Drug – bio-affecting and body treating compositions – Antigen – epitope – or other immunospecific immunoeffector
Reexamination Certificate
1995-05-30
2002-10-29
Venkat, Jyothsna (Department: 1627)
Drug, bio-affecting and body treating compositions
Antigen, epitope, or other immunospecific immunoeffector
C424S193100, C424S562000, C514S002600, C514S008100, C514S021800, C514S866000
Reexamination Certificate
active
06471963
ABSTRACT:
FIELD OF THE INVENTION
This invention relates to purified antigenic material for use in the prevention and treatment of diabetes.
BACKGROUND OF THE INVENTION
Autoantibodies which are produced by B lymphocytes are involved in the pathogenesis of a number of autoimmune diseases, such as thyroiditis or diabetes, which involve organs such as the thyroid, pancreatic islets or adrenal glands. Some autoantibodies bind cell membrane receptors (or antigens) and trigger an immune response which leads to destruction of the cell or antigen. What triggers the autoimmune response is not known. Autoantibodies can also bind antigens, causing stimulation or blockage of biological processes. The circulating levels of antoantibodies in the body may be low, but such autoantibodies are highly potent and have to neutralized to prevent damage to organs and cells.
Current evidence suggest that Type 1 diabetes mellitus is a chronic autoimmune disease involving two types of islet cell antibodies: (i) islet cell cytoplasmic antibodies (ICCA); (ii) islet cell surface antibodies (ICSA). The ICSA are believed to be central to the initial destruction of the beta cells, whereas ICCA is secondary to the damage. ICSA have been detect in 40-60% of recent-onset diabetics and are present in susceptible individuals long before clinical onset. As such, they may be used as an early predictor of diabetes and as a marker of the silent, ongoing beta cell damage in prediabetic individuals.
Baekkesov et al, Nature
(London) 298:167-169 (1982), used ICSA-positive sera to search for the autoantigen(s) recognized by ICCA and ICSA. Detailed investigations have been hampered by the small amounts of antibody available and also its polyclonality.
Baekkesov et al have shown that diabetic sera are able to immunoprecipitate surface-labelled islet proteins of 64 kDa and 38 kDa.
Hari et al, Diabetes
35:517-522 (1986), report a monoclonal antibody from the NOD mouse which recognizes a 64 kDa pancreatic protein. Similarly, Uchigata et al produced a monoclonal antibody from the BB rat which recognizes a 60 kDa and a 68 kDa glycoprotein. Their antibody bound RINm5F cells and frozen pancreas after neuraminidase treatment, suggesting that the antigen is normally hidden by sialic acid residues. Their antibody also reacted with a crude glycolipid extract (only after neuraminidase treatment) which they believe was contaminated with glycoproteins; however, their antibody bound a sequence in the glycolipid paragloboside.
Nayak et al, Diabetes
34:617-619 (1985), showed that the autoantigen recognized by diabetic sera has the properties of sialic acid-containing glycolipid. In contrast of Uchigata's monoclonal antibody, they noticed a loss of antibody-binding after neuraminidase treatment. Using preparative thin-layer chromatography of pancreatic glycolipids, they found that the upper-phase polar lipids were able to block the binding of diabetic sera to pancreatic secretions.
Various approaches have been adopted to neutralize autoantibodies, including the use of immunosuppressants, e.g. cyclosporin, and of mouse monoclonal anti-idiotypic antibody neutralization techniques, but neither has been very successful. Immunosuppressants are too non-specific and will attack all B and T cells, while the use of mouse monoclonal anti-idiotypic antibodies often result in the production of human anti-mouse antibodies in patients, considerably reducing the effectiveness of treatment.
Prior to 1998, attempts at producing autoimmune human monoclonal antibodies to islet-cell antigens from type-1 diabetics appear to have been in vain. Co-workers and I have produced numerous human monoclonal antibody-secreting lines, none of which reacts with pancreas, let alone the elusive islet-cell surface antigen.
