WO1996034886A1 - Compositions et procedes pour deceler et traiter le syndrome immunodefficitaire acquis - Google Patents

Compositions et procedes pour deceler et traiter le syndrome immunodefficitaire acquis Download PDF

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Publication number
WO1996034886A1
WO1996034886A1 PCT/US1996/006079 US9606079W WO9634886A1 WO 1996034886 A1 WO1996034886 A1 WO 1996034886A1 US 9606079 W US9606079 W US 9606079W WO 9634886 A1 WO9634886 A1 WO 9634886A1
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Prior art keywords
protein
hiv
human
precipitation
macroglobulins
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PCT/US1996/006079
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English (en)
Inventor
Harry P. Zhabilov
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Tomson, U.S.A., Ltd.
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Priority to DE69615015T priority Critical patent/DE69615015T2/de
Application filed by Tomson, U.S.A., Ltd. filed Critical Tomson, U.S.A., Ltd.
Priority to EA199700353A priority patent/EA001100B1/ru
Priority to CA002220347A priority patent/CA2220347C/fr
Priority to BR9608837-0A priority patent/BR9608837A/pt
Priority to AU58519/96A priority patent/AU721463B2/en
Priority to AT96920118T priority patent/ATE205221T1/de
Priority to EP96920118A priority patent/EP0826003B1/fr
Priority to JP53345796A priority patent/JP3816524B2/ja
Priority to NZ308708A priority patent/NZ308708A/en
Priority to DK96920118T priority patent/DK0826003T3/da
Publication of WO1996034886A1 publication Critical patent/WO1996034886A1/fr
Priority to BG102083A priority patent/BG64056B1/bg
Priority to HK98110415A priority patent/HK1009457A1/xx

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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
    • G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
    • G01N33/6803—General methods of protein analysis not limited to specific proteins or families of proteins
    • G01N33/6842—Proteomic analysis of subsets of protein mixtures with reduced complexity, e.g. membrane proteins, phosphoproteins, organelle proteins
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A61P31/18—Antivirals for RNA viruses for HIV
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/04—Immunostimulants
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
    • 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
    • G01N33/569—Immunoassay; Biospecific binding assay; Materials therefor for microorganisms, e.g. protozoa, bacteria, viruses
    • G01N33/56983—Viruses
    • G01N33/56988—HIV or HTLV
    • 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
    • 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
    • G01N33/6803—General methods of protein analysis not limited to specific proteins or families of proteins
    • G01N33/6845—Methods of identifying protein-protein interactions in protein mixtures
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies

Definitions

  • This invention relates to the area of immunology and virology, and specifically relates to compositions obtainable from mammalian thymus cells which are useful as diagnostics, vaccines, and therapeutics for human immunodeficiency virus (HIV) infection and related diseases such as acquired immunodeficiency syndrome (AIDS) and AIDS-related domplex (ARC).
  • HIV human immunodeficiency virus
  • AIDS acquired immunodeficiency syndrome
  • ARC AIDS-related domplex
  • Bone marrow produces cells which are destined to become immune cells. These cells become lymphocytes or phagocytes. Lymphocytes are small white blood cells that bear the major responsibility for carrying out the activities of the immune system.
  • the two major classes of lymphocytes are B cells and T cells.
  • B cells mature in the bone (thus the term "B cells") marrow.
  • T cells migrate to the thymus (thus the term "T cells”) where they multiply and mature into cells capable of immune response.
  • both B and T cells travel widely and continuously throughout the body.
  • T cells There are two types of T cells, regulatory and cytotoxic T cells, which contribute to the immune defenses in two major ways. Chief among the T cells are "helper/inducer" cells. Identifiable by the T4 cell marker, helper T cells are essential for activating B cells and other T cells as well as natural killer cells and macrophages. Cytotoxic T cells are killer cells which, for example, directly attack and rid the body of cells that have been infected by viruses or transformed by cancer.
  • phagocytes are monocytes and macrophages.
  • Monocytes circulate in the blood, then migrate into tissues where they develop into macrophages ("big eaters"). Macrophages are found throughout the body tissues and are versatile cells that play many roles. As scavengers, they rid the body of worn-out cells and other debris. Foremost among cells that present antigen to T cells, having first digested and processed it, macrophages play a crucial role in initiating the immune response. As secretory cells, monocytes and macrophages are vital to the regulation of immune responses. They also carry receptors for lymphokines that allow them to be "activated” to pursue microbes and tumor cells.
  • HIV Acquired Immunodeficiency Syndrome
  • HAV human immunodeficiency virus
  • HIV destroys helper T cells and is harbored in macrophages and monocytes.
  • AIDS is characterized by various unusual infections and otherwise rare cancers. HIV also damages tissue of the brain and spinal cord, producing progressive dementia.
  • HIV infection When HIV infects a human patient, it incorporates itself into the deoxyribonucleic acid (DNA) of the immune cells and for a variable period of between 3 months to 7 years, the patient may not exhibit any immunodeficiency symptoms and sometimes do not produce detectable level of antibodies against AIDS. Since an initial HIV infection may not immediately lead to detectable clinical disease symptoms or detectable level of antibodies, the term "HIV infection” as used herein encompasses both the infection and any disease resulting therefrom, the latter being termed "HIV-related diseases". Examples of HIV-related diseases are AIDS and ARC. After the above incubation period, the HIV multiplies within the infected cell and eventually bursts the host cells which release the newly formed viruses.
  • the surrogate marker that most closely correlates with the stage of HIV infection is the CD4 + , or T helper, cell count.
  • HIV-1 envelope glycoprotein, gp120 specifically binds to the CD4 receptor that is expressed in greatest concentration in a subset of T lymphocytes and in lower amounts on monocytes and macrophages.
  • Cells expressing CD4 receptors are termed the "helper/inducer" subset, reflecting their role as both helper cells for B cell responses for antigens expressed on cells bearing human leukocyte antigen (HLA) class II receptors and inducer cells that cause T cells to suppress immune responses.
  • HLA human leukocyte antigen
  • CD4 + cells results in numerous immune defects associated with susceptibility to the opportunistic infections that are the hallmark of AIDS.
