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Dive into the research topics where Laura Salvaneschi is active.

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Featured researches published by Laura Salvaneschi.


Hepatology | 1995

Differential distribution of hepatitis C virus genotypes in patients with and without liver function abnormalities

Enrico Maria Silini; Fulvia Bono; Agostino Cividini; Antonella Cerino; Savino Bruno; Sonia Rossi; Giovanni Belloni; Bruno Brugnetti; Emilio Civardi; Laura Salvaneschi; Mario U. Mondelli

Hepatitis C virus (HCV) infection persists for an indefinite length of time in a major proportion of patients, inducing chronic liver lesions that evolve to cirrhosis and hepatocellular carcinoma (HCC) in approximately 20% of cases. We studied HCV viremia and genotypes by reverse transcription–polymerase chain reaction (RT‐PCR) in 341 consecutive anti‐HCV–positive patients. Of these, 167 patients had persistently normal or near normal alanine aminotransferase (ALT) levels (fluctuations ≤5 IU above the upper limit of normal); the remaining 174 patients presented with elevated ALT and histological evidence of chronic liver disease. Seventy percent of patients with normal ALT values had circulating HCV RNA despite the absence of biochemical indicators of liver damage and mild histological forms of chronic hepatitis were detected in most patients who underwent liver biopsy. Isolated genotype III infection was significantly more prevalent in this patient group with respect to control patients with abnormal ALT values (70% vs. 39%; P < .001). Conversely, isolated genotype II was more frequently found in patients with elevated ALT values and evidence of chronic liver disease (45% vs. 23%; P < .01) and it was progressively more represented in advanced liver disease, such as cirrhosis and HCC. Virological features of HCV infection might be associated with different clinical manifestations, suggesting a potential prognostic significance on disease outcome. (HEPATOLOGY 1995;21:285–290.)


Transfusion | 2001

Extracorporeal photochemotherapy for treatment of acute and chronic GVHD in childhood.

Laura Salvaneschi; Cesare Perotti; Marco Zecca; Stefano Bernuzzi; Gianluca Viarengo; Giovanna Giorgiani; Claudia Del Fante; Paola Bergamaschi; Rita Maccario; Andrea Pession; Franco Locatelli

BACKGROUND: Extracorporeal photochemotherapy (EPC) has recently been proposed for the treatment of adults with either acute or chronic GVHD. However, data on children given this therapy are scarce. A Phase I‐II study was carried out on EPC in children experiencing GVHD after allogeneic transplantation of HPCs.


Journal of Hepatology | 1998

Association between HLA class II alleles and protection from or susceptibility to chronic hepatitis C

Claudio Zavaglia; Miryam Martinetti; Enrico Maria Silini; Riccardo Bottelli; Cristina Daielli; Margherita Asti; Aldo Airoldi; Laura Salvaneschi; Mario U. Mondelli; Gaetano Ideo

BACKGROUND/AIMS Recent studies have suggested that the course of chronic hepatitis C may be influenced by the immunogenetic background of the host. Specifically, HLA-DR11 (5) has been associated with less advanced hepatitis C virus (HCV)-related liver disease. The aim of the present study was to investigate whether HLA-DRB1*11 subtypes or HLA-DQA1 and DQB1 genes might be associated with protection from or susceptibility to chronic HCV infection, histological severity of HCV-induced liver disease and infecting HCV genotype. METHODS Ninety-nine unrelated outpatients with histologically documented chronic hepatitis C were studied and their allele frequencies were compared with those of 179 ethnically matched controls and with those of 41 HCV RNA-positive patients with persistently normal aminotransferase levels (HCV carriers). HLA-DQ types and HLA-DRB1*11 subtypes were determined by polymerase chain reaction gene amplification with sequence specific primers. RESULTS None of 10 DQA1 or 12 DQB1 alleles was significantly associated with susceptibility to or protection from chronic HCV infection or with histological staging or with HCV genotype. However, analysis of DQA1-DQB1 combinations showed that DQA1*0201-DQB1*0201 combination was significantly more frequent in patients compared to controls, both in cis (26.3% vs 16.2%, p = 0.04, odds ratio = 1.8, 95% confidence interval, 0.96-3.5) and in trans (12.1% vs. 1.1%, p = 0.0001, OR = 12.2, 95% CI, 2.6-113.7). HCV carriers did not differ from controls or from patients in the frequency of DQA1-DQB1 combinations. The extended haplotype DRB1*1104, DQA1*0501, DQB1*0301 was seen significantly less frequently in patients than in controls (8% vs 22.3%, p = 0.0025, OR = 0.31, 95% CI, 0.12-0.7) or HCV-RNA carriers (8% vs 26.8%, p = 0.003, OR = 0.24, 95% CI, 0.08-0.73). CONCLUSIONS Immunogenetic factors may play a role in determining both protection from and susceptibility to chronic hepatitis C, the trans-dimer DQA1*0201-DQB1*0201 predisposing to and the DRB1*1104, DQA1*0501, DQB1*0301 haplotype protecting from chronic hepatitis C.


