849 results on '"Andreani, M."'
Search Results
2. Origin of Fe‐Ca‐Metasomatism in Exhumed Mantle Rocks at the MARK Area (23°N, ODP Leg 153) and Implications on the Formation of Ultramafic‐Hosted Seafloor Massive Sulfide Deposits
- Author
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Coltat, R., primary, Andreani, M., additional, Patten, C. G. C., additional, Godard, M., additional, Debret, B., additional, and Escartin, J., additional
- Published
- 2023
- Full Text
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3. An exploratory work on the use of a Lagrangian-Eulerian model for simulating heat transfer of subchannels under reflooding conditions
- Author
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Badillo, A. and Andreani, M.
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- 2017
- Full Text
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4. Human leukocyte antigen evolutionary divergence influences outcomes of paediatric patients and young adults affected by malignant disorders given allogeneic haematopoietic stem cell transplantation from unrelated donors
- Author
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Merli, P., Crivello, P., Strocchio, L., Pinto, R. M., Algeri, M., Del Bufalo, F., Pagliara, D., Becilli, M., Carta, R., Gaspari, S., Galaverna, F., Quagliarella, F., Boz, G., Catanoso, M. L., Boccieri, E., Troiano, M., Fleischhauer, K., Andreani, M., Locatelli, Franco, Locatelli F. (ORCID:0000-0002-7976-3654), Merli, P., Crivello, P., Strocchio, L., Pinto, R. M., Algeri, M., Del Bufalo, F., Pagliara, D., Becilli, M., Carta, R., Gaspari, S., Galaverna, F., Quagliarella, F., Boz, G., Catanoso, M. L., Boccieri, E., Troiano, M., Fleischhauer, K., Andreani, M., Locatelli, Franco, and Locatelli F. (ORCID:0000-0002-7976-3654)
- Abstract
High genetic heterogeneity in the human leukocyte antigen (HLA) increases the likelihood of efficient immune response to pathogens and tumours. As measure of HLA diversity, HLA evolutionary divergence (HED) has been shown to predict the response of tumours to immunotherapy and haematopoietic stem cell transplantation (HSCT) in adults. We retrospectively investigated the association of HED with outcomes of 153 paediatric/young adults patients, treated for malignant disorders with HSCT from 9–10/10 HLA-matched unrelated donors. HED was calculated as pairwise genetic distance between alleles in patient HLA-A, -B, -C, -DRB1, -DQB1 and -DPB1, using the locus median to stratify patients with ‘high’ or ‘low’ HED. Patients with high HED-B and -DRB1 showed significantly improved disease-free survival (DFS), especially when combined (70.8% vs 53.7% p = 0.008). High HED-B + -DRB1 was also associated with improved overall survival (OS) (82.1 vs 66.4% p = 0.014), and concomitant reduction of non-relapse-mortality (5.1% vs 21.1% p = 0.006). The impact on OS and DFS of combined HED-B + -DRB1 was confirmed in multivariate analysis [hazard ratio (HR) 0.39, p = 0.009; and HR 0.45, p = 0.007 respectively]. Only high HED scores for HLA-DPB1 were associated, in univariate analysis, with reduced incidence of relapse (15.9% vs 31.1%, p = 0.03). These results support HED as prognostic marker in allogeneic HSCT and, if confirmed in larger cohorts, would allow its use to inform clinical risk and potentially influence clinical practice.
- Published
- 2023
5. Origin of Ca-Fe metasomatism at oceanic core complexes (23°N, MAR): implications for the formation of seafloor massive sulphide deposits
- Author
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Coltat, Remí, Andreani, M., Patten, C. G. C., Godard, M., Debret, B., Escartin, J., Coltat, Remí, Andreani, M., Patten, C. G. C., Godard, M., Debret, B., and Escartin, J.
- Published
- 2023
6. Origin of Fe-Ca-metasomatism at oceanic core complexes: implications for the formation of seafloor massive sulfide deposits (MARK area, 23°N)
- Author
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Coltat, Remí, Andreani, M., Patten, C. G. C., Godard, M., Debret, B., Escartin, J., Coltat, Remí, Andreani, M., Patten, C. G. C., Godard, M., Debret, B., and Escartin, J.
- Abstract
At (ultra)slow-spreading ridges, the circulation of hot, acidic, reduced and metal-rich fluids triggers the formation of ultramafic-hosted seafloor massive sulphides deposits (UM-SMSs). These sites display a great variability from site to site, making it difficult to build a simple genetic model. They may notably be associated with Fe-Ca metasomatism, as observed in fossil mineralized systems, thus with possible genetic implications for the formation of mineralized systems. Similar Fe-Ca metasomatism is reported in mantle rocks drilled at the Mid-Atlantic Ridge Kane (MARK) area, offering access to the vertical dimension beneath an oceanic core complex to unravel the nature and geometry of deep magmato-hydrothermal processes. At MARK, mantle rocks record complex melt-rock and fluid-rock interactions. Magma channelling and interactions with peridotite enrich mantle silicates in Fe, Co and Zn. Subsequent hydrothermal alteration produces metamorphic mineral assemblages (e.g., amphibole, clinopyroxene, chlorite, talc, ilvaite, hydro-garnet, serpentine) and is responsible for Cu leaching. It occurs during early mantle exhumation and is followed by the serpentinization of the massif during progressive mantle denudation. Considering the lithological heterogeneity at (ultra)slow-spreading ridges, metal enrichment in mantle rocks through melt-rock interactions may be widespread, eventually accounting for metal endowment at UM-SMS
- Published
- 2023
7. Origin of Fe-Ca-Metasomatism in Exhumed Mantle Rocks at the MARK Area (23°N, ODP Leg 153) and Implications on the Formation of Ultramafic-Hosted Seafloor Massive Sulfide Deposits
- Author
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International Ocean Discovery Program, German Research Foundation, Institut national des sciences de l'Univers (France), Coltat, Remí, Andreani, M., Patten, C. G. C., Godard, M., Debret, B., Escartin, J., International Ocean Discovery Program, German Research Foundation, Institut national des sciences de l'Univers (France), Coltat, Remí, Andreani, M., Patten, C. G. C., Godard, M., Debret, B., and Escartin, J.