  • the HIV core antigen p24 can be detected before the appearance of HIV antibodies. After the appearance of HIV antibodies by the screening enzyme-linked immunosorbent assay (ELISA), p24 antigenemia generally becomes undetectable, though it can occasionally persist and often will recur later in the disease. HIV-I titers found in plasma and peripheral blood mononuclear cell cultures also fall rapidly as specific antibodies are detectable, suggesting at least a transiently effective host immune response. Markers of immune stimulation includes ⁇ 2 -microglobulin.
  • CD4 + cell decline has been correlated with progression to AIDS. Serum levels of ⁇ 2 -microglobulin and detection of p24 antigen in blood were also both independently correlated with rates of progression. Combined with CD4 + cell counts, use of ⁇ 2 -microglobulin and p24 antigen increased prognostic accuracy for progression to AIDS compared with CD4 + cell count alone. However, it was rare for seroconverters to have a consistent decline in their percentage of CD4 + cells over the next three years. In the interval between visits, stable or declining levels of CD4 + cell percentages were found in 38% of subjects, with 12% experiencing declines followed by a leveling in their rates of loss of CD4 + cells. Overall, 62% experienced declines in their -CD4 + cell percentage over three years of follow-up.
  • CD4 + cell counts and other surrogate markers may be increasingly used as the sole end point for investigations of antiretroval activity, of a drug or therapy, in patients with early HIV infection.
  • compositions useful for diagnosing and treating HIV infections such as AIDS and ARC.
  • Another aspect of the invention presents methods for detecting HIV infection using the above compositions.
  • Another aspect of the invention presents methods for treating HIV infection using the above compositions.
  • Another aspect of the invention presents methods for preparing the above composition from thymus cells of non- human mammals.
  • Another aspect of the invention presents devices for in vitro detection of HIV infection using the above compositions.
  • FIG. 1 presents the chromatogram of the Thymus Factor ("TF") preparation.
  • FIG. 2 graphically presents the placement of the two-dimensional gel in its first-dimension.
  • FIG. 3 graphically presents the placement of the two-dimensional gel in its second-dimension.
  • FIGs. 4 to 11 are photographs of two-dimensional gels showing the precipitation patterns of TF with serum samples from HIV-positive or AIDS human subjects and a healthy human subject.
  • FIG. 12 graphically presents FIG. 7, and the distances measured for its analysis.
  • FIG. 13 is a photograph of a two-dimensional electrophoretic gel showing the precipitation pattern of TF with a serum sample from an HIV-negative human subject.
  • FIG. 14 is a photograph of a two-dimensional electrophoretic gel showing the precipitation pattern of TF with a serum sample from an HIV-positive human subject.
  • FIG. 15 is a photograph of a two-dimensional electrophoretic gel of the serum sample collected on May 4, 1995 from the test subject of Example 3.
  • FIG. 16 is a photograph of a two-dimensional electrophoretic gel of the serum sample collected on May 11, 1995 from the test subject of Example 3.
  • FIG. 17 is a photograph of a two-dimensional electrophoretic gel of the serum sample collected on May 18, 1995 from the test subject of Example 3.
  • FIG. 18 is a photograph of a two-dimensional electrophoretic gel of the serum sample collected on May 24, 1995 from the test subject of Example 3.
  • FIG. 19 is a photograph of a two-dimensional electrophoretic gel of the serum sample collected on May
  • the present invention presents a protein, herein referred to as Thymus Factor ("TF"), which is useful for the detection of HIV which causes the fragmentation of another protein, herein referred to as aTF, which is capable of being bound to TF.
  • TF Thymus Factor
  • HIV causes the fragmentation of aTF.
  • an individual uninfected by the HIV will have intact aTF, whereas an individual infected with HIV will have fragments of aTF.
  • the amount of aTF that are fragmented are less than at a later stage of infection.
  • the fragments are smaller in size in later stages of infection.
  • detection of aTF fragments indicates an infection by HIV.
  • the amount and size of the aTF fragments indicate the stage of the infection.
  • aTF and its fragments can be detected by their precipitation patterns with TF, in particular, by the locations of the precipitates in relation to ⁇ - , ⁇ 1 - and ⁇ 2 - macroglobulins, e.g. , in a gel electrophoresis, as described in EXAMPLE 2 below.
  • TF precipitates aTF, found in the ⁇ -, ⁇ 1 - , and ⁇ 2 - macroglobulins of healthy humans, which links the ⁇ - , ⁇ 1 -, and ⁇ 2 - macroglobulins and thus the precipitation spur is continuous alongside ⁇ - , ⁇ 1 -, and ⁇ 2 - macroglobulins.
  • aTF is fragmented, thus causing broken precipitation spurs or the absence of precipitation spurs with the macroglobulins.
  • TF precipitates with aTF found in human biological samples examples of the biological samples are bodily fluids such as: blood, serum and plasma.
  • the precipitation pattern can be detected using a number of techniques known to one skilled in the art, including methods used for detecting the immunoprecipitation pattern between antibodies and their antigen, examples of such techniques are described in Oudin, J., CR. Acad Sci., 222:115 (1946); Oudin, J., Methods in Medical Research, V: 335-78, Corcoran A.C., ed., Year Book Publishers Inc. (1952); Ouchterlony, O., Acta. Path. Microbiol. Scand.
  • TF can also be used to treat HIV infections, such as AIDS and ARC.
  • TF can exist in a methylated or an unmethylated state.
  • the present invention also presents methods for obtaining TF, in particular, from thymus cells.
  • the thymus cells are preferably from non-human mammals regardless of whether they are infected by HIV, though HIV infected non-human mammals have higher titers of TF. Examples of the non-human mammals are: monkeys, gorillas, chimpanzees, guinea pigs, cows, rabbits, dogs, mice and rats.
  • Both methylated and unmethylated TF can bind aTF and thus can be used to diagnose HIV infection, in particular AIDS. However, at least in the case of sera from human test subjects, the methylated TF suffers less from nonspecific binding with other proteins, compared to the unmethylated TF. Thus, methylated TF is preferred. Unmethylated TF can be chemically methylated using methods known in the art, for example, as described in EXAMPLE 1 below. Methylated TF can be used as a therapeutic for HIV infection, in particular AIDS.
  • TF is preferably purified from the thymus cells of freshly sacrificed, i.e. , 4 hours or less after sacrifice, mammals such as monkeys, gorillas, chimpanzees, guinea pigs, cows, rabbits, dogs, mice and rats.
