EP1206535A1 - Tumor-associated antigen (r11) - Google Patents

Abstract

The invention relates to tumor-associated antigens, immunogenic peptides derived therefrom and the DNA molecules coding therefor as well as to their utilization in cancer immunotherapy.

Description

Tumor Associated Antigen (Rll)

The invention relates to the immunotherapy of tumor diseases.

The immune system's task is to protect the organism from a variety of different microorganisms or to actively combat them. The importance of an intact immune system is particularly evident in inherited or acquired immunodeficiencies. In many cases, the use of prophylactic vaccine programs has proven to be an extremely effective and successful immunological intervention in the fight against viral or bacterial infectious diseases. It has also been shown that the immune system is also significantly involved in the elimination of tumor cells. The detection of tumor-associated antigens (TAAs) by components of the immune system plays an important role. In the broadest sense, any component (peptide or non-peptide) of a tumor cell that is recognized by an element of the immune system and that stimulates an immunological response can act as an immunogenic tumor antigen. Of particular importance are those tumor antigens that not only cause an immunological reaction, but also cause rejection of the tumor. The identification of defined antigens that can cause such an immunological reaction is an important step for the development of a molecularly defined tumor vaccine. Although it is not yet clear which elements of the immune system are responsible for rejection of the tumor, there is a consensus on this that doing CD8-expressing cytotoxic T lymphocytes (CTLs) play a major role (Coulie, 1997). A correlation between the clinical course and the increased occurrence of CD8 ⁺ and CD4 ⁺ T cells could be established, especially in those types of tumors (e.g. melanoma and kidney carcinoma) that have a relatively high spontaneous remission rate (Schendel et al., 1993; Mackensen et al., 1993; Halliday et al., 1995; Kawakami et al., 1995; Kawakami et al., 1996; Wang, 1997; Celluzzi and Falo, 1998). Specific CTL clones were obtained either from tumor infiltrating lymphocytes (TIL) or peripheral mononuclear blood cells (PBMC) after cocultivation with mostly autologous tumor cells and cytokine stimulation in vitro. In animal models as well as in human cell culture systems cultivated in vitro, the T cell response against tumor cells could be enhanced by transfection of the tumor cells with cytokines (van Elsas et al., 1997; Gansbacher et al., 1990; Tepper et al., 1989; Fearon et al., 1990; Dranoff et al., 1993).

Due to the correlation between remission and involvement of CD8 ⁺ T cells, the identification of tumor associated antigens (TAA), which are recognized by CD8 positive CTLs, is a declared main goal on the way to the development of a

Tumor vaccine (Pardoll, 1998; Robbins and Kawakami, 1996). It is still unclear whether other cell types of the immune system such as CD4 ⁺ T helper cells also play an important role; some studies with MAGE-3 / HLA-A1 peptides in melanoma patients suggest this

(Marchand et al., 1995; Boon et al., 1998). In the past few years, a number of TAAs have passed through CTLs have been identified (Boon et al., 1994; van den Eynde and van der Bruggen, 1997).

T cells recognize antigens as peptide fragments that are presented on the cell surfaces of MHC molecules (“ajor histocompatibility complex”, in humans “HLA” = “human leukocyte antigen”). There are two classes of MHC molecules: MHC-I molecules occur on most cells with a nucleus and present peptides (usually 8-10-mers) which are formed by proteolytic degradation of endogenous proteins (so-called antigen processing, "antigen processing") • Peptide: MHC-I complexes are positive CTLs detected. MHC-II molecules only occur on so-called "professional antigen-presenting cells" (APC) and present peptides of exogenous proteins that are absorbed and processed by APC during the endocytosis. Peptide: MHC-II complexes are used by CD4 helpers Interaction between T cell receptor and peptide: MHC complex can trigger various effector mechanisms that lead to apoptosis of the target cell in the case of CTLs. This happens when either the MHC (eg in the case of graft rejection), or the peptide is recognized as foreign (eg in the case of intracellular pathogens). However, not all of the peptides presented meet the structural and functional requirements for effective interaction with T cells (as described by Rammenee et al., 1995 and below).

In principle, several application forms are possible for the use of TAAs in a tumor vaccine: The antigen can either be used as a recombinant protein suitable adjuvants or carrier systems, or as cDNA coding for the antigen in plasmid (DNA vaccines; Tighe et al., 1998) or viral vectors (Restifo, 1997). Another possibility is the use of recombinant

Bacteria (e.g. Listeria, Salmonella) that recombinantly express the human antigen and have an adjuvant effect due to their additional components (Paterson, 1996; Pardoll, 1998). In all of these cases, processing and presentation of the antigen by so-called "professional antigen-presenting cells" (APC) is necessary. Another possibility is the use of synthetic peptides (Melief et al., 1996), which correspond to the corresponding T cell Epitopes of the antigen correspond and are either loaded onto the APC from the outside (Buschle et al., 1997; Schmidt et al., 1997) or taken up by the APC and transferred intracellularly to the MHC I molecules - the most therapeutically efficient form of application for a defined Antigen is generally determined in clinical studies.

The antigens or their epitopes recognized by the tumor-specific CTLs include molecules which can come from all protein classes (for example transcription factors, receptors, enzymes; for an overview, see Rammenee et al., 1995; Robbins and Kawakami, 1996). These proteins do not necessarily have to be located on the cell surface, as is required for detection by antibodies. In order to act as a tumor-specific antigen for the detection by CTLs or to be used for therapy, the proteins must fulfill certain conditions: firstly, the antigen is to be expressed mainly by tumor cells and should not occur in so-called "critical" normal tissues or only in a lower concentration than in tumors. Critical normal tissues are essential tissues; an immune reaction directed against them could have serious, sometimes lethal consequences. Second, the antigen is said to be present not only in the primary tumor, but also in the metastases. Furthermore, in view of a wide clinical use of the antigen, it is desirable if it is present in high concentration in several types of tumor. Another prerequisite for the suitability of a TAA as an effective component of a vaccine is the presence of T cell epitopes in the amino acid sequence of the antigen; Peptides derived from TAA are said to lead to an in vitro / in vivo T cell response ("immunogenic" peptide). Another selection criterion for a clinically widely applicable immunogenic peptide is the frequency with which the antigen is found in a given patient population.

The immunogenic tumor-associated antigens (TAAs), most of which have already been shown to have T cell epitopes, can be divided into several

Classify categories, including viral proteins, mutated proteins, overexpressed proteins, fusion proteins formed by chromosomal translocation, differentiation antigens, oncofetal antigens (Van den Eynde and Brichard, 1995; van den Eynde and van der Bruggen, 1997). The methods for the identification and characterization of TAAs, which are the starting point for the development of a tumor vaccine, are based on the one hand on the use of CTLs (cellular immune response) or antibodies (humoral immune response) that have already been induced in patients, or are based on the creation of differential transcription profiles between tumors and normal tissues. In the first case, the immunological approach, patient CTLs are used for screening eukaryotic tumor cDNA expression libraries which present the CTL epitopes via MHC-I molecules (Boon et al., 1994), while using high-affinity patient antisera prokaryotic cDNA expression libraries can be examined directly for the presence of TAAs via an immunoblot analysis of the individual plaques (Sahin et al., 1995). A combination of CTL reactivity and protein chemical methods represents the isolation of peptides isolated from MHC-I from tumor cells which have been preselected for reactivity with patient CTLs. The peptides are washed out of the MHC-I complex and identified using mass spectrometry (Falk et al., 1991; Woelfel et al., 1994; Cox et al., 1994). The approaches that use CTLs to characterize antigens are associated with considerable effort or not always successful due to the required cultivation and activation of CTLs.

Methods for the identification of TAAs, which are based on the comparison of the transcription profile of normal with

Tumor tissues are diverse; this includes differential hybridization, the creation of Subtraction cDNA banks ("representational difference analysis"; Hubank and Schatz, 1994; Diatchenko et al., 1996) and the use of DNA chip technology or the SAGE method (Velculescu et al., 1995). In contrast to the above-mentioned immunological method with the help of patient CTLs, the use of molecular biological methods must show that the potential antigen candidates found with them are tumor-specific (tumor-associated) and actually have T-cell epitopes that can trigger a cytotoxic T-cell response , In at least one case (NY-ESO / LAGE-1), an antigen was identified using both patient sera and RDA (Chen et al., 1997; Lethe et al. 1998), and CTL epitopes of this antigen and a simultaneous spontaneous humoral and T-cell response in one patient was described (Jager et al., 1998).

The object of the present invention was to provide a new tumor-associated antigen (TAA).

This object was achieved by first using RDA ("representational difference analysis") to produce a cDNA subtraction library between a cell line derived from a pancreatic carcinoma patient and a pool of 11 different normal tissues. To generate the cDNA fragments necessary for subtractive hybridization In deviation from the original protocol (Diatchenko et al., 1996), "fixed" and "driver" were used in a mixture of 6 different restriction enzymes. The use of a mixture of different restriction enzymes which were 6 base pairs as Require recognition sequence has the following advantages over the original protocol (Diatchenko et al., 1996): a) by selecting two restriction enzymes each, the recognition sequences of which are combined by a 6-combination of the bases A / T (eg Ssp I: AATATT) or C / G (for example Nae I: GCCGGC) or A / C / G / T (for example EcoR V: GATATC) are shown, both GC and AT-rich regions of a gene are cut equally, resulting in a homogeneous representation of the entire gene region as restriction fragments is made possible; b) it is also possible to obtain larger cDNA fragments of the candidate gene on average (approx. 800 bp), which in turn is of great advantage in the subsequent analysis (sequencing and annotation) and the cloning of the “full-size” cDNA In the original protocol (Diatchenko et al., 1996), a restriction enzyme (Rsa I) which only recognizes 4 bases is used, which leads to an average fragment length of 256 bp and cannot specifically process regions rich in CG or AT the PCR protocol was changed as described in Example 2 by the longer insert cDNA fragments to meet changed hybridization kinetics.