SUMMARY OF THE INVENTION
The present invention is based on the ability to purify islet cell membrane antigen (ICMA), from cell lines that express the antigen, and the discovery that the ICMA binds ICSA. Therefore, ICMA can be used to neutralize circulating antibodies and to target the B lymphocytes producing the autoantibodies.
Problems of the prior art, i.e. the problems associated with animal models and human autoimmune monoclonal antibody production have been overcome, by obtaining representative antibodies to the islet-cell surface antigen(s) through monoclonal anti-idiotypic antibodies.
DETAILED DESCRIPTION OF THE INVENTION
As indicated above, an anti-idiotypic monoclonal antibody strategy has been used. Assuming the patients' autoimmune antibody constituted a classic Ab1, on immunization both Ab2 and Ab3 should be produced; the latter would be expected to recognize the same antigen(s) as the patient's Ab1 . 137 hybridomas derived from a standard fusion were screened against a library of antigens on a nitrocellulose dot blot system. Ten lines were found to bind only RINm5 cell membranes (of these, 9 secreted IgM).
Preliminary data have shown that two of these antibodies strongly bind islet cells in paraffin sections of human pancreas using an immunoperoxidase system. These antibodies were also able to displace binding of diabetic serum by 50% in an enzyme-linked immunoassay used to detect islet cell membrane auto-antibodies. One of these antibodies was also able to fix complement on living RINm5 cells, suggesting that an external component of the cell membrane was recognized. These results provide evidence that monoclonal anti (anti-idiotypic)(Ab3) antibodies to islet cell surface membrane antigens have been produced.
More specifically, the present invention is based on the generation of a panel of anti-(anti-idiotypic) (Ab3) monoclonal antibodies derived from immunizing tolerant mice with polyclonal human diabetic immunoglobulins (Ab1) from a patient with high levels of ICSA.
The initial screen for the anti-(anti-idiotypic) antibodies involved a nitrocellulose dot-blot system in which 1 &mgr;g protein from RINm5 cell membranes was applied to the paper. Positive lines were subcloned and their ability to displace diabetic serum from binding RINm5F membranes in an enzyme-linked immunosorbent assay investigated. One line 55D2 was found to be able to displace the original patient's serum (Ab1) and also other newly-diagnosed diabetic patients' sera by up to 50%. This antibody was coupled to an affinity column to which solubilized RINm5F cell membranes were applied. The eluted fractions were checked on nitrocellulose with the original antibody and positive fractions run on a 5-15% (w/v) SDS/polyacrylamide gel. This revealed that a 64 kDa protein had eluted from the column.
Binding of the antibody 55D2 is not altered by neuraminidase treatment of solubilized RINm5F cell membranes. The antibody recognizes a protein bound by a lectin column derived from
Erythrina crystagalli
which recognizes D-galactose and D-galactoside groups.
Interestingly, while investigating species specificities of the antibody using human, porcine, bovine and rat pancreas, and also the rat insulinoma cell line RINm5F, it was found that even when 100 &mgr;g protein was applied to the nitrocellulose no antibody binding was observed, yet routinely 1 &mgr;g of protein from RINm5F membranes or 30 ng of the protein eluted from the
Erythrina
column was strongly positive. The antigen appears to be a relatively minor component of the membrane and it is not surprising therefore that there has been a failure to detect cross-reactivity with homogenates of other tissues.
The ability to obtain essentially pure ICMA not only provides the potential for its therapeutic and diagnostic use, but also allows its sequencing and cloning. Further, the ICMA can be digested, e.g. by a variety of enzymes or by chemical treatment, to give an epitope having a lower molecular weight, without loss of activity.
Epitopes containing the sequences specific for locking autoantibodies can be identified by standard gene-sequencing techniques. Once the amino-acid sequence is known, the peptide fragments may be synthetically produced. Synthetic production, e.g. by recombinant technology, may be the prefer
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KS Biomedix Ltd.
Venkat Jyothsna
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