Theory of single-charge exchange heavy-ion reactions

The theory of heavy-ion single-charge exchange reactions is reformulated. In momentum space, the reaction amplitude factorizes into a product of projectile and target transition form factors, folded with the nucleon-nucleon isovector interaction. The multipole structure of the transition form factors is studied in detail for Fermi-type non-spin-flip and Gamow-Teller-type spin-flip transitions, also serving to establish the connection to nuclear β decay. The reaction kernel is evaluated for central and rank-2 tensor interactions. Initial- and final-state ion-ion elastic interactions are accounted for by a distortion coefficient. Since the ion-ion interactions are dominated by the imaginary part of the optical potentials, the distortion coefficients can be evaluated in the strong absorption limit. For a Gaussian potential form factor, the distortion coefficient is evaluated in closed form, revealing the relation to the total reaction cross section. It is shown that at small momentum transfer distortion effects reduce to a simple scaling factor, allowing us to define a reduced forward-angle cross section which is given by nuclear matrix elements of β decay type. Thus we introduce new unit cross sections, as those traditionally used with light projectiles for spectroscopic purposes, for heavy-ion charge-exchange reactions. Results are discussed for τ ± excitations of 18 O and 40 Ca , respectively. Spectral distributions of nuclear-charge-changing transitions are obtained by self-consistent Hartree-Fock-Bogolubov (HFB) and quasiparticle random phase approximation (QRPA) theory and compared to spectroscopic data. The interplay of nuclear structure and reaction dynamics is illustrated for the single-charge exchange (SCE) reaction 18 O + 40 Ca → 18 F + 40 K at T lab = 270 MeV, by performing full-scale numerical calculations of the SCE cross section. We also show that the latter compare rather well with the results obtained within the strong absorption limit, thus confirming the possibility to factorize the forward-angle cross section into intrinsic nuclear transition dynamics and reaction dynamics.Programa Horizonte 2020 de la Unión Europea.654002Ministerio de Ciencia, Innovación y Universidades de España y Fondos FEDER. FIS2017- 88410-

Probing beta decay matrix elements through heavy ion charge exchange reactions

To access information on neutrinoless double beta decay (0νββ) nuclear matrix elements, it has been proposed by the NUMEN collaboration to exploit the analogies between double beta decay processes and double charge exchange (DCE) nuclear reactions, looking in particular at the conditions where the corresponding cross section can be factorized into nuclear reaction and nuclear structure terms. DCE reactions can be treated as a convolution of two correlated or uncorrelated single charge exchange (SCE) processes, resembling 0νββ and 2νββ, respectively. Thus it is important to model first SCE processes, to get a deeper insight into the possibility to factorize the corresponding cross section, so one can gain a better understanding of DCE cross section factorization. In this contribution, DCE reactions are discussed in terms of the convolution of two uncorrelated SCE processes, which should allow one to extract information on 2νββ nuclear matrix elements. These theoretical investigations are performed in close synergy with the experimental activity running at INFN-LNS within the NUMEN project

Serum amyloid A (SAA): a novel biomarker for uterine serous papillary cancer

BACKGROUND: Uterine serous papillary carcinoma (USPC) is a biologically aggressive variant of endometrial cancer. We investigated the expression of Serum Amyloid A (SAA) and evaluated its potential as a serum biomarker in USPC patients. METHODS: SAA gene and protein expression levels were evaluated in USPC and normal endometrial tissues (NEC) by real-time PCR, immunohistochemistry (IHC), flow cytometry and by a sensitive bead-based immunoassay. SAA concentration in 123 serum samples from 51 healthy women, 42 women with benign diseases, and 30 USPC patients were also studied. RESULTS: SAA gene expression levels were significantly higher in USPC when compared with NEC (mean copy number by RT\u2013PCR\ubc162 vs 2.21; P\ubc0.0002). IHC revealed diffuse cytoplasmic SAA protein staining in USPC tissues. High intracellular levels of SAA were identified in primary USPC cell lines evaluated by flow cytometry and SAA was found to be actively secreted in vitro. SAA concentrations (mgml 1) had a median (95% CIs) of 6.0 (4.0\u20138.9) in normal healthy females and 6.0 (4.2\u20138.1) in patients with benign disease (P\ubc0.92). In contrast, SAA values in the serum of USPC patients had a median (95% CI) of 15.6 (9.2\u201356.2), significantly higher than those in the healthy group (P\ubc0.0005) and benign group (P\ubc0.0006). Receiver operating characteristics (ROC) analysis of serum SAA to classify advanced- and early-stage USPC yielded an area under the ROC curve of 0.837 (P\ubc0.0024). CONCLUSION: SAA is not only a liver-secreted protein but is also a USPC cell product. SAA may represent a novel biomarker for USPC to assist in staging patients preoperatively, and to monitor early-disease recurrence and response to therapy

