody-antigen-antibody complex was formed.
  • TMB Tetramethyl benzidine
  • the set of seven galectin-3 standards was prepared by serial dilution of the standard (S1, recombinant human galectin-3, 12 ng per vial).
  • the calibration range was 0.156 ng/mL to 10.0 ng/mL.
  • one vial of the galectin-3 standard (S1) was reconstituted with 300 ⁇ L of deionized water followed by addition of 900 ⁇ L of Assay Diluent.
  • the vial was allowed to stand 15-20 minutes at room temperature with periodic vortexing and gentle inversion ensuring that the reconstitution water wets the entire surface area inside the vial. Complete dissolution of the standard was obtained prior to use.
  • Each reconstituted control (C1 and C2) was diluted 10-fold (1:10) using the Assay Diluent (AD) in a disposable borosilicate glass or polypropylene or other low protein-binding plastic test tube or vial. Each dilution was mixed by vortexing or inversion. A minimum of 25 ⁇ L of the reconstituted control was used for the dilution. Dilutions were performed externally (i.e. no in-well dilutions) and immediately before use.
  • AD Assay Diluent
  • Standards were diluted immediately before use. Six disposable tubes were labeled with numbers 2 to 7. 250 ⁇ L assay diluent (AD) were pipetted into each labeled tube. Next, 250 ⁇ L galectin-3 standard (S1) were pipetted to tube 2 and mixed gently. Then, 250 ⁇ L were transferred from tube 2 to tube 3 and vortexed gently. Next, 250 ⁇ L were transferred from tube 3 to 4, and the process was continued through tube 7.
  • AD assay diluent
  • S1 galectin-3 standard
  • Microtiter plate wells were designated for each of the controls, diluted standards and blank. All samples were tested in duplicate (i.e. blank, diluted standards, and controls).
  • the labeling antibody was diluted 1:30 with the Assay Diluent according to the dilution scheme shown in Table 8 below:
  • TMB-substrate 100 ⁇ L of TMB-substrate (TS) were pipetted to each well and the plate incubated for 20 minutes at 20-25° C. in the dark.
  • stop solution 50 ⁇ L of stop solution (ST) were pipetted to each well.
  • the contents of each well were mixed by drawing the contents up and down using a clean pipette tip, or by gently tapping the side of the plate.
  • the contents of the well turned from blue to yellow. Any bubbles were removed from the liquid surface of each well, and any dirt or liquid was removed from the well exterior.
  • the absorbance of each well was measured in a microtiter plate reader at 450 nm within 30 minutes of the stop solution addition.
  • the absorbance of each standard and control was read at 450 nm using the microplate reader.
  • a standard curve for the assay was determined using the following procedure. The average absorbance of the blank was subtracted from all data, including standards and controls. The average, standard deviation, and coefficient of variation (CV) of the absorbance (Abs 450 ) value were calculated for each set of duplicate standards and controls. If either of the controls had a duplicate CV greater than 20%, the entire plate was rejected and all specimens were re-analyzed using new reagents. Appropriate curve-fitting tools for third order polynomial curve fitting with least squares optimization of the means were used from each standard dilution.
  • the measured concentration was multiplied by 10 (dilution factor of specimens and controls) to obtain the final galectin-3 concentration. Control values were verified to be within acceptable ranges. The blank value was verified to be lower than the lowest calibrator. If the blank value exceeded the lowest calibrator value (e.g. the low calibrator value is negative when the blank is subtracted), the assay was repeated.
  • a representative calibration curve is shown in FIG. 3 and representative values for the absorbance of each diluted standard are shown in Table 9.
  • Example 2B The methods outlined in Example 2B were performed with the addition of clinical samples, incorporating the additional steps outlined below.
  • each test specimen was diluted 10-fold (1:10) using the Assay Diluent (AD) in a disposable borosilicate glass or polypropylene or other low protein-binding plastic test tube or vial.
  • AD Assay Diluent
  • Each dilution was mixed by vortexing or inversion, with a minimum of 25 ⁇ L of serum or plasma being used for the dilution. Dilutions were performed externally (i.e. no in-well dilutions) and immediately before use.
  • the absorbance of each specimen was read at 450 nm using the microplate reader.
  • the absorbance was proportional to the concentration of galectin-3 in the specimens.
  • Galectin-3 concentrations in the specimens and controls were based on the relationship of the absorbance of the specimens compared to that of the standards, which have a known concentration of galectin-3.
  • the standard curve for the assay was assigned for each individual plate using the following procedure.
  • the average absorbance of the blank was subtracted from all data, including standards, controls and test specimens.
  • the average, standard deviation, and coefficient of variation (CV) of the absorbance (Abs 450 ) value were calculated for each set of duplicate standards, controls and test specimens. Specimens with duplicate CVs greater than 20% were re-analyzed. If either of the controls had a duplicate CV greater than 20%, the entire plate was rejected and all specimens were re-analyzed using new reagants.
  • Appropriate curve-fitting tools for third order polynomial curve fitting with least squares optimization of the means were used from each standard dilution. Concentrations of unknown specimens and controls were calculated based upon the third order polynomial equation.
  • the measured concentration was multiplied by 10 (dilution factor of specimens and controls) to obtain the final galectin-3 concentration. Control values were verified to be within acceptable ranges. When an unacceptable result from assay controls was obtained, the assay was repeated. The blank value was verified to be lower than the lowest calibrator. If the blank value exceeded the lowest calibrator value (e.g. the low calibrator value is negative when the blank is subtracted), the assay was repeated.