- Abstract
At Mid-Ocean Ridges, hot, reduced, acidic, and metal-rich fluids are responsible for the formation of ultramafic-hosted seafloor massive sulfide deposits (UM-SMSs), where mantle exhumation efficiently operates. As UM-SMSs display great structural, mineralogical, and geochemical variabilities from site to site, a simple genetic model cannot be applied. Notably, fluid circulation and Fe-Ca metasomatism are reported in ultramafic-hosted hydrothermal deposits exposed in ophiolites, suggesting it might have genetic implications on the formation of mineralized systems. Similar Fe-Ca metasomatism was reported in drilled mantle rocks at the Mid Atlantic Ridge Kane (MARK) area, offering access to the vertical dimension beneath an exhumed oceanic core complex to provide an integrative study of the nature and geometry of deep magmatic and hydrothermal processes. At MARK, mantle rocks underwent complex processes of melt-rock and fluid-rock interactions. Magma channeling and interactions with surrounding rocks enriched mantle silicates in Fe, Co, and Zn. There, subsequent hydrothermal alteration allowed to stabilize Fe-rich silicates. Mineralogy and geochemistry of hydrothermal phases at MARK suggest mineral crystallization under temperatures from ∼830° down to 350°C during early mantle exhumation at a depth <6.5 km below seafloor, followed by serpentinization of the massif during progressive mantle denudation. Considering the lithological heterogeneity at (ultra)slow-spreading ridges, metal enrichment in deep mantle rocks during melt-rock interactions may be a widespread process. In ultramafic-dominated environments where extensional tectonics allow fluid flows to these deep zones, fluids may leach and transport metals to the surface, accounting for metal entrapment in UM-SMSs.
- Published
- 2023
8. Global Hydrogen Production During High‐Pressure Serpentinization of Subducting Slabs.
- Author
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Merdith, A. S., Daniel, I., Sverjensky, D., Andreani, M., Mather, B., Williams, S., and Vitale Brovarone, A.
- Subjects
HYDROGEN production ,MID-ocean ridges ,SUBDUCTION ,SUBDUCTION zones ,OCEANIC crust ,SLABS (Structural geology) ,REGOLITH ,ULTRABASIC rocks - Abstract
Serpentinization is among the most important, and ubiquitous, geological processes in crustal–upper mantle conditions (<6 GPa, <600°C), altering the rheology of rocks and producing H2 that can sustain life. While observations are available to quantify serpentinization in terrestrial and mid‐ocean ridge environments, measurements within subduction zone environments are far more sparse. To overcome this difficulty, we design a methodology to quantify and offer a first‐order estimate of the magnitude of "slab‐serpentinization" that has occurred over the last 5 Ma within the world's subduction zones by coupling four discrete tectonic and geophysical datasets—(a) raster grids of relic abyssal peridotite (peridotite exhumed from slow spreading mid‐ocean ridges but unaffected by pre‐subduction serpentinization) within ocean basins, (b) slab geometry, (c) thermal profiles and a (d) plate‐tectonic model. Averaged per year, our results suggest that 4.2–24 • 107 kg of H2 per annum could be generated from "slab‐serpentinization" within a subduction zone. Our estimate is 3–4 orders of magnitude lower than what is thought to be produced at mid‐ocean ridges, and 1–2 orders of magnitude lower than what could occur through serpentinization at trench flexure and when including possible mantle wedge serpentinization. Higher hydrogen production is correlated most strongly with the spreading history of ocean basins, underlaying the importance of the tectonic history of a slab prior to subduction. Plain Language Summary: The fate of most ocean crust formed at mid‐ocean ridges is to eventually subduct and be recycled into the mantle. Subduction zones therefore represent a key link between the rocks we see at the surface of the Earth, both in oceans and continents, and the underlaying mantle. However, subduction zones are impossible to observe directly and therefore difficult to fully understand the processes that shape them. Here, we designed a framework that coupled a series of discrete data sets to model how the composition of each subducting slab across the globe differs in order to provide an accurate estimate of "slab‐serpentinization." Serpentinization is the process that converts mantle rocks to serpentinite through exposure to water. A by‐product of this process is the formation of hydrogen gas. Using our framework, we estimated bulk fluxes of serpentinization in subducting slabs, and the corresponding flux of hydrogen. Key Points: First‐order estimate of the gross flux of "slab‐serpentinization" and the resulting (possible) hydrogen production (4.2–24 • 107 kg of H2 per annum)Seafloor spreading history and ocean basin evolution (prior to subduction) impart the strongest control on slab‐serpentinization possibility [ABSTRACT FROM AUTHOR]
- Published
- 2023
- Full Text
- View/download PDF
9. Deep alteration between Hellas and Isidis Basins
- Author
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Bultel, B., Quantin-Nataf, C., Andréani, M., Clénet, H., and Lozac’h, L.
- Published
- 2015
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10. HLA-C*18:01: A Rare Allele in the European Caucasian Population Coinciding with Difficult-to-Treat Plaque Psoriasis
- Author
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Galluzzo, M., Andreani, M., Testi, M., Chimenti, S., and Talamonti, M.
- Published
- 2016
- Full Text
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11. μXANES study of iron redox state in serpentine during oceanic serpentinization
- Author
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Andreani, M., Muñoz, M., Marcaillou, C., and Delacour, A.
- Published
- 2013
- Full Text
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12. Deformation associated to exhumation of serpentinized mantle rocks in a fossil Ocean Continent Transition: The Totalp unit in SE Switzerland
- Author
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Picazo, S., Manatschal, G., Cannat, M., and Andréani, M.
- Published
- 2013
- Full Text
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13. Identification of the novel HLA-B allele, HLA-B*44:532 by next-generation sequencing
- Author
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Galluccio, T., Locatelli, Franco, Pinto, R. M., Testa, G., Andreani, M., Locatelli F. (ORCID:0000-0002-7976-3654), Galluccio, T., Locatelli, Franco, Pinto, R. M., Testa, G., Andreani, M., and Locatelli F. (ORCID:0000-0002-7976-3654)
- Abstract
The novel HLA-B*44:532 allele differs from HLA-B*44:02:01:01 by one nucleotide substitution in Exon 3.
