Patent Application
20060182713
This invention is related to the immunology branch, particularly to a new IL-15 use for active immunization to treatment IL-15 over-expressing related diseases.
This cytokine known as IL-15 is a 14-15 KDa glycoprotein, which was simultaneously described by two groups as a T cells-activating growth factor (Grabstein, K. H. et al., Science 1994, 264, 965; Burton, J. D. et al., Proc. Natl. Acad. Sci. USA 1994, 91, 4935). IL-15 mRNA is widely present in cells and tissues, however, it is difficult to find the protein in these cells or in the cells supernatant due to a strong post-transcriptional control of its expression at the translational level and the intracellular traffic (Bamford R N. et al, J. Immunol 1998, 160: 4418-4426), (Kurys G, et al, J Biol Chem 2000, 275: 30653-30659).
The IL-15 biological effects are mediated through its binding to a cell membrane receptor composed of three subunits α, β, and γ. The IL-15Rα is a specific subunit for this cytokine to whom is bound with a very high affinity Kd 10−11, β subunit is shared with IL-2 and γ subunit is a common receptor for several cytokines, IL-2; 11-4; IL-7; IL-9; IL-15; IL-21 (Bamford R N., et al, Proc. Natl. Acad. Sci. USA 1994, 91, 4935), (Giri J G., et al, EMBO J. 1995, 14: 3654-3663).
The IL-15 is an immunostimulatory cytokine promoting proliferation and functional activity of T, B and NK cells (Giri, J. G., EMBO J. 1994, 13, 2822-2830), activates neutrophiles and modifies monokine secretion (Girard D., 1996, Blood, 88, 3176; Alleva D. G., 1997, J. Immunol., 159, 2941). This cytokine mediates different effects on several steps of the immune response, induces CD56 NK cells proliferation and acts, together with IL-12, inducing IFNγ and TNFα (Ross M E, 1997, Blood 89, 910-918; Fehniger T A, 1999, Transplant Proc, 31, 1476-1478).
The binding of the ligand to the T cell receptor induces expression of IL-15Rα and expression of several activation antigens such as CD69, CD25 and TNFRII. Also IL-15 is a chemoattractant for human blood T lymphocytes (Wilkinson 1995, J. Exp. Med. 181, 1255-1259). All these data suggest that IL-15 expressed by antigen presenting cells could be important on the early T cell activation at the inflammation site.
II-15 has been detected in the course of several diseases including Crohn's disease (Kirman I., 1996, Am. J. Gastroenterol. 91, 1789), Psoriasis (Rückert R. 2000, 165: 2240-2250), Leukemia (Yamada Y. 1999, Leukemia and Limphoma, 35(1-2): 37-45) and Rheumatoid arthritis (RA), (McInnes I. B. 1998, Immunology Today, 19, 75-79).
Feldmann et al., 1996, Annu Rv Immunol, 14: 397-440) proposed TNFα as the main cytokine in a cytokine cascade that includes IL-1β, IL-6, GM-CSF and several inflammatory cytokines such as Mip 1α, Mip 1β and IL-8, which are closely related to the development and progression of the Rheumatoid arthritis (RA). McInnes et al., found IL-15 expression abnormalities in this disease, high IL-15 concentration in the synovial fluid and its expression in synovial membrane cells. They suggested that IL-15 precedes TNFα in the cytokine cascade, proposing a mechanism dependent on cell contact, where, IL-15 activated T cells induce TNFa synthesis by macrophages. Moreover, it is proposed that IL-15 acts as an important factor on the T cell migration to the synovial fluid (McInnes, 1997, Nat Med, 3: 189-195).
Ziolkowska et al., reported that IL-15 induces IL-17 expression at joints from RA patients, it is already known that this cytokine stimulates release by synoviocytes of several inflammatory mediators such as IL-6, IL-8, GM-CSF, and prostaglandine E2 suggesting an important role for IL-15 in the RA pathogenesis (Ziolkowska y col 2000, J Immunol, 164: 2832-2838).
T cells recruitment and activation may occur as a consequence of IL-15 local synthesis and such non specific activation could bring as a result an endless inflammation. All this suggest that IL-15 inhibition could have a therapeutic potential on the disease treatment.
The use of IL-15 antagonist molecules has been shown to be effective in animal models. Ruchatz et al. generated a soluble fragment from the alpha subunit of the murine receptor (IL-15Rα) and demonstrated that this fragment inhibited collagen-induced arthritis when it was administered to DBA/1 mice (Ruchatz H. 1998, J. Immunol. 160: 5654-5660).
Other IL-15 antagonist molecules have been patented including IL-15 mutated in one or more amino acids residues and monoclonal antibodies capable to bind mature IL-15 and prevent signal transduction through its receptor (U.S. Pat. No. 6,001,973, U.S. Pat. No. 6,177,079, U.S. Pat. No. 6,168,783, and U.S. Pat. No. 6,013,480). Although their use is described in the above mentioned patent files, there are quite a few results published in scientific journals supporting their efficacy. On May 2002, Genmab Company revealed phase I/II clinical studies with an antibody against IL-15 patented by Immunex, which must correspond to previously referred U.S. Pat. No. 6,177,079, but these results have not been published yet.
Other studies have been done with the chimera protein MutlL15-Fc that binds to cells carrying the IL-15 receptor, which leads to a reduced number of activated immune cells below a critical level and induces tolerance, e.g., self-reactive activated T cells with a key role in allograft rejection are responsive to IL-15 and has been demonstrated that they can be inhibited by using MutlL15-Fc protein, which acts as an IL-15 antagonist.