In order to select the antigens overexpressed in the tumor, the cDNA clones obtained were first separated and a glycerol stock culture, a plasmid preparation and a collection of the PCR fragments representing the insert were established in 96-well plate format. First, 50 randomly selected cDNA fragments from the 3450 clones of the subtractive cDNA library of pancreatic carcinoma were selected for the selection of the im Tumor overexpressed antigens sequenced and compared with sequences available in databases. Among the genes that were annotated were 12 unknown, for which ESTs ("expressed sequence tags") entries existed in the database. One clone, Rll, was suitable for use as a TAA due to its preferred presence in fetal tissues Further investigations by means of semi-quantitative RT-PCR and Northern blot analysis confirmed the preferred expression in various tumor (breast, kidney cell and pancreatic carcinoma) as well as immune-privileged tissues (testis, placenta and adrenal gland) and no or a little Expression in normal tissues Furthermore, it can be concluded from the data obtained by Northern blot experiments that the Rll transcript has a length of approximately 7.5 kb and that splice variants or homologous genes may exist in the adrenal gland.

The human Rll cDNA was cloned from Testis, the sequence obtained is shown in SEQ ID NO: 1. The sequence of Rll shows no identity or homology to a known gene at either the nucleotide or protein level. The Rll cDNA obtained in the context of the present invention contains two separate open reading frames, each for a 401 (SEQ ID NO: 2) amino acid and for a 357 (SEQ ID NO: 3) amino acid protein. The Rll cDNA cloned in the course of the present invention has a length of 6582 bp, the presence of a polyA tail at the 3 'end of the sequence for the

Completeness of the cDNA speaks in this area. On the basis of the data obtained in the context of the present invention, it cannot be ruled out that 5 'of the sequenced cDNA is another ATG which represents the start ATG for the first open reading frame (RII-ORF-1); in this case the present cDNA contains the region coding for the C-terminal section of RII-ORF-1 at the 5 'end. Information about the 5 'end and a possibly upstream coding DNA sequence section can be obtained by standard molecular biological methods, for example by means of 5' RACE ("rapid amplification of cDNA ends"). In this method, RNA, preferably mRNA, is eliminated Cells or tissues in which Rll is transcribed (e.g. breast, kidney or

Pancreatic carcinoma tissue) reverse transcribed and then ligated with an adapter of known sequence. A PCR with an adapter primer (binds specifically to the adapter at the 5 'end of the cDNA) and an Rll-specific primer (e.g. SEQ ID NO: 26) allows the corresponding Rll fragments to be amplified. As described in Example 6, these PCR products can be cloned by standard methods and characterized, in particular by DNA sequencing.

An alternative method for characterizing the 5 'end is the screening of cDNA libraries by hybridization with DNA probes specific for RII or the analysis of cDNA expression libraries with antisera. If the screening of cDNA libraries does not lead to the desired goal due to methodological restrictions, e.g. inefficient reverse transcription due to pronounced secondary structures of the RNA, genomic libraries can be examined, for example, by hybridization with for, as in the screening of cDNA libraries Rll-specific DNA probes can be isolated from clones which contain the sequence information located upstream from the 5 ′ end of the cDNA obtained, for example the promoter region of Rll.

In the course of the complete cloning of the Rll cDNA, it can be determined whether the open reading frame of Rll-ORF-1 obtained in the area of the present cDNA section has a continuation in the 5 'area and / or whether there are alternative reading frames.

The cDNA isolated in the context of the present invention has the nucleotide sequence given in SEQ ID NO: 1; it can be assumed (see above) that it is for the C-terminal section of a tumor-associated antigen (TAA) of the designation RII-ORF-1 and for another protein which is represented by the second reading frame (RII-ORF-2) coded.

The two proteins of the two reading frames expressed by the isolated cDNA have the amino acid sequence shown in SEQ ID NO: 2 and 3.

The present invention relates to a first

Aspect, an isolated DNA molecule that contains the in

SEQ ID NO: 1 nucleotide sequence shown or a polynucleotide that hybridizes with this DNA molecule under stringent conditions.

“Stringent conditions” mean, for example: overnight incubation at 65 ° C.-68 ° C. with 6 × SSC (1 × SSC = 150 mM NaCl, 15 mM Tri-sodium citrate),

5xDenhardt's solution, 0.2% SDS, 50μg / ml salmon sperm DNA, followed by washing twice for 30 min with 2xSSC, 0.1% SDS at 65 ° C, once for 30 min with 0.2xSSC, 0.1% SDS at 65 ° C and, if necessary, with a final rinse O.lxSSC, 0.1% SDS at 65 ° C, or equivalent conditions.

In a further aspect, the present invention relates to an isolated DNA molecule which contains a polynucleotide of the sequence shown in SEQ ID NO: 1 as a partial sequence or which contains a polynucleotide which hybridizes with a polynucleotide of this sequence under stringent conditions.

The DNA molecules or fragments thereof according to the invention code for (poly) peptides of the designations R11-ORF1 and R11-0RF2, where R11-ORF2 is the amino acid sequence shown in SEQ ID NO: 3 and R11-ORF2 is the one shown in SEQ ID NO: 2 Has or contains amino acid sequence; or for protein fragments or peptides derived from RII-ORF-1 or R11-0RF2. This also includes DNA molecules which, due to the degeneration of the genetic code, have deviations from the sequence shown in SEQ ID NO: 1.

In a further aspect, the present invention relates to the tumor-associated antigens Designation Rll-ORF-1 and Rll-ORF-2, whereby in the case of Rll-ORF-1 that there is an extension of the present open reading frame in the 5 'direction, which in SEQ ID NO: 2 for Rll-ORF- 1 amino acid sequence shown is a partial sequence. The proteins with the sequences given in SEQ ID NO: 2 or 3 are products which are translated by an approximately 7.5 kb transcript or those by the transcripts of a size of approximately 3.8 kb and 2.3 kb are translated, which are derived from splice variants of the 7.5 kb transcript as found in the tissue of the adrenal gland or from transcripts of the genes homologous to them.

The amino acid sequences shown in SEQ ID NO: 2 or 3 may have deviations, e.g. those which are due to the exchange of amino acids, provided that the R11 derivatives (hereinafter “R-II”, unless otherwise stated refers to R11-ORF1 and / or R11-ORF2) are those which are desired for use in a tumor vaccine has immunogenic properties.

The natural amino acid sequence of Rll-ORF-1 or Rll-ORF-2 can optionally be modified by exchanging individual amino acids in a Rll CTL epitope in order to increase the affinity of Rll compared to the natural Rll CTL epitope -Peptides to MHC-I molecules and thus an increased immunogenicity and ultimately an increased reactivity to tumors. Modifications in the area of the Rll epitopes can be made on the total Rll protein (this is from the APCs to the corresponding Peptides processed) or on larger ones

Rll protein fragments or on Rll peptides (see below).

In a further aspect, the present invention relates to immunogenic polypeptide fragments and peptides derived from RII-ORF-1 or RII-ORF-2. The latter are referred to below as "Rll peptides". A first group are Rll peptides that trigger a humoral immune response (induction of antibodies). Such peptides are selected sections of Rll-ORF-1 or Rll-ORF-2 (at least 12 to 15 amino acids), which by means of so-called prediction algorithms such as e.g. the "surface probability plot" (Emini et al., 1985), the "hydrophobicity plot" (Kyte and Doolittle, 1982) and the "antigenic index" (Jameson and Wolf, 1988).

Also included are all those peptides which are derived from the R11 N-terminal region which may be obtained in the course of further cloning.

It is known that tumor-associated antigens can have tumor-specific mutations that contribute to an immunological differentiation between tumor and normal tissue (Mandruzzato et al., 1997; Hogan et al., 1998; Gaudi et al., 1999; Wölfel et al., 1995 ). In order to determine the presence of tumor-specific Rll-ORF-1 or Rll-ORF-2 mutations, the Rll cDNA is expediently cloned from one or more different tumors and the resulting ones, using probes from the cDNA according to the invention isolated from Testis Sequences compared with normal tissue Rll cDNA. It is to be expected that tumor Rll peptides from a sequence section mutated compared to normal tissue Rll show increased immunogenicity compared to normal tissue Rll peptides from the corresponding section. In a further aspect, the present invention thus relates to III-peptides derived from regions of a tumor-expressed III-ORF-1 and III-ORF-2 which have tumor-specific mutations.

In therapeutic use, Rll peptides are administered directly or in modified form (e.g. coupled to KLH = "keyhole limpet hemocyanine") and the formation of antibodies by means of common immunological assays, e.g. determined by ELISA.

Further Rll peptides preferred within the scope of the present invention are those which are presented by MHC molecules and which bring about a cellular immune response. There are two classes of MHC molecules, namely MHC-I molecules that are recognized by CD8-positive CTLs and MHC-II molecules that are recognized by CD4-positive T helper cells.

In order for a peptide to trigger a cellular immune response, it must bind to an MHC molecule, and the patient to be treated must have the MHC molecule in its repertoire. Determination of the MHC subtype of

With regard to the drawing of a cellular immune response, patients therefore represent one of the essential prerequisites for the effective application of a peptide to this patient. The sequence of an RII peptide to be used therapeutically is predetermined by the respective MHC molecule with regard to anchor amino acids and length. Defined anchor positions and lengths ensure that a peptide fits into the peptide binding groove of the patient's respective MHC molecule. As a result, the immune system is stimulated and a cellular immune response is generated which, in the case of using a peptide derived from a tumor antigen, is directed against the patient's tumor cells.

Immunogenic Rll peptides can be identified by known methods, one of the bases for this is the relationship between MHC binding and CTL induction.

Since the sequence of immunogenic peptides can therefore be predetermined based on their peptide binding motif, Rll peptides which represent CTL epitopes can be identified and synthesized on the basis of the Rll protein sequence. Various methods are suitable for this, which are used to identify CTL epitopes from known ones

Protein antigens have been used; e.g. the method described by Stauss et al., 1992, for the identification of T cell epitopes in human papillomavirus.

