AU2013202871A1 - Vaccine peptide combinations against cat allergy - Google Patents

Abstract

ll:\fint\Interwovn\NRPortbl\DCC\FMT\5048026 lDOC-5/042013 The present invention relates to compositions comprising peptides for preventing or treating allergy to cats, and in particular to optimal combinations of peptides.

Description

H:\fm\Intrwovn\NRPortbl\DCC\FMT\504795II.DOC-5/04/2013 VACCINE PEPTIDE COMBINATIONS AGAINST CAT ALLERGY This is a divisional of Australian Patent Application No. 2008256524, the entire contents of which are incorporated herein by reference. 5 Field of the Invention The present invention relates to compositions comprising peptides for preventing or treating allergy to cats, and in particular to optimal combinations of peptides 10 Background of the Invention T-cell antigen recognition requires antigen presenting cells (APCs) to present antigen fragments (peptides) on their cell surface in association with molecules of the major histocompatibility complex (MHC). T cells use their antigen specific T-cell receptors (TCRs) to recognise the antigen fragments presented by the APC. Such 15 recognition acts as a trigger to the immune system to generate a range of responses to eradicate the antigen which has been recognised. Recognition of external antigens by the immune system of an organism, such as man, can in some cases result in diseases, known as atopic conditions. Examples of the latter are the allergic diseases including asthma, atopic dermatitis and allergic rhinitis, hi 20 this group of diseases, B lymphocytes generate antibodies of the IgE class (in humans) which bind externally derived antigens, which are referred to in this context as allergens since these molecules elicit an allergic response. Production of allergen-specific IgE is dependent upon T lymphocytes which are also activated by (are specific for) the allergen. Allergen-specific IgE antibodies bind to the surface of cells such as basophils and mast 25 cells by virtue of the expression by these cells of surface receptors for IgE. Crosslinking of surface bound IgE molecules by allergen results in degranulation of these effector cells causing release of inflammatory mediators such as histamine, 5-hydroxtryptamine and lipid mediators such as the sulphidoleukotrienes. In addition to IgE-dependent events, certain allergic diseases such as asthma are characterised by IgE 30 independent events. Allergic IgE-mediated diseases are currently treated with agents which provide symptomatic relief or prevention. Examples of such agents are anti- WO 2008/145998 PCT/GB2008/001827 histanines, P2 agonists, and glucocorticosteroids. In addition, some IgE-mediated diseases are treated by desensitisation procedures that involve the periodic injection of allergen components or extracts. Desensitisation treatments may induce an IgG response that competes with IgE for allergen, or they may induce specific suppressor 5 T cells that block the synthesis of IgE directed against allergen. This form of treatment is not always effective and poses the risk of provoking serious side effects, particularly general anaphylactic shock. This can be fatal unless recognised immediately and treated with adrenaline. A therapeutic treatment that would decrease or eliminate the unwanted allergic-immune response to a particular allergen, without 10 altering the immune reactivity to other foreign antigens or triggering an allergic response itself would be of great benefit to allergic individuals. Approximately 10% of the worlds human population are allergic to cats (Felis domesticus) and up to 67% of asthmatic patients are sensitive to cat allergens. The major allergen produced by cats is the glycoprotein Fel dl, which elicits a response in 15 90-95% of patients suffering from cat allergy. A therapeutic or preventative treatment would therefore be of great benefit to humans that suffer or are at risk of suffering from cat allergy. Summary of the Invention 20 The present inventors have discovered that certain combinations of peptide fragments of the Fel dl protein are particularly useful in desensitising individuals to Fel dl allergen. The polypeptide combinations of the invention have been selected for their ability to bind to many MHC Class II molecules, and cause T cell proliferation with minimal histamine release. The compositions, products, vectors 25 and formulations of the invention may therefore be provided to individuals for preventing or treating allergy to cats by tolerisation. I The polypeptides of the invention were initially selected as potential T cell epitopes through use of peptide - MHC binding assays. See for example Figure 1 which demonstrates the ability of a range of peptides derived from Fel dl chains 1 30 and 2 to bind to multiple DR types in MHC class H. binding assays These candidate polypeptides were then further screened for potential use in tolerisation.

WO 2008/145998 PCT/GB2008/001827 3 A difficulty associated with approaches to desensitisation based on peptide immunisation lies in how to select an appropriate size and region of the allergen as the basis for the peptide to be used for immunisation. The size of the peptide of choice is crucial. If the peptide is too small, the vaccine would not be effective in 5 inducing an immunological response. If the peptides are too large, or if the whole antigen is introduced into an individual, there is the risk of inducing adverse reactions, such as anaphylaxis, which may be fatal. The polypeptides of the invention have been selected to retain T cell specificity whilst being small enough in size to not possess significant tertiary 10 structure that would enable them to retain the conformation of an IgE-binding epitope of the whole molecule. The polypeptides of the invention therefore do not induce significant crosslinking of adjacent specific IgE molecules on cells such as mast cells and basophils and consequently do not cause significant histamine release. The peptides of the invention are advantageous in that upon administration to 15 a sample of T cells they result in T cell proliferation whilst causing minimal histamine release. This is demonstrated in Example 2. The polypeptides of the inventions are capable of inducing a late phase response in a cat allergic individual. The composition, products and formulations of the invention comprising these polypeptides or polynucleotides that are capable of expressing these polypeptides are 20 therefore useful and effective in reducing hypersensitivity to Fel dl allergen in individuals that are sensitised to this allergen. A further advantage of the invention is the ability of the combinations of peptides to broadly target Major Histocompatibility Complex (MHC) molecules. T cell receptors (TCRs) are highly variable in their specificity. Variability is generated, 25 as with antibody molecules, through gene recombination events within the cell. TCRs recognise antigen in the form of short peptides bound to molecules encoded by the genes of the Major Histocompatibility Complex (MHC). These gene products are the same molecules that give rise to "tissue types" used in transplantation and are also referred to as Human Leukocyte Antigen molecules (HLAs) which terms may be 30 used interchangeably. Individual MHC molecules possess peptide binding grooves which, due to their shape and charge are only capable of binding a limited group of WO 2008/145998 PCT/GB2008/001827 4 peptides. The peptides bound by one MHC molecule may not necessarily be bound by other MHC molecules. When a protein molecule such as an antigen or allergen is taken up by antigen presenting cells such as B lymphocytes, dendritic cells, monocytes and macrophages, 5 the molecule is enzymatically degraded within the cell. The process of degradation gives rise to peptide fragments of the molecule which, if they are of the appropriate size, charge and shape, may then bind within the peptide binding groove of certain MHC molecules and be subsequently displayed upon the surface of antigen presenting cells. If the peptide/MHC complexes are present upon the antigen 10 presenting cell surface in sufficient numbers they may then activate T cells which bear the appropriate peptide/MHC-specific T cell receptors. Due to the polymorphic nature of the MHC, individuals in an outbred population such as man will express different combinations of MHC molecules on their cell surfaces. Since different MHC molecules can bind different peptides from 15 the same molecule based on the size, charge and shape of the peptide, different individuals will display a different repertoire of peptides bound to their MHC molecules. Identification of universal MHC-binding peptide epitopes in an outbred population such as man is more difficult than in inbred animals (such as certain strains of laboratory mice). On the basis of differential MHC expression between 20 individuals and the inherent differences in peptide binding and presentation which this brings, it is unlikely that a single peptide can be identified which will be of use for desensitisation therapy in man. The peptide combination of the invention, however, provides a broad coverage of efficacy over the human population by targeting the majority of the 25 population's MHLC. It would not, for example, be necessary to type the patient or individual to determine which MHC Class II molecules he or she possesses in order to determine what peptide or combination of peptides would be effective. A vaccine formulated with the peptides of the invention would therefore have broad utility. The inventors' work has produced peptide combinations with the following 30 characteristics: the combination binds to many different MHC Class II molecules (see WO 2008/145998 PCT/GB2008/001827 5 Figure 2 which shows the large number of combinations that do not bind to many different MHC molecules) - the combinations produce the same or less histamine release than the whole allergen and / or have a cytokine release profile equivalent to the 5 whole allergen - the peptides of the combinations are soluble. Accordingly, the present invention provides a composition for use in preventing or treating allergy to cats by tolerisation comprising: a) four or more polypeptides selected from any of SEQ ID NO: 1, 2, 3, 4, 10 5, 6, 7, 8, 9, 10, 11 or 12, and optionally b) one, two or three polypeptides having the following characteristics: (i) comprising sequence having at least 65% sequence identity to at least 9 or more contiguous amino acids in any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12 15 not selected in a); and (ii) 9 to 30 amino acids in length. Preferably, the composition of the invention comprises either: (i) at least two peptides which exhibit strong binding and at least one peptide which exhibits moderate binding to each member of a panel of HLA 20 molecules; or (ii) at least one peptide which exhibits strong binding and at least two peptides which exhibit moderate binding to each member of said panel of HLA molecules; wherein the panel of HLA molecules comprises at least seven different HLA 25 molecules encoded by different alleles which have a cumulative frequency in. an outbred human population of at least 80%; and/or (iii) wherein the composition is capable of inducing histamine release in a sample from a cat allergic individual at a level which is no higher than 5% above the histamine release induced in a sample from the same individual by whole Fel d 1 30 allergen; and/or (iv) wherein the composition induces a cytokine release profile in a PBMC WO 2008/145998 PCT/GB2008/001827 6 sample from a cat allergic individual which is equivalent to the cytokine release profile in a sample from the same individual induced by whole Fel d I allergen.. Typically the outbred human population is Caucasian, and/or the panel of HLA molecules comprises at least HLA-DRI, DR3, DR4, DR7, DRI 1, DRI3 and 5 DR15; and optionally also comprises HLA-DRB4 and DRB5. Description of the drawings Figure 1 - Peptides derived from Fel d] chains I and 2 were tested for ability to bind to multiple DR types in MHC class 1U. binding assays. Peptides that showed 10 promiscuous binding characteristics were selected and combined to generate mixtures of peptides that bind to a broad population of MHC class H types. Figure 2 - Graphical representation of peptide mixtures showing those which bind to a broad population of MHC class TI types. Figure 3 Proliferation: percentage responders and quality of response. 15 Figure 3 summarises proliferative responses to peptides and antigens. The percentage of individuals mounting a detectable proliferative response is shown in the black bars. Grey (weak), white (moderate) and hashed (strong) bars provide a breakdown of the quality of these responses. Quality is arbitrarily defined by Stimulation Index (SI: ratio of counts in the presence of antigen/peptide divided by counts in medium 20 alone). Thus for peptide 1 (MLA01), 12% of subjects made a proliferative response and of these 92% were weak, none were moderate and 8% were high. Proliferative responses to individual peptides/antigens were variable (black bar). 92% of subjects had positive proliferative responses to the positive control antigen PPD. The majority of these were strong responses (hashed bar). 75% of subjects responded to cat dander 25 extract, with 59% of the responses (i.e. 59% of the 75%) being weak. The response to the mixture of 7 preferred peptides (SEQ ID NOS: 1 TO 7) was almost identical to cat dander extract (CAT). Figure 4- Percentage of responders by cytokine. Figure 4 summarises the percentage of individuals who mounted a detectable response to each of the 30 peptides/antigens by production of the three cytokines measured. The positive control antigen PPD elicited a cytokine production in almost all individuals (1FN-y: 91%, IL- WO 2008/145998 PCT/GB2008/001827 7 13: 97% and IL-10: 96%). Whole cat allergen and the mixture of 7 peptides elicited a cytokine response in approximately 80% or more of subjects. Individual peptides elicited responses of differing frequency. In general cytokine production appeared to be a more sensitive method of detecting responses with larger percentages of 5 individuals giving positive cytokine responses than proliferative responses. In most cases, IL-10 secretion was detected in the largest number of subjects and IFN-y detected least frequently. Figure 5 - Percentage of individuals producing IFN-y and strength of response following cell culture with peptide/antigen. IFN-y responses were detected 10 in 26-44% of subjects in response to individual peptides. These responses were predominantly very low to low to moderate. Complex antigens induced more frequent responses (peptide mixture 80%, cat dander 79%, PPD 91%). These responses were low to moderate to high. PPD responses were particularly high (89 of PPD responses were above I 00pg/ml). 15 Figure 6 - Percentage of individuals producing IL-13 and strength of response following cell culture with peptide/antigen. IL-13 responses were detected in between 33-68% of subjects in response to individual peptides. These responses were predominantly very low to low, although a significant number of moderate responses were detected. This may reflect the Th2 nature of allergic sensitisation in 20 these subjects. Complex antigens induced more frequent responses (peptide mixture 85%, cat dander 93%, PPD 97%). These responses were low to moderate to high. Figure 7 - Percentage of individuals producing IL-10 and strength of response following cell culture with peptide/antigen. IL-10 responses were detected in between 46-75% of subjects in response to individual peptides. These responses 25 were predominantly very low to low. Complex antigens induced more frequent responses (peptide mixture 93%, cat dander 96%, PPD 96%). These responses were low to moderate. Very few "high" IL-10 responses were observed. Figure 8 - A representative plot showing the average LPSR area before and after treatment for all eight patients in the 12.0 nmol cohort of the clinical trial of a 30 preferred mixture of peptides of the invention.

WO 2008/145998 PCT/GB2008/001827 8 Description of the sequences mentioned herein SEQ ID NO: I to 16 provide the polypeptide sequences of the invention. SEQ ID NOS: I to 16 correspond to peptides MLA0I, MLA03, MLA04, MLA05, MLA07, MLA12,. MLA14, MLA02, MLA06, MLAI1, MLA15, MLA16, MLA08, 5 MLA09, MLA10 and MLA13 respectively in the Examples and Figure 1. Detailed description of the invention The invention provides a composition for use in preventing or treating allergy to cats by tolerisation comprising: 10 a) four or more polypeptides selected from any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12, and optionally b) one, two or three polypeptides having the following characteristics: (i) comprising sequence having at least 65% sequence identity to at least 9 contiguous amino acids in any of SEQ ID 15 NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12 not selected in a); and (ii) 9 to 30 amino acids in length. The invention also provides products and formulations comprising the polypeptides of the invention and compositions, products and vectors comprising polynucleotides capable of expressing the polypeptides of the invention for use in 20 preventing or treating cat allergy by tolerisation. Peptide fragments of Fel di protein The major allergen produced by the domestic cat Felis catus (Felis domesticus) is the glycoprotein Fel dl. This 39kDa protein is formed from two 25 17kDa subunits, each consisting of two disulphide-linked peptides (Fel dl Chain 1 and Chain 2). The amino acid sequence of Fel d1 is disclosed in WO 91/06571. The major source of the Fel dl protein is the sebaceous glands, although expression is also detected in salivary glands and the anal glands. The function of the Fel dl protein is currently unknown, although it is possibly a pheromone binding protein. 30 The peptides of the invention are derived from Fel dl. The terms "peptide" and "polypeptide" are used interchangeably herein. Fel dl is also referred to herein WO 2008/145998 PCT/GB2008/001827 9 as "the allergen". The composition of the invention comprises four or more polypeptides selected from any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12. Optionally, the composition may comprise one, two or three further polypeptides. These further 5 polypeptides relate to (i.e. are typically homologues and/or fragments of) the other sequences, i.e. SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12, that are not amongst the four or more polypeptides already selected. The one, two or three further polypeptides may be identical to any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12. The composition may therefore comprise four, five, six or seven different 10 polypeptides as provided in any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12. However, the optional one, two or three further polypeptides do not need to be 100% identical to any of'SEQ ID NO: 1, 2,3, 4,5, 6,7, 8, 9, 10, 11 or 12. They are preferably at least 65% identical to at least 9 or more contiguous amino acids in any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12, not already selected for the four 15 or more polypeptides. In other words, the invention provides a composition for use in the prevention or treatment of cat allergy by tolerisation comprising a) four or more polypeptides selected from any one of the following amino acid sequences: CPAVKRDVDLFLT (SEQ ID NO: 1); 20 EQVAQYKALPVVLENA (SEQ ID NO: 2); KALPVVLENARILKNCV (SEQ ID NO: 3); RILKNCVDAKMTEEDKE (SEQ ID NO: 4); KENALSLLDKIYTSPL (SEQ ID NO: 5); TAMKKIQDCYVENGLI (SEQ ID NO: 6); 25 SRVLDGLVMTTISSSK (SEQ ID NO: 7); LFLTGTPDEYVEQVAQY (SEQ ID NO: 8); KMTEEDKENALSLLDK (SEQ ID NO: 9); LTKVNATEPERTAMKK (SEQ ID NO:10); ISSSKDCMGEAVQNTV (SEQ ID NO:11); 30 AVQNTVEDLKLNTLGR (SEQ ID NO:12) WO 2008/145998 PCT/GB2008/001827 10 And optionally, the composition may comprise b) one, two or three further polypeptides having the following characteristics: (i) comprising sequence having at least 65% sequence identity to at least 9 or more contiguous amino acids in any of SEQ ID NO: I to 12 above not 5 selected in a); and (ii) 9 to 30 amino acids in length. The invention also provides a product containing a) four or more polypeptides selected from any one of the following amino acid sequences: CPAVKRDVDLFLT (SEQ ID NO: 1); 10 EQVAQYKALPVVLENA (SEQ ID NO: 2); KALPVVLENARILKNCV (SEQ ID NO: 3); RILKNCVDAKMTEEDKE (SEQ ID NO: 4); KENALSLLDKIYTSPL (SEQ ID NO: 5); TAMKKIQDCYVENGLI (SEQ ID NO: 6); 15 SRVLDGLVMTTISSSK (SEQ ID NO: 7); LFLTGTPDEYVEQVAQY (SEQ ID NO: 8); KMTEEDKENALSLLDK (SEQ ID NO: 9); LTKVNATEPERTAMKK (SEQ ID NO:10); ISSSKDCMGEAVQNTV (SEQ ID NO:11); 20 AVQNTVEDLKLNTLGR (SEQ ID NO:12) and optionally, the product may comprise b) one or more further polypeptides having the following characteristics: (i) comprising sequence having at least 65% sequence identity to at least 9 or more contiguous amino acids in any of SEQ ID NO: I to 12 above not 25 selected in a); and (ii) 9 to 30 amino acids in length, wherein each different polypeptide is for simultaneous, separate or sequential use in the prevention or treatment of cat allergy by tolerisation. In more detail therefore, the invention provides a product containing: 30 (a) A polypeptide selected from any one of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12; WO 2008/145998 PCT/GB2008/001827 11 (b) A polypeptide selected from any one of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12, that is not selected in (a) above; (c) A polypeptide selected from any one of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12, that is not selected in (a) or (b) above; 5 (d) A polypeptide selected from any one of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12, that is not selected in (a), (b) or (c) above; and optionally (e) A polypeptide having the following characteristics: (i) comprising sequence having at least 65% sequence identity to at least 9 or more contiguous amino acids in any of SEQ ID NO: I 10 to 12 not selected in a), b), c) or d) above; and (ii) 9 to 30 amino acids in length; and optionally (f) A polypeptide fragment of Fel dl protein having the following characteristics: (i) comprising sequence having at least 65% sequence identity to 15 at least 9 or more contiguous amino acids in any of SEQ ID NO: I to 12 not selected in a), b), c), d) or e) above; and (ii) 9 to 30 amino acids in length; and optionally (g) A polypeptide fragment of Fel dl protein having the following characteristics: 20 (i) comprising sequence having at least 65% sequence identity to at least 9 or more contiguous amino acids in any of SEQ ID NO: 1 to 12 not selected in a), b), c), d), e) or f) above; and (ii) 9 to 30 amino acids in length; for simultaneous, separate or sequential use in the prevention or treatment of cat 25 allergy by tolerisation. The composition or products of the invention may therefore comprise variants of any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12. Peptide fragments according to the invention may be derived by truncation, e.g. by removal of one or more amino acids from the N and/or C-terminal ends of a polypeptide. Fragments 30 may also be generated by one or more internal deletions, provided that the core 9 amino acids that makes up the T cell epitope is not substantially disrupted.

WO 2008/145998 PCT/GB2008/001827 12 For example, a variant of SEQ ID NO: I may comprise a fragment of SEQ ID NO: 1, i.e. a shorter sequence. This may include a deletion of one, two, three or four amino acids from the N-terminal end of SEQ ID NO: 1 or from the C-terminal end of SEQ ID NO: 1. Such deletions may be made from both ends of SEQ ID NO: 1. A 5 variant of SEQ ID NO: 1 may include additional amino acids (for example from the cat Fel d1 protein sequence) extending beyond the end(s) of SEQ ID NO: 1. A variant may include a combination of the deletions and additions discussed above. For example, amino acids may be deleted from one end of SEQ ID NO: 1, but additional amino acids from the full length Fel dl protein sequence may be added at 10 the other end of SEQ ID NO: 1. The same discussion of variants above also applies to SEQ ID NO: 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 and 12. A variant peptide may include one or more amino acid substitutions from the amino acid sequence of any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8,9, 10, 11 or 12, or a fragment thereof. A variant peptide may comprise sequence having at least 65% 15 sequence identity to at least 9 or more contiguous amino acids in any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12. More preferably a suitable variant may comprise at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, or at least 98% amino acid identity to at least 9 contiguous amino acids of any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12. This level of amino acid identity may be 20 seen at any section of the peptide, although it is preferably the core region. The level of amino acid identity is over at least 9 contiguous amino acids but it may be at least 10, 11, 12, 13, 14, 15 or at least 16 or 17 amino acids, depending on the size of the peptides of comparison. Accordingly, any of the above-specified levels of identity may be across the entire length of sequence. 25 In connection with amino acid sequences, "sequence identity" refers to sequences which have the stated value when assessed using ClustalW (Thompson et al., 1994, supra) with the following parameters: Pairwise alignment parameters -Method: accurate, Matrix: PAM, Gap open penalty: 10.00, Gap extension penalty: 0.10; Multiple alignment parameters -Matrix: PAM, 30 Gap open penalty: 10.00, % identity for delay: 30, Penalize end gaps: on, Gap separation distance: 0, Negative matrix: no, Gap extension penalty: 0.20, Residue- WO 2008/145998 PCT/GB2008/001827 13 specific gap penalties: on, Hydrophilic gap penalties: on, Hydrophilic residues: GPSNDQEKR. Sequence identity at a particular residue is intended to include identical residues which have simply been derivatized. A variant peptide may comprise 1, 2, 3, 4, 5 or more, or up to 10 amino acid 5 substitutions from any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12. Substitution variants preferably involve the replacement of one or more amino acids with the same number of amino acids and making conservative amino acid substitutions. For example, an amino acid may be substituted with an alternative amino acid having similar properties, for example, another basic amino acid, another 10 acidic amino acid, another neutral amino acid, another charged amino acid, another hydrophilic amino acid, another hydrophobic amino acid, another polar amino acid, another aromatic amino acid or another aliphatic amino acid. Some properties of the 20 main amino acids which can be used to select suitable substituents are as follows: Ala aliphatic, hydrophobic, neutral Met 1hydrophobic, neutral Cys polar, hydrophobic, neutral Asn jPolar, hydrophilic, neutral sp polar, hydrophilic, charged (-) Pro hydrophobic, neutral Glu polar, hydrophilic, charged (-) Gin polar hydrophilic, neutral -------- 1-------- Phe aromatic, hydrophobic, neutral Arg polar, hydrophilic, charged (+) ily aliphatic, neutral Ser polar, hydrophilic, neutral His aromatic, polar, hydrophilic, Thr polar, hydrophilic, neutral charged (+) -1e aliphatic, hydrophobic, neutral Val aliphatic, hydrophobic, neutral Lys polar, hydrophilic, charged(+) Trp aromatic, hydrophobic, neutral Leu aliphatic, hydrophobic, neutral Tyr aromatic, polar, hydrophobic 15 Further variants include those in which instead of the naturally occurring amino acid the amino acid which appears in the sequence is a structural analog thereof. Amino acids used in the sequences may also be modified, e.g. labelled, providing the function of the peptide is not significantly adversely affected.. 20 Where the peptide has a sequence that varies from the sequence of any of SEQ ID WO 2008/145998 PCT/GB2008/001827 14 NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12 or a fragment thereof, the substitutions may occur across the full length of the sequence, within the sequence of any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12, or outside the sequence of any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12. For example, the variations described 5 herein, such as additions, deletions, substitutions and modifications, may occur within the sequence of any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12. A variant peptide may comprise or consist essentially of the amino acid sequence of any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12 in which one, two, three, four or more amino acid substitutions have been made. A variant peptide may comprise a 10 fragment of Fel dl that is larger than any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12. In this embodiment, the variations described herein, such as substitutions and modifications, may occur within and/or outside the sequence of any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12. The variant peptides of the invention are 9 to 30 amino acids in length 15 inclusive. Preferably, they may be from 9 to 20 or more preferably 13 to 17 amino acids in length. The peptides may be the same length as the peptide sequences in any one of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12. The peptides may be chemically derived from the polypeptide allergen, for example by proteolytic cleavage or can be derived in an intellectual sense from the 20 polypeptide allergen, for example by making use of the amino acid sequence of the polypeptide allergen and synthesising peptides based on the sequence. Peptides may be synthesised using methods well known in the art. The term "peptide" includes not only molecules in which amino acid residues are joined by peptide (-CO-NH-) linkages but also molecules in which the peptide 25 bond is reversed. Such retro-inverso peptidomimetics may be made using methods known in the art, for example such as those described in Meziere et al (1997) J. Immunol.159, 3230-3237. This approach involves making pseudopeptides containing changes involving the backbone, and not the orientation of side chains. Meziere et al (1997) show that, at least for MHC class H and T helper cell responses, these 30 pseudopeptides are useful. Retro-inverse peptides, which contain NH-CO bonds instead of CO-NH peptide bonds, are much more resistant to proteolysis.