Transfusion | 2010

Extracorporeal photochemotherapy in graft-versus-host disease: a longitudinal study on factors influencing the response and survival in pediatric patients.

Cesare Perotti; Claudia Del Fante; Carmine Tinelli; Gianluca Viarengo; Luigia Scudeller; Marco Zecca; Franco Locatelli; Laura Salvaneschi

BACKGROUND: Extracorporeal photochemotherapy (ECP) is a valid therapeutic option in the treatment of acute and chronic graft‐versus‐host disease (aGVHD and cGVHD, respectively). No standard clinical and laboratory criteria of response to ECP treatment are available at the moment.


British Journal of Haematology | 2002

An estimate of the current risk of transmitting blood‐borne infections through blood transfusion in Italy

Maria Elena Tosti; S. Solinas; Daniele Prati; Laura Salvaneschi; M. Manca; M. Francesconi; M. Ciuffreda; Gabriella Girelli; Alfonso Mele

Summary. We conducted a retrospective cohort study to estimate the incidence of major blood‐borne agents among Italian blood donors and calculated the risk of infection among blood recipients using the ‘incidence/window period model’. The study was conducted among 46 180 blood donors enrolled in six blood centres between 1994 and 1999. During follow‐up, seven new infections were confirmed: three donors seroconverted for anti‐human immunodeficiency virus (HIV); two for anti‐hepatitis C virus (HCV); and two showed hepatitis B surface antigen (HBsAg) reactivity; no cases of syphilis were observed. The incidence rates per 100 000 person/years were: 4·06 (95% CI: 0·82–11·85) for HIV; 2·41 (95% CI: 0·29–8·70) for HCV; and 2·70 (95% CI: 0·32–9·77) for HBsAg; the incidence for total hepatitis B virus (HBV) infection was 9·77 per 100 000 person/years (95% CI: 1·16–35·36). The estimated risk of an infectious blood unit not being detected was: 2·45 (95% CI: 0·13–12·33) per 1 million units for HIV; 4·35 (95% CI: 0·30–22·39) for HCV; and 15·78 (95% CI: 1·16–84·23) for HBV. Overall, an estimated 22·58 per 1 million units are infected. In Italy, the risk of transfusion‐transmitted infections is low and is similar to that in other western countries. The introduction of new more sensitive screening tests could reduce the residual risk of transfusion‐transmitted infection by 40–80%.


Genes and Immunity | 2001

Family study of non-responsiveness to hepatitis B vaccine confirms the importance of HLA class III C4A locus.

A De Silvestri; Annamaria Pasi; Miryam Martinetti; Cesare Belloni; Carmine Tinelli; Giorgio Rondini; Laura Salvaneschi; Mariaclara Cuccia

Non-responsiveness to hepatitis B virus (HBV) vaccine in adults is strongly associated with HLA-C4AQ0,DRB1*0301,DQB1*02 haplotype. This association was also demonstrated in neonates who failed to mount a humoral response to challenge with HBV vaccine. About 4% of vaccinated newborns do not reach a protective antibody level (⩾10 mIU/ml) at seroconversion and 0.4% is a non-responder even after receiving a fourth dose of vaccine (true non-responders (TNR)); while 3.6% achieved an antibody level ⩾10 mIU/ml (slow responders (SR)) only when reboostered with the fourth dose. In the present study we extend the vaccination and HLA typing to 91 family members of probands to understand better the possible parent-to-child transmission of this trait. A transmission disequilibrium test (TDT), performed in 27 families, showed that the C4AQ0 allele was almost always transmitted to probands, both TNRs and SRs. Although not statistically significant, the highest LOD score was obtained with C4A locus: 1.58. These results suggest the presence of a region regulating immune response against HBV vaccination near to or coincident with the C4A locus.


International Journal of Immunopathology and Pharmacology | 2006

Hierarchy of baby-linked immunogenetic risk factors in the vertical transmission of hepatitis C virus

Miryam Martinetti; Ilaria Pacati; Mariaclara Cuccia; C. Badulli; Annamaria Pasi; Laura Salvaneschi; E. Minola; A. De Silvestri; A. M. Iannone; Anna Maccabruni

