Classifications

• • 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
  • G01N33/6872—Intracellular protein regulatory factors and their receptors, e.g. including ion channels
• • 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
  • C07K16/24—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against cytokines, lymphokines or interferons
  • C07K16/241—Tumor Necrosis Factors
• • 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
  • G01N33/6863—Cytokines, i.e. immune system proteins modifying a biological response such as cell growth proliferation or differentiation, e.g. TNF, CNF, GM-CSF, lymphotoxin, MIF or their receptors

Definitions

• the present invention relates to a method to determine Tumor Necrosis Factor (TNF) as bioactive form.
• TNF Tumor Necrosis Factor
• the present invention relates to a method to detect oligomeric, bioactive TNF, also in the presence of monomeric TNF, or TNF as complexed form with receptors, both biologically inactive.
• Alpha-TNF also designated "cachectin” is a cytokine mainly secreted by activated macrophages.
• TNF was initially identified in serum of mice infected with "Calmette Guerin” bacillus (BCG), owing to its capability of inducing the haemorrhagic necrosis of some tumors in experimental animal models.
• TNF is among the main inflammation mediators.
• TNF can cause pathologic conditions, such as septic shock and lipid dismetabolism (cachexia), typical of patients affected by infective chronic and neoplastic pathologies.
• TNF plays a role, together with other cytokines and lymphokines, in immunoregulation, angiogenesis, cellular differentiation and growth processes (Beutler B. and Cerami A., 1989, Ann. Rev. Immunol. 7, 625-655).
• TNF is thought to perfom its pleiotropic effects through receptors present on the membrane of target cells.
• two different receptor types have been purified and characterized (Smith C.A. et al., 1990, Science 248, 1019-1023; Schall T.J. et al., 1990, Cell 61, 361-370).
• soluble forms of such molecules corresponding to their extra-cellular portions, displaying powerful TNF inhibitory activity, were purified from urines of normal subjects and, in larger amount, from urines of feverish patients affected by chronic kidney failure, or from serum of patients affected by neoplastic diseases (Nophar Y. et al., 1990 EHBO J. 9, 3269-3278).
• TNF is a molecule composed by three identical sub-units of 17.5 KD, strictly associated with one another.
• Studies of analytical ultracentrifugation, gel electrophoresis, cross-linking, X ray dispersion and gel filtration showed that TNF is in oligomeric form also in solution (Wingfield P, Pain R.K. and Craig S., 1987, FEBS Lett. 211, 179-184; Arakawa T. and Yphatis D.A., 1987, J. Biol. Chem. 262, 7484-7435; Lam K.S., Scuderi P.
• TNF levels in biological fluids under normal and pathologic conditions are commonly determined by means of traditional immunologic determinations or biological assays.
• the low correlation leveI between the results obtained from both assay types on pathologic sera suggests the existence of bioinactive antigenic forms (Balkwill et al., 1987, Lancet ii, 1229), probably constituted by monomeric TNF, or soluble-receptor- complexed TNF.
• the level of TNF as bioactive form is usually determined in biological fluids by means of bioassays based on the cytotoxic effect displayed by TNF on sensible cells [e.g., L929 cells (Kramer et al., 1986, J. Immunol. Meth. 93, 210) and WEHI 164 cells (Espevik et al., 1986, J. Immunol. Heth. 95, 99)].
• sensible cells e.g., L929 cells (Kramer et al., 1986, J. Immunol. Meth. 93, 210) and WEHI 164 cells (Espevik et al., 1986, J. Immunol. Heth. 95, 99)].
• TNF antigen can reach nanomolar levels (Balkwill et al., 1987, Lancet ii, 1229).