The allele-specific requirements of each MHC-I allele product for a peptide which binds to and is presented by the MHC molecule have been summarized as a motif (eg Falk et al., 1991). A large number of both MHC peptide motifs and MHC ligands are known to date. One under the A method suitable for the present invention to search for epitopes of a known protein which fits into a particular MHC-I molecule has been described in a review article by Rammenee et al., 1995. It comprises the following steps: first, the protein sequence is examined for sections which correspond to the anchor motif, with certain variations in terms of peptide length and anchor occupation being possible. If, for example, a motif prescribes a 9-mer with Ile or Leu at the end, 10-mer with a corresponding C-terminus can also be considered, as can peptides with other aliphatic residues, such as Val or Met at the C-terminus. In this way a number of peptide candidates are obtained. These are examined for the presence of as many anchor residues as possible, which they have together with known ligands, and / or for whether they have "preferred" residues for different MHC molecules (according to the table by Rammenee et al., 1995). In order to exclude weakly binding peptides, binding assays are expediently carried out. If the requirements for peptide binding for certain MHC molecules are known, the peptide candidates can also be examined for non-anchor residues which have a negative or positive effect on the binding or which make this possible (Ruppert et al., 1993). With this approach, however, it must be considered that the peptide binding motif is not the only decisive factor in the search for natural ligands; other aspects, such as enzyme specificity during antigen processing, also contribute - in addition to the specificity of the MHC formation - contribute to the identity of the ligand. A method which takes these aspects into account and which is suitable in the context of the present invention for the identification of immunogenic Rll peptides has been used, inter alia, by Kawakami et al., 1995, to generate gplOO epitopes based on known HLA-A * 0201 motifs to identify .

The peptides can also be selected for their ability to bind to MHC-II molecules. The MHC-II binding motif spanning nine

Amino acids has a higher degree of degeneration in the anchor positions than the MHC-I binding motif. Based on the X-ray structure analysis of MHC-II molecules, methods have recently been developed which enable the exact analysis of the MHC-II

Binding motifs, and on the basis thereof, allow variations of the peptide sequence (Rammenee et al., 1995 and the original literature cited there). Peptides that bind to MHC-II molecules are typically presented to CD4-T cells by dendritic cells, macrophages or B cells. The CD4-T cells in turn then directly activate CTLs by e.g. Cytokine release and enhance the efficiency of antigen presentation by APC (dendritic cells, macrophages and B cells).

Databases and prediction algorithms have recently become available which allow the prediction of peptide epitopes which bind to a particular MHC molecule with great reliability. In the context of the present invention, using the algorithm described by Parker et al., 1994 and Rammenee et al., 1995, for the most important HLA types, in particular for HLA-Al, -A * 0201, -A3, -B7 , -B14 and -B * 4403, candidate peptides of the R11 C-terminal fragment identified which are expected to bind to the corresponding HLA molecules and are therefore immunogenic CTL epitopes; the peptides found are listed in Table 1. In a similar manner, further potential peptide epitopes can be determined, possibly using further algorithms that take into account the different characteristics of the peptides (hydrophobicity, charge, size) or requirements on the peptides, for example the 3D structure of the HLA molecule become; this also applies to peptide epitopes of other HLA types.

After selecting RII peptide candidates using the methods listed, their MHC binding is tested using peptide binding assays. Next, the immunogenicity of the peptides is good

Binding properties determined (stability of the peptide-MHC interaction correlates in most cases with immunogenicity; van der Burg et al., 1996). To determine the immunogenicity of the selected peptide or peptide

To determine equivalents, methods such as those described by Sette et al., 1994, can be used in combination with quantitative MHC binding assays. Alternatively, the immunogenicity of the selected peptide can be tested via in vitro CTL induction using known methods (as described below for ex vivo CTL induction). The principle of in Method carried out in several steps for the selection of peptides which are capable of triggering a cellular immune response is described in WO 97/30721, the disclosure of which is hereby expressly incorporated by reference. A general one

Strategy for obtaining efficient immunogenic peptides that is useful in the present invention has also been described by Schweighoffer, 1997.

Instead of using the original peptides that fit into the binding groove of MHC-I or MHC-II molecules, that is to say peptides that are derived unchanged from RII, the minimum requirements for anchor positions and long variations based on the original peptide sequence can be made , provided that the effective immunogenicity of the peptide, which is composed of its binding affinity for the MHC molecule and its ability to stimulate T cell receptors, is not only not impaired by these variations, but is preferably enhanced. In this case, artificial peptides or peptide equivalents are used, which are designed according to the requirements of the binding ability to an MHC molecule.

Peptides modified in this way are referred to as “heteroclitic peptides”. They can be obtained by the following methods:

First, the epitopes of MHC-I or MHC-II ligands or their variation are carried out, for example, according to the principle described by Rammenee et al., 1995. The length of the peptide corresponds in the case its adaptation to MHC-I molecules, preferably a minimal sequence of 8 to 10 amino acids with the required anchor amino acids.

If appropriate, the peptide can also be extended at the C- and / or at the N-terminus, provided that this extension does not impair the ability to bind to the MHC molecule or the extended peptide can be processed cellularly for the minimal sequence.

The modified peptides are then tested for recognition by TILs ("tumor-inflating lymphocytes"), for CTL induction, and for increased MHC binding and immunogenicity, as described by Parkhurst et al., 1996, and Becker et al., 1997, described.

Another method suitable for the purposes of the present invention for finding peptides with a greater immunogenicity than that of the natural Rll peptides consists in screening peptide libraries with CTLs which recognize the Rll peptides naturally occurring on tumors, as described by Blake et al. , 1996, described; in this context, the use of combinatorial peptide libraries is proposed to design molecules that mimic tumor epitopes recognized by MHC-I restricted CTLs.

The RII polypeptides of the present invention or immunogenic fragments or peptides derived therefrom can be produced recombinantly or by means of peptide synthesis, as described in WO 96/10413, the disclosure of which is hereby incorporated by reference. The same applies to the recombinant production DNA molecule inserted into an expression vector according to standard methods, transfected into a suitable host cell, the host cultivated under suitable expression conditions and the protein purified. Conventional methods can be used for the chemical synthesis of Rll peptides, for example commercially available automatic peptide synthesizers.

As an alternative to natural Rll peptides or heteroclitic peptides, substances which simulate such peptides, e.g. "Peptidomimetics" or "retro-inverse peptides" can be used. To test these molecules with regard to their therapeutic utility in a tumor vaccine, the same methods are used as above for the natural Rll peptides or Rll peptide equivalents.

The two TAAs of the designation RII-ORF-1 and Rll-ORF-2 according to the present invention and the protein fragments, peptides or peptide equivalents or peptidomimetics derived therefrom can be used in cancer therapy, e.g. by one

To induce an immune response against tumor cells that express the corresponding antigen determinants. They are preferably used for the therapy of Rll-ORF-1 and / or Rll-ORF-2-positive tumors, in particular for breast, kidney and pancreatic carcinoma.

The immune response in the form of induction of CTLs can be brought about in vivo or ex vivo.

For the in vivo induction of CTLs, a pharmaceutical composition containing is effective Component which TAAs Rll-ORF-1 and / or Rll-ORF-2 or fragments or peptide (s) derived therefrom, administered to a patient who suffers from a tumor disease associated with the TAA, the amount of TAA (peptide) being sufficient to achieve an effective CTL response to the antigen-bearing tumor.

In a further aspect, the invention thus relates to a pharmaceutical composition for parenteral, topical, oral or local administration. Preferably the composition is for parenteral administration, e.g. for subcutaneous, intradermal or intramuscular use, containing as active component TAAs R11-0RF-1 and / or RII-ORF-2 or fragments or peptides derived therefrom. The RII-TAA / peptides are dissolved or suspended in a pharmaceutically acceptable, preferably aqueous, carrier. The composition can also contain conventional auxiliaries, such as buffers, etc. The RII-TAA / peptides can be used alone or in combination with adjuvants, e.g. incomplete friend's adjuvant,

Saponins, aluminum salts or, in a preferred embodiment, polycations such as polyarginine or polylysine can be used. The peptides can also be bound to components which support CTL induction or activation, for example to T helper peptides, lipids or liposomes, or they are used together with these substances and / or together with immunostimulating substances, for example cytokines (IL -2, IFN-γ) administered. Methods and formulations which are suitable for the production and administration of the pharmaceutical composition according to the invention are in WO 95/04542 and WO 97/30721, the disclosure of which is hereby incorporated by reference.

Rll polypeptide fragments or Rll peptides can also be used to trigger a CTL response ex vivo. An ex vivo CTL response to a tumor that expresses the two possible proteins from Rll is induced by incubating the CTL progenitor cells together with APCs and Rll peptides or Rll protein. The activated CTLs are then allowed to expand, after which they are re-administered to the patient. Alternatively, APCs can be loaded with Rll peptides, which can lead to an efficient activation of cellular immune responses against Rll positive tumors (Mayordomo et al., 1995; Zitvogel et al., 1996). A suitable method for peptides on cells, e.g. Loading dendritic cells is disclosed in WO 97/19169.

In one embodiment of the invention, a combination of several different Rll peptides or Rll peptide equivalents is used. In another

In one embodiment, Rll peptides are combined with peptides derived from other TAAs. The selection of peptides for such combinations is made with a view to the detection of different MHC types in order to cover the widest possible patient population and / or it is based on the widest possible range of indications by combining peptides from several different tumor antigens. The number of peptides in a pharmaceutical composition can vary over a wide range, typically containing one clinically applicable vaccines 1 to 15, preferably 3 to 10 different peptides.