Mother-to-infant transmission of Hepatitis C Virus (HCV) represents the major cause of pediatric HCV infection today. Immunogenetic influence has been poorly investigated and mainly confined to HLA-class II serological polymorphisms. Among 290 parities, 135 from Pavia and 155 from Bergamo, of HCV-RNA-infected Italian women, 21 babies (7.24%) were HCV-RNA positive at birth and steadily positive over 20 months of life. All the 21 infected babies and 44 randomly selected uninfected ones, born to HCV-RNA+ mothers but steadily negative for HCV-RNA during a follow-up of 2 years, and their mothers were investigated for HLA-G, -C, -DRB1, -DQA1 and -DQB1 genomic polymorphisms. Among the different covariates, HLA-Cw*07, -G*010401, -DRB1*0701, -DRB1*1401 and homozigosity for HLA-G 14bp deletion can be considered as risk factors for HCV vertical transmission. On the contrary, protection was conferred by the HLA-DQB1*06, -G*0105N, -Cw*0602, DRB1*1104 and -DRB1*1302 alleles. Our initial question was: has the immunogenetic profile any role in the protection of the fetus growing in an infected milieu and, if so, is it independent from the other non-immunogenetic parameters? The answer to both questions should be yes.


American Journal of Cardiology | 1989

The morphologic spectrum of dilated cardiomyopathy and its relation to immune-response genes.

Eloisa Arbustini; Antonello Gavazzi; Roberto Pozzi; Maurizia Grasso; Pucci A; Carlo Campana; Gabriella Graziano; Miryam Martinetti; Mariaclara Cuccia; Laura Salvaneschi; Luigi Martinelli; Carlo Montemartini; Mario Viganò

Endomyocardial biopsies from 174 patients with dilated cardiomyopathy (DC) were examined. Eight patients with histologically proven myocarditis were excluded from the study. A peculiar pattern of oversized and bizarre nuclei was observed in only some of the remaining patients. Two groups were identified: those with and without this feature (groups A and B, respectively). Myocyte width, nuclear diameter and nuclear/sarcoplasmic ratio were significantly higher in group A. The mean respective values were 36 +/- 5 mu, 14 +/- 3 mu and 0.41 +/- 0.08 for group A versus 20 +/- 8 mu, 7 +/- 2 mu and 0.37 +/- 0.08 for group B. Interstitial fibrosis was similarly present in groups A and B. Endocardial thickness was significantly increased in all patients, with group A showing the highest mean value. The morphologic features showed no correlation with the clinical condition of the patients at time of presentation. HLA typing was performed in 50 consecutive patients, 38 from group A and 12 from group B. DR4 and DR5 antigens were significantly more frequent in DC patients than in a normal population control (400 blood donors), while DR3 was less frequent. Group A was more strongly associated with the DR5 antigen than group B (55.3 vs 25.0%, respectively). It was less strongly associated with the DR4 antigen compared with group B (21.5 vs 41.7%, respectively). No difference was observed between the 2 groups concerning negative association with the DR3 antigen. Endomyocardial biopsies from DC patients reveal marked morphologic changes from patient to patient.(ABSTRACT TRUNCATED AT 250 WORDS)


Transfusion | 2004

A new automated cell washer device for thawed cord blood units.

C. Perotti; Claudia Del Fante; Gianluca Viarengo; Pietro Papa; Loretta Rocchi; Paola Bergamaschi; Laura Bellotti; Andrea Marchesi; Laura Salvaneschi

BACKGROUND:  The current available techniques to wash out DMSO from thawed umbilical cord blood (UCB) units are based essentially on standard centrifugation in an open system with various degrees of cell loss.


European Radiology | 2014

Ultrasound point shear wave elastography assessment of liver and spleen stiffness: effect of training on repeatability of measurements

Giovanna Ferraioli; Carmine Tinelli; Raffaella Lissandrin; Mabel Zicchetti; Stefano Bernuzzi; Laura Salvaneschi; Carlo Filice

AbstractObjectivesTo evaluate reproducibility of measurements of spleen stiffness (SS) and liver stiffness (LS) at several sites by using point shear wave elastography (pSWE) and to investigate any training effect.MethodsHealthy volunteers were consecutively enrolled. Measurements of SS and LS were performed by an expert (observer 1) and a novice (observer 2) at three different sites of liver and spleen. To assess the effect of training the study was conducted in two periods (period 1 and period 2). Concordance correlation coefficient was used to assess intra-observer and inter-observer reproducibility.ResultsA total of 92 subjects (67 men and 25 women) were enrolled in the study. Both intra-observer and inter-observer agreement were higher for the liver than for the spleen. Overall, the highest intra-observer and inter-observer agreement were obtained for the assessment of LS through intercostal space, and for measurements at this site there was a significantly better performance of observer 2 after the training period. For both observers, training improved the repeatability of SS measurements at all sites. A good intra-observer agreement was obtained only for measurements at the spleen lower pole.ConclusionsThe results of this study show that a learning curve in pSWE acquisition should be taken into account both for SS and LS measurements.Key Points• Reproducibility of SS measurements depends on the expertise of the operator. • To achieve good reproducibility between measurements a training period is required. • A learning curve in pSWE acquisition should be taken into account. • SS measurements are less reproducible than LS measurements.

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