- Published
- 2022
14. TCRab/CD19 depleted HSCT from an HLA-haploidentical relative to treat children with different non malignant disorders
- Author
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Merli, P., Pagliara, D., Galaverna, F., Pira, G. L., Andreani, M., Leone, G., Amodio, D., Pinto, R. M., Bertaina, A., Bertaina, V., Mastronuzzi, A., Strocchio, L., Boccieri, E., Pende, D., Falco, M., Nardo, M. D., Del Bufalo, F., Algeri, M., Locatelli, Franco, Locatelli F. (ORCID:0000-0002-7976-3654), Merli, P., Pagliara, D., Galaverna, F., Pira, G. L., Andreani, M., Leone, G., Amodio, D., Pinto, R. M., Bertaina, A., Bertaina, V., Mastronuzzi, A., Strocchio, L., Boccieri, E., Pende, D., Falco, M., Nardo, M. D., Del Bufalo, F., Algeri, M., Locatelli, Franco, and Locatelli F. (ORCID:0000-0002-7976-3654)
- Abstract
Several nonmalignant disorders (NMDs), either inherited or acquired, can be cured by allogeneic hematopoietic stem cell transplantation (HSCT). Between January 2012 and April 2020, 70 consecutive children affected by primary immunodeficiencies, inherited/acquired bone marrow failure syndromes, red blood cell disorders, or metabolic diseases, lacking a fully matched donor or requiring urgent transplantation underwent TCRab/CD19-depleted haploidentical HSCT from an HLA-partially matched relative as part of a prospective study. The median age at transplant was 3.5 years (range 0.3-16.1); the median time from diagnosis to transplant was 10.5 months (2.7 for SCID patients). Primary engraftment was obtained in 51 patients, while 19 and 2 patients experienced either primary or secondary graft failure (GF), the overall incidence of this complication being 30.4%. Most GFs were observed in children with disease at risk for this complication (eg, aplastic anemia, thalassemia). All but 5 patients experiencing GF were successfully retransplanted. Six patients died of infectious complications (4 had active/ recent infections at the time of HSCT), the cumulative incidence of transplant-related mortality (TRM) being 8.5%. Cumulative incidence of grade 1-2 acute GVHD was 14.4% (no patient developed grade 3-4 acute GVHD). Only one patient at risk developed mild chronic GVHD. With a median follow-up of 3.5 years, the 5-year probability of overall and disease-free survival was 91.4% and 86.8%, respectively. In conclusion, TCRab/CD19-depleted haploidentical HSCT from an HLA-partially matched relative is confirmed to be an effective treatment of children with NMDs. Prompt donor availability, low incidence of GVHD, and TRM make this strategy an attractive option in NMDs patients. The study is registered at ClinicalTrial.gov as NCT01810120.
- Published
- 2022
15. Common and well‐documented HLA alleles over all of Europe and within European sub‐regions: A catalogue from the European Federation for Immunogenetics
- Author
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SanchezMazas, A., Nunes, J. M., Middleton, D., Sauter, J., Buhler, S., McCabe, A., Hofmann, J., Baier, D. M., Schmidt, A. H., Nicoloso, G., Andreani, M., Grubic, Z., Tiercy, J.M., and Fleischhauer, K.
- Published
- 2017
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16. Interaction of a light gas stratified layer with an air jet coming from below: Large scale experiments and scaling issues
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Studer, E., Brinster, J., Tkatschenko, I., Mignot, G., Paladino, D., and Andreani, M.
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- 2012
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17. Evaluation of a preliminary safety concept for the HPLWR
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Andreani, M., Bittermann, D., Marsault, Ph., Antoni, O., Keresztúri, A., Schlagenhaufer, M., Manera, A., Seppäla, M., and Kurki, J.
- Published
- 2012
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18. Identification of the novel HLA‐C*07:1132 allele by next‐generation sequencing.
- Author
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Galluccio, T., Cerretti, R., Battarra, M., Giustiniani, P., and Andreani, M.
- Subjects
NUCLEOTIDE sequencing ,ALLELES - Abstract
The novel HLA‐C*07:1132 allele differs from HLA‐C*07:01:01 by one nucleotide substitution in Exon 5. [ABSTRACT FROM AUTHOR]
- Published
- 2024
- Full Text
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19. European supercritical water cooled reactor
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Schulenberg, T., Starflinger, J., Marsault, P., Bittermann, D., Maráczy, C., Laurien, E., Lycklama à Nijeholt, J.A., Anglart, H., Andreani, M., Ruzickova, M., and Toivonen, A.
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- 2011
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20. Hematopoietic SCT for the Black African and non-Black African variants of sickle cell anemia
- Author
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Lucarelli, G, Isgrò, A, Sodani, P, Marziali, M, Gaziev, J, Paciaroni, K, Gallucci, C, Cardarelli, L, Ribersani, M, Alfieri, C, De Angelis, G, Armiento, D, Andreani, M, Testi, M, Amato, A, Akinyanju, O O, and Wakama, T T
- Published
- 2014
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21. BAT2 and BAT3 polymorphisms as novel genetic risk factors for rejection after HLA-related SCT
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Piras, I S, Angius, A, Andreani, M, Testi, M, Lucarelli, G, Floris, M, Marktel, S, Ciceri, F, Nasa, G La, Fleischhauer, K, Roncarolo, M G, Bulfone, A, Gregori, S, and Bacchetta, R
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- 2014
- Full Text
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22. Atomic modelling of crystal/complex fluid/crystal contacts—Part II. Simulating AFM tests via the GenMol code for investigating the impact of CO 2 storage on kaolinite/brine/kaolinite adhesion
- Author
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Pèpe, G., Dweik, J., Jouanna, P., Gouze, P., Andreani, M., and Luquot, L.
- Published
- 2010
- Full Text
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23. Protection of nascent DNA at stalled replication forks is mediated by phosphorylation of RIF1 intrinsically disordered region
- Author
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Balasubramanian, S., primary, Andreani, M., additional, Andrade, J.G., additional, Saha, T., additional, Garzón, J., additional, Zhang, W., additional, Rahjouei, A., additional, Rosen, D.B., additional, Chait, B.T., additional, Donaldson, A.D., additional, and Di Virgilio, M., additional
- Published
- 2021
- Full Text
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24. A new HLA‐B allele, HLA‐B *07:422
- Author
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Battarra, M., primary, Di Luzio, A., additional, Bianculli, A. G., additional, Pinto, R. M., additional, and Andreani, M., additional
- Published
- 2021
- Full Text
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25. Identification of the novel HLA‐DPA1 allele, DPA1 *02:53 by next‐generation sequencing
- Author
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Galluccio, T., primary, Paola, G., additional, Bianculli, A., additional, Testa, G., additional, and Andreani, M., additional
- Published
- 2021
- Full Text
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26. HLA-A-B-C-DRB1-DQB1 phased haplotypes in 124 Nigerian families indicate extreme HLA diversity and low linkage disequilibrium in Central-West Africa
- Author
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Testi, M., Battarra, M., Lucarelli, G., Isgro, A., Morrone, A., Akinyanju, O., Wakama, T., Nunes, J. M., Andreani, M., and Sanchez-Mazas, A.