WO 2008/145998 PCT/GB2008/001827 15 Similarly, the peptide bond may be dispensed with altogether provided that an appropriate linker moiety which retains the spacing between the carbon atoms of the amino acid residues is used; it is particularly preferred if the linker moiety has substantially the same charge distribution and substantially the same planarity as a 5 peptide bond. It will also be appreciated that the peptide may conveniently be blocked at its N-or C-terminus so as to help reduce susceptibility to exoproteolytic digestion. For example, the N-terminal amino group of the peptides may be protected by reacting with a carboxylic acid and the C-terminal carboxyl group of the peptide may be protected by reacting with an amine. Other examples of 10 modifications include glycosylation and phosphorylation. Another potential modification is that hydrogens on the side chain amines of R or K may be replaced with methylene groups (-NH2 -+ -NH(Me) or -N(Me) 2 ). Analogues of peptides according to the invention may also include peptide variants that increase or decrease the peptide's half-life in vivo. Examples of 15 analogues capable of increasing the half-life of peptides used according to the invention include peptoid analogues of the peptides, D-amino acid derivatives of the peptides, and peptide-peptoid hybrids. A further embodiment of the variant polypeptides used according to the invention comprises D-amino acid forms of the polypeptide. The preparation of polypeptides using D-amino acids rather than L 20 amino acids greatly decreases any unwanted breakdown of such an agent by normal metabolic processes, decreasing the amounts of agent which needs to be administered, along with the frequency of its administration. The peptides provided by the present invention may be derived from splice variants of Fel dl encoded by mRNA generated by alternative splicing of the primary 25 transcripts encoding the Fel dl chains. The peptides may also be derived from amino acid mutants, glycosylation variants and other covalent derivatives of Fel dl which retain at least an MHC-binding property of the allergen. Exemplary derivatives include molecules wherein the peptides of the invention are covalently modified by substitution, chemical, enzymatic, or other appropriate means with a moiety other 30 than a naturally occurring amino acid. Further included are naturally occurring variants of Fel dI found in different cats. Such a variant may be encoded by an WO 2008/145998 PCT/GB2008/001827 16 allelic variant or represent an alternative splicing variant. Variants as described above may be prepared during synthesis of the peptide or by post- production modification, or when the peptide is in recombinant form using the known techniques of site- directed mutagenesis, random mutagenesis, or 5 enzymatic cleavage and/or ligation of nucleic acids. In accordance with the invention, the further one, two or three peptides that the composition may comprise are preferably functional variants of any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12. That is, the peptides are preferably capable of inducing an immune response. In particular, they are capable of inducing a late 10 phase response in a cat allergic individual. This may be tested by the ability of the peptide to induce T cell proliferation in a sample of T cells. Methods of testing the induction of T cell proliferation are well known in the art and one such method is exemplified in Example 2. Preferably the one or more further peptides are capable of causing T cell proliferation in at least 20 % of samples of T cells, wherein each 15 sample is obtained from different cat allergic individuals in the population. The compositions of the invention are preferably capable of inducing T cell proliferation in 30 % or more samples of T cells obtained from of a panel of cat allergic individuals. More preferably, the compositions are capable of inducing T cell proliferation in 35% or more, 40 % or more, 45 %, 50 %, 55 %, 60 %, 65 %, 70 %, 20 75 %, 80 %, 85 %, or 90 % or more of samples obtained from sensitized individuals in a panel. The number of individuals in a panel of cat allergic individuals may be any number greater than one, for example at least 2, 3, 5, 10, 15, 20, 30, 50, 80, or at least 100 individuals. It is preferred if the peptides cause T cell proliferation, but do not lead to the release of histamine from enriched basophils or mast cell preparations 25 from a sensitised individual. There may be some histamine release, but preferably the composition does not cause significantly more histamine release than a composition comprising the 7 different polypeptides shown in SEQ ID NO: I to 7. Suitable variants capable of binding to TCRs may be derived empirically or selected according to known criteria. Within a single peptide there are certain 30 residues which contribute to binding within the MHC antigen binding groove and other residues which interact with hypervariable regions of the T cell receptor (Allen WO 2008/145998 PCT/GB2008/001827 17 et al (1987) Nature 327: 713-5). Within the residues contributing to T cell receptor interaction, a hierarchy has been demonstrated which pertains to dependency of T cell activation upon substitution of a given peptide residue. Using peptides which have had one or more T 5 cell receptor contact residues substituted with a different amino acid, several groups have demonstrated profound effects upon the process of T cell activation. Evavold & Allen (1991) Nature 252: 1308-10) demonstrated the dissociation of T cell proliferation and cytokine production. In this in vitro model, a T cell clone specific for residues 64-76 of haemoglobin (in the context of I-Ek), was challenged with a 10 peptide analogue in which a conservative substitution of aspartic acid for glutamic acid had been made. This substitution did not significantly interfere with the capacity of the analogue to bind to I-Ek. Following in vitro challenge of a T cell clone with this analogue, no proliferation was detected although IL-4 secretion was maintained, as was the 15 capacity of the clone to help B cell responses. In a subsequent study the same group demonstrated the separation of T cell-mediated cytolysis from cytokine production. In this instance, the former remained unaltered while the latter was impaired. The efficacy of altered peptide ligands in vivo was initially demonstrated in a murine model of EAE (experimental allergic encephalomyelitis) by McDevitt and colleagues 20 (Smilek et al (1991) Proc Natl Acad Sci USA 88 : 9633-9637). In this model EAE is induced by immunisation with the encephalitogenic peptide Ac -11 of MBP (myelin basic protein). Substitution at position four (lysine) with an alanine residue generated a peptide which bound well to its restricting element (Aa"Ap"), but which was non immunogenic in the susceptible PL/JxSJLFI strain and which, furthermore prevented 25 the onset of EAE when administered either before or after immunisation with the encephalitogenic peptide. Thus, residues can be identified in peptides which affect the ability of the peptides to induce various functions of T-cells. Advantageously, peptides may be designed to favour T-cell proliferation and induction of desensitisation. Metzler and Wraith have demonstrated improved 30 tolerogenic capacity of peptides in which substitutions increasing peptide-MHC affinity have been made (Metzler & Wraith(1 993) Int Immunol - : 1159-65). That an WO 2008/145998 PCT/GB2008/001827 18 altered peptide ligand can cause long-term and profound anergy in cloned T cells was demonstrated by Sloan-Lancaster et al (1993) Nature 363: 156-9. The compositions of the invention are capable of inducing a late phase response in an individual that is sensitised to Fel dl allergen. The term "late phase 5 response" includes the meaning as set forth in Allergy and Allergic Diseases (1997) A. B. Kay (Ed.), Blackwell Science, pp 1113-1130. The late phase response may be any late phase response (LPR). Preferably, the peptides are capable of inducing a late asthmatic response (LAR) or a late rhinitic response, or a late phase skin response or a late phase ocular response. Whether or not a particular peptide can give rise to a 10 LPR can be determined using methods well known in the art; a particularly preferred method is that described in Cromwell 0, Durham SR., Shaw RJ, Mackay J and Kay AB. Provocation tests and measurements of mediators from mast cells and basophils in asthma and allergic rhinitis. In: Handbook of Experimental Immunology (4) Chapter 127, Editor: Weir DM, Blackwell Scientific Publications, 1986. 15 Thus, preferably, the individual peptides of the invention are able to induce a LPR in an individual who has been sensitised to Fel dl allergen. Whether or not an individual has been sensitised to the allergen may be determined by well known procedures such as skin prick testing with solutions of allergen extracts, induction of cutaneous LPRs, clinical history, allergen challenge and radioallergosorbent test 20 (RAST) for measurement of allergen specific IgE. Whether or not a particular individual is expected to benefit from treatment may be determined by the physician based, for example, on such tests. Desensitising or tolerising an individual to Fel dl allergen means inhibition or dampening of allergic tissue reactions induced by Fel d1 in appropriately 25 sensitised individuals. It has been shown that T cells can be selectively activated, and then rendered unresponsive. Moreover the anergising or elimination of these T cells leads to desensitisation of the patient for a particular allergen. The desensitisation manifests itself as a reduction in response to an allergen or allergen derived peptide, or preferably an elimination of such a response, on second and 30 further administrations of the allergen or allergen-derived peptide. The second administration may be made after a suitable period of time has elapsed to allow WO 2008/145998 PCT/GB2008/001827 19 desensitisation to occur; this is preferably any period between one day and several weeks. An interval of around two weeks is preferred. Although the compositions of the invention are able to induce a LPR in a cat allergic individual, it should be appreciated that when a composition is used to treat a 5 patient it is preferable that a sufficiently low concentration of the composition is used such that no observable LPR will occur but the response will be sufficient to partially desensitise the T cells such that the next (preferably higher) dose may be given, and so on. In this way the dose is built up to give full desensitisation but often without ever inducing a LPR in the patient. Although, the composition or peptide is able to 10 do so at a higher concentration than is administered. The compositions of the invention preferably are capable of inducing a late phase response in 50 % or more of a panel of cat allergic individuals from the population. More preferably, the compositions are capable of inducing a LPR in 55% or more, 60 % or more, 65 % or more, 70% or more, 75% or more, 80% or more, 15 85% or more, or 90 % or more of sensitized individuals in a panel. Whether or not the compositions are able to induce a LPR in a certain percentage of a panel of subjects can be determined by methods which are well known in the art. Properties ofpeptide combinations 20 MHC binding Preferred combinations of peptides typically bind to a large number of different HLA molecules. This is advantageous in that a larger proportion of individuals in a 25 population will be tolerised by the combination. Thus preferred combinations comprise either: (iii) at least two peptides which exhibit strong binding and at least one peptide which exhibits moderate binding to each member of a panel of HLA molecules; or 30 (iv) at least one peptide which exhibits strong binding and at least two peptides which exhibit moderate binding to each member of said panel of WO 2008/145998 PCT/GB2008/001827 20 HLA molecules; wherein the panel of HLA molecules comprises at least seven different HLA molecules encoded by different alleles which have a cumulative frequency in an outbred human population of at least 80%, or at least 85%, 90%, 95% or 99%. 5 Strength of NT-IC binding may be evaluated by any suitable method. Preferred methods include competitive inhibition assays wherein binding is measured relative to a reference peptide. The reference peptide is typically a peptide which is known to be a strong binder for a given N-IC molecule. In such an assay, a peptide is a weak binder for a given HLA molecule if it has an IC5 0 more than 100 fold 10 lower than the reference peptide for the given HLA molecule. A peptide is a moderate binder is it has an IC50 more than 20 fold lower but less than a 100 fold lower than the reference peptide for the given HLA molecule. A peptide is a strong binder if it has an IC50 less than 20 fold lower than the reference peptide for the given HLA molecule. 15 The outbred human population may be any population, typically a Caucasian population. The panel of HLA molecules typically comprises at least HLA-DRI, DR3, DR4, DR7, DR.1 1, DRI3 and DRI 5; and optionally also comprises HLA DRB4 and DRB5. Suitable reference peptides for these HLA molecules are: DRI (DRB1*0101 allele): HA 306-318 (PKYVKQNTLKLAT); 20 DR3 (DRB1*0301 allele): MT216 (AKTIAYDEEARRGLE); DR4 (DRB1*0401 allele): HA 306-318 (PKYVKQNTLKLAT); DR7 (DRB1*0701 allele): YKL (AAYAAAKAAALAA); DR 11 (DRBI*1101 allele): HA 306-318 (PKYVKQNTLKLAT); DRI3 (DRBI* 1301 allele): B1 21-36 (TERVRLVTRHIYNREE); 25 DR15 (DRBI*1501 allele): A3 152-166 (EAEQLRRAYLDGTGVE); DRB4 (DRB4*0101 allele): E2/E7 (AGDLLAIETDKATI); and DRB5 (DRB5*0101 allele): IA 306-318 (PKYVKQNTLKLAT). Histamine release 30 Preferred combinations of peptides typically induce histamine release in a WO 2008/145998 PCT/GB2008/001827 21 sample from a cat allergic individual containing basophils or mast cells, which is no higher than 5%, 6%, 7%, 8%, 9% or 10% greater than the histamine release induced in a sample from the same individual or population of individuals by the whole Fel d 1 allergen. 5 Most preferably, the combination induces histamine release which is no higher than 5%, 6%, 7%, 8%, 9% or 10% greater than the histamine release induced in a sample from the same individual or population of individuals by a composition comprising the 7 different polypeptides shown in SEQ ID NO: I to 7. A sample from a cat allergic individual is typically a sample of peripheral 10 blood mononuclear cells (PBMCs) which may be prepared as is standard in the art. An example of a suitable method involves isolation of PBMCs from a heparinised blood sample obtained from a subject. PBMC's are typically isolated from such a sample by density gradient separation. Histamine release may be assessed by any suitable method, for example by 15 ELISA. A number of suitable assay kits are commercially available to test levels of histamine release from cells in response to any given histamine release agent. Typically, a sample of approximately 5x10 5 to 5x10 6 PBMCs will be incubated with a given histamine release agent at a given concentration. Histamine concentration in the incubation medium or a sample of the incubation medium will measured at the 20 end of the incubation. Incubation is typically for 30minutes at 37"C. Where the histamine release agent is a peptide or combination of peptides it will typically be administered at a number of different dilutions within a concentration range comparable to that which would be expected to be present in vivo. For example, a 10mg dose of a single peptide entering a blood volume of 5 25 litres would result in a blood concentration of 2ng/ml (2x I 0 6 mg/ml). Thus, a suitable concentration range for a peptide or combination of peptides is typically I 0mg/ml to Ing/ml. Single, duplicate or triplicate measurement may be made at each tested dilution within said range. Approximately 5x10 5 PBMCs are typically required for each measurement. Suitable positive controls will also be tested at appropriate 30 concentrations which may be readily determined by the skilled person. Suitable positive controls include whole Fel d 1 allergen or a suitable alternative such as WO 2008/145998 PCT/GB2008/001827 22 commercially available whole cat dander extract. Spontaneous histamine release by a sample of cells which is not treated with a histamine release agent may also be measured as a negative control / indicator of background histamine release. Where two or more dilutions of a peptide/allergen preparation elicit 10% or more histamine 5 release above background, or where a single value of 10% or more above background is achieved at the highest concentration tested, this will typically be considered a "positive histamine release". The histamine concentration in the incubation medium of any sample will typically be measured by ELISA. Suitable ELISA assays typically involve adding a 10 histamine acylation agent to a sample of the incubation medium together with a suitable buffer. Acylated histamine is more stable than histamine and samples treated in this way may be stored for longer prior to analysis. Analysis typically involves the addition of alkaline-phosphatase conjugated anti-acyl-histamine reagents, followed by the addition of a suitable chromogenic alkaline-phosphatase 15 substrate. Histamine concentration is determined by measurement of absorbance and comparison to a standard curve calibrated against known histamine concentrations. Cytokine release 20 Preferred combinations of peptides typically induce a cytokine release profile in a sample from a cat allergic individual containing T cells, which is equivalent to the cytokine release profile induced in a sample from the same individual or population of individuals by the whole Fel d I allergen. Most preferably, the combination induces a cytokine release profile in a 25 sample from a cat allergic individual or population of individuals containing T cells, which is equivalent to the cytokine release profile induced in a sample from the same individual or population by a composition comprising the 7 different polypeptides shown in SEQ ) NO: 1 to 7. A sample from a cat allergic individual or population is typically a sample of 30 peripheral blood mononuclear cells (PBMCs) which may be prepared as is standard in the art. Cytokine release profile may be assessed by any suitable method. Suitable WO 2008/145998 PCT/GB2008/001827 23 methods include measuring the level of one, two, three or more different cytokines released in a sample in independent assays. Suitable assays include ELISA and Luminex assays. A cytokine release profile induced in one sample is considered to be 5 equivalent to the cytokine release profile of a different sample when the level of certain specific cytokines produced is similar in both samples. More specifically, the cytokine release profiles of two different samples are considered to be equivalent when the levels of IL-10 and IL-13 produced in one sample differ by no more 5%, 6%, 7%, 8%, 9% or 10% from the levels of IL-10 and IL-13 produced in the second 10 sample. Thus, a preferred peptide combination induces production of IL-10 and IL-13 at levels which differ by no more than 10% from the levels of IL-10 and IL-13 induced in a sample from the same individual or population of individuals by the whole Fel d 1 allergen. 15 A typical cytokine release assay is as follows: 250pl of a 200pg/ml solution of the appropriate antigen or peptide concentration is distributed into the appropriate wells of, for example, 48 well plates. Plates are then incubated in a humidified 5% CO 2 incubator at 37'C for a maximum of 4 hours. 250pl of a 5x10 6 cell/ml PBMC suspension is then added to each well and the plates 20 returned to the incubator for 5 days. Samples of culture supernatant are then harvested as multiple aliquots for use in ELISA assays. The samples may be frozen and stored prior to analysis. One aliquot is tested for the presence of one cytokine. Typically the presence of a cytokine is established using an ELISA assay according to practices standard in the art. The cytokine concentrations in a sample are typically 25 determined by interpolation from standard curves generated in the same assay. ATucleic acids and vectors The individual peptides that make up the compositions and products of the invention may be administered directly, or may be administered indirectly by 30 expression from an encoding sequence. For example, a polynucleotide may be provided that encodes a peptide of the invention, such as any of the peptides WO 2008/145998 PCT/GB2008/001827 24 described above. A peptide of the invention may thus be produced from or delivered in the form of a polynucleotide which encodes, and is capable of expressing, it. Any reference herein to the use, delivery or administration of a peptide of the invention is intended to include the indirect use, delivery or administration of such a peptide via 5 expression from a polynucleotide that encodes it. Accordingly, the invention provides a composition for use in preventing or treating allergy to cats by tolerisation comprising four or more different polynucleotide sequences which when expressed cause the production of a composition for use in preventing or treating allergy to cats by tolerisation 10 comprising: a) four or more polypeptides selected from any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12; and optionally b) one,.two or three polypeptides having the following characteristics: (i) comprising sequence having at least 65% sequence 15 identity to at least 9 or more contiguous amino acids in any of SEQ[ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12. not selected in a); and (ii) 9 to 30 amino acids in length. The invention also provides a product for use in preventing or treating 20 allergy to cats by tolerisation containing: a) four or more polynucleotides capable of expressing a different polypeptide selected from SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12, and optionally b) one, two or three polynucleotides capable of expressing different 25 polypeptides having the following characteristics: (i) comprising sequence having at least 65% sequence identity to at least 9 or more contiguous amino acids in any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12 not selected in a); and 30 (ii) 9 to 30 amino acids in length, wherein each different polypeptide is for simultaneous, separate of sequential use in WO 2008/145998 PCT/GB2008/001827 25 the prevention or treatment of allergy to cats in a human. The terms "nucleic acid molecule" and "polynucleotide" are used interchangeably herein and refer to a polymeric form of nucleotides of any length, either deoxyribonucleotides or ribonucleotides, or analogs thereof. Non-limiting 5 examples of polynucleotides include a gene, a gene fragment, messenger RNA (mRNA), cDNA, recombinant polynucleotides, plasmids, vectors, isolated DNA of any sequence, isolated RNA of any sequence, nucleic acid probes, and primers. A polynucleotide of the invention may be provided in isolated or purified form. A nucleic acid sequence which "encodes" a selected polypeptide is a nucleic acid 10 molecule which is transcribed (in the case of DNA) and translated (in the case of mRNA) into a polypeptide in vivo when placed under the control of appropriate regulatory sequences. The boundaries of the coding sequence are determined by a start codon at the 5' (amino) terminus and a translation stop codon at the 3' (carboxy) terminus. For the purposes of the invention, such nucleic acid sequences can include, 15 but are not limited to, cDNA from viral, prokaryotic or eukaryotic mRNA, genomic sequences from viral or prokaryotic DNA or RNA, and even synthetic DNA sequences. A transcription termination sequence may be located 3' to the coding sequence. Polynucleotides of the invention can be synthesised according to methods 20 well known in the art, as described by way of example in Sambrook et al (1989, Molecular Cloning - a laboratory manual; Cold Spring Harbor Press). The polynucleotide molecules of the present invention may be provided in the form of an expression cassette which includes control sequences operably linked to the inserted sequence, thus allowing for expression of the peptide of the invention in 25 vivo in a targeted subject. These expression cassettes, in turn, are typically provided within vectors (e.g., plasmids or recombinant viral vectors) which are suitable for use as reagents for nucleic acid immunization. Such an expression cassette may be administered directly to a host subject. Alternatively, a vector comprising a polynucleotide of the invention may be administered to a host subject. Preferably the 30 polynucleotide is prepared and/or administered using a genetic vector. A suitable vector may be any vector which is capable of carrying a sufficient amount of genetic WO 2008/145998 PCT/GB2008/001827 26 information, and allowing expression of a peptide of the invention. The present invention thus includes expression vectors that comprise such polynucleotide sequences. Thus, the present invention provides a vector for use in preventing or treating allergy to cats by tolerisation comprising four or more 5 polynucleotide sequences which encode different polypeptides of the invention and optionally one or more further polynucleotide sequences which encode different polypeptides as defined herein. The vector may comprise 4, 5, 6, 7, 8, 9, 10, 11 or 12 polynucleotide sequences which encode different polypeptides of the invention. Furthermore, it will be appreciated that the compositions and products of the 10 invention may comprise a mixture of polypeptides and polynucleotides. Accordingly, the invention provides a composition or product as defined herein, wherein in place of any one of the polypeptide is a polynucleotide capable of expressing said polypeptide. Expression vectors are routinely constructed in the art of molecular biology 15 and may for example involve the use of plasmid DNA and appropriate initiators, promoters, enhancers and other elements, such as for example polyadenylation signals which may be necessary, and which are positioned in the correct orientation, in order to allow for expression of a peptide of the invention. Other suitable vectors would be apparent to persons skilled in the art. By way of further example in this 20 regard we refer to Sambrook et al. Thus, a polypeptide of the invention may be provided by delivering such a vector to a cell and allowing transcription from the vector to occur. Preferably, a polynucleotide of the invention or for use in the invention in a vector is operably linked to a control sequence which is capable of providing for the expression of the 25 coding sequence by the host cell, i.e. the vector is an expression vector. "Operably linked" refers to an arrangement of elements wherein the components so described are configured so as to perform their usual function. Thus, a given regulatory sequence, such as a promoter, operably linked to a nucleic acid sequence is capable of effecting the expression of that sequence when the proper 30 enzymes are present. The promoter need not be contiguous with the sequence, so long as it functions to direct the expression thereof Thus, for example, intervening WO 2008/145998 PCT/GB2008/001827 27 untranslated yet transcribed sequences can be present between the promoter sequence and the nucleic acid sequence and the promoter sequence can still be considered "operably linked" to the coding sequence. A number of expression systems have been described in the art, each of which 5 typically consists of a vector containing a gene or nucleotide sequence of interest operably linked to expression control sequences. These control sequences include transcriptional promoter sequences and transcriptional start and termination sequences. The vectors of the invention may be for example, plasmid, virus or phage vectors provided with an origin of replication, optionally a promoter for the 10 expression of the said polynucleotide and optionally a regulator of the promoter. A "plasmid" is a vector in the form of an extrachromosomal genetic element. The vectors may contain one or more selectable marker genes, for example an ampicillin resistence gene in the case of a bacterial plasmid or a resistance gene for a fungal vector. Vectors may be used in vitro, for example for the production of DNA or 15 RNA or used to transfect or transform a host cell, for example, a mammalian host cell. The vectors may also be adapted to be used in vivo, for example to allow in vivo expression of the polypeptide. A "promoter" is a nucleotide sequence which initiates and regulates transcription of a polypeptide-encoding polynucleotide. Promoters can include 20 inducible promoters (where expression of a polynucleotide sequence operably linked to the promoter is induced by an analyte, cofactor, regulatory protein, etc.), repressible promoters (where expression of a polynucleotide sequence operably linked to the promoter is repressed by an analyte, cofactor, regulatory protein, etc.), and constitutive promoters. It is intended that the term "promoter" or "control 25 element" includes full-length promoter regions and functional (e.g., controls transcription or translation) segments of these regions. A polynucleotide, expression cassette or vector according to the present invention may additionally comprise a signal peptide sequence. The signal peptide sequence is generally inserted in operable linkage with the promoter such that the 30 signal peptide is expressed and facilitates secretion of a polypeptide encoded by coding sequence also in operable linkage with the promoter.