  • the nuclei from the thymus cells are isolated using method known in the art. Part of their lysine-rich histone fractions are extracted using the pepsin degradation method of US Patent No. 4,415,553. Other degradative methods such as trypsin degradation, papain degradation, BrCN degradation appear ineffective in extracting TF.
  • the protein rich fragment of the isolate is purified by cation exchange chromatography. The proteins in the TF fractions
  • TF (methylated and unmethylated) can be concentrated by any one of several techniques well known to those skilled in the art, including high salt precipitation, for example, with ammonium sulfate, or by ultrafiltration. If TF is concentrated by precipitation, it is preferably subsequently resuspended in a suitable physiologically balanced salt solution containing protease inhibitor(s).
  • TF Administration As Therapeutics against HIV Infections Applicants observed that non-human mammals, such as cows, which were infected with HIV but did not develop AIDS, have intact TF. This invention postulates that TF plays a role in preventing the progression of HIV infections, in particular AIDS. Therefore, it would be therapeutic to administer TF to HIV infected human.
  • the TF is preferably from non-human mammals which do not develop AIDS when infected with HIV. Methylated non- mammalian TF is preferred. Further, it is preferable to provoke an immunoresponse in the infected human under treatment. To that end, TF is preferably delivered with an adjuvant, or TF is chemically conjugated to an immunogenic carrier that would provoke an antibody response in the patient. Examples of immunogenic carriers are: keyhole limpet and bovine serum albumin.
  • TF is used to vaccinate against, to treat, or cure HIV infections, especially AIDS and ARC.
  • TF is prepared for administration by mixing it at the desired degree of purity with adjuvants or physiologically acceptable carriers, i.e. carriers which are nontoxic to recipients at the dosages and concentrations employed.
  • adjuvants or physiologically acceptable carriers i.e. carriers which are nontoxic to recipients at the dosages and concentrations employed.
  • TF is desirably administered with an adjuvant, in situations where the initial inoculation is delivered with TF, boosters with TF may not require adjuvant.
  • Injections injections (intramuscular or subcutaneous) will be the primary route for therapeutic administration of the vaccines of this invention. However, intravenous delivery, delivery through catheter, or other surgical tubing may also be used.
  • Alternative routes include tablets and the like, liquid formulations, and inhalation of lyophilized or aerosolized receptors. Liquid formulations may be utilized after reconstitution from powder formulations.
  • TF may also be administered via microspheres, liposomes, other microparticulate delivery systems or sustained release formulations placed in certain tissues including blood.
  • the dosage of TF administered will depend upon the properties of the formulation employed, e.g. its binding activity and in vivo plasma half-life, the concentration of TF in the formulation, the administration route, the site and rate of dosage, the clinical tolerance of the patient involved, the pathological condition afflicting the patient and the like, as is well within the skill of the physician. Different dosages are utilized during a series of sequential inoculations; the practitioner may administer an initial inoculation and then boost with relatively smaller doses of TF.
  • TF formulation, dosage and administration schedule The patient is administered an intramuscular or subcutaneous injection containing 8 mg of TF (preferably 2 ml of a formulation containing 4 mg/ml of TF in a physiologically acceptable solution) or 57 ⁇ g of TF protein per 1 kg body weight of the patient.
  • Each treatment course consists of 16 injections, with two injections on consecutive days per week for 8 weeks.
  • the patient's disease condition is monitored by means described further below. Three months after the last injection, if the patient is still suf fering from the disease , the treatment regimen is repeated. The treatment regimen may be repeated until satisfactory result is obtained, e.g.
  • TF is formulated in an aluminum hydroxide adjuvant.
  • the final 1 ml of the final TF formulation contains: 4 mg TF, 0.016 M AlPO 4 (or 0.5 mg Al 3+ ), 0.14 M NaCl, 0.004 M CH 3 COONa, 0.004 M KCl, pH 6.2.
  • the HIV infected patient or uninfected subject may be inoculated five months later, more preferably six months to two years later, and even more preferably eight months to one year later to enhance the patient's "immune memory". See Anderson et al. , J.
  • TF can be administered in various ways and to different classes of recipients. TF can also be used to vaccinate individuals who may or may not be at risk of exposure to HIV, and additionally, the vaccines are desirably administered to seropositive individuals and to individuals who have been previously exposed to HIV.
  • TF can be administered in combination with other antigens in a single inoculation "cocktail". TF can also be administered as in a series of inoculations administered over time. Such a series may include inoculation with the same or different preparations of HIV antigens or other vaccines.
  • T cell titer may be monitored by conventional methods.
  • T lymphocytes can be detected by E-rosette formation as described in Bach, J.F., Contemporary Topics in Immunology, Vol. 2: Thymus Dependency, p. 189, Plenum Press, New York, 1973; Hoffman, T. & Kunkel, H.G., and Kaplan, M.E., et al. , both papers are in In Vitro Methods in Cell Mediated and Tumor Immunity , B.R.
  • the amount of T cell rosette formation may be assayed after the third but before the tenth week of TF treatment.
  • An over sixty-five percent rosette formation indicates a good cell mediated immune response in the patient.
  • a further indicator to monitor is aTF produced by the patient, this may be monitored by the two dimensional electrophoresis method described further below.
  • the clinical condition of the patient can be monitored for the desired effect, e.g. anti- infective effect. If inadequate anti-infective effect is achieved then the patient can be boosted with further TF treatment and the treatment parameters can be modified, e.g. to potentiate the immune response, such as by increasing the amount of TF and/or adjuvant, complexing TF with a carrier or conjugating it to an immunogenic protein, or varying the route of administration.
  • TF may optionally be administered along with other pharmacologic agents used to treat HIV infections such as AIDS and ARC.
  • pharmacologic agents used to treat HIV infections such as AIDS and ARC.
  • these pharmacologic agents are: AZT, antibiotics, immunomodulators such as interferon, anti-inflammatory agents and anti-tumor agents.
  • the device is designed to allow detection of the interaction between TF and aTF in a biological sample. More preferably, in the case where the biological sample is blood, serum, or plasma the device allows for the detection of precipitation pattern of TF in relation to ⁇ - , ⁇ 1 -, and ⁇ 2 - macroglobulins in the sample.