There are a few examples on the vaccine bibliography to generate antibodies against autologous molecules, e.g., a vaccine against EGF for the treatment of EGF dependent tumors (U.S. Pat. No. 5,894,018), its efficacy has been demonstrated in clinical trials by eliciting antibodies that block EGF activity. The generation of neutralizing antibodies against autologous proteins is very complex due to natural mechanisms to tolerate your self
In the current invention, active immunization with IL-15 in a proper formulation to generate neutralizing self-antibodies against IL-15 makes possible neutralization of the anomalous quantities of this cytokine found in patients with autoimmune diseases and leukemia.
In current invention an active immunization is done allowing generation of IL-15 neutralizing self-antibodies, being IL-15 levels regulated through an immunization scheme.
The essence and novelty of the current invention are in the vaccine composition using IL-15 for active immunization to treatment IL-15 over-expressing-related diseases.
This vaccine composition will be used in humans in order to elicit a neutralizing antibodies response against autologous IL-15.
This invention also includes IL-15 fused to a carrier protein as well as any other formulation comprising them.
The invention also contemplates the use of the vaccine alone or concurrently with anti-inflammatory drugs or other cytokines antagonists.
According to some embodiments of the invention, a mammalian expression vector comprises a DNA sequence coding for II-15 in a proper formulation for active immunization.
According to some embodiments of the invention, IL-15 is a recombinant protein obtained in E. coli, therefore, its glycosilation pattern is different from the autologous IL-15. In some embodiments of the invention, IL-15 is an active protein with a specific activity of 2-5×106 U/mg according to the CTLL-2 assay.
The IL-15 gene of the invention was isolated form LPS-activated monocytes and cloned into an E. coli expression vector and purified from this source. The protein biological activity was determined by induction of T cells proliferation on the CTLL2 assay.
According to some embodiments of this invention, fusion protein p64IL-15 was obtained by designing oligonucleotides that allow IL-15 gene amplification by PCR and insertion of this gene into an E. coli expression vector containing the gene coding for the p64k protein. The IL-15 protein was fused to the C-terminal region of the p64k carrier protein and purified from this source. The protein biological activity was determined by induction of T cells proliferation on the CTLL2 assay.
The proof-of-concept shown in this invention was demonstrated by using macacus irus monkeys as a model, their IL-15 has a 96.4% homology to human IL-15.
According to the present invention, results are provided which demonstrated that active immunization with either IL-15 or fusion protein p64kIL-15 generated both an antibody response specific for IL-15 and neutralizing antibodies on immunized animals' sera.
The object of this invention is also extensive to a DNA vaccine comprising a vector containing a DNA coding for the human IL-15 according to the present invention and its use as alternative in the gene therapy of IL-15 expression related diseases.
Described vaccine can be concurrently administered with anti-inflammatory or immunesuppressor agents or other cytokines antagonists used to treatment RA.
The following examples are provided to illustrate current invention embodiments
DNA coding for human IL-15 was isolated by RT-PCR from LPS-activated monocytes and cloned into an E. coli expression vector.
Recombinant IL-15 expressed in E. coli was extracted from cellular pellet with urea 8M and purified by a chromatography in TSK G4000SW (Merck) followed by a chromatography in RP-C4 (J. T. Baker) in a water/acetonitrile, TFA buffer system. Biological activity was measured by stimulation of the CTLL-2 cell line proliferation using MTT mitochondrial staining (Cosman y col 1984, Nature, 312: 768-771). 11-15 specific activity is 2×106 U/mg (
Obtaining Recombinant p64k-IL15 Fusion Protein
P64k-IL15 fusion protein was obtained by designing oligonucleotide primers that would amplify the IL-15 gene by PCR and insert it at the p64k c-terminus into an E. coli expression vector (
The protein is soluble after cellular rupture in a French press.
Streptomycin sulphate is added up to 0.8% to the rupture supernatant, which is kept at 4° C. for 1 h, centrifuged 15 min at 10000 rpm, and 4° C. Two precipitation steps with ammonium sulphate are carried out and pellet is suspended in Tris 20 mM, EDTA 6 mM, Urea 2 M, pefabloc 0.5 mg/mL and purified through an ionic exchange chromatography in TSK DEAE PW and gel filtration in Superdex 200.
Three groups were evaluated in a monkeys immunization scheme, immunized with IL-15; immunized with the fusion protein and placebo. The proteins were administered in amounts of 100 μg per inoculation in Freund's adjuvant. First immunization was done with Freund's complete adjuvant, second immunization with incomplete Freund's adjuvant one month later and third immunization with incomplete Freund's adjuvant was done two months later. One week after second and third immunization blood was extracted to evaluate level of anti-IL15 antibodies in the monkeys' sera. Data are shown in
The cytokine-dependent cell line CTLL-2 proliferates in presence of IL-15. IL-15 bound molecules impairing receptor depending signal transduction would inhibit this cell line proliferation.
To evaluate the neutralizing capacity of antibodies present in monkeys' sera, serial dilutions of them were done in 96 well plates (Costar, USA) in 50 μL volume of RPMI medium (Gibco) supplemented with 10% fetal bovine serum (Gibco). A sub-optimal amount of IL-15 (30 pg) was added to each well and previously washed CTLL-2 cells were added to 5×103 cells/well. Plate was incubated for 48 h at 5% CO2 and 37° C. To measure proliferation MTT mitochondrial staining was used (Cosman et al. 1984, Nature, 312: 768-771). In results shown in
Invention Advantages:
Levels of generated antibodies are more stable throughout time than antibodies obtained by a passive immunization
Lesser frequency of doses administration to patients compared to passive immunization
Required amount of protein per dose and amount of doses are quite inferior to the required for treatment with IL-15 antagonist molecules; this implies a lower production cost.
| Number | Date | Country | Kind |
|---|---|---|---|
| CU20020218 | Oct 2002 | CU | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/CU03/00010 | 10/8/2003 | WO | 8/29/2005 |