WO 2008/145998 PCT/GB2008/001827 28 Typically a signal peptide sequence encodes a peptide of 10 to 30 amino acids for example 15 to 20 amino acids. Often the amino acids are predominantly hydrophobic. In a typical situation, a signal peptide targets a growing polypeptide chain bearing the signal peptide to the endoplasmic reticulum of the expressing cell. 5 The signal peptide is cleaved off in the endoplasmic reticulum, allowing for secretion of the polypeptide via the Golgi apparatus. Thus, a peptide of the invention may be provided to an individual by expression from cells within the individual, and secretion from those cells. Alternatively, polynucleotides of the invention may be expressed in a suitable 10 manner to allow presentation of a peptide of the invention by an MHC class II molecule at the surface of an antigen presenting cell. For example, a polynucleotide, expression cassette or vector of the invention may be targeted to antigen presenting cells, or the expression of encoded peptide may be preferentially stimulated or induced in such cells. 15 Polynucleotides of interest may be used in vitro, ex vivo or in vivo in the production of a peptide of the invention, Such polynucleotides may be administered or used in the prevention or treatment of allergy to cats by tolerisation. Methods for gene delivery are known in the art. See, e.g., U.S. Patent Nos. 5,399,346, 5,580,859 and 5,589,466. The nucleic acid molecule can be introduced 20 directly into the recipient subject, such as by standard intramuscular or intradermal injection; transdermal particle delivery; inhalation; topically, or by oral, intranasal or mucosal modes of administration. The molecule alternatively can be introduced ex vivo into cells that have been removed from a subject. For example, a polynucleotide, expression cassette or vector of the invention may be introduced into 25 APCs of an individual ex vivo. Cells containing the nucleic acid molecule of interest are re-introduced into the subject such that an immune response can be mounted against the peptide encoded by the nucleic acid molecule. The nucleic acid molecules used in such immunization are generally referred to herein as "nucleic acid vaccines." 30 The polypeptides, polynucleotides, vectors or cells of the invention may be present in a substantially isolated form. They may be mixed with carriers or diluents WO 2008/145998 PCT/GB2008/001827 29 which will not interfere with their intended use and still be regarded as substantially isolated. They may also be in a substantially purified form, in which case they will generally comprise at least 90%, e.g. at least 95%, 98% or 99%, of the proteins, polynucleotides, cells or dry mass of the preparation. 5 Antigen presenting cells (4PCs) The invention encompasses the use in vitro of a method of producing a population of APCs that present the peptides of the invention on their surface, that may be subsequently used in therapy. Such a method may be carried out ex vivo on a 10 sample of cells that have been obtained from a patient. The APCs produced in this way therefore form a pharmaceutical agent that can be used in the treatment or prevention of cat allergy by tolerisation. The cells should be accepted by the immune system of the individual because they derive from that individual. Delivery of cells that have been produced in this way to the individual from whom they were 15 originally obtained, thus forms a therapeutic embodiment of the invention. Formulations and compositions The peptides, polynucleotides, vectors and cells of the invention may be provided to an individual either singly or in combination. Each molecule or cell of 20 the invention may be provided to an individual in an isolated, substantially isolated, purified or substantially purified form. For example, a peptide of the invention may be provided to an individual substantially free from the other peptides. Whilst it may be possible for the peptides, polynucleotides or compositions according to the invention to be presented in raw form, it is preferable to present 25 them as a pharmaceutical formulation. Thus, according to a further aspect of the invention, the present invention provides a pharmaceutical formulation for use in preventing or treating allergy to cats by tolerisation comprising a composition, vector or product according to the invention together with one or more pharmaceutically acceptable carriers or diluents and optionally one or more other therapeutic 30 ingredients. The carrier (s) must be 'acceptable' in the sense of being compatible with the other ingredients of the formulation and not deleterious to the recipient thereof WO 2008/145998 PCT/GB2008/001827 30 Typically, carriers for injection, and the final formulation, are sterile and pyrogen free. Formulation of a composition comprising the peptide, polynucleotides or cells of the invention can be carried out using standard pharmaceutical formulation chemistries and methodologies all of which are readily available to the reasonably 5 skilled artisan. For example, compositions containing one or more molecules or cells of the invention can. be combined with one or more pharmaceutically acceptable excipients or vehicles. Auxiliary substances, such as wetting or emulsifying agents, pH buffering substances and the like, may be present in the excipient or vehicle. These 10 excipients, vehicles and auxiliary substances are generally pharmaceutical agents that do not induce an immune response in the individual receiving the composition, and which may be administered without undue toxicity. Pharmaceutically acceptable excipients include, but are not limited to, liquids such as water, saline, polyethyleneglycol, hyaluronic acid, glycerol and ethanol. Pharmaceutically 15 acceptable salts can also be included therein, for example, mineral acid salts such as hydrochlorides, hydrobromides, phosphates, sulfates, and the like; and the salts of organic acids such as acetates, propionates, malonates, benzoates, and the like. A thorough discussion of pharmaceutically acceptable excipients, vehicles and auxiliary substances is available in Remington's Pharmaceutical Sciences (Mack Pub. Co., 20 N.J. 1991). Such compositions may be prepared, packaged, or sold in a form suitable for bolus administration or for continuous administration. Injectable compositions may be prepared, packaged, or sold in unit dosage form, such as in ampoules or in multi dose containers containing a preservative. Compositions include, but are not limited 25 to, suspensions, solutions, emulsions in oily or aqueous vehicles, pastes, and implantable sustained-release or biodegradable formulations. Such compositions may further comprise one or more additional ingredients including, but not limited to, suspending, stabilizing, or dispersing agents. In one embodiment of a composition for parenteral administration, the active ingredient is provided in dry (for e.g., a 30 powder or granules) form for reconstitution with a suitable vehicle (e. g., sterile pyrogen-free water) prior to parenteral administration of the reconstituted WO 2008/145998 PCT/GB2008/001827 31 composition. The pharmaceutical compositions may be prepared, packaged, or sold in the form of a sterile injectable aqueous or oily suspension or solution. This suspension or solution may be formulated according to the known art, and may comprise, in addition to the active ingredient, additional ingredients such as the 5 dispersing agents, wetting agents, or suspending agents described herein. Such sterile injectable formulations may be prepared using a non-toxic parenterally-acceptable diluent or solvent, such as water or 1,3-butane diol, for example. Other acceptable diluents and solvents include, but are not limited to, Ringer's solution, isotonic sodium chloride solution, and fixed oils such as synthetic mono-or di-glycerides. 10 Other parentally-administrable compositions which are useful include those which comprise the active ingredient in microcrystalline form, in a liposomal preparation, or as a component of a biodegradable polymer systems. Compositions for sustained release or implantation may comprise pharmaceutically acceptable polymeric or hydrophobic materials such as an emulsion, an ion exchange resin, a sparingly 15 soluble polymer, or a sparingly soluble salt. Alternatively, the peptides or polynucleotides of the present invention may be encapsulated, adsorbed to, or associated with, particulate carriers. Suitable particulate carriers include those derived from polymethyl methacrylate polymers, as well as PLG microparticles derived from poly(lactides) and poly(lactide-co 20 glycolides). See, e.g., Jeffery et al. (1993) Pharm. Res. 10:362-368. Other particulate systems and polymers can also be used, for example, polymers such as polylysine, polyarginine, polyornithine, spermine, spermidine, as well as conjugates of these molecules. The formulation of any of the peptides, polynucleotides or cells mentioned 25 herein will depend upon factors such as the nature of the substance and the method of delivery. Any such substance may be administered in a variety of dosage forms. It may be administered orally (e.g. as tablets, troches, lozenges, aqueous or oily suspensions, dispersible powders or granules), parenterally, subcutaneously, by inhalation, intradermally, intravenously, intramuscularly, intrasternally, transdermally 30 or by infusion techniques. The substance may also be administered as suppositories. A physician will be able to determine the required route of administration for each WO 2008/145998 PCT/GB2008/001827 32 particular individual. The compositions of formulations of the invention will comprise a suitable concentration of each peptide/polynucleotide/cell to be effective without causing adverse reaction. Typically, the concentration of each peptide in the composition 5 will'be in the range of 0.03 to 200 niol/ml. More preferably in the range of 0.3 to 200 nmol/ml, 3 to 180 nmol/ml, 5 to 75 nmol/ml or 10 to 50 nmol/ml. The composition or formulations should have a purity of greater than 95% or 98% or a purity of at least 99%. 10 Therapeutic methods and individual to be treated The present invention relates to peptides, polynucleotides, vectors and cells that are capable of desensitising or tolerising human individuals to Fel dl allergen and are therefore useful in the prevention or treatment of cat allergy. The invention provides compositions, products, vectors and formulations for use in preventing or 15 treating allergy to cats by tolerisation. The invention also provides a method of tolerising or desensitizing a cat allergic individual comprising administering, either singly or in combination the polypeptides/polynucleotides/cells of the invention as described above. The individual to be treated or provided with the composition or formulation 20 of the invention is preferably human. It will be appreciated that the individual to be treated may be known to be sensitised to Fel dl allergy, at risk of being sensitised or suspected of being sensitised. The individual can be tested for sensitisation using techniques well known in the art and as described herein. Alternatively, the individual may have a family history of allergy to cats. It may not be necessary to 25 test an individual for sensitisation to Fel dl because the individual may display symptoms of allergy when brought into proximity to a cat. By proximity is meant 10 metres or less, 5 metres or less, 2 metres or less, 1 metre or less, or 0 metres from the cat. Symptoms of allergy can include itchy eyes, runny nose, breathing difficulties, red itchy skin or rash. 30 The individual to be treated may be of any age. However, preferably, the individual may be in the age group of I to 90, 5 to 60, 10 to 40, or more preferably 18 WO 2008/145998 PCT/GB2008/001827 33 to 35. Groups of individuals that are likely to benefit from the treatment are for example cat owners, veterinarians and other cat handlers. Preferably, the individual to be treated is from a population that has MHC allele frequencies within the range of frequencies that are representative of the 5 Caucasian population. Reference population allele frequencies for 11 common DRB I allele families are shown in Table 3 of Example 2 (Data from HLA Facts Book, Parham and Barber). Reference frequencies were obtained by analysis of multiple studies reporting frequencies and the figures shown are mean values. Preferably therefore, the individual to be treated is from a population that has 10 equivalent MHC allele frequencies as the reference population for the alleles referred to Table 3 (such as for at least 1, 2, 3, 4, 5 or all of the alleles), for example within the ranges of those figures plus or minus 1, 2, 3, 5, 10, 15 or 20%. Preferably the individual is from a population where the allele frequencies of the following DRB I alleles is: 15 4 - at least 9% 7 - at least 10% 11 - at least 8%. The individual may have had allergy to cat for at least 2 weeks, I month, 6 months, 1 year or 5 years. The individual may suffer from a rash, nasal congestion, 20 nasal discharge and/or coughing caused by the allergy. The individual may or may not have been administered with other compositions/compounds which treat cat allergy. The individual may live in a population comprising at least 0.1 cats per human habitant. 25 Diagnostic method The invention also provides a method of detecting whether an individual has or is at risk of developing a disorder, wherein the disorder comprises allergic symptoms in response to cat allergen. The individual is typically a mammal, preferably a human. The individual to 30 be tested in the method is preferably between the ages of 1 year and 80 years, more preferably between the ages of 1 year and 60, 50, 40, 30 or 20 years, and most WO 2008/145998 PCT/GB2008/001827 34 preferably between the ages of 1 year and 16 years. The individual may have been diagnosed or may be suspected of suffering from a disorder which is classified as intrinsic or non-allergic, for example, intrinsic or non-allergic asthma. The individual may lack a detectable antibody response to a 5 cat allergen, in particular an IgE response to cat allergen. Suitable assays to detect IgE include the PharmaciaTM CAP system. Using this system, the individual typically scores 0 or 0/1. The individual may be a patient suffering from or diagnosed as suffering from symptoms which are typically associated with allergy such as itchy eyes, runny nose, 10 breathing difficulties, red itchy skin or rash, in the absence of an identifiable trigger. The first occurrence or diagnosis of these symptoms may occur when the individual is older than 15 years of age. For example, the individual may be at least 15, 16, 17, 18, 20, 22, 24, 26, 28 or 30 years of age at the first occurrence or diagnosis of symptoms of allergy which are typically associated with allergy. 15 The method of the invention concerns determining whether an individual has a T cell response to a cat allergen, in particular the major cat allergen, Fel d 1. Such a T cell response will be present in cat allergic individuals. Without being bound by any hypothesis, the inventors consider that intrinsic or non-allergic disorders are also in fact caused by a T cell-driven, IgE independent, immune response. Accordingly 20 these disorders also have an allergen trigger, but it does not give rise to allergen specific IgE. Rather, it gives rise to a T cell response which can be characterised by T cell proliferation or the release of cytokines. For example, the cytokines released may include IL-5, which is involved in the recruitment of eosinophils. Accordingly, the T cell response can drive the induction of eosinophilic reactions in an individual. 25 Whether an individual has a T cell response to Fel d I is determined by measuring whether or not the individual has a T cell response to a peptide or combination of peptides according to the invention. Whether or not the individual has such a response may be determined by any suitable method, typically a method which can be used to detect proliferation of allergen-experienced T cells or the 30 presence of cytokine released by allergen- experienced T cells. A positive response by the patient's T cells to the peptide or combination of the invention indicates that WO 2008/145998 PCT/GB2008/001827 35 the patient has or is more likely to develop allergy-like symptoms in response to the allergen. A negative response indicates that the patient has allergy-like symptoms which are not caused by the cat allergen, or is less likely to develop allergy-like symptoms in response to the cat allergen. 5 The T cells which respond to the peptide or combination in the method are generally T cells which have been pre-sensitised in vivo to allergen. These allergen experienced T cells are generally present in the peripheral blood of a individual, i.e. within the population of peripheral blood mononuclear cells (PBMCs) in the individual. The T cells may be CD4 and/or CD8 T cells. 10 In the method the T cells can be contacted with the peptide or combination of the invention in vitro or in vivo, preferably in vitro in a sample from the individual. Generally the T cells which are contacted in the method are taken from the individual in a blood sample, although other types of samples which contain T cells can be used. The sample may be added directly to the assay or may be processed 15 first. Typically the processing may comprise standard techniques such as gradient centrifugation to separate the T cells, with resuspension in any suitable volume. Alternatively, the processing may comprise diluting of the sample, for example with water, buffer or media. The sample may be diluted from 1.5 to 100 fold, for example 2 to 50 or 5 to 10 fold. 20 The processing may comprise separation of components of the sample. Typically mononuclear cells (MCs) are separated from the samples. The MCs will comprise the T cells and antigen presenting cells (APCs). Thus in the method the APCs present in the separated MCs can present the peptide to the T cells. In another embodiment only T cells, such as only CD4 T cells, can be purified from the sample. 25 PBMCs, MCs and T cells can be separated from the sample using techniques known in the art. Preferably the T cells used in the assay are in the form of unprocessed or diluted samples, are freshly isolated T cells (such as in the form of freshly isolated MCs or PBMCs) which are used directly ex vivo, i.e. they are not cultured before 30 being used in the method or are thawed cells (which were previously frozen). However the T cells can be cultured before use, for example in the presence of the WO 2008/145998 PCT/GB2008/001827 36 allergen, and generally also exogenous growth promoting cytokines. During culturing the allergen is typically present on the surface of APCs, such as the APC used in the method. Pre-culturing of the T cells may lead to an increase in the sensitivity of the method. Thus the T cells can be converted into cell lines, such as 5 short term cell lines. The APC which is typically present in the method may come from the same individual as the T cell or from a different individual. The APC may be a naturally occurring APC or an artificial APC. The APC is a cell which is capable of presenting the antigen to a T cell. It is typically a B-cell, dendritic cell or macrophage. It is 10 typically separated from the same sample as the T cell and is typically co-purified with the T cell. Thus the APC may be present in MCs or PBMCs. The APC is typically a freshly isolated ex vivo cell or a cultured cell. It may be in the form of a cell line, such as a short term or immortalised cell line. The APC may express empty MI-IC class II molecules on its surface. 15 i one embodiment the peptide or combination of the invention is added directly to an assay comprising T cells and APCs. As discussed above the T cells and APCs in such an assay could be in the form of MCs. In one embodiment the peptide or combination of peptides is provided to the APC in the absence of the T cell. The APC is then provided to the T cell, typically 20 after being allowed to present the allergen on its surface. The peptide or combination of peptides may have been taken up inside the APC and presented, or simply be taken up onto the surface without entering inside the APC. Typically 105 to 107, preferably 2.5x10 5 to 106 PBMCs are added to each assay. In the case where the peptide or combination or peptides is added directly to 25 the assay it is typically added as a peptide with a concentration from 10-1 to 10 3 p1g/ml, preferably 0.5 to 50pg/ml or 1 to 1 0pg/ml. Typically the length of time for which the T cells are incubated with the peptide or combination is from 4 to 24 hours (preferably 5 to 18 hours) for effector T cells or for more than 24 hours for central memory cells. When using ex vivo PIBMCs it has 30 been found that 5.0 x10 6 PBMCs can be incubated in 10p.tg/ml of peptide for 5 hours at 37*C.

WO 2008/145998 PCT/GB2008/001827 37 Proliferation of the incubated T cells may be measured by any suitable method. For example by flow cytometric measurement of incorporation of the fluorescent compound CFSE following incubation with peptide, or by measuring incorporation of the radiolabelled compound 3 H-thymidine following incubation with 5 peptide. A typical example of the latter method is as follows: 100p of the appropriate peptide concentration is distributed into the appropriate wells of 96 well plates. The plates are then placed into a humidified 5%

CO

2 incubator set at 37'C for a maximum of 4 hours. PBMC's isolated as standard in the art are prepared to a concentration of 2x 106 cells/ml in complete medium at 10 room temperature. 1OOpI of cell solution is then distributed into each of the wells of the 96 well plates containing antigen/peptide. The plates are then incubated for 6 to 8 days. The cultures are pulsed with tritiated thymidine solution by adding 1 OR] of tritiated thymidine stock solution (1 .85MBq/ml in serum-free RPMI medium) to each well. The plates are then returned to the incubator for between 8 and 16 hours. 15 Cultures are then harvested on to filter mats and dried filter mats are counted using an appropriate beta scintillation counter. Counts from wells containing peptide are compared statistically to wells containing media alone (12 wells per group). A statistically significant difference between media only wells and peptide-stimulated wells is considered a positive stimulation of PBMC's by the peptide or combination 20 of peptides. Cytokine release may be measured by any suitable method such as ELISA assay as described above. Such methods are well known in the art. Combination immunotherapy 25 Since many individuals are allergic, or may require desensitizing to several polypeptide antigens, the current invention also provides means of desensitizing individuals that are allergic to multiple antigens. "Tolerance" induced in an individual to a first polypeptide antigen or allergen can create in the individual a "tolergeneic environment" wherein inappropriate immune responses to other antigens 30 can be downregulated in order to provide tolerance to other antigens. This finding means that individuals allergic to multiple allergens can be WO 2008/145998 PCT/GB2008/001827 38 treated in a greatly reduced time period, and that individuals seriously allergic to some allergens (e.g., peanuts) but more mildly allergic to other allergens (e.g., cat dander) can benefit from a therapy wherein tolerance to the milder allergen is established and then this tolergeneic environment is used to provide tolerance to the 5 other, more extreme allergen. In. addition, individuals suffering from an autoimmune disorder who are additionally sensitised (or otherwise immune) to an unrelated antigen or allergen can benefit from a treatment regime wherein tolerance to the unrelated antigen or allergen is first established and then this tolergeneic environment is used to provide tolerance to the autoantigen associated with the autoimmune 10 disorder. A method is therefore provided for desensitising a cat allergic individual to FeldI antigen and one or more further different polypeptide antigens. The method entails, in a first step, administering to the individual a composition/product/formulation (primary composition) according to the invention 15 as described herein and wherein the administration is carried out in a manner sufficient to generate a hyporesponsive state against the Feldi antigen. Once a hyporesponsive state has been established toward Feld I antigen, or at least a shift toward desensitisation has occurred, the method entails administration of a secondary composition comprising a second, different polypeptide antigen to which the 20 individual is to be sensitised. Administration of the secondary composition is carried out in such a way as to take advantage of the tolergeneic environment established by use of the primary composition, where it is now possible to establish tolerance to the second, different polypeptide antigen. The secondary composition is coadministered with either the first primary composition or a larger fragment of Feld 1. By 25 "coadministered" it is meant either the simultaneous or concurrent administration, e.g., when the two are present in the same composition or administered in separate compositions at nearly the same time but at different sites, as well as the delivery of polypeptide antigens in separate compositions at different times. For example, the secondary composition may be delivered prior to or subsequent to delivery of the first 30 composition (or a larger fragment of Feldl) at the same or a different site. The timing between deliveries can range from about several seconds apart to about WO 2008/145998 PCT/GB2008/001827 39 several minutes apart, several hours apart, or even several days apart. Furthermore, different delivery methods can be employed. The second polypeptide antigen is preferably an allergen different to Feld I allergen. Suitable allergens for use in the methods of the invention can of course be 5 obtained and/or produced using known methods. Classes of suitable allergens include, but are not limited to, pollens, animal dander other than cat dander, grasses, molds, dusts, antibiotics, stinging insect venoms, and a variety of environmental (including chemicals and metals), drug and food allergens. Common tree allergens include pollens from cottonwood, popular, ash, birch, maple, oak, elm, hickory, and 10 pecan trees; common plant allergens include those from mugwort, ragweed, English plantain, sorrel-dock and pigweed; plant contact allergens include those from poison oak, poison ivy and nettles; common grass allergens include rye grass, Timothy, Johnson, Bermuda, fescue and bluegrass allergens; common allergens can also be obtained from molds or fungi such as Altemaria, Fusarium, Hormodendrum, 15 Aspergillus, Micropolyspora, Mucor and thermophilic actinomycetes; epidermal allergens can be obtained from house or organic dusts (typically fungal in origin), from arthropods such as house mites (Dermatophagoides pteronyssinus), or from animal sources such as feathers, and dog dander; common food allergens include milk and cheese (diary), egg, wheat, nut (e.g., peanut), seafood (e.g., shellfish), pea, 20 bean and gluten allergens; common environmental allergens include metals (nickel and gold), chemicals (formaldehyde, trinitrophenol and turpentine), Latex, rubber, fiber (cotton or wool), burlap, hair dye, cosmetic, detergent and perfume allergens; common drug allergens include local anesthetic and salicylate allergens; antibiotic allergens include penicillin, tetracycline and sulfonamide allergens; and common 25 insect allergens include bee, wasp and ant venom, and cockroach calyx allergens. Particularly well characterized allergens include, but are not limited to, the major and cryptic epitopes of the Der p I allergen (Hoyne et al. (1994) Immunology 83190-195), bee venom phospholipase A2 (PLA) (Akdis et al. (1996) J. Clin. Invest. 98:1676 1683), birch pollen allergen Bet v I (Bauer et al. (1997) Clin. Exp. Immunol. 30 107:536-541), and the multi-epitopic recombinant grass allergen rKBG8.3 (Cao et al. (1997) Immunology 90:46-51). These and other suitable allergens are commercially WO 2008/145998 PCT/GB2008/001827 40 available and/or can be readily prepared as extracts following known techniques. Preferably, the second polypeptide allergen is selected from the list of allergen sequences and database accession numbers (NCBI Entrez accession numbers) below. NCBI is the National Center for Biotechnology information and is 5 a division of the US National Institutes of Health. The NCBI web site, from which access to the database may be sought, is wwwncbi.nlmmnh.gov/. Allergen sequences and database accession numbers (NCBI Entrez accession numbers): House dust mite 10 Dermatophagoides pteronyssinus Derp 1 MKIVLAIASLLALSAVYARPSSIKTFEEYKKAFNKSYATFEDEEAARKNFLES 15 VKYVQSNGGANIILSDLSLDEFKNRFLMSAEAFEHLKTQFDLNAETNACSIN GNAPAEIDLRQMRTVTPIRMQGGCGSCWAFSGVAATESAYLAYRNQSLDLA EQELVDCASQHGCHGDTIPRGIEYIQHNGVVQESYYRYVAREQSCRRPNAQR FGISNYCQIYPPNVNKIREALAQTHSAIAVIIGIKDLDAFRHYDGRTIIQRDNGY QPNYHAVNIVGYSNAQGVDYWVRNSWDTNWGDN GYGYFAANIDLMMIEE 20 YPYVVIL Derp 2 MMYKELCLS LLVAAVARDQVDVKDCANHEIKKVLVPGCHGSEPCIIHRGKPF QLEAVFEANQNTKTAKIIiKASIDGLEVDVTGIDPNACHYMKCPLVKGQQYD 25 IKYTWNVPKIAPKSENVVVTVKVMGDDGVLACAIATHAKIRD Der p 3 MIIYNILIVLLLAINTLANPIIPA SPNATIVGGEKALAGECPYQISLQSSSHFCGG TILDEYWLTAAHCVAGQTASKLSIRYNSLKH SLGGEKISVAKIFAHEKYDSY 30 QIDNDIALIKLKSPMKLNQKNAKAVGLPAKGSDVKVGDQVRVSGWGYLEEG SYSLPSELRRVDIAVVSRKECNELY SKANAEVTDNMICGGDVANGGKDSCQ