The peptides according to the invention can also be used as diagnostic reagents. For example, the peptides can be used to test a patient's response to the humoral or cellular immune response elicited by the immunogenic peptide. This makes it possible to improve a treatment protocol. For example, depending on the dosage form (peptide,

Total protein or DNA vaccine) of the TAA, the increase in precursor T cells in the PBLs which are reactive to the defined peptide epitope can be investigated (Robbins and Kawakami, 1996 and references cited therein). In addition, the peptides or the

Whole protein or antibodies directed against the TAA can be used to characterize the course of the disease of a Rll-ORF-1 or Rll-ORF-2 positive tumor (for example by immunohistochemical analyzes of primary tumor and metastases). Such a strategy has proven to be successful several times, for example the detection of the estrogen receptor as a basis for decision-making for endocrine therapy in breast cancer; c-erbB-2 as a relevant marker in the prognosis and course of therapy for breast cancer (Ravaioli et al., 1998; Revillion et al., 1998); PSMA ("prostate specific membrane antigen") as a marker for epithelial cells of prostate cancer in serum or by using a ^nι In-labeled monoclonal antibody against PSMA in immunoscintigraphy for prostate cancer (Murphy et al., 1998 and included references); CEA ("carcinoembryonic antigen") as Serological markers for the prognosis and course in patients with colorectal cancer (Jessup and Loda, 1998).

The DNA molecules according to the invention defined above also include those which, by mutation, lead to an exchange of amino acids in the protein sequence shown in SEQ ID NO: 2 or 3, provided they are used for an RII derivative or fragments or peptides with the encode the immunogenic properties desired for use as tumor vaccines.

The RII DNA molecules of the present invention or the corresponding RNAs, which are also the subject of the present invention, are used, like the (poly) peptides encoded thereby, for the immunotherapy of cancer diseases.

In one embodiment of the invention, DNA molecules encoding natural RII polypeptides are used. As an alternative to the natural Rll cDNA or fragments thereof, modified derivatives can be used. These include sequences with modifications which code for a protein (fragment) or peptides with a higher immunogenicity, the same considerations applying to the modifications at the DNA level as for the peptides described above. Another type of modification is the stringing together of numerous sequences, coding for immunologically relevant peptides, in the manner of a string of pearls ("string-of-beads"; Toes et al., 1997). The sequences can also be modified by adding auxiliary elements, such as functions that a Ensure more efficient delivery and processing of the immunogen (Wu et al., 1995). For example, by adding a localization sequence into the endoplasmic reticulum ("ER targetting sequence"), the processing and thus the presentation and ultimately the immunogenicity of the antigen can be increased.

In a further aspect, the present invention relates to a recombinant DNA molecule which contains the III-DNA according to SEQ ID NO: 1 or a partial sequence, in particular the sequence coding for the polypeptide III-ORF-1 or III-ORF-2.

The RII DNA molecules of the present invention can be administered, preferably in recombinant form as plasmids, directly or as part of a recombinant virus, or bacterium. In principle, any gene therapy method for the immunotherapy of cancer based on DNA ("DNA vaccine") on Rll-DNA can be used, both in vivo and ex vi vo.

Examples of m vivo administration are the direct injection of "naked" DNA, either intramuscularly or by means of a gene gun, which has been shown to lead to the formation of CTLs against tumor antigens. Examples of recombinant organisms are vaccinia virus, adenovirus or Listeria monocytogenes (an overview was given by Coulie, 1997). Furthermore, synthetic carriers for nucleic acids, such as cationic lipids, microsphere, microsphere or liposome for the in vivo administration of nucleic acid molecules, coding for Rll peptide can be used. Similar to peptides, various adjuvants that enhance the immune response can be co-administered, for example cytokines, either in the form of proteins or plasmids encoding them. The application can optionally be combined with physical methods, eg electroporation.

An example of ex vivo administration is the transfection of dendritic cells, as described by Tuting, 1997, or other APCs which are used as cellular cancer vaccines.

In a further aspect, the present invention thus relates to the use of cells which express RII, either on their own or, in optionally modified form, after transfection with the corresponding coding sequence, for the production of a cancer vaccine.

In a further aspect, the invention relates to antibodies against R11-0RF-1 or Rll-ORF-2 (hereinafter “anti-Rll antibodies”) or fragments thereof.

Polyclonal anti-Rll antibodies can be obtained in a conventional manner by immunizing animals, in particular rabbits, by injection of the antigen or fragments thereof, and subsequent purification of the immunoglobulin.

Monoclonal anti-Rll antibodies can be obtained according to standard protocols according to the principle described by Kohler and Muster, 1975, by immunizing animals, in particular mice, followed by antibody-producing cells of the immunized animals be immortalized, for example by fusion with myeloma cells, and the supernatant of the hybridomas obtained is screened for monoclonal anti-Rll antibodies by means of standard immunological assays. For therapeutic or diagnostic use in humans, these animal antibodies can optionally be chimerized in a conventional manner (Neuberger et al., 1984, Boulianne et al., 1984) or humanized (Riechmann et al., 1988, Graziano et al., 1995) ,

Human monoclonal anti-Rll antibodies (fragments) can also be obtained from so-called “phage display libraries” (Winter et al., 1994, Griffiths et al., 1994, Kruif et al., 1995, Mc Guiness et al., 1996) and by means of transgenic animals (Brüggemann et al., 1996, Jakobovits et al., 1995).

The anti-Rll antibodies according to the invention can be used in immunohistochemical analyzes for diagnostic purposes.

In a further aspect, the invention relates to the use of Rll-ORF-1 and Rll-ORF-2-specific antibodies in order to selectively bring any substances into or into a tumor which Rll-ORF-1 and / or Rll- ORF-2 expressed. Examples of such substances are cytotoxic agents or radioactive nuclides, the effect of which is to damage the tumor on site. Due to the tumor-specific expression of Rll-ORF-1 or Rll-ORF-2, no or only minor side effects are to be expected. In a further aspect, substances for visualization can be used with the help of RII-ORF-1 and / or RII-ORF-2 antibodies of tumors that express RII. This is useful for the diagnosis and evaluation of the course of therapy. Therapeutic and diagnostic uses of are described in WO 95/33771.

The TAAs of the designation RII-ORF-2 and Rll-ORF-2 according to the present invention and the protein fragments, peptides or peptide equivalents or peptidomimetics derived therefrom can be used in cancer therapy, e.g. B. to induce an immune response against tumor cells that express the corresponding antigenic determinants. They are preferably used for the therapy of Rll-ORF-1 and / or Rll-ORF-2 positive tumors, in particular in breast, kidney and pancreatic carcinomas.

In a further application, R11 can be used as the target molecule of a directed chemotherapy.

Chemotherapy means the therapeutic administration of substances which, by interfering with the metabolism of malignant cells, their signal transduction and their cell division processes, are either cytostatic or cytotoxic-cytolytic.

In principle, these chemotherapeutic agents have an effect on all dividing cells; However, tumor cells show a higher sensitivity to these substances than healthy cells, since mainly proliferating cells are attacked. In contrast to the immunological therapy approaches mentioned above, the prerequisite for using the tumor-associated RII as a target for chemotherapy is knowledge of the function of the RII proteins R11-ORF-1 and R11-ORF2 or the gene coding therefor.

As a first step in the so-called "down-stream" functional analysis of Rll, a bioinformatic analysis is expediently carried out, which is trend-setting for the experimental validation of Rll as a target for chemotherapy.

For this analysis, the biomformatics concepts based on similarity and modular structure represent an essential basis. Established bioinformatic aids for determining similarities are BLAST

(http://www.ncbi.nlm.nih.gov/BLAST, Altschul et al., 1997) or FASTA (Pearson & Lipman, 1988), the specialized databases such as Pfam (http: // www.sanger. ac. uk / Pfam, Bateman et al., 2000) and SMART (http: // smart. embl-heidelberg. de, Schultz et al., 2000), which take into account domain structures. To refine the analysis, applications such as Clustal (http: // www2. Ebi .ac.uk / clustalw, Higgins et al., 1996) HMMer (http: // hmmer. Wustl. Edu, Durbin et al., 1998), PSI-BLAST (Altschul et al., 1997) and the PROSITE database (http: // www. Expasy. Ch / prosite, Hofmann et al., 1999) are used. Statistical analysis methods that are not based on homologies allow the prediction of further structure and function-relevant properties like that Secondary structure and the appearance of transmembrane segments and helix-turn-helix motifs. Methods for predicting the secondary structure of proteins are available; Jpred (http: // barton. ebi. ac. uk / servers / jpred. html, Cuff et al., 1998) is particularly worth mentioning. The secondary structure prediction can support functional hypotheses, for example if the structure of the suspected homologue is known.

Subsequently, Rll is subjected to a biochemical and biological analysis.

After performing the sequence analysis described above, RII-ORF-1 and RII-ORF-2 are subjected to a biochemical and biological analysis. The selection of the methods used for further analyzes is based on the result of the bioinformatics analysis carried out.

An example of the functional analysis is the analysis of partly theoretically derived proteins of chromosome III of the yeast genome. (Such an analysis succeeded in using bioinformatics to predict more than 70% of the gene functions, some of which have already been confirmed experimentally (Bork, P. et al., 1992; Sharp, PM et al., 1993 and Koonin EV et al., 1994)).

In all of the studies to be carried out, it is important to make a pre-selection of those domains of the protein to be analyzed with unknown function that have striking structural complexity because of little structural information (eg globular areas) does not contribute any essential information content. A comprehensive summary of examples of successful function prediction based on protein sequences has been published in Nature Genetics by Bork and Koonin (Bork and Koonin, 1998).

In the functional analysis of RII-ORF-1 carried out in the context of the present invention, it was found that, according to the bioinformatics analysis, it is a protein that belongs to the family of zinc finger-containing transcription factors.

By suitable experiments, e.g. "Mobility shift", southwestern, UV crosslinking etc. can be used to demonstrate direct and / or indirect interaction with nucleic acids, particularly in promoter regions. Suitable methods are known from the literature (for example Ausubel et al., 1994 ).