- Published
- 2015
- Full Text
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27. HLA-haploidentical TCRab1/CD191-depleted stem cell transplantation in children and young adults with Fanconi anemia
- Author
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Strocchio, L., Pagliara, D., Algeri, M., Pira, G. L., Rossi, F., Bertaina, V., Leone, G., Pinto, R. M., Andreani, M., Agolini, E., Girardi, K., Gaspari, S., Grapulin, L., Bufalo, F. D., Novelli, A., Merli, P., and Locatelli, Franco
- Subjects
HLA-haploidentical tranpslant ,Settore MED/38 - PEDIATRIA GENERALE E SPECIALISTICA - Published
- 2021
28. Identification of a new HLA-B*44 allele, HLA-B*44:02:68, by next generation sequencing
- Author
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Troiano, M., Locatelli, Franco, Giustiniani, P., Bianculli, A. G., and Andreani, M.
- Subjects
next generation sequencing ,new allele ,Settore MED/38 - PEDIATRIA GENERALE E SPECIALISTICA ,HLA-B*44:02 NEW - Published
- 2021
29. Fluid circulation along an oceanic detachment fault: insights from fluid inclusions in silicified brecciated fault rocks (Mid‐Atlantic Ridge at 13°20’N)
- Author
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Verlaguet, A., Bonnemains, D., Mével, C, Escartín, J., Andreani, M., Bourdelle, F., Boiron, M.‐c., Chavagnac, V., Verlaguet, A., Bonnemains, D., Mével, C, Escartín, J., Andreani, M., Bourdelle, F., Boiron, M.‐c., and Chavagnac, V.
- Abstract
The MAR 13°20’N corrugated detachment fault is composed of pervasively silicified mafic cataclastic breccias, instead of ultramafics and gabbros commonly found at other detachments. These breccias record overplating of hangingwall diabases, with syntectonic silicification due to important influx of silica‐iron‐rich fluids, able to leach alkalis and calcium. Fluids trapped in quartz inclusions show important salinity variations (2.1‐10 wt.% NaCl eq.) indicating supercritical phase separation. Fluid inclusions also contain minor amounts of H2±CO2±CH4±H2S, with high H2/CO2 and H2/H2S ratios, signatures typical of ultramafic‐hosted vent fluids. We propose that seawater infiltrated the hangingwall upper crust at the axis adjacent to the active detachment, reaching a reaction zone at the dyke complex base (∼2 km). At >500°C, fluids become Si‐rich during diabase alteration (amphibolite‐facies alteration in clasts), and undergo phase‐separation. Brines, preferentially released in the nearby detachment fault during diabase brecciation, mix with serpentinite‐derived fluids bearing H2 and CH4. Cooling during detachment deformation and fluid upward migration triggers silica precipitation at greenschist‐facies conditions (quartz+Fe‐rich‐chlorite±pyrite). Important variations in fluid inclusion salinity and gas composition at both sample and grain scales record heterogeneous fluid circulation at small spatial and short temporal scales. This heterogeneous fluid circulation operating at <2 km depth, extending both along‐axis and over time, is inconsistent with models of fluids channeled along detachments from heat sources at the base of the crust at the fault root. Present‐day venting at detachment footwall, including Irinovskoe, is instead likely underlain by fluid circulation within the footwall, with outflow crossing the inactive detachment fault near‐surface. Plain language summary Here we present constraints on fluid circulation along the 13°20′N oceanic detachment fault along
- Published
- 2021
- Full Text
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30. Identification of the novel HLA-DPB1*1149:01
- Author
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Galluccio, T., Locatelli, Franco, Troiano, M., Giustiniani, P., Andreani, M., Locatelli F. (ORCID:0000-0002-7976-3654), Galluccio, T., Locatelli, Franco, Troiano, M., Giustiniani, P., Andreani, M., and Locatelli F. (ORCID:0000-0002-7976-3654)
- Abstract
The new allele HLA-DPB1*1149:01 differs from HLA-DPB1*09:01:01 by one nucleotide substitution in Exon 4.