GDSGGPVVDVKNNQVVGIVSWGYGCARKGYPGVYTRVGNFIDWIESKRSQ

WO 2008/1145998 PCT/GB2008/001 827 41 Der p 4 KY) HLPFIGXRS VITXLMIF 5 Derp 5 MKFlaIIAFFVATLAVMTVSGEDKKHDYQNEFDFLLM-. \ERIH EQIIKKGELALFYLQ EQINHFEEKPTKEMKIVAEMDTIIAMIDGVTRGVIDRLMQRKDILDIFEQY-N LEMAKKSGDILERDLKKEAR VKKIEV 10 Derp 6 AIGXQPAAEAEAPFQISLMK Der p 7 MM4KlLLTIAAAAFVAVSADPLIHYDKITEEINXAVDEAV.AAIEKSETFDPMKVP 15 DHSDKFERH-IG11DL.KGELDMR.N1QVRIGLKQMlKRVGDAN~rKSEDGVVKAHL LVGVH1DDVVSMIEYDLAYKLGDLI)NTHVISDIQDFVVELSLEVSEEGNMTLT SFEVRQFANVVNI-IGGLSILDPIFAVLSDVLTAIFQDTVRAEMTKVLAPAFKK ELERNNQ 20 Der p9 IVGGSNASPGDAVYQLAL Dermatophagoides farinae 25 DerflI MKFVILAAS.LLVLT'VYARP3ASIKT'FEFKKAN 1 KNYATVEEEEVARKiNFLESLK YVEANKGAJNI-ILSDLS LDEFKNRYLM4SAEAFEQLKTQFDLNAETSACRINSV iNVSEL.Dl.RSLRTrVTIPIRMQGGCGSCWAFSGVAATESAYLAYRNTSLDLSEQ ELVDCASQHG3'CH GDIPRGIEYLQQNGVVEERSYPYVA-REQRCRRNSQHYG 30 ISLNYCQIYPPDVKQIREALTQTHTAJAVIIGIKDLRAFQIYDGRTIIQIDNGYQP NYHAVNIVGYGSTQGDDY- rv'RNSWDTTWGDSGYGYrFQAGNNL MIEQY WO 2008/145998 PCT/GB2008/001827 42 PYVVIM Der f2 MISKILCLSLLVAAVVADQVDVKDCANNEIKK.VMVDGCHGS DPCIIHRGKPF 5 TLEALFDANQNTKTAKIEIKIASLDGLEIDVPGIDTNACHFFMKCPLVKGQQYDI KYTWNVPKIAPKSENVVVTVKLIGDNGVLACAIATHGKIRD Der f 3 MMILTIVVLLAANILATPILPSSPNATIVGGVKAQAGDCPYQISLQSSSHFCGG io SILDEYWILTAAHCVNGQSAKKLS IRYNTLKHASGGEKIQVAEIYQHENYDS MTIDNDVALIKLKTPMTLDQTNAKPVPLPAQGSDVKVGDKIRVSGWGYLQE GSYSLPSELQRVDIDVVSREQCDQLYSKAGADVSENMICGGDVANGGVDSC Q GD SGGPVVDVATKQIVGIVSWGYGCARKGYP GVYTR VGNFVD WIESKRS Q 15 Der f 4 AVGGQDADLAEAPFQISLLK Der f 7 20 MMIKFLLIAAVAFVAVSADPIHYDKITEEINKAIDDAIAAIEQSETIDPMKVPDH ADKFERIHVGIVDFKGELAMRNIEARGLKQMKRQGDANVKGEEGIVKAHLLI GVHDDISMEYDLAYKLGDLHPTTHVISDIQDFVALSLEISDEGNITMTSFE VRQFANVVNI-IGGLSILDPIFGVLSDVLTAIFQDTVRKEMTKVLAPAFKRELE KN 25 Additional mite allergen sequences (NCBI entrez accession): 1170095; 1359436; 2440053; 666007; 487661; 1545803; 84702; 84699; 625532; 404370; 1091577; 1460058; 7413; 9072; 387592. 30 WO 2008/145998 PCT/GB2008/001827 43 Cat Felis sequences (NCBI entrez accession): 5 539716;539715;423193;423192;423191;423190; 1364213; 1364212; 395407; 163827; 163823; 163825; 1169665; 232086; 1169666. Latex Hevea sequences: 10 Hev b 1 MAEDEDNQQGQGEGLKYLGFVQDAATYAVTTFSNVYLFAKDKS GPLQPGV DIIEGPVKNVAVPLYNRFSYIPNGALKFVDSTVVASVTIIDRSLPPIVKDASIQV VSAIRAAPEAARSLASSLPGQTKILAKVFYGEN 15 Hev b 3 MAEEVEEERLKYLDFVRAAGVYAVDSFSTLYLYAKDISGPLKPGVDTIENVV KTVVTPVYYIPLEAVKFVDKTVDVSVTSLDGVVPPVIKQVSAQTYSVAQDAP RIVLDVASS VFNTGVQEGAKALYANLEPKAEQYAVITWRALNKLPLVPQVA 20 NVVVPTAVYFS.EKYNDVVRGTTEQGYRVSSYLPLLPTEKITKVFGDEAS Additional Hevea sequences (NCBI entrez accession): 3319923; 3319921; 3087805; 1493836; 1480457; 1223884; 3452147; 3451147; 1916805; 232267; 123335; 2501578; 3319662; 3288200; 1942537; 2392631; 25 2392630; 1421554; 1311006; 494093; 3183706; 3172534; 283243; 1170248; 1708278; 1706547; 464775; 266892; 231586; 123337; 116359; 123062; 2213877; 542013; 2144920; 1070656; 2129914; 2129913; 2129912; 100135; 82026; 1076559; 82028; 82027; 282933; 280399; 100138; 1086972; 108697; 1086976; 1086978; 1086978; 1086976; 1086974; 1086972; 913758; 913757; 913756; 234388; 1092500; 30 228691; 1177405; 18839; 18837; 18835; 18833; 18831; 1209317; 1184668; 168217; 168215; 168213; 168211; 168209; 348137.

WO 2008/145998 PCT/GB2008/001827 44 Rye grass Lolium sequences: 5 126385 Lol p 1 MASS SSVLLVVALFAVTLGSAIIGIAKVPPGPNITAEYGDKWLDAKSTWYGK PTGAGPKDNGGACGYKNVDKAPFNGMTGCGNTPIFKDGRGCGSCFEIKCTK PESCSGEAVTVTITDDNEEPIAPYHFDLSGHAFGSMAKKGEEQNVRSAGELEL QFRR VKCKYPDDTKPTFH VEKASNPNYLAILYKYVDGDGDVVAVDIKEKGK 10 DKWIELKESWGAVWRIDTPDKLTGPFTVRYTTE GGTKSEFEDVIPEGWKADT SYSAK 126386 Lol p 2a AAPVEFTVEKGSDEKNLALSIKYNKEGDSMAEVELKEHGSNEWLALKKNGD 15 GVWEIKSDKPLKGPFNFRFVSEKGMRNFDDVVPADFKVGTTYKPE 126387 Lol p 3 TKVDLTVEKGSDAKTLVLNIIKYTRPGDTLAEVELRQHGSEEWEPMTKKGNL WEVKSAKPLTGPMNFRFLSK.GGMKNVFDEV JIPTAFTVGKTYTPEYN 20 2498581 Lol p 5a MAVQKYTVALFLRRGPRGGPGRSYAADAGYTPAAAATPATPAATPAGGWR EGDDRRAEAAGGRQRLASRQPWPPLPTPLRRTSSRSSRPPSPSPPRASSPTSA AKAPGLIPKLDTAYDVAYKAAEAHPRGQVRRLRICPHRSLRVIAGALEVHA 25 VKPATEEVLAAKIPTGELQIVDKIDAAFKIAATAANAAPTNDKFTVFESAFNK. ALNECTGGAMRPTSSSPPSRPRSSRPTPPPSPAAPEVKYAVFEAALTKAITAM TQAQKAGKPAAAAATAAATVATAAATAAAVLPPPLLVVQSLISLLIYY 2498582 Lol p 5b 30 MAVQKHTVALFLAVALVAGPAASYAADAGYAPATPATPAAPATAATPATP ATPATPAAVPS GKATTEEQKLIEKINAGFKAAVAAAAVVPP ADKYKTFVETF WO 2008/145998 PCT/GB2008/001827 45 GTA'NKAFVEGLASGYADQSKNQLTS KLDAALKLAYEAA QGATPEAKYDA YVATLTEALRVIAGTLEVHAVKPAAEEVKVGAIPAAEVQLIDKVDAAYRTA ATAANAAPANDKFTVFENTFNNAIKVSLGAAYDSYKFIPTLVAAVKQAYAA K.QATAPEVKYTVSETALKKAVTAMSEAEKEATPAAAATATPTPAAATATAT 5 PAAAYATATPAAATATATPAAATATPAAAGGYKV 455288 Lol p isoform 9 MAVQKIITVALFLAVALVAGPAASYAADAGYAPATPATPAAPATAATPATP ATPATPAAVPSGKATTEEQKLIEKINAGFKAAVAAAAVVPPADKYKTFVETF 10 GTATNKAFVEGLASGYADQSKNQLTSKLDAALKLAYEAAQGATPEAKYDA YVATLTEALRVIAGTLEVHAVKPAAEEVKVGAPAAEVQLIDKVDAAYRTA ATAANAAPANDKFTVFENTFNNAIKVSLGAAYDSYKFIPTLVAAVKQAYAA KQATAPEVKYTVSETALKKAVTAMS EAEKEATPAAAATATPTPAAATATAT PAAAYATATPAAATATATPAAATATPAAAGGYKV 15 1582249 Lol p 11 DKGPGFVVTGRVYCDPCRAGFETNVSHNVEGATVAVDCRPFDGGESKLKAE ATTDKDGWYKIEIDQDHQEEICEVVLAKSPDKSCSEIEEFRDRARVPLTSNXG IKQQGIRYANPIAFFRKEPLKECGGILQAY 20 Additional Lolium sequences (NCBI entrez accession): 135480; 417103; 687261; 687259; 1771355; 2388662; 631955; 542131; 542130; 542129; 100636; 626029; 542132; 320616; 320615; 320614; 100638; 100634; 25 82450; 626028; 100639; 283345; 542133; 1771353; 1763163; 1040877; 1040875; 250525; 551047;515377; 510911;939932; 439950; 2718; 168316; 168314; 485371; 2388664;2832717;2828273;548867. Olive tree 30 Olive sequences WO 2008/145998 PCT/GB2008/001827 46 416610 Ole e I EDIPQPPVSQFHIQGQVYCDTCRAGFITELSEFIPGASLRLQCKD KEN GDVTF' EVGYTRAEGLYSMLVERDHKNEFCEITLISSGRKDCNEIPTEGWAKPSLKFKL NTVNGTTRTVNPLGFFKKEALPKCAQVYNKLGMYPPNM 5 Parietaria Parietaria sequences: 2497750 Parj P2 10 MRTVSMAALVVLAAALAWTSSAEPAPAPAPGEEACGKVVQDIMPCLHFVKG EEKEPSKECCSGTKKLS EEVKTTEQKREACKCIVRATKGISGIKNELVAEVPK KCDIKTTLPPITADFDCSKIQSTIFRGYY 1352506 Parj P5 15 MVRALMPCLPFVQGKEKEPSKGCCSGAKRLDGETKTGPQRVHACECIQTAM KTYSDII)GKLVSEVPKHCGIVDSKLPPIDVNMDCKTVGVVPRQPQLPVSLRH GPVTGPSDPAIKARLERPQIRVPPPAPEKA 1532056 Parj P8 20 MRTVSMAALVVIAAALAWTSSAELASAPAPGEGPCGKVVHHIMPCLKFVKG EEKEPSKSCCSGTKKLSEEVKTTEQKREACKCIVAATKGISGIKNELVAEVPK KCGITTTLPPITADFDCSKIESTIFRGYY 1532058 Parj P9 25 MRTVSAPSAVALVVIVAAGLAWTSLASVAPPAPAPGSEETCGTVVRALMPC LPFVQGKEKEPSKGCCSGAKRLDGETKTGLQRVHACECIQTAMKTYSDIDGK LVSEVPKHCGIVDSKLPPIDVNMDCKTLGVVPRQPQLPVSLRHGPVTGPSDPA HKARLERPQIRVPPPAPEKA 30 2497749 Par j P9

MRTVSARSSVALVVIVAAVLVWTSSASVAPAPAPGSEETCGTVVGALMPCL

WO 2008/145998 PCT/GB2008/001827 47 PFVQGKEKEPSKGCCSGAKRLDGETKTGPQRVHACECIQTAMKTYSDIDGKL VSEVPKHCGIVDSKLPPIDVNMDCKTLGVLHYKGN 1086003 Parj 1 5 MVRALMPCLPFVQGKEKEPSKGCCSGAKRLDGETKTGPQRVIACECIQTAM KTYSDIDGKLVSEVPKHCGIVDSKLPPIDVNMDCKTVGVVPR.QPQLPVSLRH GPVTGPSRSRPPTKHGWRDPRLEFRPPHRKKPNPAFSTLG Additional Parietaria sequences (NCBI entrez accession): 10 543659; 1836011; 1836010; 1311513; 1311512; 1311511; 1311510; 1311509; 240971. Timothy grass 15 Phleum sequences: Phl p 1 MASSSSVLLVVVLFAVFLGSAYGIPKVPPGPNITATYGDKWLDAKSTWYGKP TGAGPKDNGGACGYKDVDKPPFSGMTGCGNTPIFKSGRGCGSCFEIKCTKPE 20 ACSGEPVVVHITDDNEEPIAPYHFDLSGHAFGAMAKKGDEQKLRSAGELELQ FRRVKCKYPEGTKVTFHVEKGSNPNYLALLVKYVNGDGDVVAVDIKEKGK DKWIELKE SWGAIWRIDTPDKLTGPFT VRYTTEG GTKTEAEDVIPEGWKADT SYESK 25 Phl p I MASSSSVLLVVALFAVFLGSAHG[PKVPPGPNITATYGDKWLDAKSTWYGKP TAAGPKDNGGACGYKDVDKPPFSGMTGCGNTPIFKSGRGCGSCFEIKCTKPE ACSGEPVVVHITDDNEEPIAAYHFDLSGIAFGSMAKKGDEQKLRSAGEVEIQF RRVKCKYPEGTKVT.FHVEK.GSNPNYLALLVKFSGDGDV VAVDIKEKGKDK 30 WIALKESWGAIWRIDTPEVLKGPFTVRY'ITEGGTKARAKDVIPEGWKADTA

YESK

WO 2008/1145998 PCT/GB2008/00i 827 48 PhIp 2 MSM.ASSSS SSLLAMAVLAALFAGAWC"VPK VTFT VEKGS'NEKHLA'VLVKYE GDTN4AEVELREHGSDEWV)AMTKGFGGVWTFDSEEPL QGPFhNFRFLTEKGM4 5 KNVFDDVVPEKYTIGATYAPEE Phi p 5 ADLGYGGYPATPAAPAEAAPAGKATTEEQKL.IEK-INDGFKAALA-AAAGV7PPA DKYKTFVA.TFGAASNKAFAEGLSAEPKGAAE SSSKAAL TSKLDAAYKIAYK 10 TNEGATPEAK.YDAYVATLSEALRIIIAGTLEVIIAkvKPAAEEVKVIPAGELQVLE KVDSN-FKV ;AATA ANAAP)ANDKFTVFEAAFNN AKSTGGAYESYKFULl:ALEA AVKQAYAATVATAPEVKYTrVFETIALKKATAM4SEAQKAAKPATEATATIAT' A-AVGAATG.AATAAkTGGYKV 15 Phlp 5 ADLGYGGPATPAAPAEAAPAGKATTEEQKLIEKINGFKAALAAAAGVPPA. DKYKTFVATFGAA.SNCAFAEGLSAEPKGAAESSSKAALTSKLDAAYKLAYK TrAEGATPEA-KYDAY'iVATL.SEALRIIAGTILE\'HAVKP)AAEEVKVIPAGELQVIE KVDSAFKV;AATAAN AAPANDKFTVFEAAFNNAIKAST'GGAkYESYKFIPALEA 20 AVKQAYAATVATAPEVKYTVFETALKKAITAMSEAQKAAKPATEATATAT AAVGANIATGATAATGGYKV Phi p 5b AAAAVPRRGPRGlPGRSYTrADAGYAPATPAAAGAAAGKA.TTEEQKLTIEDIN 25 VGFK.AAVAAA-ASVPAADKFKTrFEAAFTSS SKAAA GLVPKLDAAYSVA YKAAV ;GATPEAKFDSFVASLTrEALIRVIAGALEVHAVKPVTEEPG--MKIAGE LQIDKIDAAFKVAATAAATAPADDKFT-VFEAAFiIKESTGGAYDTYKCIP SLEAAVKQAYAATVAAAPQVKYAVFEAALTKAITAMSEVQKVSQPATGAA. TVAAGAA.TTAAGAASGYAAT'VAAGGYKV 30 Ph p 5a WO 2008/1145998 PCT/GB2008/001 827 49 ADLGYGPATIPAAPAAGYTPATP.AAPAGADAA GKATTEEQKL1E:KINAGFKA ALAGAGVQI)ADKYRTFVATFGPA.SNKAFAEGLSGEPKGAAESSSKAALTrSK LDAAYKLAYKT'AEGAkTPEAKYDAYVATILSEALR1AGTLEVHAVKPAAEEV KVIPAGELIQVIEKVDAAFKVAATAANAAANDKFTV-FEAAFNDEIK-ASTGGiAL 5 YESYKFLPAL]-EAAVKQAYAAT VAT APE VKYT VEETALKKATAMSEA QKAA KPAA-AATATATAAVGAATGAATAATGGYKV Phi p 5 MAVQKYTVAIF1LAVALVAGPAASYAADAGYAPATP)AAAGAEAGKATTEEQ o0 KIEDINGFKAAVAAAASVPAADKFKTFEAAFTSSSKAATA -GLVPKL-D AAYSVSYKAAVGjATPEAKFDSFVASLTEALRVIAGALLEVHA-VKPVTEEPGMN ,<AGELQIII)KIDA AFKVA ATAAAT-APADTVFEAkAFNK AIESTGGAYDTY ,KCJIPSLEAAVKQAYAAkTVAAAI)QVKYAVFEAA-L-TKAIJTAMSEVTQKVSQPAT GAATIVAAGAATTAAGAASGAAT'VAAGGYKV 15 Phi p 5 MAVQKYTVALFLAVALVAGPAAS YAADAGYAPATPAAAGAEAGKA'irEEQ KLIIED INVGjFKA-AVAA-AASVPAADKFKTIFEAAFTSSSKAATAKAPGLVPKLD AAYSVAYKAkAV GATPEA DSFVASLTIEALRVJ-AGALEVHALVKPVTEDPAW 20 PKIPAGELIQUIDKIDAAFKVTAATAAATAPADDKF'VFEA-AFNKTKMESTGGAY DT-YKCIPSILE AAVKQAYAATVAA4APQVKYAVFEAALTKAITAMSEVQKVSQ PATGAATVAAGAA~virATGA-,SGAATVAAGGYKV Phi p 5 25 ADAGYAPATPAAAGAEAGKATT'EEQKJJEDINVGFKAAVAAAAS VPAADKF KTrFEAAFTS SSKAATAKAPGil.VP KLDAAYS VAYKAA kVGATPE AKFD SF VAS ILTEALRVJAGALEVHAVKPVTEEPGiMAK-IPAGELQIIDKIDAAFKVAATAAATr APADDKFTV-FEAAFNKAIIKESTGGAYDTYKCIPSLEFAAVKQAY, ATVAAP Q VKYA- \-FEAALTKAI TAM SEVQ K VSQPAT GAAT VAAGAATT-AAGA AS GAA 30 TVAAGGYKVT WO 2008/145998 PCT/GB2008/001827 50 Phl p 5 SVKRSNGSAEVHRGAVPRRGPRGGPGRSYAADAGYAPATPAAAGAEAGKA TTEEQKIUEDINVGFKAAVAAAASVPAADKFKTFEAAFTSSSKAATAKAPGL VPKLDAAYSVAYKAAVGATPEAKFDSFVASLTEALRVIAGALEVHAVKPVT 5 EEPGMAKIPAGELQIIDKIDAAFKVAATAAATAPADDKFTVFEAAFNKAIKES TGGAYDTYKCIPSLEAAVKQAYAATVAAAPQVKYAVFEAALTKAITAMSEV QKVSQPATGAATVAAGAATTAAGAASGAATVAAGGYKV Phl p 5 10 MAVHQYTVALFLAVALVAGPAGSYAADLGYGPATPAAPAAGYTPATPAAP AGAEPAGKATTEEQKLIEKINAGFKAALAAAA.GVPPADKYRTFV ATFGAAS NKAFAEGLSGEPKGAAESSSKAALTSKLD AAYKLAYKTAEGATPEAKYDAY VATVSEALRIIAGTLEVHAVKPAAEEVKVIPAGELQVIEKVDAAFKVAATAA NAAPANDKFTVFEAAFNDAIKASTGGAYESYKFIPALEAAVKQAYAATVAT 15 APEVKYTVFETALKKAITAMSEAQKAAKPAAAATATATAAVGAATGAATA ATGGYKV Phl p 5 ADLGYGGPATPAAPAEAAAGKATTEEQKLIEKINDGFKAALAAAAGVPPA 20 DKYKTFVATFGAASNKAFAEGLSAEPKGAAESSSKAALTSKLDAAYKLAYK TAEGATPEAKYDAYVATLSEALRIIAGTLEVHAVKPAAEEVKVIPAGELQVIE KVDSAFKVAATAANAAPANDKFTVFEAAFNNAIKASTGGAYESYKFIPALEA AVKQAYAATVATAPEVKYTVFETALKKAFTAM SEAQKAAKPATEATATAT AAVGAATGAATAATGGYKV 25 Phl p5b AAAAVP RRGPRGGPGRSYTADAGYAPATPAAAGAAAGKATTEEQKLIEDIN VGFKAAVAAAASVPAADKFKTFEAAFTSSSKAAAAKAPGLVPKLDAAYSVA YKAAVGATPEAKFDSFVASLTEALRVIAGALEVHAVKPVTEEPGMAKIPAGE 30 LQIIDKIDAAFKVAATAAATAPADDKFTVFEAAFNKALKESTGGAYDTYKCIP

SLEAAVKQAYAATVAAAPQVKYAVFEAALTKAITAMSEVQKVSQPATGAA

WO 2008/1145998 PCT/GB2008/00i 827 51 TVAAGAATTAAGYAASGAATVAAGC GYKV Phi p5a At4DLGYGPATPAAPAAGYTPATPAAPAGADAAGKATTEEQKLIEKI-NAGFKA 5 ALAGiAG\'QPADKYRTFVATFGPASNKAFAF-GLSGFPKGAAESS SKAALTSK LDA AYKLAYKTAEGATPEAKYDAY'VA.TLSEALRAGTLEVHAVKPAAEEV K VIPAGELQ VIEK VDAAFK VAATAANAAP AND KFTVFEAAF7NDEIKAST'GGA YESYK-FIPALEAAVKQAYAATVAT-APEVKYTVFETALKKAr'rAMSEAQKAA KP3AAAKAATATAAVGAATGAATAATGGYKV 10 Phi p 5 AVPRRGPRGGPGYRSYAADAGYAPATPA-AAGAEAGKA.TTEEQKL-IEDINVGF KAAVAAAASVPAGDKFKTFEAAFTSSSKAATAKAPGLVPKL-DAAYSVAYKA AVGATPEAKFDSFVASLT:EALRVIAGALEVHA-vKPVTEEPGMAKIPAGELQI 15 DKIDAA-FKVAATAAATFAPAtDDKFTXTl-EAANAIFSTGGAYDT~yKC.LPSI.E AGAATTATGAASGAATVAAGGiYKV Phi p 5b 20 MIAVPRRGPRGGPGRSYTADAGYAPATPAAAGA AAGKATTIEEQKLIEDINV G FKAAVAARQRPAADKFKT FEAASPRHiPRPILRQGiAGiLVPKEDAt AYSVAYKAA VGATPEAKFDSFVASLTEALRVIAGAL ,EHAVKPVTEE PGMAKPA.CELQLID KIIDAAF-KVAATAAATAPADDKFT'VFEAAFN YAKSTGGAYDTYKCIPSLEA AVKQAYAATrVAAAEVKYAVFFEAALTKATAMSEVQKVSQPATGAATVAA 25 GAATTAAGA, ASGiAAT'VAAGGYKV; Phil p 5 MAVHIQYTVALFLAVALVAGPAASYAADLGYGPATPAAPAA GYTPATPA AP AE.AAPAGKATT'EEQKLIEKINAGFKAALAAAAGVQPADKYRTFVATFGA-AS 30 NKAFAEGLSGEP3KGA AESSSKAALTSKLDAAYKLAYKT.AEGATPEAKYD-AY VATLSEALRflAGT'LEVHAVKPAAEEVK'v'IPAGELQVIEKV -DAAFKVA-ATAA WO 2008/1145998 PCT/GB2008/00i 827 52 NAAPA-NDKFT~vFEAAFNDA STGGAYESYKFIPAIEAA VKQA.YAAT VAT APEYKYT'VFETA' LKKAIT AMSEAQKAAKPAAAATlA TATAAVGA, ATGA ATA ATGGYKV 5 Ph p 5 EA-PAGKATTEEQKLIEKINAGFKAAL kRQPADKYRTFVATFGP AS.NK-AFA EGLS GEPKGAAESS SKAA[TISKLDAAYiKLAYKTAIEGAkTPEAKYD.AYVATL.S EALR IGTLFv1]-IAVKPAAEEVKVIIPAAELQVIEKVDAAFKVAATAANAAPA NDKFTVFEAAFNDEIKASTGGAYESYKFIPALEAAVKQAYAATVATAPEVKY 10 TVFFETALKKrAMSEA.QKAAKJPPLPPPPQPI)PLAATGAATAATGGYKV Phi p 5 MAVHQYTVALFLAVALVAGPAASYAADLGYGiPATPAAPAAGYTPATPAAP AEAAPAGKATTEEQKLIEKINAGFKAALAAAAGVQPADKYRTFVATFGAAS 15 NKAFAEGLSGEPKG-AAESSSKAALTSKLDAAYKLAYKTFAEGATPEAKY-DAY VAT'LSE ALRILAGTLETHAVKPAAEEVKVIPAGELQVLEK