A clear homology to a retroviral pol polyprotein was shown for the first 280 amino acids of the protein derived from the RII-ORF-2 region. Rll-ORF-2 could therefore be a possible retrotransposon.

Once the function of Rll-ORF-1 or Rll-ORF-2 has been determined, the importance of the Rll gene and its function or the function of the proteins encoded by it for the tumor process is analyzed. This can e.g. by

Proliferation assays in vitro or in animal models using tumor cells that overexpress the gene to be examined (constitutive or inducible) and expressed as a control either in deleted (inactive) form or downregulated via antisense (see eg Grosveld and Kollias, 1992).

Rll can be used in screening assays to identify substances that modulate, in particular inhibit, the activity of R11-0RF-1 or Rll-ORF-2. In one embodiment, such an assay may e.g. B. consist of Rll-ORF-1 or Rll-ORF-2 or an active fragment thereof, in cells that react to the activity of Rll with proliferation, or the corresponding Rll-cDNA section in the cell Bring expression, and to determine the proliferation of the cells in the presence and in the absence of a test substance.

An example of test cells are cells with a low division rate, e.g. primary cells that have no endogenous Rll. In order to determine the suitability of the cells for a screening assay, these are transformed with Rll cDNA, grown and analyzed using standard assays, e.g. Thymidine incorporation, on their

Proliferation ability tested. Due to a significant increase in their proliferation properties after Rll expression, they can be used as test cells, e.g. in High Throughput Screening Proliferation Assays. examples for

Proliferation assays in high throughput format, e.g. based on the MTS assay, are described in WO 98/00713.

Rll inhibitors with proliferation-inhibiting effects can be used to treat tumors with strong Rll expression can be used, particularly in breast, renal cell or pancreatic carcinoma.

Figure About Looks

Fig. 1: Transcription of Rll in tumor and

Normal tissues: semiquantitative RT-PCR

Fig. 2: Transcription of Rll in tumor tissues and normal tissues: Qualitative PCR

Fig. 3: Northern blot analysis of Rll in normal tissues

Fig. 4: R11 transcription: Qualitative RT-PCR from RNA from human tumor cell lines

Fig. 5: Modified region of the pCR3.1 (+) vector.

example 1

Cell culture of the cell lime MZ derived from a human pancreatic carcinoma. PC2 m7 # l B7.1 # 3 and isolation of the poly A ⁺ RNA

The cell lime MZ. PC2 m7 # 1 B7.1 # 3 is derived from human pancreatic carcinoma (MZ.PC2); it was obtained as follows: First, the tumor cells were passaged once in the mouse and a clone was selected for further studies (MZ.PC 2m7 # 1). This clone was developed under standard conditions (Ausubel et al., 1994) with a eukaryotic vector (pEF-BOS; promoter comes from the human EF-lalpha gene, selection marker: Puromycm;

Mizushima and Nagata, 1990) of the human cDNA B7.1 gene (Selvakumar et al., 1992) contains, transfected. A clone MZ-PC2 m7 # 1 B7.1 # 3 was selected and grown up in T150 cell culture flasks. RPMI 1640 (Gibco plus 4 g / L glucose) with 10% heat-inactivated, fetal calf serum and 2 mM L-glutamine was used as the nutrient medium. Every 3 to 4 days, the cells were cleaved by trypsinization 1: 5 for propagation. After reaching about 80% confluency, 4 ml of a trypsin solution (data per liter: 8 g NaCl, 0.2 g KC1, 1.13 g Na ₂ HP0 ₄ -water-free, 0.2 g KH ₂ P0 ₄ , 100 ml 2.5) were obtained per T150 cell culture bottle % Trypsin solution, 1 g EDTA-Na salt; pH 7.2-7.4) was used to harvest the cells. A total of 2 × 10 ⁷ cells were used to isolate the RNA according to the manufacturer's protocol (RNeasy Minikit, QIAgen). Starting from approx. 100 μg total RNA, the Oligotex Kit (QIAgen) was used to isolate polyA ⁺ RNA in accordance with the manufacturer's protocol. Following this, starting from approx. 0.5 mg polyA + RNA, the cDNA synthesis was carried out according to the

Manufacturer (Clontech marathon protocol) carried out.

Example 2

Representative Difference Analysis (RDA) of the

Pancreatic carcinoma cell line MZ. PC2 m7 # l B7.1 # 3 versus a pool of 11 normal tissues

Starting from approx. 0.5 μg poly-A (+) of the pancreatic tumor cell line MZ. PC2 m7 # l B7.1 # 3 and a pool of 2.5 μg poly-A (+) RNA from 11 normal tissues (Clontech) Bone marrow, heart, kidney, liver, lung, pancreas, skeletal muscle, spleen, thymus, small intestine and stomach were the RDA study (Diatchenko et al., 1996; Hubank and Schatz, 1994) using the PCR-select ™ Kit (Clontech, Palo Alto) according to the

Manufacturer protocol carried out: the RNA of the pancreatic tumor cell line was used as "solid", that of the normal tissue pool as "driver" according to the manufacturer protocol. In contrast to the original protocol, after the synthesis of double-stranded cDNA using oligo-dT, the cDNA with 6 restriction enzymes: EcoRV, Nael, Nrul, Seal (Promega), Sspl, StuI (TaKaRa) in Promega buffer A for 2 hours at 37 ° C and after increasing the NaCl concentration to 150 mM, cut at 37 ° C. for a further 2 hours. The use of this mixture of 6 different restriction enzymes allowed the generation of approximately 800 bp long cDNA fragments, which were used for the representative difference analysis.

Equal parts of "tester cDNA" were ligated either with the adapters A or B and then hybridized separately with an excess of "driver cDNA" at 68 ° C. The two batches were then combined and subjected to a second hybridization with freshly denatured “driver cDNA”. The enriched “solid” -specific cDNAs were then PCR-treated with primers of the kit specific for the adapters A and B, with an elongation time of 2 minutes at 72 ° C amplified exponentially, 27 cycles (10 "94 ° C, 30" 66 ° C, 2 '72 ° C). For further enrichment, an aliquot of this reaction was a second PCR with specific inside subjected to "nested" primers of the kit with an elongation time of 2 minutes at 72 ° C., 10 cycles

(10 "94 ° C, 30" 66 ° C, 2 '72 ° C). The product resulting from this reaction was divided into 3 different specially modified pCR3.1 (+) vectors (InVitrogen): vector (l.ORF), vector (2nd ORF) and vector (3rd ORF)

(Fig. 5: CMV cytomegalovirus; BGH Bovine Growth Hormone; ORF Open Reading Frame) ligated and then in competent E. coli (OneShot ™, Invitrogen) transformed. These vectors enable expression in eukaryotic cells in 3 different reading frames.

For the construction of the 3 vectors, the pCR3.1 (+) vector (InVitrogen) was cut with Nhel and Hindlll (Promega) and each with a dsDNA

Oligomer produced by annealing two ssDNA oligomers (SEQ ID NO: 4 and 5; vector ORF1) or (SEQ ID NO: 6 and 7; vector ORF2) or (SEQ ID NO: 8 and 9; vector ORF3) Standard protocols ligated (e.g. Ausubel et al., 1994; Sambrook et al. 1989). The 3 vector types have a start codon and a cloning site for expression in a reading frame that is different from the other two vectors.

The transformation of competent E. Carried out in three approaches (vector I. ORF, 2. ORF and 3. ORF). coli (OneShot ™, Invitrogen) with the cDNA of the subtractive cDNA library resulted in approximately 9600 clones. These were checked for the presence and length of the insert cDNA by means of PCR analysis. The procedure was as follows: the 9600 clones were in 96-well blocks cultivated in LB-Amp medium for 48 h at 37 ° C. Subsequently, 5 μl aliquots of the E. coli suspensions in 500 μl TE buffer were heated at 100 ° C. for 10 minutes and 1.5 μl thereof was used as a template for a PCR in which the insert of the vector with flanking primers (SEQ ID NO: 10 and 11) was amplified, 35 cycles (1 '94 ° C, 1' 55 ° C, 2 '72 ° C). The PCR products were detected by agarose gel electrophoresis and Ethidiu bromide staining. The remaining bacterial cultures were stored as gycerin stock cultures at -80 ° C.

This gave a cDNA subtraction library of 3450 individual clones, which was named E. coli glycerol stock cultures were available and their insert length was known by agarose gel electrophoresis. As expected, an average length of the inserted cDNA fragments of approximately 800 bp could be detected.

Example 3

DNA sequencing and annotation of clones of the subtractive cDNA library of the pancreatic tumor cell line MZ.PC2 m7 # l B7.1 # 3

The plasmid DNA of 50 clones randomly selected from the subtractive cDNA library was isolated according to the manufacturer's instructions (QIAgen) and sequenced using the Sanger method on an ABI-Prism device. The sequences determined in this way were annotated by BLAST search (National Center for Biotechnology Information) and EST database comparisons were made subjected. This allowed the identification of 38 known and 12 unknown genes. Only EST entries existed for the latter. The expression profile was estimated for the 12 unknown genes: the starting tissue for the corresponding cDNA library was checked for all ESTs with> 95% identity (BLAST) for the experimentally determined sequence in databases. There was a subdivision into i) critical normal tissue, ii) fetal, "dispensable" and immune privileged

Tissue and iii) tumors and tumor cell lines. Based on this "virtual mRNA profile", 4 clones (R2, R8, Rll and R12) were selected for further experimental analysis.