• TNF on sensible cells shows a series of problems connected with execution difficulties: such tests require accurate specificity checks, special equipment for cellular cultures, keeping cellular lines in culture for long time periods, and a specialistic experience in cell cultivation, all the above not always being available. Furthermore, execution of assay normally requires from 3 to 4 days; it is decidedly long and laborious and does not make it possible the analysis of a large number of samples to be carried out. As a consequence, such a methodology is decidedly inadequate for routine analyses in clinic laboratories.
• the execution of the biological assay requires that the sample is diluted in a suitable medium for cellular growth, normally containing, serum, or other factors produced by the same cells and therefore uncontrollable, which may alter the actual concentration of TNF as bioactive form in the analysed sample.
• an Object of the present invention is a method to detect TNF as bioactive form comprising the steps of:
• a capturing reactant capable of only reacting with TNF molecules as oligomeric form, but not with TNF as complexed form with the receptor or TNF as monomeric form;
• said detector reactant is capable of only reacting with molecules of TNF in oligomeric form, but not with TNF as complexed form with a receptor or TNF as monomeric form conjugated with a detection system; said capturing reactant has an affinity constant for oligomeric TNF higher than 10 9 M - 1 and an affinity constant for receptor-complexed TNF Lower than 10 5 M -1 .
• said capturing reactant and said detector reactant comprise the same reactant molecule and oligomeric TNF contains at least two binding sites for said reactant molecule.
• said capturing reactant and said detector reactant comprise polyclonal or monoclonal anti-TNF antibodies, which preferably are neutralizers of TNF/receptor bond, still more preferably, monoclonal Hab-78 antibody (GB patent application No. 9028123.1; Barbanti P. et al. "2 nd Int. Congress on Trauma, Shock and Sepsis: Hechanisms and Therapeutic Approaches", 1991, Kunststoff).
• said capturing reactant and said detector reactant comprise TNF receptors or synthetic molecules or recombinant molecules.
• said substrate comprises titration microslabs or polystyrene tubes or poly-(vinyl chloride) tubes
• said detection system comprises enzymatic molecules of fluorescent compounds or chemoluminescent compounds or radioactive compounds or colloidal metals, or coloured latex particles.
• Said enzymatic molecules are preferably comprised within the group consisting of peroxidase, alkaline phosphatase, urease, beta-galactosidase and said colloidal metals are comprised within the group consisting of gold, silver, copper, platinum, copper hydroxide, aluminum hydroxide, vanadium oxide, manganese hydroxide.
• said measurement is carried out by causing said detector reactant to react with chromogenic or fluorogenic substrates, and reading the signal.
• a further Object of the present invention is a kit to detect, from a sample, TNF as bioactive form, which kit comprises:
• a capturing reactant immobilized on a substrate capable of only reacting with TNF molecules in oligomeric form, but not with receptor-complexed TNF or TNF in monomeric form;
• a detector reactant capable of only reacting with TNF molecules in oligomeric form, but not with receotor- complexed TNF or TNF in monomeric form, conjugated with a detection system
• said capturing reactant and said detector reactant comprise Mab-78 antibody
• said kit also comprises a detection system for total TNF.
• the monoclonal antibody endowed with TNF neutralizing activity, was immobilized on poly-(vinyl chloride) slabs, as follows: to each well of 96-well slabs, 50 ⁇ l of 50 mM sodium phosphate buffer pH 7.3, containing 0.15 M sodium chloride (PBS) and 10 ⁇ g/ml of monoclonal Mab-78 antibody (GB patent application No. 9028123.1; Barbanti P. et al. "2 nd Int. Congress on Trauma, Shock and Sepsis: Mechanisms and Therapeutic Approaches", 1991, Kunststoff) were added.