  • the device contains a site for TF and a site for the test sample. Since a two-dimensional gel electrophoresis, as described in the following EXAMPLE 2 is preferred, the device most preferably consists of a gel with slots for containing TF and the test sample such as serum sample, respectively.
  • the device is also preferably packaged with a kit with containers for the reagents necessary for conducting the test, such as buffer solution and TF.
  • the device has its own electrical source, such as a battery, to allow for a two-dimensional electrophoresis to be conducted. Otherwise, it is preferably designed such that it can be connected to outside electrical source.
  • the following experiment shows the isolation, purification, and characterization of TF from calf thymus 4 hours after sacrifice.
  • the thymus tissue and its associated connective tissues were separated from a calf within 4 hours of its sacrifice.
  • the tissues were washed with a solution containing 0.14 M NaCl, and 0.005 M EDTA-Na 3 at 4°C for 5 minutes.
  • the wash solution was decanted and the tissues were washed a second time under the same conditions. After decantation of the wash solution, the tissues were weighed.
  • the tissues were homogenized in 0.14 M NaCl, 0.005 M KCl, 0.005 M MgCl 2 , 0.003 M CaCl 2 , 0.15 M TRIS- HCl, pH 7.6, 0.25 M sucrose in a tissue homogenizer (Brinkman Polytron Homogenizer, Brinkman Instruments, Inc., Westbury, New York), at 4°C and at an rpm and for the duration of time recommended by the manufacturer of the homogenizer for removal of cell nuclei.
  • the ratio of the tissue to the buffer was 1:4 (weight/weight).
  • the tissue homogenate was then filtered through gauze pad by vacuum. The filtrate was centrifuged at 1,000 g at 4°C for 90 minutes. The supernatant was discarded. The pellet was resuspended in 0.008 NaCl, 0.003 M CaCl 2 , 0.003 M MgCl 2 , 0.08 M NaH 2 PO 4 , 0.002 M TRIS- HCl, 0.25 M sucrose, pH 5.2. The ratio of the pellet to the buffer was 1:4 (weight/weight). The resuspension was homogenated in a beaker with a magnetic stirrer at 200 rpm, at 4°C for 5 minutes.
  • the homogenate was then centrifuged at 3500 g, at 4°C, for 60 minutes. The supernatant was discarded. The pellet was resuspended in 0.014 M NaCl, 0.001 M CaCl 2 , 0.002 M MgCl 2 , 0.001 M EDTA- Na 3 , 0.002 M TRIS-HCl, 0.25 M sucrose, pH 4.2 at a ratio of pellet to buffer of 1:4 (weight/weight). The resuspension was homogenated in a beaker with a magnetic stirrer at 200 rpm, at 4°C for 5 minutes. The homogenate was then centrifuged at 8000 g, at 4°C for 60 minutes. The supernatant was discarded.
  • the pellet was resuspended at a ratio of 1:4 (weight/weight) with a previously prepared buffer containing: 1 part volume/volume) Solution 1, 2 parts Solution 2, and 17 parts Buffer 4.
  • Solution 1 consisted of: 10% sodium dodecyl sulfate in water/ethanol (at 55:45 v/v).
  • Solution 2 consisted of 10% Tween 80 (in distilled water).
  • Buffer 4 consisted of: 0.011 M NaH 2 PO 4 and 0.19 M Na 2 HPO 4 , pH 7.4.
  • the resuspension was homogenated in a beaker with a magnetic stirrer at 200 rpm, at 4°C for 15 minutes. The homogenate was then centrifuged at 12000 g, at 4°C for 60 minutes. The supernatant was discarded. The pellet was weighed and resuspended in 0.05 M Na 3 C 6 H 5 O 7 , 0.05 M CH 3 COONa, 0.1 N HCl, pH 2.8 at a ratio of pellet to buffer of 1:4 (weight/weight). The resuspension was homogenized by tissue homogenizer at 1000 rpm, at 4°C for 1 minute.
  • Pepsin (catalog number P 7000, Sigma Chemical Company, St. Louis, Missouri) diluted in distilled water at 1:10000, with activity of 800-2500 units per mg protein, was added to the homogenate at a pepsin (powder) to pellet after homogenization weight ratio of 100:1.8.
  • the mixture was placed in a beaker and stirred, under nitrogen atmosphere, with a magnetic stirrer at 45 rpm, at 4°C for 12 hours. The resulting mixture was then centrifuged at 12000 g, at 4°C for 60 minutes. The pellet was discarded. The supernatant was removed and precipitated with a solution consisting of saturated
  • the protein in the dialysate was measured by the Lowry method.
  • the solution was diluted to obtain 2 mg/ml of protein.
  • the pH of the solution was then adjusted to 7.2 by 0.1 N NaOH.
  • a solution of 0.2 M bromoacetic acid was prepared separately by dissolving bromoacetic acid in 10 ml or less of water and the pH was adjusted to 7.0 by 0.1 N NaOH.
  • the resulting bromoacetic acid solution was added to the protein solution and the mixture was stirred by magnetic stirrer for 48 hours under nitrogen atmosphere.
  • the pH of the mixture was maintained at 7.2 throughout the reaction.
  • the ammonium sulfate precipitation step was repeated up to the step of measuring the protein concentration by the Lowry method.
  • the final solution was diluted or concentrated, as needed, to obtain 4 mg/ml of the protein TF from 200 g of calf thymus cells.
  • the molecular weight of the collected TF fraction was determined by silver stained 11% non-reducing SDS-
  • the larger band was unmethylated TF which constituted 98% of the TF fraction.
  • the smaller band was methylated TF which constituted the remaining 2% of the TF fraction.
  • unmethylated TF was determined to have a molecular weight of about 35 Kilodalton (Kd) and methylated TF has a molecular weight of about 28 Kd.
  • the TF composition (including methylated and unmethylated TF) has a pH of between about 7.64 and 8.6 by pH titration.
  • the isoelectric point of the TF composition is about 5.6 ⁇ 0.1 as determined by immunoelectrical focusing.
  • the TF was methylated to form a methylated TF preparation for use in the following EXAMPLES.
  • the methylation was conducted as follows.
  • TF was mixed with CH 2 BrCOOH in sufficient quantity to produce a final solution of 0.2 M CH 2 BrCOOH.