- Published
- 2021
31. Vernal keratoconjunctivitis in twins: case report and literature review
- Author
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Artesani, M. C., Esposito, M., Mennini, M., Andreani, M., Locatelli, Franco, Buzzonetti, L., Fiocchi, A., Locatelli F. (ORCID:0000-0002-7976-3654), Artesani, M. C., Esposito, M., Mennini, M., Andreani, M., Locatelli, Franco, Buzzonetti, L., Fiocchi, A., and Locatelli F. (ORCID:0000-0002-7976-3654)
- Abstract
no abstract
- Published
- 2021
32. Use of DPB1 T-cell epitope algorithm among italian transplant centers: A survey on behalf of Associazione Italiana di Immunogenetica e Biologia dei Trapianti
- Author
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Crocchiolo, R., Mele, L., Testi, M., Scollo Chiara, M., Murgia, B., Rossi, A., Vecchiato, C., Grammatico, P., Mininni, D., Longhi, E., Manfroi, S., Giuliodori, S., Castellani, L., Carella, G., Lai, S., Azzaro Maria, P., Mazzi, B., Perotti, L., Penta, R., Lombardo, C., Tognellini, R., Andreani, M., Albergoni Maria, P., Nesci, S., Cappuzzo, V., Chiusolo, Patrizia, Garino, E., Cappucci, G., Ceschini, N., Bevilacqua, E., Guizzardi, E., Tagliaferri Cinzia, M., Piazza, A., Carcassi, C., Miotti, V., Chiusolo P. (ORCID:0000-0002-1355-1587), Crocchiolo, R., Mele, L., Testi, M., Scollo Chiara, M., Murgia, B., Rossi, A., Vecchiato, C., Grammatico, P., Mininni, D., Longhi, E., Manfroi, S., Giuliodori, S., Castellani, L., Carella, G., Lai, S., Azzaro Maria, P., Mazzi, B., Perotti, L., Penta, R., Lombardo, C., Tognellini, R., Andreani, M., Albergoni Maria, P., Nesci, S., Cappuzzo, V., Chiusolo, Patrizia, Garino, E., Cappucci, G., Ceschini, N., Bevilacqua, E., Guizzardi, E., Tagliaferri Cinzia, M., Piazza, A., Carcassi, C., Miotti, V., and Chiusolo P. (ORCID:0000-0002-1355-1587)
- Abstract
The HLA-DPB1 locus has been demonstrated to have a significant role on patients' outcome after allogeneic HSCT, and the so-called T-cell epitope (TCE) algorithm has been incorporated in international guidelines for the selection of unrelated donors. The purpose of the present study is to measure, through a national survey conducted on behalf of the Associazione Italiana di Immunogenetica e Biologia dei Trapianti (AIBT), the extent of awareness and use of HLA-DPB1 TCE-based algorithms during the donor search. 89% of the HLA laboratories answered to a short questionnaire and the results showed a progressive increase of the laboratories typing DPB1 in patients and their potential donors during the search (from 44% to 79% during the 2010–2019 period) as well as the application of a TCE-based algorithm for the donor choice whenever possible (from 24% to 65% during the same period). The DP-permissiveness status is detailed in the official HLA typing report by 12%, 32% and 50% of laboratories in 2010, 2015 and 2019, respectively. The present data indicate an encouraging raise in the awareness of the HLA-DPB1 role in unrelated donor selection; noteworthy, mentioning the TCE-based permissiveness status in the HLA typing report of each potential unrelated donor represents a notable mean to raise awareness among transplant physicians and to support them in their task of choosing the best donor. Nonetheless, despite the compelling evidence of the predictive ability of TCE-based algorithms, further efforts are still needed to extend its application to all transplant centers in Italy.
- Published
- 2021
33. Allelic HLA Matching and Pair Origin Are Favorable Prognostic Factors for Unrelated Hematopoietic Stem Cell Transplantation in Neoplastic Hematologic Diseases: An Italian Analysis by the Gruppo Italiano Trapianto di Cellule Staminali e Terapie Cellulari, Italian Bone Marrow Donor Registry, and Associazione Italiana di Immunogenetica e Biologia dei Trapianti
- Author
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Picardi, A., Sacchi, N., Miotti, V., Lorentino, F., Oldani, E., Rambaldi, A., Sessa, M., Bruno, B., Cerno, M., Vago, L., Bernasconi, P., Arcese, W., Benedetti, F., Pioltelli, P., Russo, D., Farina, L., Fagioli, F., Guidi, S., Saporiti, G., Zallio, F., Chiusolo, Patrizia, Borghero, C., Papalinetti, G., La Rocca, U., Milone, G., Lamparelli, T., Carella, A. M., Luppi, M., Olivieri, A., Martino, M., Carluccio, P., Celeghini, I., Andreani, M., Gallina, A. M., Patriarca, F., Pollichieni, S., Mammoliti, S., Micciche, S., Mangione, I., Ciceri, F., Bonifazi, F., Chiusolo P. (ORCID:0000-0002-1355-1587), Picardi, A., Sacchi, N., Miotti, V., Lorentino, F., Oldani, E., Rambaldi, A., Sessa, M., Bruno, B., Cerno, M., Vago, L., Bernasconi, P., Arcese, W., Benedetti, F., Pioltelli, P., Russo, D., Farina, L., Fagioli, F., Guidi, S., Saporiti, G., Zallio, F., Chiusolo, Patrizia, Borghero, C., Papalinetti, G., La Rocca, U., Milone, G., Lamparelli, T., Carella, A. M., Luppi, M., Olivieri, A., Martino, M., Carluccio, P., Celeghini, I., Andreani, M., Gallina, A. M., Patriarca, F., Pollichieni, S., Mammoliti, S., Micciche, S., Mangione, I., Ciceri, F., Bonifazi, F., and Chiusolo P. (ORCID:0000-0002-1355-1587)
- Abstract
HLA molecules are important for immunoreactivity in allogeneic hematopoietic stem cell transplantation (HSCT). The Gruppo Italiano Trapianto di Cellule Staminali e Terapie Cellulari, Italian Bone Marrow Donor Registry, and Associazione Italiana di Immunogenetica e Biologia dei Trapianti promoted a retrospective observational study to evaluate HLA matching and the impact of allelic HLA mismatching and non-HLA factors on unrelated Italian HSCT outcomes. From 2012 to 2015, 1788 patients were enrolled in the study. The average donor age was 29 years and the average recipient age was 49 years. As a conditioning regimen, 71% of the patients received myeloablative conditioning. For GVHD prophylaxis, 76% received either antithymocyte or anti-T lymphocyte globulin, cyclosporine A, and methotrexate. Peripheral blood was the stem cell source in 80%. The median duration of follow-up was 53 months. Regarding HLA matching, 50% of donor-recipient pairs were 10/10 matched, 38% had 1 mismatch, and 12% had 2 or more mismatches. A total of 302 pairs shared Italian origin. Four-year overall survival (OS), progression-free survival, GVHD-free relapse-free survival, and relapse rates were 49%, 40%, 22%, and 34%, respectively. The 4-year NRM was 27%, and the 100-day cumulative incidence of grade ≥II acute GVHD (aGVHD) was 26%. In multivariate analysis, 9/10 and ≤8/10 HLA allele-matched pairs were associated with worse OS (P = .04 and. 007, respectively), NRM (P = .007 and P < .0001, respectively), and grade III-IV aGVHD (P = .0001 and. 01, respectively). Moreover, the incidences of grade II-IV aGVHD (P = .001) and chronic GVHD (P = .002) were significantly lower in Italian pairs. In conclusion, 10/10 HLA matching is a favorable prognostic factor for unrelated HSCT outcome in the Italian population. Moreover, the presence of 2 HLA-mismatched loci was associated with a higher NRM (P < .0001) and grade II-IV aGVHD (P = .006) and a poorer OS (P = .001) compared with 1 HLA-mismatched loc
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- 2021
34. Allogeneic cellular gene therapy in hemoglobinopathies—evaluation of hematopoietic SCT in sickle cell anemia
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Lucarelli, G, Gaziev, J, Isgrò, A, Sodani, P, Paciaroni, K, Alfieri, C, De Angelis, G, Marziali, M, Simone, M D, Gallucci, C, Roveda, A, Saltarelli, F, Torelli, F, and Andreani, M
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- 2012
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35. Higher CD3+ and CD34+ cell doses in the graft increase the incidence of acute GVHD in children receiving BMT for thalassemia
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Gaziev, J, Isgrò, A, Marziali, M, Daniele, N, Gallucci, C, Sodani, P, Simone, M D, Adorno, G, Paciaroni, K, Andreani, M, Lanti, A, Del Proposto, G, Testi, M, De Angelis, G, Roveda, A, Alfieri, C, Saltarelli, F, and Lucarelli, G
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- 2012
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36. A benchmark exercise on the use of CFD codes for containment issues using best practice guidelines: A computational challenge
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Andreani, M., Haller, K., Heitsch, M., Hemström, B., Karppinen, I., Macek, J., Schmid, J., Paillere, H., and Toth, I.
