T 0840/07 (Immunomodulatory peptide/CELLACT PHARMA) 14-09-2011

I. The appeal lies from the decision of the examining division to refuse European patent application 02777137.7, published as WO 03/025000. The decision is on the application as filed with amended claims 1-10 of a main and auxiliary request both filed with a letter of 27 October 2006.

Claim 1 of the main request read:

"1. An immunomodulatory peptide of up to 50 amino acid residues comprising a fragment of the amino acid sequence of HLA-(Human Leukocyte associated Antigen) class II alpha 2 chain, said peptide comprising or consisting of an amino acid sequence shown in SEQ ID NO:3 or SEQ ID NO:4, or a fragment of at least 6 consecutive amino acids thereof wherein said peptide is capable of inhibiting proliferation of peripheral

blood mononuclear cells (PBMCs)." (emphasis added by the board)

Claim 1 of the auxiliary request read:

"1. An immunomodulatory peptide of up to 50 amino acid residues comprising a fragment of the amino acid sequence of HLA-(Human Leukocyte associated Antigen) class II alpha 2 chain, said peptide comprising or consisting of (i) an amino acid sequence shown in SEQ ID NO:3 or SEQ ID NO:4; (ii) a fragment of at least 10 consecutive amino acids of(i), or (iii) an amino acid sequence of (i) or (ii) containing conservative amino acid substitutions, wherein said peptide is capable of inhibiting proliferation of peripheral blood

mononuclear cells (PBMCs)." (emphasis added by the board)

II. The examining division refused the application for the sole reason that the claims lacked unity within the meaning of Article 82 EPC for the following reasons:

Claim 1 of the request before the examining division, defined chemical alternatives, i.e. a so-called Markush grouping, and unity of invention should be considered to be present if the alternatives are of a similar nature.

The problem underlying the application resided in the provision of compounds for the inhibition of an immune response. As a solution, peptides derived from HLA-class II alpha 2 chain, up to 50 amino acids long, were provided. The technical feature which a priori could be considered to unify different solutions was thus a peptide derived from HLA-class II alpha 2 chain being up to 50 amino acids long.

However, such a solution had already been proposed in prior art document (D2), i.e. US 5,827,516, which disclosed a 23-mer peptide derived from the HLA-class II alpha 2 chain corresponding to amino acids 158-180 of SEQ ID NO:1 of the application. The peptide was useful for therapeutic intervention in disease conditions characterized by autoreactivity, such as rheumatoid arthritis or multiple sclerosis, and might also be used to reduce transplant rejection (see (D2) SEQ ID NO: 231, table 8 and column 2).

The objective problem to be solved was therefore the provision of further peptides derived from the HLA-class II alpha 2 chain that are up to 50 amino acids long. While peptides of SEQ ID NO:3 and 4 had a common activity or property, i.e. the inhibition of the proliferation of peripheral blood mononuclear cells and the inhibition of the proliferation of immune cells respectively, a significant structural element shared by both peptides, which could fulfil the role of a "special technical feature" in the sense of Rule 30(1) EPC 1973, was missing. There was no common amino acid sequence motif present in SEQ ID NO:3 and 4 that might be considered as a significant structural element that was shared by said peptide and that could link both peptides together. As there were no other special technical features, inventions (1) and (2), directed to peptides of SEQ ID NO:3 and SEQ ID NO:4 respectively, were not so linked as to form a single general inventive concept (Rule 30(2) EPC 1973). The examining division noted that an additional search on 30 October 2006 had revealed several documents that were "detrimental to the issue of novelty" and cited three specific documents. The examining division specified however that the application was not refused under Article 54(1) and (2) EPC vis-à-vis these documents, because the applicant had had no chance to comment on the objection.

The examining division was furthermore of the opinion that the applicant was given sufficient opportunity in writing and by telephone to file a request that met the requirements of the EPC and decided not to issue a further communication or to telephone the applicant again prior to the oral proceedings.

III. The appellant filed a new main request with the notice of appeal dated 16 February 2007 and two auxiliary requests with the statement of grounds of appeal dated 17 April 2007.

Claim 1 of the new main request read:

"1. Use of a peptide of up to 100 amino acid residues, wherein said peptide is capable of inhibiting proliferation of peripheral blood mononuclear cells (PBMCs), and having at least 6 consecutive amino acids of the amino acid sequence of HLA-(Human Leukocyte associated Antigen) class II alpha 2 chain, for the preparation of a pharmaceutical composition for inhibition of an immune response by interfering with the interaction of TIRC7 with its ligand." (emphasis added by the board)

IV. The board summoned the appellant for oral proceedings to take place on 14 September 2011.

V. Further arguments were filed by the appellant with a letter dated 30 May 2011. On 12 September the appellant informed the board that it would not attend the oral proceedings.

VI. The appellant (applicant) requested that the decision under appeal be set aside and a patent be granted on the basis of the main request filed with the notice of appeal dated 16 February 2007 or on the basis of the first or second auxiliary requests filed with the statement of grounds of appeal dated 17 April 2007. The appellant requested furthermore reimbursement of the appeal fee.

