Vaccination and methods against diseases resulting from...

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Carbohydrate doai

Reexamination Certificate

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C435S069100, C435S320100, C435S372300, C435S455000, C536S023100, C536S023500

Reexamination Certificate

active

06207645

ABSTRACT:

BACKGROUND OF THE INVENTION
This invention relates to the immune system and, more specifically, to methods of modifying pathological immune responses.
Higher organisms are characterized by an immune system which protects them against invasion by potentially deleterious substances or microorganisms. When a substance, termed an antigen, enters the body, and is recognized as foreign, the immune system mounts both an antibody-mediated response and a cell-mediated response. Cells of the immune system termed B lymphocytes, or B cells, produce antibodies that specifically recognize and bind to the foreign substance. Other lymphocytes termed T lymphocytes, or T cells, both effect and regulate the cell-mediated response resulting eventually in the elimination of the antigen.
A variety of T cells are involved in the cell-mediated response. Some induce particular B cell clones to proliferate and produce antibodies specific for the antigen. Others recognize and destroy cells presenting foreign antigens on their surfaces. Certain T cells regulate the response by either stimulating or suppressing other cells.
While the normal immune system is closely regulated, aberrations in immune response are not uncommon. In some instances, the immune system functions inappropriately and reacts to a component of the host as if it were, in fact, foreign. Such a response results in an autoimmune disease, in which the host's immune system attacks the host's own tissue. T cells, as the primary regulators of the immune system, directly or indirectly effect such autoimmune pathologies.
Numerous diseases are believed to result from autoimmune mechanisms. Prominent among these are rheumatoid arthritis, systemic lupus erythematosus, multiple sclerosis, Type I diabetes, myasthenia gravis and pemphigus vulgaris. Autoimmune diseases affect millions of individuals world-wide and the cost of these diseases, in terms of actual treatment expenditures and lost productivity, is measured in billions of dollars annually. At present, there are no known effective treatments for such autoimmune pathologies. Usually, only the symptoms can be treated, while the disease continues to progress, often resulting in severe debilitation or death.
In other instances, lymphocytes replicate inappropriately and without control. Such replication results in a cancerous condition known as a lymphoma. Where the unregulated lymphocytes are of the T cell type, the tumors are termed T cell lymphomas. As with other malignancies, T cell lymphomas are difficult to treat effectively.
Thus, a long-felt need exists for an effective means of curing or ameliorating T cell mediated pathologies. Such a treatment should ideally control the inappropriate T cell response, rather than merely reducing the symptoms. The present invention satisfies this need and provides related advantages as well.
SUMMARY OF THE INVENTION
The present invention provides vaccines and a means of vaccinating a vertebrate so as to prevent or control specific T cell mediated pathologies. The vaccine is composed of a substantially pure T cell receptor (TCR) or an immunogenic fragment thereof corresponding to a TCR present on the surface of T cells mediating the pathology. The vaccine fragment can be a peptide corresponding to sequences of TCRs characteristic of the T cells mediating said pathology.
The invention additionally provides specific &bgr;-chain variable regions and their immunogenic segments, and in particular three T cell receptors, designated V&bgr;3, V&bgr;14 and V&bgr;17, which are associated with the pathogenesis of autoimmune diseases, for example rheumatoid arthritis (RA) and multiple sclerosis (MS). Additional VDJ junctional (CDR3) regions associated with other autoimmune diseases are also provided. The present invention further relates to means for detecting, preventing and treating RA, MS and other autoimmune diseases.
The invention further provides methods of preventing or treating T cell mediated pathologies, including RA and MS, by gene therapy. In these methods, pure DNA or RNA encoding for a TCR, an immunogenic fragment thereof or an anti-idiotype antibody having an internal image of a TCR or an immunogenic fragment is administered to an individual. Vectors containing the DNA or RNA and compositions containing such vectors are also provided for use in these methods.