  • CH 2 BrCOOH 2.78 g CH 2 BrCOOH was dissolved in 10 ml distilled water and added to 100 ml TF containing 700 mg TF (7 mg/ml). The pH of the mixture was adjusted to and maintained at 7.24 with 0.1 M in NaOH. The mixture was allowed to incubate from 6 to 8 hours. The TF protein in the resulting aqueous fraction was concentrated by ammonium sulfate precipitation, using techniques known in the art. To 10 ml of the methylated TF fraction was added an equal volume of saturated ammonium sulfate.
  • the mixture was refrigerated 12 hours and then centrifuged 20,000 rpm for 60 minutes. The pellet was removed and dissolved in a final buffer containing 0.1 M NaCl, 0.1 M sodium citrate, 0.02 M thiodiglycol. The mixture was then dialyzed against the same buffer, to remove the ammonium sulfate, for 24 hours.
  • the methylated TF obtained from EXAMPLE 1 was used to determine whether a given human serum sample was from a patient infected with HIV. The experiment was conducted as follows:
  • the human serum samples in this Example were provided by AIDS Health Foundation, Los Angeles, California.
  • the Foundation had tested the samples using commercially available enzyme-linked immunosorbent assay
  • ELISA Western blot which detected the patient's antibodies against the HIV.
  • the ELISA was conducted first. If the ELISA indicated HIV infection (HIV- positive), Western blot was conducted as a confirmation test.
  • the equipment used was a submarine mini gel electrophoresis unit. (Catalog No. E 0638, Sigma Chemical Company).
  • the unit contained a buffer chamber with a capacity for 800 ml of buffer.
  • the unit was also equipped with a peristaltic pump for recycling the buffer.
  • the power source had an output range of 20 to 240 V, 0 to 100 mA, with a constant current and voltage output.
  • the gel was prepared with 1% agarose (Catalog No. A 4679, Sigma Chemical Company).
  • the gel buffer consisted of: 0.0257 M TRIS-HCl, 0.009 M sodium borate decahydrate, 0.067 M glycine, 0.0034 M sodium acetate trihydrate, 0.015 M 2-mercaptoethanol and 0.015 M thiodiglycol, pH 7.64. 14.25 ml of the 1% melted agarose gel was applied to the electrophoretic gel plate.
  • the solidified gel was 0.2 cm thick and at a dimension of 7.5 cm x 7.5 cm. The gel was overlaid with the same buffer.
  • FIG. 2 schematically presents the arrangement for the first- dimension gel, 1 denotes the well for the serum sample.
  • FIG. 3 schematically presents the arrangement for the second-dimension gel, 2 denotes the trough.
  • the trough was filled with 100 ⁇ l of methylated TF of EXAMPLE 1. The same voltage and current was applied to the gel for 50 minutes at 14°C. Throughout the two- dimensional electrophoresis, the buffer was recirculated at 25 ml/min. After the last run, the power was turned off, and the gel was removed after a few seconds.
  • the gel was then simultaneously fixed and stained, for 45 minutes, in a solution containing: 3 parts methanol, 1 part ethanol, 12% acetic acid and 0.1% bromophenol blue (Catalog No. B-8026, Sigma Chemical Company).
  • the gel was destained by soaking it in distilled water for 3 to 4 hours and dried.
  • FIG. 4 The positions of serum proteins on the two- dimensional electrophoretic gel were shown in FIG. 4.
  • the immunoglobulin stain 3 appeared next to the serum well 1 containing the patient's serum sample, so did ⁇ -macroglobulin 4, further from the serum well were ⁇ 2 -macroglobulin 5, ⁇ 1 -macroglobulin 6, and albumin 7.
  • precipitation spurs The patterns of these precipitation spurs indicate whether the test subject has
  • test subject's HIV infection such as
  • FIG. 5 shows broken precipitation spurs 9 which indicate that the subject was HIV-positive.
  • This subject's serum was taken and tested HIV-positive by ELISA and the test of the present invention. At the time the serum was taken, the subject did not show any clinical symptoms of AIDS.
  • FIGs. 6 to 9 show position 10, where ⁇ -macroglobulin was located and where a healthy subject's precipitation spur would be adjacent to, and the spur would be a continuous spur spanning alongside the locations of ⁇ - , ⁇ - , and ⁇ 2 - macroglobulins (as in FIG. 4).
  • the subjects' precipitation spurs 11 were broken (i.e. not continuous alongside the locations of ⁇ - , ⁇ - , and ⁇ 2 - macroglobulins) and below position 10.
  • the positions of the test subject's precipitation spurs indicated that they were of lesser molecular weight than the precipitation spurs of a healthy subject.
  • gels with precipitation spurs that are further away in distance, from the location of spurs expected of a healthy subject indicate smaller fragments of aTF and thus a more severe case of AIDS than gels with precipitation spurs that are closer to the expected location of the spurs of a healthy patient.
  • this distance can be determined based on the relative distance of the first precipitation spur, i.e. the spur closest in vertical distance to the serum hole 1, from the expected spur of a healthy subject should be. The further the relative distance, in both the horizontal and vertical directions from the location of the health subject's spur, the more severe the disease.
  • the disease is less severe for the subject who has a gel showing spur(s) that are more intense and lesser in number. Lesser number of precipitation spurs and a heavier precipitation indicate aTF that is less fragmented and at a higher level, and therefore, a less severe case of AIDS.
  • the first precipitation spur is the one closest in vertical distance 15 from the baseline 14 (see FIG. 12). Since a healthy subject's precipitation spur would stretch from adjacent to the locations of ⁇ - and ⁇ 1 -macroglobulins, to the location of ⁇ 2 - macroglobulins (as in FIG. 4), one can measure the relative distance from either the location of ⁇ - , ⁇ - , or ⁇ 2 - macroglobulins. In this case, the location of ⁇ - macroglobulin 10 was chosen.
  • the baseline can be another position that is standardized for all the gel photographs, and the relative distances can be measured from another point that is located in the spread of the serum, as long as these points are consistent for all the photographs being compared and consistently used to measure the relative distances.
  • Other variations that do not depart from the spirit of the first analysis can be used.
  • FIG. 10 is significant in that at the time the serum for this test was taken, the subject tested HIV-negative on the ELISA. However, the test of the present invention indicated that the subject was HIV-positive as shown by broken precipitation spur 11. Two months after the serum for the test was drawn, the subject tested HIV-positive on the ELISA. Thus, the figure confirms that the test of the present invention is capable of an earlier detection of HIV infection than the conventional ELISA.
