[en] Abstract only

[en] The PSA2 work package (PSA2 WP) is a part of the Joined Programme Activity of the European Severe Accident Network (SARNET) related to level 2 PSA methodologies. The general objectives of this work package is to provide a comparison of the different methodologies used or under development for level 2 PSA application by the partners involved in the work package and to promote their harmonization. The PSA2 WP is organized into three main topics: methodologies in general, methodologies for uncertainties assessment, and dynamic reliability methods. The different tasks initially defined for these three topics are shortly described and the partners involved identified. Attention is then paid on the methodologies used so far by the different partners to assess the uncertainties in their level 2 PSA. A review of partners approaches to assess - as far as possible - the different sources of possible uncertainties is done for the different following topics: - uncertainties propagated from the level 1 PSA, - uncertainties (in sense of approximation) due to the binning of the level 1 sequences in Plant Damage, - uncertainties related to the structure of the Accident Progression Event Tree, - uncertainties related to the probabilities of stochastic events (system failure or recovery, human actions, some physical phenomena such as ignition of hydrogen combustion or triggering of steam explosion), - uncertainties elated to the modelling of the different physical phenomena, - uncertainties related to the cut-off frequency used in the probabilistic quantification of the Accident Progression Event Tree; - uncertainties related to the binning of level 2 sequences in Release Categories (variables not considered, values of eventual continuous variables). First conclusions of the comparison are given in terms of improvement needs and then of perspectives of the work for the following period of work. (authors)

[en] Three peptides, D1 (amino acid residues 175-201), D2 (a.a. 434-467), and TM (a.a. 1128-1159), corresponding to the spike protein (S) of severe acute respiratory syndrome corona virus (SARS CoV) were synthesized and their immunological functions were investigated in three different animals models (mice, guinea pigs, and rabbits). The peptides mixture formulated either with Freund's adjuvant or synthetic adjuvant Montanide ISA-51/oligodeoxy nucleotide CpG (ISA/CpG) could elicit antisera in immunized animals which were capable of inhibiting SARS/HIV pseudovirus entry into HepG2 cells. The neutralizing epitopes were identified using peptides to block the neutralizing effect of guinea pig antisera. The major neutralizing epitope was located on the D2 peptide, and the amino acid residue was fine mapped to 434-453. In BALB/c mice T-cell proliferation assay revealed that only D2 peptide contained T-cell epitope, the sequence of which corresponded to amino acid residue 434-448. The ISA/CpG formulation generated anti-D2 IgG titer comparable to those obtained from Freund's adjuvant formulation, but generated fewer antibodies against D1 or TM peptides. The highly immunogenic D2 peptide contains both neutralizing and Th cell epitopes. These results suggest that synthetic peptide D2 would be useful as a component of SARS vaccine candidates