VII. The appellant's arguments as far as they are relevant for the present decision can be summarised as follows:

Unity of invention

The decision held erroneously that a technical feature in the sense of Article 82 and Rule 30(2) EPC 1973 had to be a "significant structural element" in the form of a common amino acid sequence motif. This was apparently also the reason for rejecting the auxiliary request, which had been filed with a letter of 4 September 2006 in response to the summons to attend oral proceedings and which was now the main request in the appeal proceedings (cf. result of consultation of 23 October 2006).

Document (D2) taught to solve the problem of inhibiting an undesired immune response by introducing into, or intracellularly expressing in, antigen presenting cells (APC) of a patient a sort of self-peptides, which were assumed to prevent association of the MHC class II alpha/beta chain complex. The blocking peptides of document (D2) therefore specifically blocked the binding of immunogenic peptides inside APCs by binding to the well defined peptide-binding pockets of the MHC class I or II molecules resulting in MHC molecule/blocking peptide complexes which were only subsequently expressed on the cell surface of APCs.

In contrast, the peptides of the invention were required to interact with TIRC7 in order to prevent its interaction with its natural ligand (see description e.g. page 3, line 27 to page 4, line 12). The peptides of the present invention and those disclosed in (D2) were directed towards different sites of pharmacological action.

The claims of the main request before the board now were "use" claims, contrary to the claims underlying the impugned decision. The purpose of the use of the peptides was now explicitly the "preparation of a pharmaceutical composition for inhibition of an immune response by interfering with the interaction of TIRC7 with its ligand"(emphasis added by the board). This feature was common to all peptides and specific sequences described in the claims.

Neither document (D2), nor any other cited prior art document, did indicate or suggest any interference between the peptides and TIRC7.

The novel and inventive feature of the present invention was the effect that the peptides were characterized by the functional feature of being capable of interfering with the interaction of TIRC7 with its ligand. This was now explicitly reflected in the claims and was thus to be considered to constitute the contribution of the claimed invention as a whole over the prior art. Consequently, it was not only novel and inventive over the prior art including document (D2) but also a "special technical feature" in the sense of Rule 30(1) EPC 1973, second sentence.

This special technical feature, i.e. the capability of interfering with the interaction of TIRC7 with its ligand, was also present if the peptides base amino acid sequence of HLA class II alpha 2 chain was further defined by reference to either of SEQ IDs NO: 3 and 4. Consequently, the requirements of Article 82 and Rule 30 EPC were fully met.

Reimbursement of the appeal fee

The reimbursement of the appeal fee pursuant to Rule 67 EPC 1973 (now Rule 103(1)(a) EPC) was equitable by reason of a substantial procedural violation.

The applicant had been adversely affected by the manner in which the examination proceedings had been conducted. Although the applicant made every effort to comply with each communication, the examining division "went on throwing spanner [sic] in the works" so that the application had to fail.

After the applicant had dealt with the unsubstantiated objections against the breadth of the claims in the second communication, the examining division took the applicant by surprise by summons to oral proceedings with an annexed communication introducing for the first time document (D2) as the justification for the oral proceedings and another "reason" for rejection of the application. The applicant filed two new sets of claims with its letter of 4 September 2006, asked for the examination to be continued in writing and for a telephone discussion of any minor issues, but requested oral proceedings in the examination division considered refusal of the application.

In the subsequent first telephone consultation on 23 October 2006, the applicant's representative explained that the summons to attend oral proceedings was premature and allowance should be made for the applicant's limited resources. No reason was given why the requests filed on 4 September 2006 were bad. The primary examiner refused to cancel the oral proceedings and to continue the proceedings in writing and gave the applicant until 27 October 2006 to file new sets of claims. The applicant's representative filed an amended second auxiliary request on 26 October 2006 and a further telephone consultation took place on 27 October 2006 in which he was told that this request was inadmissible and he was given a last chance to file amended claims by 16.00 hours on that date.

The present appeal proceedings would not have been necessary if only the examining division would have conformed to the usual practice in the EPO and discussed the substantive issues in a sensible or at least reasonable way. In any case, the unjustified summons to attend oral proceedings on the grounds of a newly-introduced document on which the applicant had not been given a previous opportunity to comment during the written proceedings alone amounted to a substantial procedural violation, not to mention the attitude of the primary examiner with respect to applicant's attempts to cancel the oral proceedings.

The examining division had deprived the applicant of fair and reasonable proceedings by its piecemeal delivery of objections and cited documents, culminating in the issue of the summons to attend oral proceedings for reason of a document, i.e. document D2, which had not been considered before and had not been cited in the search report. This amounted to a substantial procedural violation, in particular in view of the fact that the objections raised in the previous communications of the examining division had all been dealt with by the applicant.

Moreover, in response to the summons to attend oral proceedings, the examining division was respectfully requested to grant the applicant at least one further opportunity to continue the substantive examination in writing because of the newly cited document (D2). However, contrary to the well-established principle to provide an applicant sufficient opportunities to address the objections raised by the examining division for the first time, the examining division simply stated that it "does not want to cancel the oral proceedings and does not want to continue the procedure in writing" (result of telephone conversation of 23 October 2006).

As can be inferred from the subsequent result of consultation of 27 October 2006, the opportunity given by the examining division to the applicant to file a new set of claims on short notice only and of having a further telephone interview was not quite helpful and at last resulted in the contested decision.

VIII. Oral proceedings were held on 14 September 2011. The representative of the appellant had informed the board on 12 September 2011 that she would not attend the oral proceedings.