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- 2008
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37. Influence of the HLA characteristics of Italian patients on donor search outcome in unrelated hematopoietic stem cell transplantation
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Testi, M., Andreani, M., Locatelli, F., Arcese, W., Troiano, M., Battarra, M., Gaziev, J., and Lucarelli, G.
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- 2014
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38. RESULTS OF HLA-HAPLOIDENTICAL STEM CELL TRANSPLANTATION AFTER REMOVAL OF ALPHA/BETA+ T CELLS AND OF CD19+ B CELLS IN CHILDREN WITH ACUTE LEUKEMIA: PH-O106
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Bertaina, A., Pagliara, D., Pende, D., Rutella, S., Falco, Emma M., Bauquet, A., Spagnoli, A., Lucarelli, B., Brescia, Pomponia L., Merli, P., Andreani, M., Pira, G. Li, Ceccarelli, S., Grapulin, L., Palumbo, G., Bernardo, M. E., Biagini, S., Moretta, F., Milano, Maria G., Airoldi, I., Moretta, A., Moretta, L., and Locatelli, F.
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- 2014
39. Mixed chimerism in haemoglobinopathies: from risk of graft rejection to immune tolerance
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Andreani, M., Testi, M., and Lucarelli, G.
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- 2014
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40. Early detection with speckle tracking echocardiography of biventricular systolic dysfunction, and its relationship with fatigue, in patients with multiple sclerosis
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Michelotto, E, primary, Oliva, MC, additional, Amoruso, MT, additional, Giovannetti, G, additional, Battista, C, additional, Andreani, M, additional, Mazzilli, D, additional, Amico, AP, additional, Tota, A, additional, Megna, M, additional, D"agostino, C, additional, Palmieri, VO, additional, and Colonna, P, additional
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- 2021
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41. Amnioinfusion in preterm PROM: effects on amnion and cord histology
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Locatelli, A, Andreani, M, Ghidini, A, Verderio, M, Pizzardi, A, Vergani, P, and Salafia, C M
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- 2008
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42. Association of kidney disease measures with risk of renal function worsening in patients with type 1 diabetes 11 Medical and Health Sciences 1103 Clinical Sciences
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Mirijello, A, Viazzi, F, Fioretto, P, Giorda, C, Ceriello, A, Russo, G, Guida, P, Pontremoli, R, De Cosmo, S, Cimino, A, Fava, D, Meloncelli, I, Nicolucci, A, Pellegrini, F, Rossi, M, Turco, S, Vespasiani, G, Graziano, G, Lucisano, G, Memmo, R, Pellicciotta, E, Paciotti, V, Pupillo, M, Armentano, G, Giovannini, C, Armentano, V, Laudato, M, Acquati, S, Ciardullo, A, Laffi, G, Felace, G, Taboga, C, Tortul, C, Santantonio, G, Suraci, C, Ghisoni, G, Raffa, M, Genovese, S, Lovagnini-Scher, C, Rampini, P, Rocca, A, Ruggeri, P, Tortato, E, Cotti, L, Cristofaro, M, Tagliaferri, M, Comoglio, M, Fornengo, R, Gentile, F, Gigante, A, Mastinu, F, Di Benedetto, A, Pata, P, Arcangeli, A, Orsini, P, Acler, P, De Blasi, G, Cicioni, G, Pocciati, S, Marangoni, A, Nogara, A, Lanero, M, Bertero, M, Damassino, R, Bergonzini, C, Schumtz, L, Seksich, L, Pipitone, A, Boaretto, M, Manfroi, I, Parmesan, L, Conte, B, Soccol, F, Pagano, A, Papini, E, Rinaldi, R, Petrucci, L, Graziano, F, Chianelli, M, Silvagni, S, Rosco, M, Ansaldi, E, Malvicino, F, Battezzati, M, Maresca, P, Palenzona, C, Boemi, M, Rabini, R, Brandoni, G, Lanari, L, Gatti, C, Testa, I, Cherubini, V, Doveri, G, Pecorelli, L, Ciccarelli, A, Gallardini, M, Courthoud, R, Sara Bredy, S, Ricciardi, G, Vitalone, G, Setti, D, Contrini, P, Corsi, A, Ghigliotti, V, Oddone, G, Ponzani, P, Valbonesi, G, Mazzini, V, Di Berardino, P, Colleluori, P, Montani, V, Trosini, V, Velussi, M, Alfidi, P, Verdecchia, B, Baliva, L, Di Pietro, A, Franchi, G, Luce, R, Pianta, A, Ferrari, M, Balzano, S, Beltranello, G, Dal Fabbro, S, Arico, C, Cervo, L, Zanon, R, Rossa, S, Di