  • the measuring range of the galectin-3 assay with clinical specimens was demonstrated to be from 1.32 to 96.6 ng/mL.
  • the assay was calibrated with seven standards spanning the range of approximately 0.1 to 10.0 ng/mL. Each test sample (i.e. control or subject specimen) was pre-diluted 1:10 prior to assay allowing the measurement to occur within the range bracketed by the calibrators.
  • the linearity of the assay was established according to the recommendations of the Clinical Laboratory Standards Institute Evaluation Protocol 6 (CLSI-EP6). Serum and plasma specimens were prepared and diluted to span a clinically-meaningful measurement range of galectin-3 concentrations.
  • the assay was demonstrated to be linear up to 96.6 ng/mL. The lower end of the measuring range is defined by the limit of quantitation (LoQ), which was determined to be 1.32 ng/mL.
  • Galectin-3 assay Galectin-3 Test mean within run Run to run Day to day Total Specimen (ng/mL) SD CV % SD CV % SD CV % SD CV % Low 6.1 0.3 5.7 0.6 10.5 0.0 0.0 0.7 12.0 Mid 20.7 0.7 3.4 1.4 6.7 0.3 1.7 1.6 7.7 High 72.2 2.4 3.3 4.3 6.0 2.9 4.0 5.7 8.0
  • the analytical sensitivity of the galectin-3 assay was established according to the recommendation of the CLSI EP17-A Guidelines.
  • LoB Limit of Blank
  • LoD Limit of Detection
  • LoD 1.13 ng/mL
  • Limit of Quantitation (LoQ): LoQ 1.32 ng/mL
  • the galectin-3 assay displayed no significant cross-reactivity when tested in the presence of the following compounds: galectin-1, galectin-2, galectin-4, galectin-7, galectin-8, galectin-9, galectin-12, collagen I and collagen III, all at a concentration of 500 ng/mL.
  • the mean % cross-reactivity of the above potential cross-reactants is at or below 0.3%.
  • the measuring range of the galectin-3 assay is from 1.32 ng/ml to 96.6 ng/mL.
  • the galectin-3 assay was evaluated for the effects of potential interfering substances, both endogenous and exogenous, according to the recommendations of the CLSI EP7-A.
  • Conjugated bilirubin up to 5 mg/dL
  • unconjugated bilirubin up to 15 mg/dL
  • albumin up to 12 g/dL
  • triglycerides up to 3000 mg/dL
  • cholesterol up to 250 mg/dL
  • creatinine up to 5 mg/dL
  • Purified hemoglobin up to 500 mg/dL did not show interference in the galectin-3 assay; however, packed blood cell lysate does show interference.
  • Human anti-mouse antibodies (HAMA) and rheumatoid factor (RF) cause significant positive interference with the galectin-3 assay.
  • the galectin-3 assay was not significantly affected when tested in the presence of 34 common pharmaceutical substances; including HF drugs (refer to Table 11).
  • galectin-3 levels were measured in 181 banked EDTA-plasma samples from the Acute Decompensated Heart Failure (ADHF) study.
  • the ADHF study was a prospective observational study conducted in the United States that enrolled subjects who presented with dyspnea in the emergency department (4).
  • Blood plasma galectin-3 concentration was measured in baseline samples for 181 subjects diagnosed with acute decompensated HF. Subjects were followed-up for four years.
  • the galectin-3 threshold value of 17.6 ng/mL, derived from the reference range population (described in Example 2D), was used to define a category of subjects with elevated baseline galectin-3 (n 68).
  • the Chronic HF Study II enrolled patients with chronic NYHA class III or IV HF.
  • a diagnosis of HF was established by typical clinical signs and symptoms of HF in conjunction with echocardiographic or radionuclide ventriculographic findings of a reduced left ventricular systolic function or left ventricular ejection fraction (LVEF), or of a diastolic dysfunction with preserved left ventricular systolic function.
  • Patients were stable with standard medication at the time of enrollment.
  • Galectin-3 concentration was measured using the galectin assay on baseline samples for 232 subjects.
  • the galectin-3 threshold value of 17.6 ng/mL, derived from the reference range population (described in Example 2D), was used to define a category of subjects with elevated baseline galectin-3 (n 118).
  • patients in the highest quartile of galectin-3 levels compared to the lowest quartile showed an approximately 2-fold higher hazard of death over a 3-6 year follow-up period.
  • Cox regression survival analysis and Kaplan-Meier analysis demonstrated that elevated baseline galectin-3 is a significant predictor of risk of mortality, even after adjustment for age, gender, New York Heart Association (NYHA) class, left ventricular ejection fraction, smoking status, and diabetes status (see FIG. 6 ).
  • NYHA New York Heart Association

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MX2011004501A (es) 2011-11-18
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CN104198712A (zh) 2014-12-10
CN102257390B (zh) 2015-04-01
WO2010096126A1 (fr) 2010-08-26
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US20170370944A1 (en) 2017-12-28
JP5903270B2 (ja) 2016-04-13
EP3971570A3 (fr) 2022-11-09
JP2014199261A (ja) 2014-10-23
BRPI0919975A2 (pt) 2015-12-15
AU2009340423B2 (en) 2014-07-24
CN102257390A (zh) 2011-11-23
KR20110104930A (ko) 2011-09-23
EP2359143A1 (fr) 2011-08-24
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AU2009340423A1 (en) 2010-08-26

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