  • FIG. 11 is significant in that the serum sample was taken after a clinically diagnosed AIDS subject had been transfused with blood from a healthy donor.
  • the precipitation spur caused by the donor's serum is indicated by the arrow 12 at the location of higher molecular weight, which tends to show that the initial small amount of fragmentation of whole aTF from the healthy donor, and thus the location of the spur was closer to the molecular weight expected of a healthy subject and more indicative of an earlier stage of infection, as shown by the relatively similar locations of this spur with the spur in FIG. 10.
  • the precipitation spur caused by the serum of the AIDS subject is indicated by the arrow 13, at a location of lower molecular weight, which indicates fragmented and thus smaller aTF from the patient and HIV-infection.
  • the two-dimensional gel electrophoresis shown herein can be mass-produced as an in vitro device for testing of biological fluid samples for the presence of HIV infection from the test subjects.
  • the gels can be dried for easy packaging and transportation.
  • the packaged gel may contain a preformed well for samples, and a trough for TF.
  • the TF can be stored in a container and sold separately or together with the gel as a kit.
  • the kit may also contain containers for the electrophoretic buffer, the stains and/or molecular weight standards.
  • the kit may further contain containers with serum sample(s) from healthy subject(s).
  • kits containing reagents and materials needed for these assays are also included in the present invention.
  • This example describes a study in which an AIDS patient (also referred to as "test subject" in this EXAMPLE 3) was therapeutically treated with the TF composition of the present invention. The patient did not receive any other treatments or drugs during the study.
  • the patient was a 27 year old White homosexual male, weighing 138 pounds at the beginning of the trial. Eighteen months ago, the patient's serum tested positive for HIV antibodies. The patient was also diagnosed as HIV positive based on his clinical symptoms, p24 antigen count, CD4 + and CD8 + on cell counts in absolute numbers (cells/ ⁇ l) and lymphocyte subset percentages, as shown in Table 1 below for the tests conducted on the patient's blood sample taken on April 12, 1995, two weeks before he started his TF treatment. The patient was not suffering from AIDS before and during the TF treatment.
  • the treatment started on April 27, 1995.
  • the patient received 14 mg of TF per week in two intramuscular injections, one injection on Tuesday and another on Wednesday.
  • Each injection contained 7 mg of TF (in 2 ml of a formulation containing 3.5 mg/ml of TF).
  • the TF was purified as described in Example 1 above and the sterilized TF formulation contained: 3.5 mg/ml methylated TF, 8.1 mg/ml sodium chloride, 1.9 mg/ml sodium acetate, 2.6 mg/ml sodium tri-phosphate, 2.1 mg/ml aluminum chloride, pH 6.2.
  • Table 1 presents the results of the experiment.
  • the dates are the dates on which blood samples were taken from the patient.
  • the tests were conducted by Unilab Corporation (Tarzana, California), using generally accepted clinical assays.
  • RBC red and white blood cell counts, respectively (x 10 3 /mm 3 ).
  • HEMOGLOBIN and “PLATELET COUNT” denote the haemoglobin counts (in g/dL) and platelets counts (x 10 3 /mm 3 ), respectively.
  • POLYS denotes neutrophil cell counts measured as a percentage of white blood cell counts.
  • CD4% and CD8% denote the lymphocyte subset percentages of CD4 + and CD8 + cells, respectively.
  • CD4 ABS and “CD8 ABS” denote the absolute cell numbers (in cells/ ⁇ l) of CD4 + and CD8 + cells, respectively.
  • the CD4 + and CD8 + cell counts were determined by flow cytometry.
  • RATIO H/S denotes the ratio of the Helper versus the Suppressor cells and was obtained by dividing the number of "CD4 ABS” with the number for "CD8 ABS".
  • TOTAL PROT denotes the total blood serum protein in g/dL in the patient's sample, as determined by colorimetric method using Olympus AU 5000 instrument (Olympus Co., Ltd., Tokyo, Japan).
  • ARB denotes albumin
  • APHA-1 denotes alpha-1 globulin
  • APHA-2 denotes alpha-2 globulin
  • BETA denotes beta-globulin
  • GAMMA denotes gamma-globulin.
  • P/24" denotes p24 viral core antigen which was determined by p24 antigen EIA test kit (Abbott Laboratories, Abbott Park, Illinois). Further, the blood samples collected on the time points specified in Table 1 also tested positive for HIV- 1 antibodies as determined by HIV ELISA test kit of Organon Technica (Raleigh, North Carolina). The patient gained 7 pounds in weight between his first TF injection and up to May 24, 1995.
  • the above tests show a trend of increasing CD4 + cell counts and decreasing CD8 + cell counts after the start of the TF treatment. Additionally, the p24 antigen tests showed negative results after the start of the TF treatment, though the test subject tested positive before and at the start of the TF treatment. The HIV antibody assays remained positive as residual antibodies remained in the test subject. These test results tend to suggest that the TF treatment was effective in combating HIV- infection and the progression of the disease caused by HIV.
  • FIGs. 13 and 14 are photographs of two-dimensional electrophoretic gels of serum samples from two controls: a human subject whose serum sample tested negative for
  • the precipitation spur 9 is a continuous spur spanning alongside the locations of ⁇ -, ⁇ 1 - , and ⁇ 2 - macroglobulins, which indicate a healthy HIV negative subject.
  • the precipitation spur 9 in FIG. 13 is a continuous spur spanning alongside the locations of ⁇ -, ⁇ 1 - , and ⁇ 2 - macroglobulins, which indicate a healthy HIV negative subject.
  • FIGs. 15 to 19 present the resulting photographs of the two-dimensional electrophoretic gel tests for the test subject, on the serum samples collected on May 11, May 18, May 24 and May 31, 1995, respectively.
  • test subject's serum sample tested negative for HIV infection As shown in FIG. 15, after a week of receiving the above TF treatment, on May 4, 1995 the test subject's serum sample tested negative for HIV infection, as indicated by the continuous precipitation spur 9 alongside the locations of ⁇ - , ⁇ 1 -, and ⁇ 2 - macroglobulins.