T

D AAFK-VAATAA NAAPANDKFTVFEA-AFNDAIKASTGGAYESYKFIPALEAAVKQAYAAT'VAT APE VKYT VFET'ALKKATAMSEAQK-AAKPAAAATATATAAVGAATlGAAT'A ATO G'YKV 20 Phi p 5b MAVPRRGPRGGPGiRSYTFADAGY-APATPAA-AGAA-AGKATTEEQKLIEDIN7G FKAAVAARQRPAADKFKTFEAASPRHPRPJLR:QGAGLVPKLDAAYSVAYKAA VGATPEAKFDSF VASILTEAR VIAGYAL.E VHAVKPVTrEEPG AIAGELQ]ID 25 KIDAAFKVAATAAATAPADDKFTVFEAAF-NKAIKjESTGGAYDTrYKCIPSLEA A\TKQAYAATVAAAAEV7KYAV-FhAAL]-TKAITAM SEV QKVSQPATrGAA'VA GAATrTAAGAASGAATVAAGQYKV Ph p 5a 30 AkDLGYGPATPAAPAAGYTPATPAAPAGADAAGKATTEEQKLIEKINAGFKA ALAGAGVQPADKYRTFVkTIFGPASNKAFAEF-GLSGEPKGAAESSSKAALTSK WO 2008/1145998 PCT/GB2008/00i 827 53 LDAAYK-LAYKTAEGATPEAKY-DAYVATLSEALRIIAGTILEVHAVKI)AAEEV KVIPACGELQVIEKVDAAFKVTAAT-AA-NAAPANDKFTV-FhEAAFNDE[FKASTGGA YESY-KFII)ALEAAVKQAYAATVATAPEVKYTVFETALKKAITAMSE AQKAAk KPPPLP1PPQP)PPLAATGAATAATGGYKV 5 Phi p 5 MAVIHQYTVAlFLAVALVAGPAASYAADLGYGPATPAAPAAGYTPATPAMU) AEAA-PAGKAkTTEEQKL[EKIN\AGFKAALAAAAGVQPADKYRTFVATFGAAS NKAFAEGL.SGEFPKGCAAESSSKAALTISKLDAAYKLAYKTAEGATPEAKYD.AY 10 VATLSEA1,RfAGTLEVHAVKPAAEEVKVWPAGELQ'vIEKYDAAFKVA-ATAA NAAPA NDKFT VFEF AAFNDAIKAST'GGAYESYKFIPALEAAVKQAYAAT VAT APEVKYTVFETAL-KKAITAMSEAQK AAKP1AAAATATATAAVGAATGAATA ATGGYKV 15 Ph p 6 MAAHKF\4MLAVAVVLGLATS PTAE-GGKATTEEQKLIEDVNASFRAA -M ATTANVPPADKYKTFEAA-FTVS SKRNLADAVSKAPQLVPKEDEVYNA AYNA ADHAAPEDKY-EAFVLKFSEALRIIAGTPEVHAVKPGA, 20o Phlp 6 SKAPQLVP KLDEVY NAAYNAADHAAPEDKYEAFVLHFSEALHIIAGTPEVHA VKPGA Phi p 6 25 -ADKYKTFEAAFTVSSKR-NLADAV SKAPQLVI)KLDEVY-NAAYNAADHAAP)E DKYENAFVLHFSEAllHiIAGTPEVIIAVKPGA WO 2008/1145998 PCT/GB2008/00i 827 54 Phi p 6 T'EEQKLIEDVINASFRAMTTANVPPADKYKTLEAAFTVSSKRi\I--ADAVSK APQLVPKLDE-VYNAAYNAADHIAAPE DKYEAkFVLHFS.EALIIA4GTPEV}{AVK P3GA 5 PI p 6 MAAHKFMVAMIFLAVAVVLGLATSPTAEGGKATTEEQKIJED IINASFR AAMA TTAiNYPPADKYKTlFEAAFTVSSKRNADAkVSKAPQLV7PKLDEVYNAAYNAA DHIAAPEDKYEAF'VLIL{FSEALHIIAGTPEVHAVKPGA 10 PI p 6 MVAMFLAVAVVLGLATSPTAEGGKATTEEQKLIEDVNASFRAAMATTA-NrVP PADKYKTFEAAFTIV SSKRNLADAVISKAPQLV PKLDEVYNAAYN-AADHAAP EDKYEAFVL.H-FSEALR[IAGTP)EVHAVKPGA 15 Phi p 7 MADDM-NER-IFKRFDTNGDGKISL SELTDALRT'LGST'SADEVQRMMA-EIDTDGD GFIDF-N.E FJSFCNA-NPGLM-N-KDV.AK'vF 20 Phipl11 MS WQTYiVDEHL-MCEIEGHHLASAAITLGHDGTVWAQSADFPQ FKPEEITGJM4 KDFDEPGHLAPTG iFVAGAKYMVIQGEPGRVIRGKKGAGGITIKKTGQALV ; VGIYDEI)MTPGQCNM'VVERLGDYLVEQGMN 25 Additional Phleurn sequences (NCBJ entrez accession): 458878; 548863; 2529314; 25293'08; 2415702; 2415700; 2415698; 542168; 5421671; 626037; 542169; 541814; 542171; 253337; 253336; 453976; 439960. 30 Y 2{ nd elated Ves,_pul sequences: WO 2008/1145998 PCT/GB2008/001 827 55 465054 ALLERGEN VES V 5 .MEISGLVYLIIIVTIIDLPIYGKANCKICLKGGVH-TACKYGSLKPNCGNKV VVSYGILTKQEKQDJLKEHNDFRQKIARGLETRG-NPGPQPPAK-NMKNILVWND 5 ELAYVAQVWANQCQYGHDTCRDVAKYQVGQNVALTGST-AAYDDPVKLV KMNWEDEVKDY-NPKKKFSGNDFLKTGHYTlQMVWANTKEVGCGSIKYIQEK AXXKHYVCNYGPSGNF MNEELYQTK 1709545 ALLERGEN YES M 1 10 GPKCPFNSDTVSIEETRENRNRDLYTLQTLQ'NHPEFKKKTITRPY ;VFITHGFTS SASEK-NFINLAK-ALVDKDNYMVISIDWQTAACTFNEYP1GLKYAY-YPTAASNT RLVGQYIATITQKLVIKDYKISMAN}IRTIGHI-SLGAH-V SGFAGKRVQELKLGKYS EIIGLDPARPSFDSNHCSERLCETDAEYVQHHITSNYL.GTEKILGTrVDFYMNNG KNNPIGCGRFFSEVCSHTRAVIYMAECIKH-ECCLIG1PRSKSSQPISRCTFKQECV 15 C VGLNAKKYP SRGSFYVP-VHS TAPFCiN-N GKH 1352699 ALLERGEN VES V I MEENMNLKYLLLFVYFVQVLiNCCYGHGDPLSYELDRGPKCPFNSDTVSUIET RENR-NRDILYTIQTLQNHIPEFKKKITIRPN;VITHGFTSSASETNTINLA VD 2o KDNYMvVISIDWQTAACTrNEAAGLKYLYY1PTAAR-NTRLVGQYIAT1TQKLVK HYKISMAN~NILIGH-SLGCAHASGiFAGKKVQELKLGKYSEIIGLDPAR.PSFDSMI CSERLCETDAEYVQIIHiTS NYLGTEKTFLGTVDFYMlNNGKNQPGCGRFFSEVC SHSR-AV1YM4AECIK-ECCILTGIPKSKSSQPISSCTlKQECVCVGLN-AKKYP)SRGS FYiVPVESTA.PFCNNKGKII 25 1346323 ALLERGEN VES V 2 SERPKRVFNTh NWPTFMCHQYDLYFDEVTN URSKDDFQGYDKTAIFYD PGEFPALLSLKDGKYKKRGGV~PQEGNITIHLQKE-IENLDKIYPNR.NFSGIlGVI DFERWRP1FRQNTWGNT4K FNSIDLV7RNE1{PTW.NKKMA1ELEASKRFEKYA 30 RFFMEETlLKLAKKTRKQADWGYYGY-PYCFNM IvSPNNLV PECDVTAMH-ENDK

MSWFNNQNVLLPSVY-VRQELTPDQRIGLVQGRVKEAVRISNNIKHSPKVLS

WO 2008/145998 PCT/GB2008/001827 56 YWWYVYQDETNTFLTETDVKKTFQEIVINGGDGIIIWGSSSDVNS LSKCKRL QDYLLTVLGPIAINVTEAVN 549194 ALLERGEN VES VI 5 5KVNYCKIKCLKGGVIHTACKYGTSTKPNCGKMVVKAYGLTEAEKQEILKVH NDFRQKVAKGLETRGNPGPQPPAKNMNNLVWNDELANIAQVWASQCNYG HIDTCKDTEKYPVGQNIAKRSTTAALFDSPGKLVKMWENEVKDFNPNIEWSK NNLKKTGHYTQMVWAKTKEIGCGSVKYVKDEWYTHYLVCNYGPSGNFRN EKLYEKK 10 Additional vespula sequences (NCBI entrez accession): 549193; 549192; 549191; 549190; 549189; 117414; 126761; 69576; 625255; 627189; 627188; 627187; 482382; 112561; 627186; 627185; 1923233; 897645; 897647;745570;225764; 162551. 15 Tree allergy (mainly birch sequences: 114922 Bet v I MGVFNYETETTSVIPAARLFKAFILDGDNLFPKVAPQAISSVENIEGNGGPGTI 20 KKISFPEGFPFKYVKDRVDEVDHTNFKYNYSVIEGGPIGDTLEKISNEIKIVAT PDGGSILKISNKYHTKGDHEVKAEQVKASKEMGETLLRAVESYLLAI-ISDAY N 130975 Bet v 2 25 MSWQTYVDEHLMCDIDGQASNSLASAIVGHDGSVWAQSSSFPQFKPQEITGI MKDFEEPGHLAPTGLHLGGTKYMVIQGEAGAVIRGKKGSGGITIKKTGQALV FGIYEEPVTPGQCNMVVERLGDYLIDQGL 1168696 Bet v 3 30 MPCSTEAMEKAGHGHASTPRKRSLSNSSFRLRSESLNTLRLRRIFDLFDKNSD GIITVDELSRALNLLGLETDLS ELESTVKSFTREGNIGLQFEDFISLHQSLNDSY WO 2008/145998 PCT/GB2008/001827 57 FAYGGEDEDDNEEDMRKSILSQEEADSFGGFKVFDEDGDGYISARELQMVL GKLGFSEGSEIDRVTEKMIVSVDSNRDGRVDFFEFKDMMRSVLVRSS 809536 Bet v 4 5 MADDHPQDKAERERIFKRFDANGDGKISAAELGEALKTLGSITPDEVKHM4 AEIDTDGDGFISFQEFTDFGRANRGLLKDVAKIF 543675 Que a I - Quercus alba=oak trees (fragment) GVFTXESQETSVIAPAXLFKALFL 10 543509 Car b I - Carpinus betulus=hornbeam trees (fragment) G'TNYEAETPSVIPAARLFKSYVLDGDKLIPKVAPQAIXK 543491 Aln g I - Alnus glutinosa=alder trees (fragment) 15 GVFNYEAETPSVIPAARLFKAFILDGDKLLPKVAPEAVSSVENI 1204056 Rubisco VQCMQVWPPLGLKKFETLSYLPPLSSEQLAKEVDYLLRKNLIPCLEFELEHGF VYREHNRSPGYYDGRYWTMWKLPMFGCNDSSQVLKELEECKKAYPSAFIRI 20 IGFDDK Additional tree allergen sequences (NCBI entrez accession number): 131919; 128193; 585564; 1942360; 2554672; 2392209; 2414158; 1321728; 25 1321726; 1321724; 1321722; 1321720; 1321718; 1321716; 1321714; 1321712; 3015520; 2935416; 464576; 1705843; 1168701; 1168710; 1168709; 1168708; 1168707; 1168706; 1168705; 1168704; 1168703; 1168702; 1842188; 2564228; 2564226;2564224;2564222;2564220;2051993;1813891;1536889;534910; 534900; 534898; 1340000; 1339998; 2149808; 66207; 2129477; 1076249; 30 1076247;629480;481805;81443;1361968;1361967; 1361966;1361965;1361964; 1361963; 1361962; 1361961; 1361960; 1361959; 320546; 629483 ; 629482; WO 2008/145998 PCT/GB2008/001827 58 629481; 541804; 320545; 81444; 541814:; 629484; 474911; 452742; 1834387; 298737; 298736; 1584322; 1584321; 584320; 1542873; 1542871; 1542869; 1542867; 1542865; 1542863; 1542861; 1542859; 1542857; 1483232; 1483230; 1483228;558561;551640;488605;452746;452744;452740;452738;452736; 5 452734;452732;452730;452728;450885;17938; 17927; 17925;17921;297538; 510951;289331;289329;166953. Peanut Peanut sequences 10 1168391 Ara h I MRGRVSPLMLLLGILVLASVSATHAKSSPYQKKTENPCAQRCLQSCQQEPDD LKQKACESRCTKLEYDPRCVYDPRGHTGTTNQRSPPGERTRGRQPGDYDDD RRQPRREEGGRWGPAGPREREREEDWRQPREDWRRPSHQQPRKIRPEGREG 15 EQEWGTPGSHVREETSRNNPFYFPSRRFSTRYGNQNGRIRVLQRFDQRSRQF QNLQNHRIVQIEAKPNTLVLPKIADADNILVIQQGQATVTVANGNNRKSFNL DEGHALR]PSGFISYILNRHDNQNLRVAKISMPVNTPGQFEDFFPASS RDQSSY LQGFSRNTLEAAFNAEFNEIRRVLLEENAGGEQEERGQRRWSTRS SENNEGVI VKVSKEHVEELTKHAKSVSKKGSEEEGDITNPINLREGEPDLSNNFGKLFEVK. 20 PDKKNPQLQDLDMMLTCVEIKEGALMLPHFNSKAMVIVVVNKGTGNLELV AVRKEQQQRGRREEEEDEDEEEEGSNREVRRYTARLKEGDVFIMPAAHPVAI NASSELHLLGFGINAENNHRIFLAGDKDNVIDQIEKQAKDLAFPGSGEQVEKL IKNQKESHFVSARPQSQSQSPSSPEKESPEKEDQEEENQGGKGPLLSILKAFN 25 Ragweed Ambrosia sequences 113478 Amb a I MGIKHCCY[LYFTLALVTLLQPVRSAEDLQQILPSANETRSLTTCGTYNIIDGC 30 WRGKADWAENRKALADCAQGFAKGTIGGKDGDIYTVTSELDDDVANPKEG

TLRFGAAQNRPLWBIFI:ARDMVIRLDREILAINNDKTIDGRGAKVEIINAGFAIYN

WO 2008/1145998 PCT/GB2008/00i 827 59 VKBII~vIHDI\VNPGGLIKSHDGPPVPRKGSDGDAJGISGGSQIWIDHCSLS KAVDGLIDAKGSTIIFTVSNCLFTQHQYLLL1FWDFDERGMLCTVAFNKFTD

NVDQRMPNLRHGFVQVV

1 ± -NYERWGSYAILGGSAGPTILSQCGNRFIASDrKK EVVGRYGESAMSESINTWNWRSX XTDFE-NGATFVPSGVDPVITPEQNAGMEP 5 AEPGEAVLRLTS SAG VLSCQPGAPC 113479 Amb a 2 MGIKHICCYILIYFTLALVTrLVQAGRLGEEVDILPSPNDTRRLQGCEA IIK CWRCKPDWAENRQALGNCAQGFGKATHGGKWNGDIYMVTSDQDDDNVKP 10 KEGTLRFGYATQDRPILWflFQRDMI1YLQQEMVVTSDKTDGRGAKVNELVYGGI TMNV-KNVIHINIDIH-DVPRVLPGGR]JKSNGGPALPRHQSDGDAIHVTGSSDIW DH CTILSKSFDGLVDVNWGSTGVT1ISNCKFTIHHEKAVILLGASDTL{FQDLKMH VTLAYNIFTNTVTIIERMPRCRFGFFQIVNNFYDRWDKYAIGGSSNP)TISQGNK FVAPDFIYKKNVCLRTGAQEPEWMTWNWRTQNDVLENGC)A]FVASGSDPVLT' 15 AEQNkG-TMMQAEPGDMVPQLT.MNAGxVLTCSPGtAPC 113477 Amb a 1.3 MGIKQCCYITLALVALLQPVRSAEGVGELPSVNETRSQACEALNIIDKC WVRGKADWENNQALADCAQGFAKGTYGGKWGDVYTVTSNL.DDDVANPK 20 ECGTLRFAAkQiNRPJL'WTWKNDM-vITh1LNQELNVN1SDKTIDGRG-vKVEIINGGLT LMNVKNIflHNINIHDVKVLPGGIKSNDGPPILRQASDGDTINVAGSSQrW9ID HCS LSKSFDGLVDVTILGSTHVTISNCKFTQQSKAILGADDTHVQDKGMLAT VAFNMFTIDNVDQR MPRCRFGiFFQVV-NNDRWGTYAIGGSSAPTILCQGNR FLAPDDQIKKNVLARTIGTGAAESMAWNWRSDKDLLENGAIFVTSGSDPVLTr 25 PVQSAGMIPAEPGEAA1KLTSSAGVFSCHPGAPC 113476 Amb a 1.2 MGTKHCCYILYFTIALVTLLIQPVRSAEDVEFLPSANETIRRS LKACEAHNDIDK. CWNRCK-ADWAN-NRQALADCAQGFAKGTIYGGiKHGDVYTrVTSDKDDDVANP 30 KEGTLRFAAAQNRPLWH IFKRNMVHLNQELVVNSDKTIIDGRGiVKVNI/NAG LTLMNKN{-N1N[H'DIIKVCPGGMIKSNDGP1PILRQQSDGDAINVAGSSQIWI WO 2008/1145998 PCT/GB2008/001 827 60 DIICSLSKASDGLLDITLGSSHVTVSNC'KFTQHQFVLLLGADDTHYQDK.GML ATVAFNMFT-DH VDQRMVPRCRFGFFQ V VNNNYDR WGTYAIGGS SAPTIS QG NRFFAPDDLIKKNVWLARTGTGNAESMS W-NWRTDRDLLENGA]IFLPSGSDPVL TPEQ'KAGiMIPAEPGEAVLRLTSSAGVLSCHQGAPC 5 113475 Arnb a I.I mGiKiHccy1L-YFTrLALVTLLQPVRSAEDLQEIIPVNETrRRLTTSGAYNNDGCW RGKADW.AENRKALADCAQGFGKGTVGGK-DGDIY TVTrSELDDDVANPKEGT LRFGAAQNPLWUEFERDM-vVIRIDKEMVVNSDKTFIDGjRGAK-VEnNAGFTL.NG 10 VKNVMBHN[NMIIDVKVN--PGGLIKSNDGPAAPRAiS DGDAISISGS SQIW7IDIHCS LSKSVDil.VDAKLcGT[RLTVSNSLFTQHQFVIFGAGiDENIEDRGMLATVAF NTFTDNrVDQRMVPR.CRHGFFQVV