Example 4

Transcriptional analysis of the candidate clones in tumor and normal tissue

Between 2 and 5 μg total RNA from tumor or normal tissues were reverse transcribed using SuperScriptll (GibcoBRL) or AMV-RT (Promega) according to the manufacturer's recommendations. For each individual RNA sample, a second approach without reverse transcriptase as a control for contamination by chromosomal DNA was carried out. The quality and amount of the cDNAs were determined by PCR with β-actin-specific primers (SEQ ID NO: 14 and 15) and GAPDH-specific primers (SEQ ID NO: 16 and 17) after 30 and 35 cycles (1 '95 ° C, 1' 55 ° C, 1 '72 ° C), checked. The 4 candidate genes were analogous with specific ones Analyzed primers. The PCR products were detected using agarose gel electrophoresis and ethidium bromide staining. A candidate who was designated “Rll” showed a relatively specific tumor / testis transcription profile after 35 cycles with Rll-specific primers (SEQ ID NO: 12 and 13); the semiquantitative RT-PCR of RNA from breast cancer om, Lung adenocarcinoma, pulmonary pith epithelial carcinoma, kidney carcinoma, colon carcinoma, heart, lung, liver, kidney, colon, spleen and testis is shown in Fig. 1. Another qualitative PCR of cDNA from patient tissue from 3 human pancreatic tumors with the same Rll-specific primers (SEQ ID NO: 12 and 13) showed the expression in human pancreatic tumors (Fig. 2). Furthermore, an additional qualitative PCR of cDNA from different tumor cell lines of human lung (LC 6, 16), gallbladder (GB 1) and Pancreatic tumors (PC 1, 2) and two melanomas (Mel 2, 7) were carried out with the same Rll-specific primers (SEQ ID NO: 12 and 13), which gave a clear expression in all tumor cell lines (FIG. 4) this analysis was proceeded according to the protocol of Perkin Elmer (GeneAmp RNA PCR Kit, # N808-0017) (RT reaction: (lx) 15 '/ 42 ° C - 5' / 99 ° C - 5 '/ 4 ° C; PCR reaction: (35x) 2 '/ 95 ° C - l' / 95 ° C - l '/ 60 ° C and (lx) 7 ^' / 72 ° C - 4 ° C (Fig. 4). As described above, the PCR products were detected by agarose gel electrophoresis and ethidium bromide staining. A lkb large marker from Gibco BRL was used as the large marker. Example 5

Rll transcription profile in normal tissues

For the Northern blot analysis, "Human Multiple Tissue Northern Blots" (Clontech, Palo Alto and Invitrogen) were hybridized with the [α- ³² P] dCTP (NEN, Boston) labeled approximately 1000 bp Rll PCR product at 68 ° for 2 h The visualization was carried out using standard autoradiographs (Hyperfilm, Amersham). FIG. 3 shows the result of this analysis: of 19 normal tissues (pancreas, adrenal medulla, thyroid gland,

Adrenal cortex, testis, thymus, small intestine, stomach, brain, heart, skeletal muscle, colon, muscle, kidney, liver, placenta, lungs, leukocytes). For Rll, a prominent 7.5 kb long transcript can be seen in the placenta, adrenal medulla, adrenal cortex and in testis.

A very weak band of 7.5 kb can also be detected in the brain. Since all of these normal tissues have an immune privileged status (Streile, 1995), an attack by CTL can be ruled out in immunotherapy based on this antigen.

Additional transcripts of 3.8 kb and 2.3 kb, which may represent splice variants of the 7.5 kb transcript or are derived from a homologous gene, were identified in the adrenal medulla and the adrenal cortex (FIG. 3). Example 6

Cloning of Rll cDNA

The cloning of the human Rll cDNA was carried out as follows: a BLAST analysis showed that the Rll

"Original sequence" (796 bp) an overlapping fragment AF038197 and a large number of overlapping ESTs, such as N42343, W69539, H82474, H51766, N28313, could be identified. Starting from the sequence AF038197, the EstExtractor was used on TigemNet

(http://gcg.tigem.it/cgi-bin/uniestass.pl) found a contig overlapping with the clone Rll. The overlap of the contig and the 796 bp Rll "original sequence" could be by PCR-aplification with a Rll "original sequence" specific primer and one located on the contig

Primers (SEQ ID NO: 18 and 19) from a SuperScript ™ Human Testis cDNA Library (GibcoBRL) and subsequent sequencing are verified. From the SuperScript ™ Human Testis cDNA Library, a Rll-specific primer (SEQ ID NO: 20) and a vector-specific primer (SEQ ID NO: 21) were used to PCR, using the Advantage cDNA PCR Kit ( Clontech) and the standard protocol described there. Knowledge of these new sequences in turn enabled PCR approaches with Rll-specific primers (SEQ ID NO: 22 and 23) and the vector-specific primer (SEQ ID NO: 21).

For the further extension of the Rll cDNA, a human Testis Rapid-Screening cDNA Library panel (OriGene Technologies, Ine) with specific for Rll was used Primers (SEQ ID NO: 24 and 25) screened under the standard PCR conditions specified by the manufacturer. An aliquot of the positive cells was amplified as a template for a PCR with an Rll-specific and a vector-specific primer (SEQ ID NO: 26 and 27) using the Advantage cDNA PCR Kit (Clontech) and the standard protocol described there

For the sequence analysis, aliquots of the PCR batches were ligated directly into the pCR2.1 vector (Invitrogen) and then into competent E. coli (OneShot ™,

Invitrogen) and, as described in Example 3, sequenced.

Based on these newly identified sequences, it was possible to clone from a SuperScript ™ Human Testis cDNA library (GibcoBRL) with the following further RII-specific oligonucleotide primers (SEQ ID NO: 28 to 43) 5 'sequence regions located higher upstream. The primers were combined with a plasmid-specific primer already described above (SEQ ID NO: 21) or with each other

PCR cloning using the Advantage cDNA PCR Kit (Clontech) was used.

The cloned region of the RII cDNA is 6582 bp, the presence of a polyA tail at the 3 'end of the sequence indicating the completeness of the cDNA in this region. Two separate continuous reading frames were identified. The first 5'-sided reading frame (Rll-ORF-1; SEQ ID NO: 2) is at position 218 and the stop codon (TAG) at position 1421 in SEQ ID NO: 1 by the start codon represents. Since no database entries of known genes exist for this gene, no statement can be made about the function. An analysis of the protein profile (http://www.expasy.ch/prosite/) indicated 3 possible N-glycosylation sites (positions # 62-65, 76-79 and 117-120 in SEQ ID NO: 2), a cAMP - and cGMP-dependent protein kinase phosphorylation site (position # 11-14 in SEQ. ID. N0: 2), further 7 possible PKC phosphorylation sites (position * 9-11, 14-16,

78-80, 119-121, 183-185, 202-204 and 210-212 in SEQ ID N0: 2) and 6 possible casein kinase II phosphorylation sites (position # 119-122, 127-130, 183-186, 256- 259, 295-298 and 358-361 in SEQ ID N0: 2). The zinc finger motif (zf-CCHC; E = 0.11, Pfam-A HMM) from position # 371 to position # 384 in SEQ ID NO: 2 could be of particular interest for the prediction of a possible function of R11-0RF-1 ( CLYCGTGGHYADNC). Members of the protein family that have these motifs are known to have none

Have insertions or deletions in the motif itself; which also applies to the R11-0RF-1 protein. Although no typical SH3 binding sequence can be found, it is quite conceivable that the P-rich region (position # 36-56 in SEQ ID NO: 2) could interact with an SH3 domain. By using the COILS algorithm, a coiled-coil structure can be predicted with a probability of over 99% for the amino acid residues in the range from position # 80 to about 125. Because of these two domains, Zinfingermotiv and coiled-coil domain, it can be concluded that R11-0RF-1 may be one Transcription factor, whose oligomerization is controlled via these two domains.

In the second open reading frame, R11-0RF-2, which is defined by a start codon at position # 1498 and a stop codon (TAA) at 2569, in addition to the two obvious proline-rich sections (positions # 128-141 and 330-351 in SEQ ID NO: 2), potential motifs for two N-glycosylation sites (104-107 and 251-254), one protein kinase C phosphorylation site (108-110), five casein kinase II

Phosphorylation sites (99-102, 165-168, 198-201, 200-203 and 274-277) and a region similar to the active site of eukaryotic and viral aspartate proteinases (16-27) were identified. Of particular note is the clear homology of the first 280 amino acids from RII-ORF-2 to the retroviral pol polyprotein. In contrast, no homologies could be found in the C-terminus. Amino acids from position # 9 to 277 in blastp clearly align with the fugu pol polyprotein (position # 104-365; 2e ^{~ 22} ). The above-mentioned aspartate protease pattern # 16-27 comprises the active nucleophile Asp (# 19) of the active site of the prot region of the pol region; Positions # 215 through # 277 correspond to part of the reverse transcriptase domain. The protein derived from RII-ORF-2 is therefore a possible retrotransposon. Example 7

Potential MHC-binding peptides in the regions coding for the two reading frames of Rll, Rll-ORF-1 and Rll-ORF-2

Potential peptide epitopes within the two

Reading frames from R11 according to SEQ ID NO: 2 and 3) were determined using the method described by Parker et. al., algorithms described in 1994 were carried out on the basis of known motifs (Rammenee et al. 1995). For the most important HLA types, in particular for HLA-Al, - A * 0201, -A3, -B7, -B14 and -B 403, 9-mer candidate peptides have been identified which are expected to match the bind corresponding HLA molecules and therefore represent immunogenic CTL epitopes; the peptides found are in Tab. 1 (Rll-ORF-1) and

Tab. 2 (Rll-ORF-2) listed. Using an analogous procedure, further potential peptide epitopes for other HLA types or 8- and 10-mer peptides can be determined.

Table 1

Immunogenic peptide candidates from RII-ORF-1 (401 amino acids)

Table 2

Immunogenic peptide candidates from RII-ORF-2 (357 amino acids)

literature

Altschul, S.F., Madden, T.L., Schäffer, A.A., Zhang, J., Zhang, Z., Miller, W. and Lipman, D.J. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 25, 3389-3402 (1997).

Ausubel, F.M., Brent, R., Kingston, R.E., Moore, D.D., Smith, J.A., Seidman, J.G., Struhl, K. (Eds), (1994),

Vol. 1 + 2 "Current Protocols in Molecular Biology", John Wiley & Sons. Inc.