Pace, M, Ciavarella, A, Giangiulio, S, Grimaldi, M, Mustacchio, A, Fattor, B, Monauni, T, Cristini, M, Orion, G, Crazzolara, D, Amor, F, Eisath, J, Lintner, S, Garavelli, S, Calari, T, Marini, P, Sandri, O, Scala, M, Stroppa, C, Trentin, A, Carlin, R, Carli, B, Sandona, M, Zortea, C, Bonet, L, Pradel, L, Reato, S, Buschini, M, Bonfiglioli, D, Mones, D, Beldi, F, Morea, A, Bondesan, L, Perbellini, S, Valentini, U, Agosti, B, Corsini, R, Girelli, A, Zarra, E, Rocca, L, Bergmann, M, Pradi, I, Unterkircher, S, Piok, M, Pichler, M, Trinchera, A, Palama, G, Palma, P, Carboni, L, Murtas, M, Mudadu, T, Turco, M, Floris, M, Delogu, A, Farris, L, Songini, M, Piras, G, Seguro, R, Floris, R, Corona, G, Lai, M, Piras, E, Contini, P, Cocco, S, Pilosu, R, Sannia, M, Spanu, F, Busciantella Ricci, N, Cartechini, M, Agostinelli, G, Fiorelli, C, Nuzzi, A, Ballauri, C, Lesina, A, Romeo, F, Giudici, G, Maciejewska, E, Deroma, A, Paduano, M, Rossi, L, Vagnini, C, Dolci, M, Mori, M, Baccetti, F, Gregori, G, Straface, E, Pozzuoli, G, Barone, M, Stasio, G, Tondini, S, Borgoni, F, Grosso, J, Scarsellato, C, Sciulli, A, De Marco, F, Confortin, L, Marin, N, Lamonica, M, Gialdino, S, Borzi, V, Gatta, C, Rapisard, R, Strano, S, Calabro, M, Puccio, L, Zolli, M, Coracina, A, Starnone, V, Del Buono, A, Terracciano, A, Monda, M, Castro, F, Guaglianone, A, Maccari, V, Corsi, L, Versari, G, Falivene, M, Boletto, N, Corsi, S, Marafetti, L, Vitacolonna, E, Capani, F, Caputo, L, Di Nisio, L, Simonetti, F, Boscolo Bariga, A, Ballarin, G, De Boni, S, Di Benedetto, S, Chiambretti, A, Di Vito, L, Pascuzzo, M, Urli, P, Rumi, P, Balzarini, B, Galli, P, Castellan, M, Giannetti, A, Russotti, C, De Blasi, A, Perna, A, Campanelli, C, Ranchelli, A, Biccheri, D, Dadi, G, Massa, L, Baldi, G, Sciacca, F, Costanzo, E, Spada, M, Paolini, G, Ziller, P, Portolan, F, Pasolini, G, Ghilardi, G, Fiorina, P, Grata, M, Capretti, L, Speroni, G, Fugazza, L, Massafra, C, Lovagnini Scher, A, Cimicchi, M, Percudani, C, Risolo, T, Sacco, P, Gidoni Guarnieri, G, Piccolo, D, Bravin, C, De Noni, E, Scarpel, M, Marcon, M, Giacon, F, Panebianco, G, Tadiotto, F, Da Tos, V, D'Ambrosio, M, Pellizzola, D, Zampini, M, Frezzati, E, Mari, E, Raminelli, E, Gaiti, D, Bosi, E, Chierici, G, Pilla, S, Copelli, M, Zanichelli, P, Bertelli, L, Caretta, P, Vezzani, V, Bodecchi, S, Longobucco, A, Di Lembo, S, Spotti, E, Carrai, E, Degli Innocenti, A, Manini, L, Persico, R, Rossi, C, Magro, G, Marelli, G, Vilei, V, Andrioli, M, Bellato, L, Fedeli, M, Merlini, A, Pinelli, G, Marin, G, Contin, M, Gallo, A, Parlato, P, Pecchielan, W, Jacovacci, J, Placentino, G, Richini, D, Molinari, S, Strazzeri, R, Fabbri, T, Di Bartolo, P, Garrapa, G, D'Incau, F, Lagomanzini, P, Conte, P, Todesco, F, Foglini, P, Pantanetti, P, Bedetta, C, Maricotti, R, Tomasi, F, Monesi, M, Graziani, R, Beretta, F, Penna, L, Guberti, A, Dazzi, D, Forte, E, Gasbarrone, A, Marrocco, T, Moschetta, R, Tuccinardi, F, De Meo, F, Coppola, A, Pirolozzi, P, Placitelli, E, Vallefuoco, R, Catone, B, Ceschia, S, Urban, M, Fabbri, F, Torresani, M, Crovetto, R, Battistini, M, Carosia, P, Viviani, G, Durante, A, Pais, F, Lilliu, V, Quieto, C, D'Ugo, E, Squadrone, M, Amenduni, T, Iovannisci, M, Della Penna, L, Potente, F, Delle Donne, T, Massa, C, Ulisse, M, De Berardinis, S, Guarnieri, I, Pace, S, Splendiani, M, Di Giuseppe, R, Brunato, B, Assaloni, R, Muraro, R, Loro, R, Bucciol, S, Lavacca, C, Sabbatini, G, Quadri, F, Sambuco, L, Santacroce, C, Paola Caretta, D, Marino, C, Micheletti, A, Petrelli, A, Corda, A, Pisano, L, Guaita, G, Deias, C, Trevisan, G, Coletti, I, Iannarelli, R, De Luca, A, Minnucci, A, Antenucci, D, Di Florio, C, Angelicola, G, Bosco, A, Fresco, R, Di Marco, G, Ugolotti, D, Cadossi, T, Di Caro, P, Mazzocchetti, M, Buzzetti, R, Leto, G, Gnessi, C, Cipolloni, L, Foffi, C, Moretti, C, Venditti, C, Meniconi, R, Bertoli, S, Cosimi, S, Di Cianni, G, Turco, A, Richini, A, Marconi, S, Sannino, C, Lemmi, P, Giuntoli, S, Manfre, N, Giannini, F, Di Carlo, A, Casadidio, I, Melandri, P, Maolo, G, Polenta, B, Piccinini, N, Vincenti, C, Pastore, N, Mega, P, Magurano, E, Cananiello, A, Francescutto, C, Brussa Toi, E, Gaspardo, G, Angeli, L, Ronchese, L, Sciangula, L, Ciucci, A, Contartese, A, Banfi, E, Castelli, E, Tatti, P, Bloise, D, Di Mauro, P, Masselli, L, Lo Presti, A, Scarpitta, A, Gambina, F, Venezia, A, Morea, R, Lagonigro, G, Copeta, G, Iannucci, V, Milano, V, Trupo, M, Lochmann, A, Marchetto, P, Incelli, G, De Paola, G, Steiger, M, Gamper, M, Breitenberger, S, Holzner, M, Frischmann, J, Lambiase, C, Di