  • the test subject's serum formed a continuous precipitation spur 9 alongside the locations of ⁇ - and ⁇ 1 - macroglobulins, which is a more continuous precipitate spur than that observed for the control HIV-positive patient of FIG. 14.
  • the two-dimensional electrophoretic tests tend to suggest that the TF treatments of the present invention is effective against HIV-infection and/or disease progression.
  • This Example provides further data regarding six human patients who were therapeutically treated with the TF composition of the present invention. These patients did not receive any other treatments or drugs during and after the six weeks of treatment period.
  • the TABLES below also show patients' data at nine months (for Patient Nos. 1-5), and two months (for Patient No. 6) after the end of the treatment period.
  • each patient received 14 mg of TF per week in two intramuscular (IM) injections, one injection on Tuesday and another on Wednesday per week.
  • Each injection contained 7 mg of TF (in 2 ml of a formulation containing 3.5 mg/ml of TF).
  • the TF was purified as described in EXAMPLE 1 above and the sterilized TF formulation contained: 3.5 mg/ml methylated TF, 8.1 mg/ml sodium chloride, 1.9 mg/ml sodium acetate, 2.6 mg/ml sodium tri-phosphate, 2.1 mg/ml aluminum chloride, pH 6.2.
  • TABLES 2 to 7 present the results of the study for each patient. The tests were conducted by laboratories using generally accepted clinical assays.
  • HIV-Ab ELISA
  • ELISA denotes HIV-1 antibodies as determined by ELISA.
  • CD4 abs.” and CD8 abs.” denote the absolute cell numbers (in cells/ ⁇ l) of CD4 and CD8 cells, respectively.
  • p24 Ag denotes p24 viral core antigen which was determined by p24 antigen immune complex disruption (ICD) EIA; this EIA for HIV-1 antigen detects p24 core protein after disruption of immune complexes.
  • HIV-1 RNA, PCR denotes quantitative estimate of number of copies of HIV-1 ribonucleic acid (RNA) per ml of plasma tested by polymerase chain reaction (PCR) amplification. Increases/decreases in the number of copies of viral RNA detected are associated with increases/decreases in plasma viremia.
  • HIV-1 Plasma Culture denotes HIV-1 titers found in plasma and peripheral blood mononuclear cell cultures.
  • HIV-1 Plasma Quantitative denotes HIV-1 viral infectivity expressed as infectious unit per ml (IU/ml).
  • Poly Cells denotes white blood cell counts in absolute numbers (cells/ ⁇ l).
  • ⁇ -1 macroglobulin (denoted as "alpha-1 Macro"), ⁇ -2 macroglobulin (denoted as “alpha-2 Macro"), and gamma-immunoglobulin (“IgG”) were determined by serum protein electrophoresis. The number (with %) indicated is the percentage distribution of the specific serum globulin among all the serum globulins.
  • the IgG, IgA and IgM are expressed in mg/DL serum.
  • HLA-DR denotes a product of Human Major Histocompatibility complex located on chromosome 6.
  • Patient No. 1 (a 21-year old female) had full blown AIDS with cerebral damage and mental disorders, a CD4 count of 36, and a life expectancy in the range of six-twelve months. Her CD4 count increased from 36 (at the start of treatment) to 108 (nine months after the end of the treatment period).
  • the p24 core antigen was negative, i.e., at less that 5 ⁇ g/ml. This negative p24 core antigen reading indicates lack of viral activity as of the fourth week of treatment.
  • HIV-1 culture tested negative as of the fourth month of treatment The negative plasma HIV-culture reading indicates that this patient's T-cells isolated from plasma were non-infective when mixed with T-cells of uninfected control blood in the in vitro assay -- i.e. , negative plasma culture.
  • positive plasma culture was produced when T-cells from control HIV-1 infected blood were mixed with uninfected control blood in the in vitro assay.
  • Increases in IgG, ⁇ -1 and ⁇ -2 macroglobulin activities were observed during and after TF treatment.
  • the patient no longer had full blown AIDS (e.g., no opportunistic diseases), though she was still HIV positive (i.e., tested positive for antibodies against HIV in an ELISA).
  • Patient No. 2 (a 30- year old male) was HIV positive (i.e. , tested positive for antibodies against HIV in an ELISA), however he did not suffer from all the symptoms of AIDS.
  • His CD4 cell counts increased from 193 (before TF treatment) to 305 (nine months from the end of treatment).
  • His p24 core antigen remained negative before, during and after TF treatment -- indicating low viral activity.
  • His plasma culture was converted to negative at fourth month after treatment, indicating non-infectivity of the his plasma in the in vitro assay.
  • Increase in his humoral immunity was indicated by increases in the IgG, ⁇ -1 and ⁇ -2 macroglobulin levels.
  • the patient still did not show any sign of AIDS.
  • Patient No. 3 (a 24- year old female) was HIV positive (i.e. , tested positive for anitbodies against HIV in an ELISA), however she did not suffer from all the symptoms of AIDS.
  • CD4 -cell counts increased from 404 (pretreatment) to 636 (nine months from the end of treatment).
  • Her p24 core antigen test was negative throughout the study.
  • Her plasma culture converted to negative at fourth month after treatment.
  • the increase in humoral immunity of the patient was indicated by increases in her IgG, ⁇ -1 and ⁇ -2 macroglobulins.
  • the patient did not show any sign of AIDS.
  • the patient Before treatment, the patient (a 27-year old male) was HIV positive (i.e. , tested positive for anitbodies against HIV in an ELISA), and had full blown AIDS symptoms (Grade 3, with opportunistic infections in the throat and upper part of the lung). His CD4 cell counts increased from 389 (before treatment) to 599 (nine months from the end of treatment). His p24 core antigen converted to negative after four weeks of treatment and remained negative. His HIV plasma infectivity was converted to non-infective after six weeks of treatment and remained non-infective. The increased in humoral immunity of the patient was indicated by the increase in his IgG, ⁇ -1 and ⁇ -2 macroglobulins. Twelve months after the end of the treatment, the patient did not show any sign of AIDS.
  • the patient was HIV positive
  • the patient had full blown AIDS (at a grade between 3 and 4, suffering from e.g., retinitis, cytomegalovirus infection, fungal infection in the throat, lung, trachea, and bronchi, and bedridden).
  • His CD4 count was slightly increased after two months of treatment.
  • His p24 core antigen converted to negative after four weeks of treatment and remained negative.