• the slabs were then incubated at room temperature (r.t.) for 2 hours and were then blocked with a 3% calf serum albumine solution, for 2 hours at r.t..
• the slabs prepared in that way can be stored some weeks at 4°C.
• Monoclonal Mab-t8 antibody was biotinylated as follows: a solution containing 1 mg of Mab-78/ml, 600 ⁇ l, was mixed with 6 ⁇ l of N-hydroxysuccinimidic ester of D-biotinyl-6-amino-caproic acid, 10 mg/ml in dimethyl-suIfoxide, and was incubated for a 4-hour time at r.t.. Then 60 ⁇ l of a 1 M lysine solution was added. The mixture was further incubated for 1 hout at r.t., and was then dialyzed overnight against PBS. The product was diluted to 3 ml with PBS, and was stored at -20oC.
• TNF in oligomeric form The slabs sensibilized with Mab-8 antibody as disclosed in Example 1, were washed by filling the wells with PBS, and emptying them (3 times). The wells were then filled with the samples to be analysed, suitably diluted with PBS containing 1% BSA (PBS-B). The slab was incubated again overnight at 4°C and was washed with PBS containing 0.05% Tween 20 (PBS-T). At the end, to each well 50 ⁇ l of biotinylated Nab-Neu, diluted in the ratio of 1:200 with PBS-B containing 0.05% Tween 20 (PBS-BT) was added.
• PBS-BT biotinylated Nab-Neu
• the slabs were washed with PBS-T, were filled with 50 ⁇ l/well of a solution of streptavidine-peroxidase, available from the market (Sigma Chemical Co.), diluted in the ratio of 1:1000 with PBS-BT, and were then incubated again for 1 hour at 37°C.
• the slab was stained with a chromogenic solution containing ABTS [2,2'-azino-di-(3-ethyl-benzylthiazoline sulfonate) ], available from the market (from Kirkegaard and Perry Laboratories Inc.).
• Oligomeric and monomeric TNF were prepared by dissociation of recombinant DNF with 0.1% Triton X-100, as described in literature [Smith R.A., Baglioni C. (1987), J. Biol. Chem. 262, 0951-09543 and were separated by HPLC gel-filtration on TSK3000SW chromatographic column (LKB-Pharmacia) (flow rate: 0.5 ml/minute).
• the chromatographic fractions corresponding to monomeric TNF resulted to be totally inactive at the assay for oligomeric TNF.
• the presence of monomeric TNF in such fractions was checked by means of a conventional assay performed with polyclonal ant-TNF antibodies as described in Example 6.
• Polyclonal anti-TNF Mab-78 antibody was prepared by immunization of Balb/c mice and was purified according to known methods from literature (Bringman et al., 1987, Hybridoma 5, 489). Purified immunoglobulins were immobilized on poly-(vinyl chloride) slabs, as follows: to each well of 96-well slabs, 50 ⁇ l of 50 mM sodium phosphate buffer pH 7.3, containing 0.15 M sodium chloride (PBS) and 10 ⁇ g/ml of immunoglobulins were added. The slabs were then incubated 2 hours at r.t. and were then blocked with a 3% calf serum albumine solution, for 2 hours at r.t.. The slabs prepared in that way can be stored some weeks at 4°C.
• the slabs were washed with PBS-T, were filled with 50 ul/well, of a solution, available from the market (Sigma Chemical Co.), of goat anti-rabbit- immunoglobuIin globulins conjugated with peroxidase, diluted 1:1000 with PBS-BT, and were incubated again, for 1 hour at 37°C.
• the slab was stained with a chromogenic solution containing ABTS [2,2'-azino-di-(3-ethyl-benzyIthiazoline sulfonate)], available from the market (from Kirkegaard and Perry Laboratories Inc.).

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• 1991
  • 1991-09-23 IT ITRM910710A patent/IT1249708B/it active IP Right Grant
• 1992
  • 1992-09-17 EP EP92921308A patent/EP0605635A1/en not_active Withdrawn
  • 1992-09-17 JP JP5505949A patent/JPH07502113A/ja active Pending
  • 1992-09-17 AU AU26905/92A patent/AU2690592A/en not_active Abandoned
  • 1992-09-17 WO PCT/IT1992/000116 patent/WO1993006489A1/en not_active Application Discontinuation

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