T

-iDKWG SYAIGGSASPTRESQGMUFCA P DERSKKNVLGRHIGEAAAESMIKWNWRTNKDVLE NGAWFVASGVDPVLTPE QSAGMI4PAEPGESALSL TSSAGjVLSCQPGAPC 15 Cedar sequences 493634 Cryj IB precursor -MDSPCL VALLVFSFVIGSCFSDNPIDSCWRGDSNWAQNrRMKIADCAVGFGS 20 STMGGK.GGDLYTVTNSDDDPV(.NPPGYTLRYGiATRDRPLVUFSGNMNIKLKM PMYIAGYKTrFDGRGAQVYIGNGGiPCVFLKRVSNVUEHGLYLYGCSTSVLGCNVL INESFGVEPVHPQDGDAILTLRTATNTWIDIINSFSNSSDGLVDVTLTSTGiVTISN NLFFNHHl-K.VMSLGHDDAYSDDKSMXKVTVAFNQFGPNCGQRMIPRARYGLV HX,'NTN7NYDPWTIrYAIGGSSNIPTILSEGNSFTAPNES YKKQVTIRIGCKTSSSCS 25 NWVWQSTQDVFY.NGAYFVSSGKY-EGG-NIYTKKEAFiNVENGNATrPHLTQNA GVLTFCSLSKRC 493 632 Cry j IA precursor MNDSPCLVALLVLSFVIGSCFSDNP)IDSCXVRGDSNWAQNRM-KLADCAVGFGS 30 STMGGKGGDL.YTVTNSDDD)V NIAPGTLRYGATRDRPLWIIFSGNN]IK MPMYJIAGYKTFDGiRGA QVYICGNGGPCVFIKRVSN-VIIHGLHLYGCSTSVLGN WO 2008/145998 PCT/GB2008/001827 61 VLINESFGVEPVHPQDGDALTURTA'INIWIDHNSFSNSSDGLVDVTLSSTGVTI SNNLFFiNHHKVMLLGHDDAYS:DDKSMKVTVAFNQFGPNCGQRMPRARYGL VHVANNNYDPWTIYAIGGSSNPTILSEGNSFTAPNESYKKQV TIRIGCKTSSSC SNWVWQSTQDVFYNGAYFVSSGKYEGGNIYTKKEAFNVENGNATPQLTKN 5 AGVLTCSLSKRC 1076242 Cry j II precursor - Japanese cedar MAMKLIAPMAFLAMQLIIMAAAEDQSAQIMLDSVVEKYLRSNRSLRKVEHS RHDAINIFNVEKYGAVGDGKHDCTEAFSTAWQAACKNPSAMLLVPGSKKFV 10 VNNLFFNGPCQPHFTFKVDGIIAAYQNPASWKNNRIWLQFAKLTGFTLMGKG VIDGQGKQWWAGQCKWVNGREICNDRDRPTAIKFDFSTGLI[QGLKLMNSPE FHLVFGNC EGVKIIGISITAPRDSPNTDGIDIFASKNFHLQKNTIGTGDDCVAIG TGSSNIVIEDLICGPGHGISIGSLGRENSRAEVSYVHVNGAKFIDTQNGLRIKT WQGGSGMA-Si I]YENVEMINSENPILINQFYCTSASACQNQRSAVQIQDVTYK 15 NIRGTSATAAAIQLKCS:DSMPCKDIKLSDISLKLTSGKIASCLNDNANGYFSGH VIPACKNLSPSAKRKESKSHKHPKTVMVENMRAYDKGNRTRILLGSRPPNCT NKCHGCSPCKAKLVVHRIMPQEYYPQRWICSCHGKYHP 1076241 Cry j II protein - Japanese cedar 20 MAMKFIAPMAFVAMQLUMAAAEDQSAQIMLDSD.IEQYLRSNRSLRKVEHSR HDAINIFNVEKYGAVGDGKHDCTEAFSTAWQAACKKPSAMLLVPGNKKFV VNNLFFNGPCQPHFTFKVDGILAAYQNPASWKNNR]WLQFAKLTGFTLMGKG VIDGQGKQWWAGQCKWVNGREICNDRDRPTAIKFDFSTGLIIQGLKLMNSPE FHLVFGNCEGVKIIGISITAPRDSPNTDGIDIFASKNFHLQKNTIGTGDDCVAIG 25 TGSSNIVIEDLICGPGHGISIGSLGRENSRAEVSYVHVNGAKFIDTQNGLRIKT WQGGSGMASHIIYENVEMINSENPIINQFYCTSASACQNQRSAVQIQDVTYK NIRGTSATAAAIQLKCSDSMPCKDIKLSDISLKLTSGKIASCLNDNANGYFSGH VIPACKNLSPSAKRIKESKSHKHPKTVMVKNMGAYDKGNRTRILLGSRPPNCT NKCHGCSPCKAKLVIVHRIMPQEYYPQRWMCSRHGKIYHP 30 541803 Cry j I precursor - Japanese cedar WO 2008/145998 PCT/GB2008/001827 62 IMDSPCLVALLVLSFVIGSCFSDNPIDSCWRGDSNWAQNRMKLADCAVGFGS STMGGKGGDLYTVTNSDDDPVNPPGTLRYGATRDRPLWIIFSGNMNIKLKM PMYIAGYKTFDGRGAQVYIGNGGPCVTIKRVSNVIIHGLHLYGCSTSVLGNVL INESFGVEPVHPQDGDALTLRTATN1WIDHNSFSNSSDGLVDVTLSSTGVTISN 5 NLFFNHHKVMLLGHDDAYSDDKSMKVTVAFNQFGPNCGQRMPRARYGLV HVANNNYDPWTIYAIGGSSNPTILSEGNSFTAPNESYKKQVTIRIGCKTSSSCS N WV WQSTQD VFYNGAYF VSSGKYEGGNIYTKKEAFNVENGNATPQLTKNA GVLTCSLSKRC 10 541802 Cry j I precursor- Japanese cedar .MDSPCLVALLVFSFVIGSCFSDNPIDSCWRGDSNWAQNRMKLADCAVGFGS STMGGKGGDLYTVTNSDDDPVNPAPGTLRYGATRDRPLWIIFSGNMNIK MPMYIAGYKTFDGRGAQVYIGNGGPCVFIKRVSNVIIHGLYLYGCSTSVLGN VLINESFGVEPVHPQDGDALTLRTATNIWIDHNSFSNSSDGLVDVTLTSTGVTI 15 SNNLFFNHHKVMSLGHDDAYSDDKSMKVTVAFNQFGPNCGQRMPRARYGL VHVANNNYDPWTIYAIGGSSNPTILSEGNSFTAPNESYKKQVTIRIGCKTSSSC SNWVWQSTQDVFYNGAYFVSSGKYEGGNIYTKKEAFNVENGNATPHLTQN AGVLTCSLSKRC 20 Dog Canis sequences: Can f I MKTLLLT iiFSLIAILQAQDTPALGKDT VAVS GKWYLKAMTADQE VPEKPDS 25 VTPMILKAQKGGNLEAKITMLTNGQCQNITVVLHKTSEPGKYTAYEGQRVV FIQPSPVRD:HYILYCEGELHGRQIRMAKLLGRDPEQSQEALEDFREFSRAKGL NQEILELAQSETCSPGGQ Serum albumin fragment 30 EAYKSEIAHRYNDLGEEHFRGLVL WO 2008/145998 PCT/GB2008/001827 63 Serum albumin fragment LSSAKERFKCASLQKFGDRAFKAWSVARLSQRFPKADFAEISKVVTDLTKVH KECCHGDLLECADDRADLAKYMCENQDSISTKLKECCDKPVLEKSQCLAEV ERDELPGDLPSLAADFVEDKEVCKNYQEAKDVFLGTFLYEYSRRHPEYSVSL 5 LLRLAKEYEATLEKCCATDDPPTCYAKVLDEFKPLVDEPQNLVXTNCELFEK LGEYGFQNALLVRYTKKAPQVSTPTLVVEVSRKLGKVGTKCCKKPES TERMS CADDFLS Can f 2 10 MQLLLLTVGLALICGLQAQEGNHEEPQGGLEELSGRWHSVALASNKSDLIKP WGHFRVFIHSMSAKDGNLHGDILIPQDGQCEKVSLTAFKTATSNKFDLEYWG HINDLYLAEVDPKSYLILYMIN QYNDDTSLVAHLMVRDLSRQQDFLPAFESVC EDIGLHKDQIVVLSDDDRCQGSRD 15 Additional dog allergen protein (NCBI entrez accession): 1731859 Horse 20 Equus sequences: 1575778 Equ cl MKLLLLCLGLILVCAQQEENSDVAIRNFDISKISGEWYSIFLASDVKEKIEENG SMRVFVDVIRALDNSSLYAEYQTKVNGECTEFPMVFDKTEEDGVYSLNYDG 25 YNVFRISEFENDEHIILYLVNFDKDRPFQLFEFYAREPDVSPEIKEEFVKIVQKR GIVKENE[DLTKIDRCFQLRGNGVAQA 3121755 Equ c 2 SQXPQSETDYSQLSGEWNTIYGAASNTXK 30 WO 2008/1145998 PCT/GB2008/001 827 64 Euro gIvphus (mite) Euroglyphus sequences: Eur m I (variant) 5 TYACSIINSVSLPSELDLRSLRTVTP MQGGCGSCWAFSGVASTrESAYLAYRN MSLD LAEQELVDCASQNGCHGDTIPRGIEYIQQNGVVQEIYYPYVAR:EQSC IHRPNAQRYGiLKNYCQISPPDSNKIRQALTQTHTAVAVIIGIKDINAFRHIYDGR TriMQH-DNGYQPNYI]AVNIVGYGNTQGNIDYW AI-vRPNSWDTTWGDNG'(-YGYFA, ANNhIL 10 Eur mn I (variant) TYACSI.NSVSLPSEL.DLRsLwrvTrPIRMQGGCGSCWAFSGVASTESAYL.AYRN MSLDLAEQELIVI)CA.SQNGCH7GDTrIPRGIEYIQQNGV-VQEH{YYPYVAREQSC I{RNAQRYGLKNYCQISPPDSNKJIRQALT-QTrHTAVAVIIGIKDLNAFRHYDGR 15 TTM4QEDNGYQPNYHAVNIrVGYGNT'QGVDYWIVR-NSWDTTWGDNGYGY FA Eur m I (variant) ETINACSINGNAPAEIDLRQMRTVTPIRMQGGCGSCWAFSGVAAT-ESAY-LAY 2o RNQSLDLAEQELVDCASQHGCHGDTIPRGIEYIQHENGVVQES YYRYVAREQS CRRPNAQRFGJISNYCQI-YPPNANKIkEALAQTHSATAVIIGIKDLDAFRH-YDGR TIIQRDNGYQPNYHAVNIVGYSNAQGVDYWTV7RNSWDTNWGDNGYGYTFAA NIDL 25 Eur mlI(variant) ETSACRJNSV NVSEL DLRSLRTVTPIRMQGGCGSCWAFSGVAATESAY]LAY RNTSLDLSEQELVDCASQH-GCIIGDTIPRGIEYIQQNGWVVEERSYPYVAREQQ CRRPNSQHYGIS NYCQIYPPD- YKQIREALTQTrHTMAAIIG1KDLR-AFQHYDGR TIIQHDNGYQPNYHAVNrVGYGsTrQGVDYWYVRNSWDTTWGDSGYGY-FQA 30 GNNL WO 2008/1145998 PCT/GB2008/001 827 6-5 Poa_(grass )__giqW jce~s 113562 POLLEN ALLERGENPOA P 9 MAVQKYTVALFLIVALVVGP)AASYA-ADLSYGAPATP-AAPAAGYTPA-APAGA 5 APKATTDEQKMIEK1INVGFKAAVAAAGGVR ANYKTFVATFGA-ASNKAFA E.ALSTEPKGAA VD SSKAAL.TSKLDAAYKLAYKSAEGATPE AKYD DY-VA. TLS EALR IGTLEVHGVKPAAEEVKATPAGELQVIDKVIDAAFKVAATAANAAPA. NDKFITFEAAFNrDAIKASTGGAYQSY-KFIIPALEAAVI(QSYAATVATAPAVK YTrVFET-ALKATA-MSQAQKAAKPAiAATGiTATAAVGAATGAATAAAGGY j.o KV 113561 POAP19 MA VHQYT VALE LA VAL VAGPAASYAAD VGYGAP3ATLATPATPAAPAAGYT PAAPAGAAPKA,:irDEQKLIEK]NAGFKAAVAAAAGiV PAVDKYKTFVATFGT 15 ASN-AFAEALSTEP)KGAAAASSNAVLTSKLDAAYKLAYKSAkEGATPEAKYD AYVATLSEALRILAGTrLEVHAVKAGEEVKAITPA.GELQVIDKVDA-AEKVAAT AANAAPAND'KFT'VFEAAFNDAIKASTGGAYQSYKFIPALEAAkVKQSYAATV ATAPAVKYTVFETALKLKAITAMSQAQKAAKPAAAVTATIAT-GAVGAATGAV GAATGAATAAAGGYKT lGAATPITAGGYKV, 20 113560 POA P 9 MDKANGAYKTALKAA kSAVAPAEKFPVFQATIFD KIBOLS GPDAVGFAKK LDAFIQTSY-LSTKAAEPKEKFDL.FVL.SL'EV LRFMAGAVKAPPASKFPAKAP KVAtAYTPIAAPAG AAPKATTDEQKLIEKINIVGFKAAVAAAAGVPAASKYKTF PEAK YDAY-VATLS EALR GTLEVI-GVKPAAEEVKAIPAGiELQVIDKVDAA FKVAATAAN AAPANDKFTVFEAANAKSTGGAYQSYKFIPALEAAVKQ SYAATVATAPAVKYTVFET.ALKKAIT-AMSQAQKAAKPAA AVTGTATSAVG AATGAATAAAtGGYKV 30 WO 2008/1145998 PCT/GB2008/00i 827 66 Cockroach sequences 2833325 Cr pl MIKTrALVFA AVVAFVAARFPDH-KDYKQLA DKQFLAKQRDVLRLFHRVHQIN 5 ILNDQVEVG1PIMTSKQTSATTvPPSGEAVH-GVLQEGHAPJ3RGEPFSVNYEK}I REQAIMLYDLLYFANDYDTFYKTACWARDRVNEGMFMY SFSLAVFHRDDM QGV-MLPP)PYEVY3Y-LFVIDHV -MQKYWMX-NAGSGEHH SHVIPVN-FTLR TQDHLL-AYFTISDV-NLNAFNTYYiRYYYPSWYNTTILYGI-NIDRRGEQFYYTYK QWYARYIFLIERLSNDLI)DVYPFY-YSKPVKSAYNPNLRYHINGEEMPVRPSNM4Y 10 VT.NFDIYYIADIKNYEKRVEDAIDFGYAFDEHMLNKPIISL.YH-DVHG-MEY-LADM IEGNMDSPNrFYFYGSJYHMYHSMivGHIVDPYliKIMGLAPSLEH-PETVLIRDP'VF YQLWKRVDHLIFQKYK-NRLPRYTHDELA-FEG-v-KVEN'vDVGKLIYTYFEF-QYD MSLDMAVYVNNVDQ[SNVDVQLAVRLI HKFTYMTEVSSDK-AQDVYVAVF LGPKYDYLGREYDL.NDRRHYFVEMDRFPY1HVGAGKTVIERNSHDSNIIAPER 15 DSYRTFYKKVQEAYEGKSQYYVDKGI{NYCGY-PENLLIPKGKKGGQAYTFY -'/IVTPY-V-KQDBHiDFEPYNYKAFSY'CGVGSERKY'PDNKPLGYTFDRKIYSNDF YTPNMYFKDVIIFI{TKKYDEVGiVQGH 2231297 Cr p2 20o INEII{SIGLPPFVrPPSRRARGVCINGILIDDVI A]LP)VDELYKA4LFQEKLETSPD FKAitLYDAIRSPEFQSISTLNAMQRSBHHIQINLR-DK.GVDDHFIQLIRALFGLSR AARNLQDDLNDFLHSLEPISPRHRGLPRQRRRSARVSAYLHADDFHKIIIE AL1PEFANFY NFLKEHGLDV VDYINETHSIIGLPPF'vrPPSRRH-ARRGCGINGI.IDD VIAILPVDELKALFQEKLETSPDFKALYDAIRSPEFQSIISTLNA-MPEYQEIlLQN 25 I.RDK.GVDVDHFIRVDQCGrLRT'LSSGQRN-LQDDLNDFLALIPTDQH-.LkMDY ANDAEU-VQEIVAYLQSDDFHKlITrEALP3EF.ANFYNFLKEHGLDVVDILNEIHS IIGLPPFVPPSQRHIARRGVGINGLIDDVLAIPVDELKALFQEKLETSPDFKAILY DAU)LRSSRA 30 1703445 Bla g 2 M1GLKLV ;TVLFXAVA1TI'HAAELQRVPLYKVH-VFINTQYAGITKIG NQNFLITV WO 2008/145998 PCT/GB2008/001827 67 FDSTSCNVVVASQECVGGACVCPNLQKYEKLKPKYISDGNVQVKFFDTGSA VGRGIEDSLTISNLTTSQQDIVLADELSQEVCILSADVVVGIAAPGCPNALKGK TVLENFVEENLIAPVFSIHHARFQDGEHFGEIIFGGS:DWKYVDGEFTYVPLVG DDSWKFRLDGVKIGDTTVAPAGTQAIIDTSKAIIVGPKAYVNPLNEAIGCVVE 5 KTTTRRICKLDCSKIPSLPDVTFVINGRNFNISSQYYIQQNGNLCYSGFQPCGH SDHFFIGDFFVDHYYSEFNWENKTMGFGRSVE Sv 1705483 Bla g 4 10 AVLALCATDTLANE:DCFRHESLV PNLDYERFRGSWIIAAGTSEALTQYKCWI DRFSYDDALVSKYTDSQGKNR TTIRGRTKFEGNKFTIDYNDKGKAFSAPYSV LATDYENYAIVEGCPAAANGHVIYVQIRFSVRRFHPKLGDKEMIQ:HYTLDQV NQHKKAIEEDLKHFNLKYEDLHSTC H 15 2326190 Bla g 5 YKLTYCPVKALGEPIRFLLSYGEKDFEDYRFQEGDWPNLKPSMPFGKTPVLEI DGKQTH QSVAISRYLGKQFGLSGKDDWENLEIDMIVDTISDFRAAANY HYD ADENSKQKKWDPLKKETIPYYTKKFDEVVKANGGYLAAGKLTWADFYFVA ILDYLNIHMAKEDLVANQPNLKALREKVLGLPAIKAWVAKRPPTDL 20 Additional cockroach sequences (NCBI Entrez accession numbers): 2580504; 1580797; 1580794; 1362590; 544619; 544618; 1531589; 1580792; 1166573;1176397;2897849. 25 Allergen (general) sequences; NCBI accession numbers 2739154; 3719257; 3703107; 3687326; 3643813; 3087805; 1864024; 1493836; 1480457; 2598976; 2598974; 1575778; 763532; 746485; 163827; 163823; 3080761; 30 163825; 3608493; 3581965; 2253610; 2231297; 2897849; 3409499; 3409498; 3409497; 3409496; 3409495; 3409494; 3409493; 3409492; 3409491; 3409490; WO 2008/145998 PCT/GB2008/001827 68 3409489;3409488;3409487;3409486;3409485;3409484;3409483;3409482; 3409481;3409480;3409479;3409478;3409477;3409476;3409475;3409474; 3409473;3409472;3409471;3409470;3409469;3409468;3409467;3409466; 3409465;3409464;3409463;3409462;3409461;3409460;3409459;3409458; 5 3409457; 3409456; 3318885; 3396070 ; 3367732; 1916805; 3337403; 2851457; 2851456;1351295;549187;136467;1173367;2499810;2498582;2498581; 1346478;1171009;126608;114091;2506771;1706660;1169665;1169531; 232086;416898;114922;2497701;1703232;1703233; 1703233; 1703232; 3287877;3122132;3182907;3121758;3121756;3121755;3121746;3121745; 10 3319925;3319923;3319921;3319651;3318789;3318779;3309647;3309047; 3309045;3309043;3309041;3309039;3288200; 3288068;2924494;3256212; 3256210;3243234;3210053;3210052;3210051; 3210050;3210049;3210048; 3210047;3210046;3210045;3210044;3210043;3210042;3210041;3210040; 3210039;3210038;3210037;3210036;3210035;3210034;3210033;321 0032; 15 3210031;3210030;3210029;3210028;3210027;3210026;3210025;3210024; 3210023;3210022;3210021;3210020;3210019;3210018;3210017;3210016; 3210015;3210014;3210013;3210012;3210011;3210010;3210009;3210008; 3210007;3210006;3210005;3210004;3210003;3210002;3210001;3210000; 3209999;3201547;2781152;2392605;2392604;2781014;1942360;2554672; 20 2392209; 3114481;3114480;2981657;3183706; 3152922;3135503 ;3135501; 3135499;3135497;2414158;1321733;1321731;1321728;1321726;1321724; 1321722;1321720;1321718;1321716; 1321714;1321712;3095075;3062795; 3062793;3062791;2266625;2266623;2182106; 3044216;2154736;3021324; 3004467;3005841;3005839;3004485; 3004473;3004471;3004469;3004465; 25 2440053; 1805730; 2970629; 2959898; 2935527; 2935416; 809536; 730091; 585279;584968;2498195;2833325;2498604;2498317;2498299;2493414; 2498586; 2498585; 2498576; 2497749; 2493446; 2493445; 1513216 ; 729944; 2498099;548449;465054;465053;465052;548671;548670;548660;548658; 548657;2832430;232084;2500822;2498118;2498119;2498119;2498118; 30 1708296;1708793;416607;416608;416608;416607;2499791;2498580;2498579; 2498578;2498577;2497750;1705483;1703445;1709542;1709545;1710589; WO 2008/145998 PCT/GB2008/001827 69 1352699;1346568; 1346323; 1346322; 2507248; 1352240; 1352239; 1352237; 1352229;1351935;1350779;1346806;1346804;1346803; 1170095;1168701; 1352506;1171011;1171008;1171005;1171004;1171002; 1171001;1168710; 1168709; 1168708;1168707;1168706;1168705;1168704; 1168703;1168702; 5 1168696; 1168391;1168390;1168348;1173075;1173074;1173071;1169290; 1168970;1168402;729764;729320;729979;729970;729315; 730050;730049; 730048;549194;549193;549192;549191;549190;549189;549188;549185; 549184;549183;549182;549181;549180;549179;464471;585290;416731; 1169666;113478;113479;113477;113476;113475;130975;119656;113562; io 113561;113560;416610;126387; 126386;126385;132270;416611;416612; 416612;416611;730035;127205;1352238;125887;549186;137395;730036; 133174;114090;131112;126949;129293;124757;129501;416636;2801531; 2796177;2796175;2677826;2735118;2735116;2735114;2735112;2735110; 2735108; 2735106 ; 2735104; 2735102 ;2735100 ; 2735098 ; 2735096 ; 2707295; 15 2154730;2154728; 1684720; 2580504;2465137; 2465135; 2465133; 2465131; 2465129;2465127;2564228;2564226;2564224;2564222;2564220;2051993; 1313972; 1313970; 1313968; 1313966; 2443824 ; 2488684; 2488683; 2488682; 2488681; 2488680; 2488679; 2488678; 2326190; 2464905; 2415702; 2415700; 2415698; 2398759; 2398757; 2353266 ; 2338288; 1167836; 414703 ; 2276458; 20 1684718 ; 2293571 ; 1580797; 1580794 ; 2245508 ; 2245060; 1261972; 2190552; 1881574 ; 511953 ; 1532058; 1532056; 1532054; 1359436; 666007; 487661; 217308;1731859;217306;217304;1545803;1514943;577696;516728;506858; 493634;493632;2154734;2154732;543659;1086046;1086045;2147643; 2147642;1086003;1086002;1086001;543675;543623;543509;543491;1364099; 25 2147108;2147107;1364001;1085628;631913;631912;631911;2147092;477301; 543482;345521;542131;542130;542129;100636;2146809;480443;2114497; 2144915;72355;71728;319828;1082946;1082945;1082944;539716;539715; 423193;423192;423191;423190;1079187;627190;627189;627188;627187; 482382;1362656;627186;627185;627182;482381;85299;85298;2133756; 30 2133755;1079186;627181;321044;321043;112559;112558;1362590;2133564; 1085122;1078971;627144;627143;627142;627141;280576;102835;102834; WO 2008/145998 PCT/GB2008/001827 70 102833;102832;84703;84702;84700;84699;84698;84696;477888;477505; 102575;102572;478272;2130094;629813;629812;542172;542168;542167; 481432;320620;280414;626029;542132;320615;320614;100638;100637; 100635;82449;320611;320610;280409;320607;320606;539051;539050; 5 539049;539048;322803;280407;100501;100498;100497;100496;1362137; 1362136;1362135;1362134;1362133;1362132;1362131;1362130;1362129; 1362128;100478;2129891;1076531;1362049;1076486;2129817;2129816; 2129815;2129814;2129813;2129812;2129805;2129804;2129802;2129801; 2129800;2129799;479902;479901;2129477;1076247;629480;1076242; 10 1076241;541803;541802;280372;280371;1361968;1361967;1361966;1361965; 1361964;1361963;1361962;1361961;1361960;1361959;320546;2119763; 543622;541804;478825;478824;478823;421788;320545;81444;626037; 626028;539056;483123;481398;481397;100733;100732;100639;625532; 1083651;322674;322673;81719;81718;2118430;2118429;2118428;2118427; 15 419801;419800;419799;419798;282991;100691;322995;322994;101824; 626077; 414553 ; 398830; 1311457; 1916292; 1911819; 1911818; 1911659; 1911582; 467629; 467627; 467619 ; 467617 ; 915347; 1871507; 1322185; 1322183; 897645 ; 897647; 1850544; 1850542; 1850540; 288917; 452742; 1842045 ; 1839305;1836011;1836010;1829900;1829899;1829898;1829897;1829896; 20 1829895;1829894; 1825459; 1808987; 159653 ; 1773369; 1769849; 1769847; 608690; 1040877; 1040875;1438761;1311513;1311512;1311511;1311510; 1311509;1311689;1246120;1246119;1246118;1246117;1246116;1478293; 1478292;1311642;1174278;1174276;1086972;1086974;1086976;1086978; 1086978;1086976;1086974;1086972;999009;999356;999355;994866;994865; 25 913758;913757;913756;913285;913283;926885;807138;632782;601807; 546852;633938;544619;544618;453094;451275;451274;407610;407609; 404371;409328;299551;299550;264742;261407;255657;250902;250525; 1613674;1613673;1613672;1613671;1613670;1613304;1613303;1613302; 1613240;1613239;1613238;1612181;1612180;1612179;1612178;1612177; 30 1612176;1612175;1612174;1612173;1612172;1612171;1612170;1612169; 1612168;1612167;1612166;1612165;1612164;1612163;1612162;1612161; WO 2008/145998 PCT/GB2008/001827 71 1612160; 1612159; 1612158; 1612157; 1612156; 1612155; 1612154; 1612153; 1612152; 1612151; 1612150; 1612149; 1612148; 1612147; 1612146; 1612145; 1612144;1612143;1612142;1612141;1612140;1612139;1093120;447712; 447711; 447710; 1587177; 158542; 1582223; 1582222; 1531589 ; 1580792 ; 5 886215; 1545897; 1545895; 1545893; 1545891; 1545889; 1545887; 1545885; 1545883; 1545881; 1545879; 1545877; 1545875; 166486 ; 1498496 ; 1460058; 972513; 1009442 ; 1009440 ; 1009438 ; 1009436 ; 1009434 ; 7413 ; 1421808 ; 551228; 452606 ; 32905; 1377859 ; 1364213; 1364212; 395407; 22690; 22688; 22686; 22684 ; 488605 ; 17680 ; 1052817 ; 1008445 ; 1008443 ; 992612; 706811 10 886683; 747852 ; 939932 ; 19003 ; 1247377 ; 1247375; 1247373; 862307 ; 312284; 999462; 999460 ; 999458 ; 587450 ; 763064 ; 886209 ; 1176397 ; 1173557 ; 902012; 997915; 997914; 997913; 997912; 997911; 997910; 99790; 997908; 997907;997906;997905;997904;997903;997902;997901;997900;997899; 997898;997897;997896;997895;997894;997893;997892;910984;910983; 15 910982; 910981; 511604; 169631; 169629; 169627; 168316; 168314 ;607633; 555616; 293902 ; 485371 ;455288; 166447; 166445 ;166443; 166435 ;162551; 160780; 552080; 156719; 156715 ;515957 ;515956 ;515955 ;515954 ;515953 459163; 166953 ; 386678; 169865. 20 Delivery methods Once formulated the compositions of the invention can be delivered to a subject in vivo using a variety of known routes and techniques. For example, a composition can be provided as an injectable solution, suspension or emulsion and administered via parenteral, subcutaneous, epidermal, intraderrnal, intramuscular, 25 intraarterial, intraperitoneal, intravenous injection using a conventional needle and syringe, or using a liquid jet injection system. Compositions can also be administered topically to skin or mucosal tissue, such as nasally, intratracheally, intestinal, rectally or vaginally, or provided as a finely divided spray suitable for respiratory or pulmonary administration. Other modes of administration include oral 30 administration, suppositories, sublingual administration, and active or passive transdermal delivery techniques.