Bateman, A., Birney, E., Durbin, R., Eddy, S.R., Howe, K.L. and Sonnhammer, E.L. The Pfam Protein Families Database. Nucleic Acids Res. 28, 263-266 (2000).

Becker, D., Kuhn, U., Lempertz, ü., Enk, A., Saloga, J., and Knop, J. (1997), J. Immunol. Methods 203, 171-180.

Blake, J., Johnston, J.V., Hellström, K.E., Marquardt, H., and, Chen, L. (1996), J. Exp. Med. 184, 121-130.

Boon, T, J.C. Cerottini, B. Van den Eynde, P. van der Bruggen, and A. Van Pel (1994), Annu. Rev. Immunol. 12: 337-365

Boon T, (1998), Tumor antigen recognized by cytolytic T cells. Cancer Vaccine Week - International Symposium, New York, Oct 1998; abstract S01 Bork, P. et al. (1992). What's in a genome? Nature 358: 287.

Bork, P. and Koonin, E.V. (1998). Predicting functions from protein sequences - where are the bottlenecks? Nature Genetics 18: 313-318.

Boulianne, G.L., et al., (1984) Nature 312, 643-646

Brüggemann, M. and Neuberger, M.S., (1996), Immunol. Today 17, 391-397

Buschle M, Schmidt W, Zauner W, Mechtler K, Trska B, Kirlappos H, Birnstiel M (1997), Proc. Natl. Acad. Be. U.S.A. 94, 3256-3261

Celluzzi, CM and Falo, LD, Jr. (1998), J. Immunol. 160, 3081-3085

Chen, Y.T., Scanlan, M.J., Sahin, U., Tureci, 0., Gure, A.O., Tsang, S., Williamson, B., Stockert, E., Pfreundschuh, M., and Old, L.J. (1997) Proc. Natl. Acad. Be. U.S.A. 94, 1914-1918.

Coulie, P.G. (1997) Mol. Med. Today 3, 261-268

Cox, AL, Skipper, J, Chen, Y, Henderson, RA, Darrow, TL, Shabanowitz, J, Engelhard, VH, Hunt, DF, and Slingluff, CL, Jr. (1994) Science 264, 716-719

Cuff, JA, Clamp, ME, Siddiqui, AS, Finlay, M. and Barton, GJ Jpred: a consensus secondary structure prediction server. Bioinformatics 14, 892-893 (1998).

Diatchenko, L., Lau, YF, Campbell, AP, Chenchik, A., Moqadam, F., Huang, B., Lukyanov, S., Lukyanov, K., Gurskaya, N., Sverdlov, ED, and Siebert, PD (1996) Proc. Natl. Acad. Be. U.S.A. 93, 6025-6030.

Dranoff, G., Jaffee, E., Lazenby, A., Golumbek, P., Levitsky, H., Brose, K., Jackson, V., Hamada, H.,

Pardoll, D., and Mulligan, R. (1993) Proc. Natl. Acad. Be. U.S.A. 90, 3539-3543.

Durbin, R., Eddy, S., Krogh, A., and Mitchison, G. (1998), Biological Sequence Analysis: Probabilistic Models of Proteins and Nucleic Acids, Cambridge University Press

Elble, R., Widom, J., Gruber, A.D., Abdel-Ghany, M., Levine, R., Goodwin, A., Cheng, H.-C, and Pauli, B.U. (1997), J. Biol. Chem. 272, 27853-27861.

Emini, EA, Hughes, J, Perlow, D, and Boger, J (1985), J. Virol. 55, 836-839

Falk, K., Rötzschke, 0., Stevanovi'c, S., Jung, G., and Rammenee, H-G (1991), Nature 351, 290-296.

Fearon, ER, Pardoll, DM, Itaya, T., ^' Golumbek, P., Levitsky, HI, Simons, JW, Karasuyama, H.,

Vogelstein, B., and Frost, P. (1990), Cell 60, 397-403. Gansbacher, B., Zier, K., Daniels, B., Cronin, K., Bannerji, R., and Gilboa, E. (1990), J. Exp. Med. 172, 1217-1224.

Gaudi C, Kremer F, Angevin E, Scott V, Triebel F (1999), J Immunol 162: 1730-1738

Graziano, R.F., et al., (1995), J. Immunol. 155, 4996-5002

Griffiths, A.D., et al., (1994), EMBO J. 13, 3245-3260

Grosveld, F. and Kollias, G. Transgenic Animals, Academic Press (1992).

Halliday, GM, Patel, A, Hunt, MJ, Tefany, FJ, and Barnetson RS (1995), World J. Surg. 19, 352-358

Higgins, D.G., Thompson, J.D. and Gibson, T.J. Using CLUSTAL for Multiple Sequence Alignments. Methods Enzymol. 266, 383-402 (1996).

Hofmann, K., Buchner, P., Falquet, L. and Bairoch, A. The PROSITE database, its Status in 1999. Nucleic Acids Res. 27, 215-219 (1999).

Hogan KT, Eisinger DP, Cupp SBC, Lekstrom KJ, Deacon DD, Shabanowitz J, Hunt DF, Engelhard VH, Slingluff CL, Ross MM (1998), Cancer Res 58: 5144-5150

Hubank, M. and Schatz, DG, (1994), Nucleic. Acids. Res. 22, 5640-5648. Jager, E., Chen, YT, Drijfhout, JW, Karbach, J., Ringhoffer, M., Jager, D., Arand, M., Wada, H., Noguchi, Y., Stockert, E., Old, LJ, and Knuth, A. (1998), J. Exp. Med. 187, 265-270.

Jakobovits, A., (1995), Curr. Opin. Biotechnol. 6, 561-566

Jameson, BA and Wolf, H (1988), The antigenic index: a novel algorithm for predicting antigenic determinants. Comput. Appl. Biosci. 4, 181-186

Jessup, JM and Loda, M (1998), Prognostic markers in reetal carcinoma. Semin. Surg. Oneol. 1_5, 131-140.

Kastan, M. B. (ed.) "Genetic Instability and Tumorigenesis" in Curr. Top. Microbiol. Immunol. 221 (1997).

Kawakami, Y., Eliyahu, S., Jennings, C, Sakaguchi, K., King, X., Southwood, S., Robbins, P.F., Sette, A., Appella, E., and Rosenberg, S.A. (1995), J. Immunol. 154, 3961-3968.

Kawakami, Y, Robbins, PF, and Rosenberg, SA (1996), Keio J. Med. 45, 100-108

Koonin, EV, Bork, P., and Sander, C. (1994). Yeast chromosome III: New gene functions. EMBO J. 13: 493-503. Koehler, G. and Milstein, C. (1975) Nature 265, 495-497

Kruif, J., et al., (1995), Proc. Natl. Acad. Be. USA 92, 3938-3942

Kyte, J and Doolittle, RF (1982) J. Mol. Biol. 157, 105-132

Lethe, B, Lucas, S, Michaux, L, De Smet, C, Godelaine, D, Serrano, A, De Plaen, E, and Boon, T (1998), Int. J. Cancer 76, 903-908

Mackensen A, Ferradini L, Careelain G, Triebel F, Faure F, Viel S, and Hercend T (1993), Cancer Res. 53, 3569-3573

Mandruzzato S, Brasseur F, Andry G, Boon T, van der Bruggen P (1997), J Exp Med 186: 785-793

Marchand M, Weynants P, Rankin E et al (1995), Int. J. Cancer 63: 883-885

Mayordomo, J.I., Zorina, T., Storkus, W.J., Zitvogel, L., Celluzzi, C, Falo, L.D., Melief, C.J., Ildstad, S.T., Käst, W.M., DeLeo, A.B., and Lotze, M.T. (1995) Nature Medicine 1, 1297-1302.

McGuinnes, B.T., et al., (1996) Nature Biotechnol. 14, 1149

Melief CJ, Offringa R, Toes RE, Käst WM (1996), Curr. Opin. Immunol. 8, 651-657 Mizushima, S. and Nagata, S. (1990), Nucleic Acids Res 18, 5322.

Murphy, G.P., Elgamal, A.A., Su, S.L., Bostwick, D.G., and Holmes, E.H. (1998) Cancer 83, 2259-2269

Neuberger, M.S., et al., (1984) Nature 312, 604-608

Pardoll, D.M. (1998) Nature Medcine 4, 525-531

Parker, K.C., M.A. Bednarek, and J.E. Coligan. (1994), J. Immunol. 152, 163.

Parkhurst, M.R., Salgaller, M.L., Southwood, S., Robbins, P.F., Sette, A., Rosenberg, S.A., and Kawakami, Y. (1996), J. Immunol. 157, 2539-2548.

Paterson Y, Ikonomidis G (1996), Curr. Opin. Immunol. 5, 664-669

Pearson, W.R. and Lipman, D.J. Improved tools for biological sequence comparison. Proc. Natl. Acad. Be. USA 85: 2444-2448 (1988).

Pusztai, L., Lewis, C.E., and Yap, E. (eds.) "Cell Proliferation in Cancer" Oxford University Press (1996).

Rammenee HG, Friede T, Stevanovic S (1995), Immunogenetics 41, 178-228 Rapellino, M, Pecchio, F, Baldi, S, Scappaticei, E, and Cavallo, A (1995), Anticancer Res. 15, 1065-1070

Ravaioli, A., Bagli, L., Zucchini, A., and Monti, F. (1998), Cell. Prolif. 31, 113-126

Revillion, F, Bonneterre, J, and Peyrat, JP (1998), Eur. J. Cancer 34, 791-808

Restifo NP (1996), Curr. Opin. Immunol. 5, 658-63

Riechmann, L., et al., (1988) Nature 332: 323-327

Robbins, PF and Kawakami, Y (1996), Curr. Opin. Immunol. 8, 628-636

Ruppert, J., Sidney, J., Celis, E., Kubo, R.T., Gray, H.M., and Sette, A. (1993), Cell 74, 929-937.