REFERENCES:
patent: 4886743 (1989-12-01), Hood et al.
patent: 5185250 (1993-02-01), Brenner et al.
patent: 5614192 (1997-03-01), Vandenbark
patent: 0 340 109 A3 (1989-04-01), None
patent: WO 90/11294 (1990-10-01), None
patent: WO 91/01133 (1991-02-01), None
patent: WO 91/15225 (1991-10-01), None
patent: WO 92/12996 (1992-08-01), None
Maniatis et al., ‘Molecular Cloning: A laboratory manual’, Second Edition, Cold Spring Harbor Press 1989.*
Donahue et al JEM 176: 1125, 1992.*
Coghlan New Scientist, pp. 14-15, Nov. 25, 1995.*
Marshall Science 270: 1751, 1995.*
Orbin & Motulsky “Report & Recommendation . . . Gene Therapy” Dec. 7, 1995.*
Rattner, M. Biotechnology 7:207 (1989) “Can the Antisense Message be Delivered?”.*
Simons, M., et al., Nature 359:67-70 (1992), “Antisense C-mxb Oligonucleotides Inhibit Intimal Arterial Smooth Muscle Cell Accumulation in vivo”.*
Brostoff, et al., “T Cell receptors, immunoregulation, and autoimmunity”Clinical Immunology and Immunopathology.62:1-7 (1992).*
Ben-Nun et al., Vaccination against autoimmune encephalomyelitis with T-lymphocite line cells reactive against myelin basic protein. Nature 292:60-61 (1981).*
Acha-Orbea et al., Limited heterogeneity of T cell receptors from lymphocytes mediating autoimmune encephalomyelitis allows specific immune intervention. Cell 54:263-273 (1988).*
Urban et al., Restricted use of T cell receptor V genes in murine autoimmune encephalomyelitis raises possibilities for antibody therapy. Cell 54:577-592 (1988).*
Owhashi and Heber-Katz, Protection from experimental allergic encephalomyelitis conferred by a monoclonal antibody directed against a shared idiotype on rat T cell receptors specific for myelin basic protein. J. Exp. Med. 168:2153-2164 (1988).*
Burns et al., Both rat and mouse T cell receptors specific for the encephalitogenic determinant of myelin basic protein use similar V &agr; and V &bgr; chain genes even though the major histocompatiblity complex of encephalitogenic determinants being recognized are different. J. Exp. Med. 169:27-39 (1989).*
Chluba et al., T cell receptor &bgr; chain usage in myelin basic protein-specific rat T lymphocytes. Eur. J. Immunol. 19:279-284 (1989).*
Wucherpfennig et al., Shared human T cell receptor VB usage to immunodominant regions of myelin basic protein. Science 248:1016-1019 (1990).*
Kimura et al., Sequences and repertoire of the human T cell receptor &agr; and &bgr; chain variable region genes in thymocytes. Eur. J. Immunol. 17:375-383 (1987).*
Sedgwick, J., Long-term depletion of CD8′ T cells in vivo in the rat: no observed role for CD8 (cytotoxic/suppressor) cells in the immunoregulation of experimental allergic encephalomyelitis, Eur. J. Immunol. 18:495-502 (1988).*
Urban et al., Restricted use of T cell receptor V genes in murine autoimmune encephalomyelitis raises possibilities for antibody therapy. Cell 54:577-592 (1988).*
Lider et al., Anti-idiotypic network induced by T cell vaccination against experimental autoimmune encephalomyelitis. Science 239:181-183 (1988).*
Sun et al., Suppression of experimentally induced autoimmune encephalomyelitis by cytolytic T-T cell interactions. Nature 332:843-845 (1988).*
Offner et al., Lymphocyte vaccination against experimental autoimmune encephalomyelitis: evaluation of vaccination protocols. J. Neuroimmunol. 21:13-22 (1989).*
Choi et al., Interaction ofStaphylococcus aureustoxin “superantigens” with human T cells. Proc. Natl. Acad. Sci. USA 86:8941-8945 (1989).*
White et al., The VB-specific superantigen staphylococcal enterotoxin B: stimulation of mature T cells and cloncal deletion in neonatal mice. Cell 56:27-35 (1989).*
Pullen et al., Identification of the region of T cell receptor &bgr; chain that interacts with t

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