WO 2008/145998 PCT/GB2008/001827 72 Where a peptide of the invention is to be administered, it is preferred to administer the peptide to a site in the body where it will have the ability to contact suitable antigen presenting cells, and where it, or they, will have the opportunity to contact T cells of the individual. Where an APC is to be administered, it is preferred 5 to administer the APC to a site in the body where it will have the ability to contact, and activate, suitable T cells of the individual. Delivery regimes Administration of the peptides/polynucleotides/cells (such as the composition 10 containing a plurality of peptides) may be by any suitable method as described above. Suitable amounts of the peptide may be determined empirically, but typically are in the range given below. A single administration of each peptide may be sufficient to have a beneficial effect for the patient, but it will be appreciated that it may be beneficial if the peptide is administered more than once, in which case typical 15 administration regimes may be, for example, once or twice a week for 2-4 weeks every 6 months, or once a day for a week every four to six months. As will be appreciated, each peptide or polynucleotide, or combination of peptides andlor polynucleotides may be administered to a patient singly or in combination. Dosages for administration will depend upon a number of factors including 20 the nature of the composition, the route of administration and the schedule and timing of the administration regime. Suitable doses of a molecule or a combination of molecules of the invention may be in the order of upto 10 Rg, up to 15ug, up to 20g, up to 25 jg, up to 30pg, up to 35ig, up to 50jig, up to 100jig, up to 500 p1g or more per administration. Suitable doses may be less than 15ig, but at least Ing, or at 25 least 2ng, or at least 5ng, or at least 50ng, or least 1Ong, or at least 500ng, or at least Ijig, or at least 1Opg. For some molecules or combinations of the invention, the dose used may be higher, for example, up to I mg, up to 2 mg, up to 3 mg, up to 4 mg, up to 5 mg or higher. Such doses may be provided in a liquid formulation, at a concentration suitable to allow an appropriate volume for administration by the 30 selected route. It will be understood that the above doses refer to total dose in the case of a combination of molecules. For example, "up to 35pg" refers to a total WO 2008/145998 PCT/GB2008/001827 73 peptide concentration of up to 35pg in a composition comprising a combination of more than one peptide. Kits 5 The invention also relates to a combination of components described herein suitable for use in a treatment of the invention which are packaged in the form of a kit in a container. Such kits may comprise a series of components to allow for a treatment of the invention. For example, a kit may comprise four or more different peptides, polynucleotides and/or cells of the invention, or four or more peptides, 10 polynucleotides or cells of the invention and one or more additional therapeutic agents suitable for simultaneous administration, or for sequential or separate administration. The kit may optionally contain other suitable reagent(s) or instructions and the like. 15 The invention is illustrated by the following Examples. Example 1: Screening of peptide mixtures for MIHC binding characteristics Binding-assas 20 Peptides The following peptides that encompass the sequences of Fel dl were investigated for their capacity to bind the nine HLA-DR molecules: DRI, DR3, DR4, DR7, DRI 1, DRI3, DRI5, B4 and B5. 25 SEQ ID NO: MLA1 H 2 N EICPAVKRDVDLFLTGT COOHIDerived from Fel dl chain 1 1 MLA2 H 2 N LFLTGTPDEYVEQVAQY COOHIDerived from Fel dl chain 1 8 MLA3 H 2 N EQVAQYKALPVVLENA COOH Derived from Fel dl chain 1 2 MLA4 H 2 N KALPVVLENARILKNCV COOH Derived from Fel dl chain 1 3 MLA5 H 2 N RILKNCVDAKMTEEDKE COOH Derived from Fel dl chain 1 4 MLA6 H 2 N TEEDKENALSLLDK COOH Derived from Fel dl chain 1 9 jMLA7 H 2 N IKENALSVLDKIYTSPL COOH Derived from Fel dl chain 1 5 MLA8* H 2 N| VKAE TCPIFYDVFFA COOH Derived from Fel dl chain 2 13 IMLA9* H2N [CPIFYDVFFAVANGNEL COOH Derived from Fel dl chain 2 14 MLAIO* H 2 N GNELLLKLSLTKVNAT COOH Derived frorn Fel d1 chain 2 15 WO 2008/145998 PCT/GB2008/001827 74 MLA11 H 2 N LTKVNATEPERTAMKK COOH Derived from Fel dl chain 2 10 MLA12 H 2 N TAMKKIQDCYVENGLI COOH Derived from Fel dl chain 2 6 MLA13* H 2 N CYVENGLISRVLDGLV COOH Derived from Fel dl chain 2 16 MLA14 H 2 N SRVLDGLVMTTTSSSK COOH Derived from Fel dl chain 2 7 2NISSSKDCMGEAVQNTV COOH Derived from Fel dl chain 2 11 MLA16 H 2 N AVQNTVEDLKLNTLGR COOH Derived from Fel d1 chain 2 12 *Peptides shown in italics were assessed for binding but not considered further in these experiments due to relatively poor solubility. 5 Binding conditions jbr MHC binding assays EBV homozygous cell lines were used as sources of human HLA class II molecules (Tab. 4). HLA-DR molecules were purified by affinity chromatography using the monomorphic Mab L243 (ATCC, Rockville, USA) coupled to protein A sepharose CL 4B gel (Pharmacia, France). Briefly, cells were lysed on ice at 5x108 cells/ml in 1o 150 mM NaCl, 10 mM Tris HCl pH==:8.3 buffer containing 1% Nonidet P40 (NP40), 10 mg/I aprotinin, 5 mM EDTA and 10 mM PMSF. After centrifugation at 100 000 g for I h, the supernatant was applied to a sepharose 4B and protein A-sepharose 4B columns and then to the specific affinity column. HLA-DR, molecules were eluted with 1.1 mM n-dodecyl b-D-maltoside (DM), 500 mM NaCl and 500 mM Na2CO3 15 pH=1 1.5. Fractions were immediately neutralized to pH=::7 with 2 M Tris HCI pH=:6.8 buffer and extensively dialysed against 1 mM DM, 150 mM NaCl, 10 mM phosphate pH=:7 buffer. For HLA-DR molecules beyond lot number 40 the 1 mM DM in dialysis buffer was replaced by 1 mM NOGP. 20 HLA-DR molecules were diluted in 10 mM phosphate, 150 mM NaCl, 1 mM DM, 10 mM citrate, 0.003% thimerosal buffer with an appropriate biotinylated peptide and serial dilutions of competitor peptides. Binding conditions of each molecule are detailed in Tab 4. Samples (100 pl per well) were incubated in 96-wells polypropylene plates (Nunc, Denmark) at 37*C for 24 h to 72 h. After neutralization 25 with 50 pl of 450 mM Tris HCI pH=7.5, 0.003% thimerosal, 0.3% BSA, 1 mM DM buffer, samples were applied to 96-well maxisorp ELISA plates (Nunc, Denmark) previously coated with 10 mg/ml L243 Mab and saturated with 100 mM Tris HCI pH=7.5, 0.3% BSA, 0.003% thimerosal buffer. They were allowed to bind to the WO 2008/145998 PCT/GB2008/001827 75 antibody-coated plates for 2h at room temperature. Bound biotinylated peptide was detected by incubating streptavidine-alkaline phosphatase conjugate (Amersham, U.K.), and after washings, by adding 4-nethylumbelliferyl phosphate substrate (Sigma, France). Emitted fluorescence was measured at 450 nm upon excitation at 5 365 nm on a Wallac Victor2 1420 multilabel counter fluorimeter (Perkin Elmer). Maximal binding was determined by incubating the biotinylated peptide with the MHC Himolecule in the absence of competitor. Binding specificity was assessed by adding an excess of non biotinylated peptide. Background did not significantly differ from that obtained by incubating the biotinylated peptide without MHC H molecules. 10 Data were expressed as the peptide concentration that prevented binding of 50% of the labeled peptide (IC50). Binding ability was then evaluated relative to known strong binding control (reference) peptide. Suitable reference peptides for the HLA alleles tested in these experiments are: DRI (DRBI*0101 allele): HA 306-318 (PKYVKQNTLKLAT); DR3 (DRB1*0301 allele): MT216 15 (AKTIAYDEEARRGLE); DR4 (DRB1I*0401 allele): HA 306-318 (PKYVKQNTLKLAT); DR7 (DRB1*0701 allele): YKL (AAYAAAKAAALAA); DRB1*1101: HA 306-318 (PKYVKQNTLKLAT); DR13 (DRB1*1301 allele): BI 21-36 (TERVRLVTRHIYNREE); DR15 (DRBI*1501 allele): A3 152-166 (EAEQLRRAYLDGTGVE); DRB4 (DRB4*0101 allele): E2/E7 20 (AGDLLAIETDKATI); and DRB5 (DRB5*0101 allele): HA 306-318 (PKYVKQNTLKLAT). Results Binding and non-binding peptides were first discriminated on the basis of an upper 25 1000 nM threshold as it is generally described in the literature (Southwood et al (1998). J Immunol 160:3363; Geluk et al (1998) Proc Natl Acad Sci U S A 95:10797), but are additionally assessed by comparison to reference peptides. The reference peptides are selected from among the best binding peptides of each given HLA molecule. Relative to the reference peptides, a peptide is a weak binder for a 30 given HLA molecule if it has an IC50 more than 100 fold lower than the reference peptide for the given HLA molecule. A peptide is a moderate binder is it has an IC50 WO 2008/145998 PCT/GB2008/001827 76 more than 20 fold lower but less than a 100 fold lower than the reference peptide for the given HLA molecule. A peptide is a strong binder if it has an IC50 less than 20 fold lower than the reference peptide for the given HLA molecule. 5 Analysis ofpreferredpeptide mixtures The nine HLA alleles used for these experiments encompass a high proportion of the Caucasian population. (Reference frequencies of HLA alleles in the population are provided in Table 3 of Example 2). Accordingly, combinations of peptides were evaluated to determine which would give the broadest coverage of different HLA 10 molecules. The target criteria for a mixture was therefore defined as follows: For a given HLA molecule, a mixture must comprise either 2 strong binding peptides and I moderate binding peptide, or I strong binding peptide and 3 moderate binding peptides. Preferred mixtures achieve these criteria for all nine tested HLA types. Only the peptides with sequences corresponding to SEQ ID NOS: I to 12 were 15 considered in this analysis as peptides with sequences corresponding to SEQ ID NOS: 13 to 16 were found to be poorly soluble. From SEQ ID NOS: I to 12 there are over 3000 possible combinations of peptides which could potentially fulfill the target criteria set out above. To enable visualization of these combinations, a binary scoring system was applied 20 such that for each HLA type, where a combination of peptides achieves one of the above criteria a score of "1" was entered and where the criteria were not met a score of "0" is entered. The scores across all HLA types are then added up, such that a mixture which fulfills the criteria for none of the HLA types will score 0, whereas a mixture which fulfills the criteria for all nine ILA types scores 9. The scores for 25 each peptide combination are plotted in Figure 1 A to Q. The highest score of nine was achieved by the 10 mixtures shown below: Figure A point 16 MLA 01, 02, 03, 04, 05, 12, 14 Figure B point 272 MLA 01, 03, 04, 05, 07, 12, 14 Figure C point 472 MLA 02, 03, 04, 05, 06,12,14 Figure C point 482 MLA 02, 03, 04, 05, 07, 12,14 Figure C point 488 MLA 02, 03, 04, 05,11, 12,14 Figure C point 494 MLA 02, 03, 04, 05,12,14,15 WO 2008/145998 PCT/GB2008/001827 77 Figure C point 495 MLA 02, 03, 04, 05,12,14, 16 Figure D point 699 MLA 03, 04, 05, 07, 12, 14, 15 Figure D point 700 MLA 03, 04, 05, 07, 12, 14, 16 Figure G point 1271 MLA 02, 03, 04, 05, 12, 14 Thus theses mixtures are preferred combinations of peptides for use in vaccination. Example 2: Cross-sectional screening of cat allergic subjects for T cell responses 5 and basophil histamine release by Fel d 1-derived, MHC characterised T cell peptide epitopes. L Introduction 11 Histamine release assay 10 The purpose of this assay was to identify individual peptides that are capable of activating blood basophils (as a surrogate for tissue mast cells) resulting in histamine release that may result in allergic reactions during therapy. Peptides or combinations of peptides that induce histamine release frequently may be considered unsuitable for inclusion in the peptide vaccine. 15 Histamine release requires the crosslinking of adjacent specific IgE molecules on the surface of the basophil. The peptides being evaluated were small (13 to 17 amino acids in length) and should not, therefore, possess significant tertiary structure that would enable them to retain the conformation of an IgE-binding epitope of the whole molecule. Furthermore, peptide monomers in solution, even if they are bound 20 by IgE, should not be able to crosslink adjacent IgE molecules. It should be noted however, that some of the peptides contain cysteine residues that may result in disulphide bond formation between single peptides and also between different peptides in a mixture. Thus, diners of peptides may be generated that may have IgE crosslinking potential In the present analysis, no excipients were used in peptide 25 formulation to prevent or reduce dimer formation through disulphide linkage. Histamine release from fresh peripheral whole blood from cat allergic subjects was evaluated. Peripheral blood basophils were used as a surrogate for tissue mast cells which were not practical to assay. Blood was incubated in vitro with WO 2008/145998 PCT/GB2008/001827 78 9 individual peptides from the sequence of the major cat allergen Fel d I (MLA01, 03, 04, 05, 07, 12, 14, 15 and 16). These peptides were selected as potential T cell epitopes following peptide-MHC binding assays as explained in Example 1. Additionally, responses to a preferred mixtures of a mixture of 7 peptides identified 5 in Example I were analysed. The tested preferred mixture of 7 peptides consisted of peptides MLA01, 03, 04, 05, 07, 12, 14 (SEQ ID NOS: I to 7). Histamine release in response to whole cat dander allergen extract acted as a positive control. 12 Proliferation Assay 10 The purpose of the proliferation assay was to determine the percentage of the population that responded to each individual peptidelback-up peptide and the preferred mixture of 7 peptides. 1.3 Cytokine Assays 15 The purpose of the cytokine assays was two-fold; (1) to determine the percentage of the population that responded to each individual peptide and the preferred mixture of 7 peptides, and (2) to identify individual peptides possessing intrinsic Th2 (IL-13)-inducing characteristics which would be undesirable in a peptide vaccine for allergic disease, and also to identify individual peptides 20 possessing intrinsic IL-10-inducing characteristics which may be beneficial for a peptide vaccine for allergic disease. 2. Materials and Methods 2.1 Isolation of Peripheral Blood Mononuclear Cells 25 Peripheral blood mononuclear cells (PBMC) were isolated from the heparinised blood sample obtained from the subject. PBMC's were isolated by Ficoll-Hypaque density gradient separation. Once isolated, the cells were used in the cell proliferation assay, histamine release and ELISA assay and the cytokine release assay. 30 2.2 Histamine Release Assay and Histamine ELISA Assays were performed on PBMC (which contain basophils). Each peptide WO 2008/145998 PCT/GB2008/001827 79 and combinations of peptides was compared with whole allergen molecules in a histamine release assay. Histamine concentrations were measured by ELISA. The assay required 3x10 6 PBMC's per subject. The assay was performed using the Immunotech Histamine Release Immunoassay kit according to the 5 manufacturer's instructions. Following the histamine release assay, acylated samples were tested by histamine ELISA. The histamine ELISA used 50P 1 l of the 100pl1 acylated sample generated by the histamine release assay. The remaining 50p.l of sample was retained, by freezing at -20*C until the data analysis section of the ELISA has been completed. Once the results had been analysed and the ELISA 10 performed in a satisfactory manner, the samples were discarded. Peptides were assayed for their ability to induce histamine release over a 5 logo range (10tg/ml to Ing/ml). The concentration range assayed was selected based on theoretical in vivo doses of peptide that may be achieved during therapy. For example, a 10pg dose of peptide entering a blood volume of 5 litres, would result in a 15 blood concentration of 2ng/ml (2x10~ 6 mg/ml), at the lower end of the histamine release assay dose range. Whole cat dander extract (C.B.F. LETI) was used as a positive control for release over a slightly higher concentration range (I OIg to lOng/mi). Single measurements (i.e. not duplicate or triplicate) were performed for each dilution. One duplicate blood sample was assayed for spontaneous histamine 20 release and the mean value of these samples was subtracted from all peptide/allergen results. After completion of the histamine ELISA, individual histamine levels were determined by interpolation for the standard curve generated in the ELISA assay. Results from samples were adjusted to allow for any dilution of the samples. Where 25 two or more dilutions of a peptide/allergen preparation elicited 10% or more histamine release above background, or where a single value of 10% or more above background was achieved at the highest concentration tested, this was considered a "positive histamine release". 30 2.3 Cell Proliferation Assay The cell proliferation assay was performed on PBMC's (140x10 6 cells WO 2008/145998 PCT/GB2008/001827 80 required for all parameters to be tested). Proliferation was measured by the incorporation of the radiolabelled compound 3 H-thymidine. In more detail, I 00ptl of the appropriate antigen or peptide concentration was distributed into the appropriate wells of 96 well plates. The plates were then placed 5 into a humidified 5% CO 2 incubator set at 37 0 C for a maximum of 4 hours. PBMC's isolated as described above were prepared to a concentration of 2x1 06 cells/mI in complete medium at room temperature. I 00pl of cell solution was then distributed into each of the wells of the 96 well plates containing antigen/peptide. The plates were then incubated for 6 to 8 days. The cultures were pulsed with tritiated 10 thymidine solution by adding I Oil of tritiated thymidine stock solution (1.85MBq/ml in serum-free RPMI medium) to each well. The plates were then returned to the incubator for between 8 and 16 hours. Cultures were then harvested using a Canberra Packard FilterMate 196 cell harvester. Dried filter mats were counted using an appropriate beta scintillation counter. 15 Counts from wells containing peptide were compared statistically to wells containing media alone (12 wells per group). The non-parametric Mann-Whitney test was used. The same statistical test was used for all subjects. A statistically significant difference between media only wells and peptide-stimulated wells was considered a positive stimulation of PBMC's by the peptide. 20 2.4 Cytokine release assay Cytokine secretion profiles from PBMC's was analysed in response to the peptide stimulation. Supernatants from the cytokine release assay were tested for the presence of 3 cytokines, IFN,-y IL-10 and IL-13, using ELISA assays. 25 The cytokine release assay required 40x 106 PBMC's per subject. In more detail, 250pl of a 200pg/ml solution of the appropriate antigen or peptide concentration was distributed into the appropriate wells of 48 well plates. Plates were the incubated in a humidified 5% CO 2 incubator at 37*C for a maximum of 4 hours. 2 50pl of a 5x10 6 cell/ml PBMC suspension'was then added to each well and 30 the plates returned to the incubator for 5 days. Following stimulation, samples of culture supernatant were harvested into 3 WO 2008/145998 PCT/GB2008/001827 81 aliquots and frozen until the ELISA assays could be performed. One aliquot was tested for the presence of one cytokine (therefore all 3 aliquots were required to test for the 3 cytokines). The cytokine levels in the samples were determined by interpolation from standard curves also generated in the assay. 5 3. Results. Results Overview. 3.1 Histamine Release 10 Table 1 - Histamine Release Overview Subject Positive control Individual peptide Peptide mixture (release 10% above (release 10% above (release 10% above baseline) baseline) baseline) 2 or more Highest 2 or more Highest 2 or more Highest dilutions conc dilutions conc dilutions conc only only only %age of 70.4 7.4 17.3 18.5 2.5 2.5 subjects showing release Total 77.8 30.9* 5 percentage showing histamine release per group * in some subjects some peptides caused release at 2 or more concentrations and others at the highest dose only. Thus the two numbers cannot simply be added as they are for cat dander extract and the peptide mixture. Similarly, values for individual WO 2008/145998 PCT/GB2008/001827 82 peptide release cannot be added to values for the mixture of peptides since 2 of the subjects with histamine release to the mixture also had release to individual peptides. Histamine release from peripheral blood basophils was observed in response 5 to both positive control and peptides. Table I shows the percentage of individuals in which histamine release (as defined by the acceptance criteria) occurred. Histamine release to one or more individual peptide occurred frequently but this rarely translated into histamine release from the mixture of 7 preferred peptides. However, a total of 5% of individuals displayed histamine release in response to the peptide 10 mixture. The details of dose and number of consecutive doses of peptide mixture that elicit release of histamine are relevant to the interpretation of these results and are discussed in more detail below. Table 2- Individual Peptide Histamine Release Overview MLA01 MLA03 MLA04 MLA05 MLA07 MLA12 MLA14 MLA15 MLA16 (Related (SEQ ID (SEQ ID (SEQ ID (SEQ ID (SEQ ID (SEQ ID to SEQ NO: 2) NO: 3) NO: 4) NO: 5) NO: 6) NO: 7) ID NO:1) 4 6 6 1 6 6 2 7 11 15 Table 2 shows the number of individuals in whom histamine release was detected in response to each individual peptide. MLA.15 and MLAI 6 most commonly released histamine. 3.2 Proliferation Assay Overview 20 Figure 3 summarises proliferative responses to peptides and antigens. The percentage of individuals mounting a detectable proliferative response is shown in the black bars. Grey (weak), white (moderate) and hashed (strong) bars provide a breakdown of the quality of these responses. Quality is arbitrarily defined by Stimulation Index (SI: ratio of counts in the presence of antigen/peptide divided by 25 counts in medium alone). Thus for peptide I (MLAO 1), 12% of subjects made a proliferative response and of these 92% were weak, none were moderate and 8% were high. Proliferative responses to individual peptides/antigens were variable WO 2008/145998 PCT/GB2008/001827 83 (black bar). 92% of subjects had positive proliferative responses to the positive control antigen PPD. The majority of these were strong responses (hashed bar). 75% of subjects responded to cat dander extract, with 59% of the responses (i.e. 59% of the 75%) being weak. The response to the mixture of 7 preferred peptides (SEQ ID 5 NOS: I TO 7) was almost identical to cat dander extract (CAT). Peptides MLA15 and MLA16 induced more frequent responses that four of the preferred peptides. However, MLA 15 and MLA 16 induced the most frequent basophil histamine release responses (see section 3.1). Few individual peptides induced strong proliferative responses as expected (low precursor frequency of peptide-specific precursor T 10 cells). 3.3 Cytokine Assay Overview Figure 4 summarises the percentage of individuals who mounted a detectable response to each of the peptides/antigens by production of the three cytokines 15 measured. The black bars represent production of IFN-7, the grey bars L-13 and the white bars IL-10. The positive control antigen PPD elicited a cytokine production in almost all individuals (IFN-y: 91%, IL-13: 97% and IL-10: 96%). Whole cat allergen and the mixture of 7 peptides elicited a cytokine response in approximately 80% or more of subjects. Individual peptides elicited responses of differing frequency. In 20 general cytokine production appeared to be a more sensitive method of detecting responses with larger percentages of individuals giving positive cytokine responses than proliferative responses. In most cases, IL-10 secretion was detected in the largest number of subjects and IFN-y detected least frequently. 25 3.4 Tissue Typing Table 3 DRB1 1 3 4 7 8 11 12 13 14 15 16 % 6.4 147 15.7 8.8 3.4 8.3 3.9 14.7 2.9 17.6 2.5 R e f e r e c e-9 . 1 - - - -- 1.1 1 . 1 3- --1-42 .- 1 2 3.-- - 20 3 6 Reference 9.4 11.1 12.8 13.2 3.7 13.4 12.3 10.2 3.2 10.7 3.6 WO 2008/145998 PCT/GB2008/001827 84 population Tissue typing was performed in order to ensure that the study population (predominantly Caucasian) was representative of the general Caucasian population in which the vaccine will be used. Eleven common DRB I allele families are shown. 5 Allele frequencies in 102 typed study subjects are shown, not the percentage of individuals expressing an allele, since each individual has two DRB I alleles and some individuals are homozygous for particular alleles. Reference population allele frequencies are also shown for comparison (Data from HLA Facts Book, Parham & Barber). Reference frequencies were obtained by analysis of multiple studies 10 reporting frequencies and the figures shown are mean values. All of the frequencies detected in the current analysis were within the ranges reported in the reference data. Therefore the population examined in the current study is representative of a Caucasian population.