Sahin, U., Türeci, Ö., Schmitt, H., Cochlovius, B., Johannes, T., Schmits, R., Stenner, F., Luo, G., Schobert, I., and Pfreundschuh, M. (1995) Proc. Natl. Acad. Be. U.S.A. 92, 11810-11813

Sambrook, J., Fritsch, E.F., and Maniatis, T. Molecular Cloning: A Laboratory Manual. ColdSpring Harbor Laboratory Press, 1989

Schendel DJ, Gansbacher B, Oberneder R, Kriegmair M, Hofstetter A, Riethmuller G, and Segurado OG (1993), J. Immunol. 151, 4209-4220 Schmidt W, Buschle M, Zauner W, Kirlappos H, Mechtler K, Trska B, Birnstiel M (1997), Proc. Natl. Acad. Be. USA 94, 3262-3267

Schultz, J., Copley, R.R., Doerks, T., Ponting, C.P. and Bork, P. SMART: A Web-based tool for the study of genetically mobile domains. Nucleic Acids Res. 28, 231-234 (2000).

Schweighoffer, T. (1997), One. Res. 3, 164-176

Seeber, S. and Schütte, J. (ed.) "Therapy Concepts Oncology" Springer Verlag 1998.

Selvakumar, A., Mohanraj, B.K., Eddy, R.L., shows,

T.B., White, P.C., and Dupont, B. (1992) Immunogenetics 36, 175-181.

Sette, A., Vitiello, A., Reherman, B., Fowler, P., Nayersina, R., Käst, WM, Melief, CJM, Oseroff, C, Yuan, L., Ruppert, J., Sidney, J ., del Guercio, M.-F., Southwood, S., Kubo, RT, Chesmut, RW, Gray, HM, and Chisari, FV (1994), J. Immunol. 153, 5586-5592.

Sharp, P.M. and Lloyd, A.T. (1993). Regional base composition variation along yeast chromosome III: Evolution of chromosome primary structure. Nucleic Acids Res. 21: 179-183.

Stauss, HJ, Davies, H., Sadovnikova, E., Chain, B., Horowitz, N., and Sinclair, C. (1992), Proc. Natl. Acad. Be. USA 89, 7871-7875. Streilein, JW (1995) Science 270, 1158-1159.

Tepper, R.I., Pattengale, P.K., and Leder, P. (1989), Cell 57, 503-512.

Tighe H, Corr, M, Roman M, and Raz E (1998), Immunol. Today 19, 89-97

Toes, R.E., Hoeben, R.C., Van der Voort, E., Ressing,

M.E., Van-der-Eb, A.J. Melief, C.J.M., and Offringa, R. (1997), Proc. Natl. Acad. Be. U.S.A. 94, 14660-14665

Tuting, T., DeLeo, A.B., Lotze, M.T., and Storkus, W.J., (1997), Eur. J. Immunol. 27, 2702-2707 ,.

Van den Eynde, B. and Brichard, V.G. (1995), Curr. Opin. Immunol. 1_, 674-681.

Van den Eynde, BJ, and van der Bruggen, P (1997), Curr. Opin. Immunol. 9, 684-693

van der Bruggen, P., C. Traversari, P. Chomez, C. Lurquin, E. De Plaen, B. Van den Eynde, A. Knuth, and T. Boon. (1991) Science 254, 1643-1647

van der Burg, S.H., et al., (1996), J. Immunol. 156, 3308-3314

van Elsas, A., van der Minne, CE, Borghi, M., van der Spek, CW, Braakman, E., Osanto, S., and Schrier, PI (1996), CTL Reeognition of an IL-2 Producing Melanoma Vaccine. In: Immunology of human melanoma. Tumor-host interaction and immunotherapy, edited by M. Maio, Amsterdam: IOS, 1996, p. 165-173

van Elsas, A., Aarnoudse, C, van der Minne, C.E., van der Spek, C.W., Brouwenstijn, N., Osanto, S., and Schrier, P.I. (1997), J. Immunother. 20, 343-353.

Vaughan, T.J., et al., (1998) Nature Biotechnol. 16, 535-539

Velculescu, VE, Zhang, L, Vogelstein, B, and Kinzler, KW (1995), Science 270, 484-487

Wang, L., et al., (1997) Mol. Immunol. 34, 609-618

Wang, RF (1997) Mol. Med. 3, 716-731

Winter, G., et al. , (1994), Annu. Rev. Immunol. 12, 433-455

Wölfel T, Schneider, J, Zum Buschenfelde, Meyer, KH, Rammenee, HG, Rotzschke, 0, and Falk, K (1994), Int. J. Cancer 57_, 413-418

Wölfel T, Hauer M, Schneider J, Serrano M, Wölfel C, Klehmann-Hieb E, De Plaen E, Hankeln T, Meyer zum Büschenfelde KH, Beach D (1995), Science 269: 1281-1284

Wu, TC, Guarnieri, FG, Staveley-0 'Carroll, KF, Viscidi, RP, Levitsky, HI, Hedrick, L., Cho, KR, August, JT, and Pardoll, DM (1995), Proc. Natl. Acad. Be. USA 92, 11671-11675. Zhang, Y. et al. (1994). Positional eloning of the mouse obese gene and its human momologue. Nature 372 425-432.

Zhu, D., Cheng., C.-F., and Pauli, B.U. (1992) J. Clin. Invest. 89, 1718-1724.

Zitvogel, L., Mayordomo, J.I., Tjandrawan, T., DeLeo, A.B., Clarke, M.R., Lotze, M.T., and Storkus, W.J. (1996), J. Exp. Med. 183, 87-97.

Claims

claims

1. Isolated DNA molecule which has the nucleotide sequence shown in SEQ ID NO: 1 or a polynucleotide which hybridizes with this DNA molecule under stringent conditions, or a fragment thereof.

2. An isolated DNA molecule according to claim 1, containing a DNA sequence coding for a tumor-associated antigen with the immunogenic properties of the

Polypeptide of the amino acid sequence according to SEQ ID NO: 2 or a tumor-associated antigen, of which the polypeptide shown in SEQ ID NO: 2 is a partial sequence, or for fragments thereof.

3. An isolated DNA molecule according to claim 1, containing a DNA sequence coding for a tumor-associated antigen with the immunogenic properties of the polypeptide with the amino acid sequence according to SEQ ID NO: 3, or for fragments thereof.

4. Tumor-associated antigen of the name

Rll-ORF-1, characterized in that it has the amino acid sequence defined in SEQ ID NO: 2 or contains this as a partial sequence.

5. Immunogenic protein fragment or peptide, characterized in that it is derived from the tumor-associated antigen defined in claim 4.

6. Immunogenic (poly) peptide according to claim 5, which triggers a humoral immune response.

7. Immunogenic (poly) peptide according to claim 5, or its degradation products are presented by MHC molecules and trigger a cellular immune response.

8. Immunogenic peptide according to claim 7, selected from the group of peptides according to SEQ ID NO: 88 to 102.

9. Immunogenic (poly) peptide according to one of claims 5 to 8 for the immunotherapy of cancer in vivo or ex vivo, wherein the (poly) peptide induces an immune response against tumor cells of the patient that express RII.

10. Pharmaceutical composition for parenteral, topical, oral or local administration, characterized in that it contains one or more immunogenic (poly) peptides according to one of claims 5 to 9 as an effective component.

11. Pharmaceutical composition according to claim 10, characterized in that it is different from

Rll-ORF-1 derived immunogenic peptides.

12. Pharmaceutical composition according to claim 10 or 11, characterized in that it contains one or more peptides derived from RII-ORF-1 in a mixture with peptides derived from other tumor-associated antigens.

13. Pharmaceutical composition according to claim 11 or 12, that the peptides bind to at least two different HLA types.

14. Tumor-associated antigen of the designation R11-0RF-2, characterized in that it is the in

SEQ ID NO: 3 defined amino acid sequence.

15. Immunogenic protein fragment or peptide, characterized in that it is derived from the tumor-associated antigen defined in claim 14.

16. Immunogenic (poly) peptide according to claim 15, which triggers a humoral immune response.

17. Immunogenic (poly) peptide according to claim 15, or its degradation products are presented by MHC molecules and trigger a cellular immune response.

18. Immunogenic peptide according to claim 17, selected from the group of peptides according to SEQ ID NO: 44 to 87.

19. Immunogenic (poly) peptide according to one of claims 15 to 18 for the immunotherapy of cancer diseases in vivo or ex vivo, wherein the (poly) peptide induces an immune response against tumor cells of the patient, which express RII.

20. Pharmaceutical composition for parenteral, topical, oral or local administration, characterized in that it contains as active component one or more immunogenic (poly) peptides according to one of claims 15 to 19.

21. Pharmaceutical composition according to claim 20, characterized in that it contains various immunogenic peptides derived from RII-ORF-2.

22. Pharmaceutical composition according to claim 21, characterized in that it contains one or more peptides derived from RII-ORF-2 in a mixture with peptides derived from other tumor-associated antigens.

23. A pharmaceutical composition according to claim 21 or 22, that the peptides bind to at least two different HLA types.

24. Recombinant DNA molecule containing a DNA molecule according to one of claims 1 to 3.

25. DNA molecule according to one of claims 1 to 3 or 24, for the immunotherapy of cancer, wherein the (poly) peptide Rll-ORF-1 or Rll-ORF-2 or a fragment thereof expressed by the DNA molecule Immune response against tumor cells of the patient, which express Rll-ORF-1 and / or Rll-ORF-2.

26. Use of cells which express the antigen defined in claim 4 and / or 14 for the production of a cancer vaccine.

27. Antibodies against a (poly) peptide defined in one of the tips 4 to 9.

28. Antibodies against a (poly) peptide defined in one of the tips 14 to 19.

29. Antibody according to claim 27 or 28, characterized in that it is monoclonal.

30. Antibody according to one of claims 27 to 29 for the therapy and diagnosis of cancer diseases which are associated with the expression of Rll.