Self-adjuvanting polymer-peptide conjugates as therapeutic vaccine candidates against cervical cancer

Dendrimers are structurally well-defined, synthetic polymers with sizes and physicochemical properties often resembling those of biomacromolecules (e.g. proteins). As a result they are promising candidates for peptide-based vaccine delivery platforms. Herein, we established a synthetic pathway to conjugate a human papillomavirus (HPV) E7 protein-derived peptide antigen to a star-polymer to create a macromolecular vaccine candidate to treat HPV-related cancers. These conjugates were able to reduce tumor growth and eradicate E7-expressing TC-1 tumors in mice after a single immunization, without the help of any external adjuvant

A constrained analysis of the 40Ca(18O,18F)40K direct charge exchange reaction mechanism at 275 Mev

The40 Ca(18 O,18 F)40 K single charge exchange (SCE) reaction is explored at an incident energy of 275 MeV and analyzed consistently by collecting the elastic scattering and inelastic scattering data under the same experimental conditions. Full quantum-mechanical SCE calculations of the direct mechanism are performed by including microscopic nuclear structure inputs and adopting either a bare optical potential or a coupled channel equivalent polarization potential (CCEP) constrained by the elastic and inelastic data. The direct SCE mechanism describes the magnitude and shape of the angular distributions rather well, thus suggesting the suppression of sequential multi-nucleon transfer processes

Induction of tumour-specific CD8+ cytotoxic T lymphocytes by tumour lysate-pulsed autologous dendritic cells in patients with uterine serous papillary cancer

Uterine serous papillary carcinoma is a highly aggressive variant of endometrial cancer histologically similar to high grade ovarian cancer. Unlike ovarian cancer, however, it is a chemoresistant disease from onset, with responses to combined cisplatinum-based chemotherapy in the order of 20% and an extremely poor prognosis. In this study, we demonstrate that tumour lysate-pulsed autologous dendritic cells can elicit a specific CD8+ cytotoxic T lymphocyte response against autologous tumour target cells in three patients with uterine serous papillary cancer. CTL from patients 1 and 2 expressed strong cytolytic activity against autologous tumour cells, did not lyse autologous lymphoblasts or autologous EBV-transformed cell lines, and were variably cytotoxic against the NK-sensitive cell line K-562. Patient 3 CD8+ T cells expressed a modest but reproducible cytotoxicity against autologous tumour cells only at the time of the first priming. Further priming attempts with PBL collected from patient 3 after tumour progression in the lumboaortic lymph nodes were unsuccesful. Cytotoxicity against autologous tumour cells could be significantly inhibited by anti-HLA class I (W6/32) and anti-LFA-1 MAbs. Highly cytotoxic CD8+ T cells from patients 1 and 2 showed a heterogeneous CD56 expression while CD56 was not expressed by non-cytotoxic CD8+ T cells from patient 3. Using two colour flow cytometric analysis of intracellular cytokine expression at the single cell level, a striking dominance of IFN-γ expressors was detectable in CTL populations of patients 1 and 2 while in patient 3 a dominant population of CD8+ T cells expressing IL-4 and IL-10 was consistently detected. Taken together, these data demonstrate that tumour lysate-pulsed DC can be an effective tool in inducing uterine serous papillary cancer-specific CD8+ CTL able to kill autologous tumour cells in vitro. However, high levels of tumour specific tolerance in some patients may impose a significant barrier to therapeutic vaccination. These results may have important implications for the treatment in the adjuvant setting of uterine serous papillary cancer patients with active or adoptive immunotherapy

Recent results on Heavy-Ion induced reactions of interest for 0νββ decay

An updated overview of recent results on Heavy-Ion induced reactions of interest for neutrinoless double beta decay is reported in the framework of the NUMEN project. The NUMEN idea is to study heavy-ion induced Double Charge Exchange (DCE) reactions with the aim to get information on the nuclear matrix elements for neutrinoless double beta (0νββ) decay. Moreover, to infer the neutrino average masses from the possible measurement of the half- life of 0νββ decay, the knowledge of the nuclear matrix elements is a crucial aspec

Recent results on heavy-ion direct reactions of interest for 0νββ decay at INFN LNS

Neutrinoless double beta decay of nuclei, if observed, would have important implications on fundamental physics. In particular it would give access to the effective neutrino mass. In order to extract such information from 0νββ decay half-life measurements, the knowledge of the Nuclear Matrix Elements (NME) is of utmost importance. In this context the NUMEN and the NURE projects aim to extract information on the NME by measuring cross sections of Double Charge Exchange reactions in selected systems which are expected to spontaneously decay via 0νββ. In this work an overview of the experimental challenges that NUMEN is facing in order to perform the experiments with accelerated beams and the research and development activity for the planned upgrade of the INFN-LNS facilities is reported