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0 N-' Cl ~ '~ C C l~ r.OOd)~ Q2c i WO 2008/145998 PCT1/GB2008/001827 89 000 00~00, 00~ 0 z 7 ~~~~)~V - u_ ____ - 0 , w ci 0 0000 o o o m z -- --------- --- --- WO 2008/145998 PCT1/GB2008/001827 90 w w 00 '0 0)C) , z zz zz _____~~ZI __ _i Z 1 ZZ___ ZI Z Z~ __ ~~zlilz Z Z~z_ 0 ~~7. 'A1 -0 L~ .. . . .... . . . .. ... - - . .. . .. . -- - - - - - WO 2008/145998 PCT1/GB2008/001827 91 - ------ 00 r0 0 >ct 00 01 Cd~ 075 0 Ini 0o Ur WO 2008/145998 PCT/GB2008/001827 92 A total of 94 histamine release assays were completed during the study. Of these 13 assays were rejected, mainly due to unacceptably high levels of spontaneous release. Assays with spontaneous'histamine release of 20% or more of the total histamine release were rejected. Those assays with a spontaneous release of between 5 10% and 20% are indicated in Table 4. All other assays had spontaneous release values of less than 10%. Approximately 78% of the subjects assayed demonstrated positive histamine release to the sensitising allergen. Existing literature reports 10-20% of allergic individuals being resistant to allergen-induced basophil histamine release. 10 Histamine release was considered positive if (a) the highest concentration of peptide alone induced release of 10% or more of the total release value or (b) if two consecutive values were 10% or more of the total release. Approximately 31% (25/81) of subjects showed histamine release to one or more individual peptide. Of these, 6/81 (7.4%) had not positive control release to whole cat allergen extract. 15 In two individuals the mixture of 7 peptides also induced histamine release in addition to certain individual peptides. In two further individuals, only the mixture of 7 peptides induced release. Thus, 4/81 individuals (--5%) displayed histamine release with the mixture of peptides. Subject 044 showed release (28% of total release) at the highest concentration 20 (10ug/ml) of peptide only. Subject 055 showed release at 0. lug/ml (72% of total) and lug/ml (47% of total) only. Subject 056 showed release at 0.0lug/ml (11%), 0.1ug/ml (12%), 1.0ug/ml (17%) and 10ug/ml (10ug/ml). Subject 103 showed histamine release (33%) at the highest concentration (1 Oug/ml) of peptide only. 25 4.2 Proliferation Assay For the proliferation assay, individual proliferation data for all subjects and all peptide concentrations was analysed. Stimulation indices to each peptide/antigen were summarised for the entire population of 100 subjects. Complex antigens such as cat dander extract and PPD induce significant 30 proliferative responses in the population as a whole. The peptides that induce significant responses are those that elicit proliferative responses in a larger WO 2008/145998 PCT/GB2008/001827 93 percentage of the population. Stimulation indices of less than I arise when counts in wells containing peptides are lower than those containing culture medium alone. Such an effect may be attributable to slight changes in pH upon the addition of peptides which are 5 prepared in acid solution. The absence of a proliferative response to the peptide would then result in counts slightly lower than those in the medium alone wells. 4.3 Cytokine Release Assay Figures 4 to 6 show, for each peptide/antigen, the percentage of individuals 10 who made a response of any detectable magnitude (i.e. production of detectable IFN y, IL-13 or IL-10). The strength of those responses is then split into four levels of cytokine production. For example, 35% of the study population may have made an IFN-y response. Of that 35% of individuals, half (50%) made a very weak response, 20% a weak response, 15% a moderate response and 15% a strong response (giving a 15 total of 100% of the responders). The boundaries of each cytokine level were arbitrarily assigned based on the detection range of the ELISA assay. The boundaries are different between IFN-y/IL-10 and IL-13 since for IFN-y and IL-10 the detection range was approximately 1-I 00pg/ml whereas the range for the IL- 13 assay was approximately 0.5-50pg/ml. 20 4.3.1 Interferon-y production Figure 4 shows the percentage of individuals producing IFN-y and the strength of the response following cell culture with peptide/antigen. IFN-y responses were detected between 26-44% of subjects in response to individual peptides. These 25 responses were predominantly very low to low to moderate. Complex antigens induced more frequent responses (peptide mixture 80%, cat dander 79%, PPD 9 1%). These responses were low to moderate to high. PPD responses were particularly high (89 of PPD responses were above 100pg/ml). 30 4.3.2 IL-13 Production WO 2008/145998 PCT/GB2008/001827 94 Figure 5 demonstrates the percentage of individuals producing IL-13 and strength of the response following cell culture with peptide/antigen. IL-13 responses were detected in between 33-68% of subjects in response to individual peptides. These responses were predominantly very low to low, although a significant number 5 of moderate responses were detected. This may reflect the Th2 nature of allergic sensitisation in these subjects. Complex antigens induced more frequent responses (peptide mixture 85%, cat dander 93%, PPD 97%). These responses were low to moderate to high. 10 4.3.3 IL-J0 Production Figure 6 demonstrates the percentage of individuals producing IL-10 and strength of the response following cell culture with peptide/antigen. IL-10 responses were detected in between 46-75% of subjects in response to individual peptides. These responses were predominantly very low to low. Complex antigens induced 15 more frequent responses (peptide mixture 93%, cat dander 96%, PPD 96%). These responses were low to moderate. Very few "high" IL-10 responses were observed. 5. Discussion 5.1 Histamine Release Assay 20 In interpreting the histamine release results it is important to consider several points relating to the assay design: 1) The estimated blood dose of peptides that will be achieved during treatment lies towards the bottom of the dose response curve employed in the assay. For example, a I Oug dose of peptide entering a blood volume of 5 litres, would 25 result in a blood concentration of 2ng/ml (2x 1 0mg/ml; this assumes that no peptide is degraded which is unlikely). This concentration is just above the lower dose limit of the assay (Ing/ml). The 2 lowest concentrations of peptide used in the assay correspond approximately to injected doses of 5pig (lng/ml) and 50ig (1Ong/mi). Thus, the assay is designed to detect histamine release at 30 or above doses of peptide used for therapy. In only 3 instances was histamine release associated with the lowest two (consecutive values above 10%) WO 2008/145998 PCT/GB2008/001827 95 concentrations of peptide. In two of these cases values were less than 11%. The 7 peptide mixture did not show any release at the lowest 2 concentrations of peptide. Thus, although histamine release in response to individual peptides or the mixture was relatively common, it was generally not seen at 5 the concentrations of peptide that will be achieved during therapy. 2) For reasons of cost and complexity, only single wells were assayed for each concentration of peptide. This increases the risk that any one value may be spurious. This is particularly relevant to the second condition defined for a positive result; that the highest concentration alone of peptide/antigen shows 10 release of 10% or more of the total release. Several cases of histamine release to individual peptides were only associated with the single highest concentration of peptide and this was also true for 2/4 individuals with histamine release triggered by the mixture of 7 peptides. 3) In some cases, histamine release from peptides was not associated with 15 histamine release from cat dander extract (absence of positive control). 4) Peptides with cysteine residues (.MLAOI, MILAO4, MLA05, MLA12 and MLA 15) were previously shown to be capable of varying degrees of homo dimerisation. Although not formally quantified, these peptides when mixed are likely to also form hetero-dimers (i.e. within the SEQ ID NOS: I TO 7 20 mixture). Dimers may be sufficient to crosslink IgE molecules on the surface of mast cells and basophils giving rise to histamine release. No excipients to reduce disulphide bond formation between homologous or heterologous peptides were used in this study. Clinical preparations of the vaccine will contain thioglycerol to block disulphide bond formation. 25 Approximately 78% of the subjects assayed demonstrated positive histamine release to the sensitising allergen. This is slightly lower than reports in the literature which suggest that 10-20% of allergic individuals are resistant to allergen-induced basophil histamine release. 30 30.9% of subjects showed histamine release to one or more individual peptide. Histamine release was also detected in 5% of subjects (4/81) to the mixture WO 2008/145998 PCT/GB2008/001827 96 of 7 peptides (SEQ ID NOS: I TO 7; likely vaccine candidates). Two of these 4 individuals displayed release to individual peptides and 2 did not. In several subjects showing histamine release to individual peptides (6/81; 7.4%), release only occurred with peptide MLAI5 or MLA16, which are not included in the SEQ ID NOS: I TO 7 5 mixture. MLA16 was the peptide most frequently associated with histamine release. Adjusting values for individual peptide release to include only those peptides in the preferred 7 vaccine candidates, 23.5% of subjects displayed histamine release to individual components of the vaccine. 10 5.2 Proliferation Assay Proliferation of PBMC was assayed in response to culture with 3 concentrations of individual peptides, a mixture of 7 peptides (selected by MHC binding assays) and whole cat dander allergen extract. Responses to PPD at a single concentration were also measured as a marker of a positive recall response. 15 PPD responses: 92% of subjects mounted a detectable proliferative response to PPD. The response is largely dependent upon prior vaccination with BCG. Non responders may have originated from countries in which BCG is not mandatory (e.g. USA), or may not have received the immunisation for other reasons. The majority of responses (92%) resulted in an SI of greater than 10. These were arbitrarily assigned 20 as "strong" responses. Cat dander allergen extract responses: 75% of subjects mounted a detectable proliferative response to cat dander allergen extract. More frequent responses were detected through measurement of cytokines highlighting the importance of assaying multiple parameters of activation to determine reactivity. The majority of responses 25 were weak (SI 2-5; 59%) although significant numbers of moderate (SI 5-10; 24%) and strong (S1 10+; 17%) were observed. Peptide mixture (P1-7): 71% of subjects mounted a response to the peptide mixture, similar to cat dander allergen extract. A similar percentage of weak (52%), moderate (34%) and strong (14%) responses were observed. Proliferative responses 30 to cat dander allergen extract and peptide mixture correlated closely indicating that the majority of T cell reactivity to cat dander can be accounted for by the epitopes WO 2008/145998 PCT/GB2008/001827 97 contained within the peptide mixture. Individual peptide responses: Proliferative responses to individual peptides were generally weak to moderate. Most peptides generated 70-80% of their responses in the weak category with 20-30% in the moderate category. Few peptide elicited 5 strong responses. Weaker responses to individual peptides than to complex antigens or mixtures of peptides is an expected finding resulting from lower precursor frequencies of T cells specific for individual epitopes. The strongest proliferative responses to an individual peptide were to P12 from Fel d I chain 2 (43%) and the weakest to P4 from chain 1 (6%). However, 10 cytokine responses to all peptides were detected more frequently than proliferative responses. 5.3 Cytokine Assays Cytokine measurement proved to be the most sensitive method of measuring 15 responses to the peptides. Generally a higher percentage of subjects displayed measurable cytokine responses compared to measurable proliferative responses. Production of each of the three cytokines varied with IL- 10 generally being produced by a greater proportion of subjects than IL-13 and IFN-7. The lowest frequency of response was detected with IFN-7. The atopic allergic status of these subjects is likely 20 to mean that the memory T cell response to Fel d I and its epitopes will be dominated by Th2 responses which may account for the less frequent Th1 (IFN-y) response. The high frequency of IL- 10 responses was a surprise. IL- 10 is considered to be a Th2 cytokine in the murine system but this is not well established in the human system. IL- 10 is generally regarded as a regulatory/immunosuppressive cytokine. Previous 25 reports have suggested that some peptide sequences may have intrinsic IL-10 inducing properties. Such peptides were not observed in this study. The detection of such responses in other systems may simply reflect the nature of T cell priming to whole allergen which is recalled by culture of memory T cells with peptide. Thus, production of IL-10 may be a recall response rather than the result of intrinsic IL-10 30 inducing characteristics of the peptide. No single peptide induced the preferential production of a particular cytokine.

WO 2008/145998 PCT/GB2008/001827 98 Thus, none of the peptides screened induced a particularly unfavourable Th2 (IL- 13) response which would have been considered undesirable for inclusion in the peptide vaccine. 5 5.4 Tissue Typing Tissue typing results show that a representative population was assayed in this study. 6. Conclusion 10 6.1 Histamine Release Assay Individual peptides induced histamine release in some individuals. The mixture of preferred peptides SEQ ID NOS: I TO 7 induced histamine release in 4 individuals although in 2 of these the release was detected at a single point (highest concentration). MLA16 caused most frequent release but is absent from SEQ ID 15 NOS: I TO 7. Some positive release was observed with peptides in the absence of "positive control release" from whole cat dander. The assay was designed to detect histamine release at concentrations of peptide approximating to treatment doses and above. Histamine release at concentrations of peptide corresponding to treatment doses was extremely rare (only one clear example) and only occurred with individual 20 peptides, not with SEQ ID NOS: I TO 7. The results of the in vitro histamine release assay are likely to over-represent the histamine releasing potential of the vaccine since no steps were taken to minimise disulphide bond formation between peptides. Histamine was released by basophils from the majority of individuals in the 25 presence of whole cat dander extract. Histamine release occurred in a dose-dependent fashion in many subjects in contrast to release with peptides which frequently occurred at concentrations in the middle of the dose range. In individuals where histamine was released by peptides, sensitivity to cat dander extract was usually apparent at lower doses of extract. 30 6.2 Proliferation assay WO 2008/145998 PCT/GB2008/001827 99 Proliferative responses to peptides were weaker than to peptide mixtures or complex protein antigens as expected. Most individual peptide elicited proliferative responses in less than 20% of individuals. Considerable variation was seen between peptides but no single peptide failed to elicit proliferative responses in at least some 5 subjects, although one of the preferred 7 peptides MLA04 was poor at inducing proliferation. Peptides MLA15 and MLA16 were more potent in induction of proliferation than several of the preferred 7 peptides but gave the highest histamine release, 10 6.3 Cytokine assays Cytokine production was a more sensitive method than proliferation for detecting responses to peptides in this study. No evidence was obtained to support the idea that certain peptides may have an intrinsic ability to induce a particular pattern of cytokine production. No single peptide preferentially elicited a Thl, Th2 or 15 Treg (IL- 10) response. IFN-y responses tended to be less common than IL- 13 and IL 10. The cytokine assay data does not indicate that any of the preferred peptide mixture be substituted nor that any single peptide or the mixture will preferentially induce a Th2 response in vivo. 20 Example 3: Clinical trial of preferred combination A preferred mixture of 7 peptides consisting of peptides MLAO1, 03, 04, 05, 07, 12, 14 (SEQ ID NOS: I to 7) has been tested in a randomised, placebo-controlled, blind clinical trial. The efficacy of this mixture in reducing allergic symptoms was evaluated. The study design of the clinical trial was in accordance with good clinical 25 practice guidelines. Baseline skin responses to cat allergen for all subjects were established using a Baseline Challenge which took place between 6 and 8 days prior to study medication administration. Two intradermal injections of 0.010 HEP (histamine equivalent prick) units of commercially available standard cat allergen (supplied by 30 Laboratorios Leti, Spain) were administered, separated by a 30 minute time interval, into the volar surface of the left and right forearms respectively. Subjects were WO 2008/145998 PCT/GB2008/001827 100 assessed to ensure that they experience a Late-Phase Skin Response (LPSR) to whole cat allergen, and the magnitude of the baseline reaction was recorded as follows: Eight hours after each injection the outline of any late-phase response was drawn onto the skin with a ballpoint pen. The longest and orthogonal diameters were 5 measured and recorded for each response, and the area of the response in each arm was calculated. The average area of response in both arms of each subject was then calculated to provide the baseline reaction. Subjects who produced a suitable baseline reaction were assigned to dosing groups, randomised and entered into the Treatment Phase. 10 The Treatment Phase consisted of a period of 21 days for each subject. During this period one group of subjects received a single intradernal injection of either the preferred mixture (0.03, 0.3, 3, 12 nmol of each peptide per dose) or diluent placebo at Treatment Phase Visit I on day one. A cohort of 8 subjects received treatment at each dose level (6 received the preferred mixture and 2 15 placebo). The first cohort of the intradermal group received 0.03 nmol of each peptide in the mixture and each subsequent cohort in the group received the next higher dose level. Intradernal injections were made into the flexor surface of the left forearm. The total volume of the injection was 60 pL for all injections. After treatment, 20 subjects had their skin response to whole allergen retested at Treatment Phase Visit 2 on day 21 (1-3 days). Skin responses to cat allergen were assessed by measurement of the late-phase responses 8 hours following intradermal administration of 0.010 HEP (histamine equivalent prick) units of commercially available standard cat allergen (supplied by Laboratorios Leti, Spain) as described above. The average area of 25 response for both arms of each subject was then calculated as described above. This average LPSR area after treatment was then compared to the baseline LPSR area for each subject. The overall change in LPSR area for all eight patients in each cohort was then evaluated. The results of this analysis are shown in the table below. This analysis was performed without unblinding the data. 30 WO 2008/145998 PCT/GB2008/001827 101 DOSE (nmol) REDUCTION IN LPSR AREA I FOLLOWING TREATMENT 0.03 0.3 ++ 3.0 ++ 12.0 ++ Figure 8 is a representative plot showing the average LPSR area before and after treatment for all eight patients in the 12.0 nmol cohort. Taken together, these data indicate that the preferred mixture of peptides is effective at reducing the LPSR to 5 whole allergen in cat allergic individuals.

Claims (16)

1. A composition for use in preventing or treating allergy to cats by tolerisation comprising: 5 a) four or more polypeptides independently selected from any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12; and optionally b) one, two or three polypeptides having the following characteristics: (i) comprising sequence having at least 65% sequence identity to at least 9 or more contiguous amino acids in any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 10 8, 9, 10, 11 or 12 not selected in a); and (ii) 9 to 30 amino acids in length.

2. The composition according to claim 1, wherein the peptides selected in (a) comprise or consist of: 15 i) SEQ ID NOS: 1, 2, 3, 4, 5, 6 and 7; or ii) SEQ ID NOS: 2, 3, 4, 10, 6 and 7; or iii) SEQ ID NOS: 2, 3, 4, 5, 6, 7 and 11; or iv) SEQ ID NOS: 2, 3, 4, 5, 6, 7 and 12; or v) SEQ ID NOS: 8, 2, 3, 4, 6 and 7; 20 vi) as in (v) with one additional peptide selected from SEQ ID NOS: 1, 5, 9, 11 or 12; and optionally wherein the composition comprises no further peptides.

3. The composition according to any one of the preceding claims comprising 25 at least one polypeptide as defined in b), wherein said polypeptide is capable of causing T cell proliferation in at least 20% of samples of T cells, wherein each sample is obtained from different cat allergic individuals in the population.

4. The composition according to any one of the preceding claims comprising 30 at least one polypeptide as defined in b), wherein said polypeptide is capable of inducing a late phase response in a cat allergic individual and/or wherein the WO 2008/145998 PCT/GB2008/001827 103 composition is used to prevent or treat allergy to cats in an individual whose MHC alleles are unknown.

5. The composition according to any one of the preceding claims, wherein the 5 composition is capable of tolerising at least 50% or at least 60% of a panel of cat allergic individuals in the population.

6. The composition according to any one of the preceding claims, comprising at least one polypeptide as defined in b), wherein said polypeptide is 9 to 20 or 13 10 to 17 amino acids in length and/or wherein said polypeptide has at least 70% sequence identity to any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12.

7. The composition according to any one of the preceding claims wherein said polypeptide as defined in b) has at least 70%, 80%, 90%, 95% or 99% 15 sequence identity to at least one, two or more different sets of 9 contiguous amino acids in the amino acid sequence of any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12 not selected in a), wherein said 9 contiguous amino acids optionally comprise a T cell epitope. 20 8. The composition according to claim 9, wherein the one or more polypeptides in b) are selected from the amino acid sequence of any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12 not selected in a) and/or wherein the composition is used to treat an individual who has had an allergy to cats for at least one year. 25

9. The composition according to any one of the preceding claims, wherein one or more of the polypeptides in a) and/or b) have one or more modifications selected from the following: 30 (i) N terminal acetylation; (ii) C terminal amidation; WO 2008/145998 PCT/GB2008/001827 104 (iii) one or more hydrogen on the side chain amines of Arginine and/or Lysine replaced with a methylene group; (iv) glycosylation; and (v) phosphorylation. 5

10. The composition according to any one of the preceding claims wherein each polypeptide as defined in a) or b) of claim I has a concentration in the range of 0.03 to 200 nmol/ml, 0.3 to 200 nmol/ml or 10 to 50 nmol/ml. 10 11. A composition for use in preventing or treating allergy to cats by tolerisation comprising four or more different polynucleotide sequences which when expressed cause the production of a composition as defined in any one of claims I to 11.

12. The composition according to claim 11, wherein each polynucleotide 15 sequence capable of expressing a different polypeptide is present in the same or different polynucleotide vectors.

13. A vector for use in preventing or treating allergy to cats by tolerisation comprising four or more polynucleotide sequences which encode different 20 polypeptides as defined in claim I a) and optionally one or more polynucleotide sequences which encode different polypeptides as defined in claim 1b).

14. A vector for use in preventing or treating allergy to cats by tolerisation comprising different polynucleotide sequences, wherein each polynucleotide 25 sequence encodes one of the polypeptides as shown in the following combinations: i) SEQ ID NOS: 1, 2, 3, 4, 5, 6 and 7; or ii) SEQ ID NOS: 2, 3, 4, 10, 6 and 7; or iii) SEQ ID NOS: 2, 3, 4, 5, 6, 7 and 11; or iv) SEQ ID NOS: 2, 3, 4, 5, 6, 7 and 12; or 30 v) SEQ ID NOS: 8, 2, 3, 4, 6 and 7; vi) as in (v) with one additional peptide selected from SEQ ID NOS: 1, WO 2008/145998 PCT/GB2008/001827 105 5, 9, 11 or 12;

15. A compositon for use in preventing or treating allergy to cats by tolerisation containing three or more polypeptides independently selected from: 5 a) any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12; and b) any polypeptide having the following characteristics: (i) comprising sequence having at least 65% sequence identity to at least 9 or more contiguous amino acids in any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12 not selected in a); and 10 (ii) 9 to 30 amino acids in length. wherein the composition comprises either: (i) at least two peptides which exhibit strong binding and at least one peptide which exhibits moderate binding to each member of a panel of HLA molecules; or 15 (ii) at least one peptide which exhibits strong binding and at least two peptides which exhibit moderate binding to each member of said panel of HLA molecules; wherein the panel of HLA molecules comprises at least seven different HLA molecules encoded by different alleles which have a cumulative frequency in an 20 outbred human population of at least 80%; and/or (iii) wherein the composition is capable of inducing histamine release in a sample from a cat allergic individual at a level which is no higher than 5% above the histamine release induced in a sample from the same individual by whole Fel d I allergen; and/or 25 (iv) wherein the composition induces a cytokine release profile in a PBMC sample from a cat allergic individual which is equivalent to the cytokine release profile in a sample from the same individual induced by whole Fel d 1 allergen.

16. The composition according to claim 15 wherein the outbred human 30 population is Caucasian, and/or wherein the panel of HLA molecules comprises at least HLA-DR1, DR3, DR4, DR7, DR 11, DR13 and DR15; and optionally also WO 2008/145998 PCT/GB2008/001827 106 comprises HLA-DRB4 and DRB5.

17. A product for use in preventing or treating allergy to cats by tolerisation containing: 5 a) four or more polypeptides independently selected from any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12; and optionally b) one, two or three polypeptides having the following characteristics: (i) comprising sequence having at least 65% sequence identity to at least 9 or more contiguous amino acids in any of SEQ ID 10 NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12 not selected in a); and (ii) 9 to 30 amino acids in length. wherein each different polypeptide is for simultaneous, separate of sequential use in the prevention or treatment of allergy to cats in a human. 15 18. A product for use in preventing or treating allergy to cats by tolerisation containing: a) four or more polynucleotides capable of expressing a different polypeptide selected from SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12, and optionally 20 b) one, two or three polynucleotides capable of expressing different polypeptides having the following characteristics: (i) comprising sequence having at least 65% sequence identity to at least 9 or more contiguous amino acids in the amino acid sequence of any of SEQ ID NO: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12 25 not selected in a); and (ii) 9 to 30 amino acids in length, wherein each different polynucleotide is for simultaneous, separate or sequential use in the prevention or treatment of allergy to cats in a human. 30 19. A pharmaceutical formulation for use in preventing or treating allergy to cats by tolerisation comprising a composition according to any one of claims 1 to WO 2008/145998 PCT/GB2008/001827 107 12 or 15 to 16; a vector according to any one of claims 13 or 14; or a product according to any one of claims 17 or 18; and a pharmaceutically acceptable carrier or diluent. 5 20. The composition, vector or product according to claim 19, formulated for intradermal administration, oral administration, nasal administration, subbcutaneous administration, sublingual administration or for administration by inhalation or by injection. 10 21. The composition as defined in any one of claims I to 12 or 15 to 16, or product as defined in claim 17 or 18, additionally comprising a further polypeptide allergen for use in tolerising an individual to the further polypeptide allergen. 15 22. An in vitro method of determining whether an individual has or is at risk of a condition wherein the condition is characterized by allergic symptoms in response to a cat allergen, the method comprising testing whether the individual has T cells which respond to a composition as defined in any one of claims I to 12 or 15 to 16, thereby determining whether the individual has or is at risk of the. 20 condition.

23. A method according to claim 22 wherein a T-cell immune response to said composition is measured by contacting the composition with T cells in a sample taken from the subject, under conditions which allow the composition and 25 the T cells to interact; and determining whether or not any of the T cells are stimulated and thereby determining whether or not a T-cell immune response is present or absent.