  • His plasma culture was positive before treatment and was converted to negative and non-infective after treatment.
  • the peripheral blood cell cultures are positive in a patient with CD4 count of less than 100 and viral loads of 5x10 5 .
  • no HIV was detected in the peripheral blood cells at one and two months of treatment.
  • the viral load of the patient had decreased from 5x10 5 to 3x10 4 copies of viral RNA. This is close to a 1.5 log decrease in viral RNA.
  • Patient No. 6 had also gained 15 pounds of weight since the start of treatment. Three months after the end of treatment, the patient did not have AIDS.
  • This Example shows that HIV viral activity was stopped as seen by P24 core antigen converting to less that 5 ⁇ g/ml, the limit of test method. Dramatic increase of CD4 count in the HIV patient was also shown. This increase is more dramatic over time than those observed for antiviral products commercially available in the United States, such as AZT and others.
  • This Example also shows dramatic decreases in viral load of the patients as determined by quantitative RNA polymerase chain reaction.
  • the patients' plasma cultures converted to negative. In in vitro systems, the patients' blood plasma was non-infective.
  • the patients' T-cells were unable to infect non-infected (normal) patients' T-cells in vitro . The foregoing may indicate lack of virus in the plasma. It may also indicate the patient might have been immunized, and thus unable to infect other non-infected patients.
  • peripheral blood mononucleocytes tested negative for HIV.
  • the treatment transformed full blown

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Abstract

L'invention se rapporte à l'immunologie et la virologie, et plus précisément à des compositions obtenues à partir de cellules de thymus de mammifères. Ces compositions sont utiles pour les diagnostics, les vaccins et le traitement pour l'infection à virus d'immunodéficience humaine (VIH) et des maladies apparentées telles que le syndrome immunodéficitaire acquis (SIDA) et le para-sida. On décrit par ailleurs des procédés de diagnostic, de vaccination et de traitement, ainsi que des dispositifs mettant en æuvre ces compositions.
PCT/US1996/006079 1995-05-01 1996-05-01 Compositions et procedes pour deceler et traiter le syndrome immunodefficitaire acquis WO1996034886A1 (fr)

Priority Applications (12)

Application Number Priority Date Filing Date Title
AT96920118T ATE205221T1 (de) 1995-05-01 1996-05-01 Zusammensetzungen und verfahren zur detektion und behandlung des erworbenen immun-defizienz- syndroms
EA199700353A EA001100B1 (ru) 1995-05-01 1996-05-01 Фракция обогащенного лизином гистонового тимусного фактора (tf), способ получения фракции и способ выявления вич-инфекции у человека
CA002220347A CA2220347C (fr) 1995-05-01 1996-05-01 Compositions et procedes pour deceler et traiter le syndrome immunodefficitaire acquis
BR9608837-0A BR9608837A (pt) 1995-05-01 1996-05-01 "composição obtida de células para detectar uma infecção por vìrus da imunodeficiência humana, aparelho, kit e métodos para sua detecção, purificação da proteìna e sua obtenção e tratamento do ser humano"
AU58519/96A AU721463B2 (en) 1995-05-01 1996-05-01 Compositions and methods for detecting and treating acquired immunodeficiency syndrome
DE69615015T DE69615015T2 (de) 1995-05-01 1996-05-01 Zusammensetzungen und verfahren zur detektion und behandlung des erworbenen immun-defizienz-syndroms
EP96920118A EP0826003B1 (fr) 1995-05-01 1996-05-01 Compositions et procedes pour deceler et traiter le syndrome immunodefficitaire acquis
DK96920118T DK0826003T3 (da) 1995-05-01 1996-05-01 Præparater og fremgangsmåder til påvisning og behandling af erhvervet immundefekt syndrom
NZ308708A NZ308708A (en) 1995-05-01 1996-05-01 Compositions and methods for detecting and treating acquired immunodeficiency syndrome
JP53345796A JP3816524B2 (ja) 1995-05-01 1996-05-01 後天性免疫不全症候群を検出しそして処置するための組成物および方法
BG102083A BG64056B1 (bg) 1995-05-01 1997-11-28 Състави и методи за откриване и лечение на спин
HK98110415A HK1009457A1 (en) 1995-05-01 1998-09-03 Compositions and methods for detecting and treating acquired immunodeficiency syndrome

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EP2323680A2 (fr) * 2008-07-25 2011-05-25 Viral Genetics, Inc. Protéines pour utilisation dans le diagnostic et le traitement d'une infection et d'une maladie
US8957031B2 (en) 2007-10-23 2015-02-17 Regents Of The University Of Colorado, A Body Corporate Competitive inhibitors of invariant chain expression and/or ectopic clip binding

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US4415553A (en) * 1973-08-06 1983-11-15 Dso "Pharmachim" Compositions, processes for their preparation and method for treatment of neoplasms
EP0149468A2 (fr) * 1984-01-12 1985-07-24 SYMBIOTEC Gesellschaft zur Forschung und Entwicklung auf dem Gebiet der Biotechnologie GmbH Substance biologiquement active à caractères hormonaux, procédé de préparation et utilisation d'histones dans des buts médicinaux
EP0392315A1 (fr) * 1984-01-12 1990-10-17 SYMBIOTEC Gesellschaft zur Forschung und Entwicklung auf dem Gebiet der Biotechnologie GmbH Histone H1 pure utilisable dans des procédés thérapeutiques
WO1989005455A1 (fr) * 1987-12-02 1989-06-15 The Regents Of The University Of California Test d'anticorps anti cellules t relatif au sida
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8957031B2 (en) 2007-10-23 2015-02-17 Regents Of The University Of Colorado, A Body Corporate Competitive inhibitors of invariant chain expression and/or ectopic clip binding
US10420813B2 (en) 2007-10-23 2019-09-24 The Regents Of The University Of Colorado, A Body Corporate Competitive inhibitors of invariant chain expression and/or ectopic clip binding
EP2323680A2 (fr) * 2008-07-25 2011-05-25 Viral Genetics, Inc. Protéines pour utilisation dans le diagnostic et le traitement d'une infection et d'une maladie
EP2323680A4 (fr) * 2008-07-25 2013-05-01 Viral Genetics Inc Protéines pour utilisation dans le diagnostic et le traitement d'une infection et d'une maladie

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