Vece, T, D'Aniello, M, Fezza, M, Giordano, C, Leo, F, Saitta, G, Cucinotta, D, Di Vieste, G, Pintaudi, B, Mancuso, T, Musacchio, N, Giancaterini, A, Pessina, L, Salis, G, Schivalocchi, F, Testori, G, Cerutti, N, Morpugo, P, Cavaletto, M, Bonino, G, Morreale, F, Mariani, G, Ragonesi, P, Bollati, P, Colapinto, P, Falqui, L, Bortolato, L, Cosma, A, Pistolato, P, Centenaro, B, Ceccato, A, Campobasso, G, Zaurino, F, Mazzotta, G, Manti, R, Da Ros, R, Carlucci, S, Narduzzi, L, Bortolotto, D, D'Acunto, L, Stanic, L, Volpi, A, Cospite, A, Manicardi, V, Michelini, M, Finardi, L, Borghi, F, Manicardi, E, Lombardi, S, Tommasi, C, Iaccarino, M, Cozza, S, Binotto, M, Marini, F, Mecenero, I, Massignani, S, Stecco, P, Urbani, E, Massariol, W, Parolin, R, Gatti, A, Bonavita, M, Creso, E, Giannettino, R, Gobbo, M, Iovine, C, 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M., Manicardi V., Michelini M., Finardi L., Borghi F., Manicardi E., Lombardi S., Tommasi C., Iaccarino M., Cozza S., Binotto M., Marini F., Mecenero I., Massignani S., Stecco P., Urbani E., Massariol W., Parolin R., Gatti A., Bonavita M., Creso E., Giannettino R., Gobbo M., Iovine C., Riccardi G., Iazzetta N., Giannattasio C., Egione O., Galdieri S., Velotti A., Azzolina A., Annicelli G., Sorrentino T., Gaeta I., Zenari L., Bertolini L., Sorgato C., Grippaldi F., Stroppiana M., Popolizio R., Carbone N., Grasso S., Abate S., Gaggero G. C., Strazzabosco M., Brun E., Carlesi G. P., Garrone S., Cicalo A. M., Clausi C., Cau R., Manconi A., Carboni A., Angius M. F., Pinna A. A., Caria S., Filigheddu G. D., Tonolo G., Carta I., Calebich S., Burlotti C., Saglietti G., Schellino A., Madau G., Cossu M., Mulas F., Zoccheddu S., Balsanelli M., Fetonti M., Rotolo A., Sambo P., Secchi E., Angotzi M. A., Loddoni S., Brundu I., Careddu F., Becciu A., Gabriella Piras G., Novara F., Cipro F., Torchio G., Palumbo P., Bianchi A., Colucci G., La Motta G., Tiengo A., Avogaro A., Bruttomesso D., Crepaldi C., Fadini G., Guarnieri G., Lavagnini M. T., Maran A., Vedovato M., De Kreutzenberg V., Fedele D., Lapolla A., Sartore G., Bax G., Cardone C., Dalfra M. G., Masin M., Toniato R., Piarulli F., Mattina G., Fulantelli M. A., Gioia D., Conti M., Ridola G., D'Agati F., Grossi G., Zavaroni I., Dei Cas A., Franzini L., Usberti E., Antonimi M., Anelli N., Poli R., Ridolfi V., Michela M., Haddoub S., Prampolini G., Muoio A., Filippi D., Bucci F., Tardio S. M., Calderini M. C., Magotti M. G., Quarantelli C., Vernazza M. A., Carolfi A., Saracca R., Picchio E., Del Sindaco P., Spalluto A., Maggiulli L., Torreggiani V., Rastelletti S., Ugolini C., Pucci N., Magi S., Muratori S., La Penna G., Consoli A., Galeone F., Magiar A. V., Gherardini V., Moretti L., Bientinesi M., Landi L., Bernardi A., Del Prato S., Miccoli R., Bianchi C., Penno G., Venditti F., Anichini R., De Bellis A., Bruschi T., Butelli L., Gioffredi M., Gori R., Picciafuochi R., Malagoli R., Bernini A., Gelisio R., Zanon M., Del Bianco A., Bamiston A., Signorato M., Citro G., Calabrese M., Ianni L., Lorenzetti M., Marsocci A., Guizzotti S., Memoli G., Cabasino F., Farci F., Atzori A., Sanna A., Ghiani M., Siotto I., Sedda M., Manis A., Loddo C., Loddo I., Seguro P., Cuomo A., Orlando L., Olanda G. B., Pucci A., Massenzo M., Sardu C., Perrone G., Corazziere F., La Puzza I., Tripodi P. F., Riggio S., Giampaolo A., Mannino D., Aleandri A. R., Guidi M. V., Battisti B., Faraglia M. R., Lilli V., Leotta S., Visalli N., Gagliardi A., Fontana L., Altomare M., Carletti S., Abbruzzese S., Chiaramonte F., Giordano R., Rossini M., Migneco G., Cappelloni D., Urbani A., Piergiovanni F., Simonetta A., Massimiani F., Bulzomi R., Giuliano M., Pennafina M. G., Di Perna P., D'Accinni M. P., Paolucci D., D'Ubaldi A., D'Angelo M. T., Masaro G., Pietrantoni M., Fratini M., La Rosa R., Poggi M., Piccirilli F., Pisano R., Saponara C., Conforti I., Penza A., Scalpone R., Lo Pinto S., Iacovella L., Caccamo C., Sposito S., Teodonio C., Restuccia M. G., Mirto G., Girardello R., Gennaro R., De Moliner L., Bettini E., Mattuzzi A., Speese K., Frisinghelli F., Locatelli F., Nicoletti M., Trojan N., Centis R., L Volsi P., Levis E., Zanette G., Comba G., Ballatore L., Cattaneo A., Aglialoro A., Guido R., Patrone M., Zecchini M., Clementi L., Galetta M., Marconi V., Bordin P., Perale L., Vinci C., Sira Zanon M., Geretto L., Toffolo C., Furlan M. G., Mazzanti G., Vinci M., Sica V., Armeni M., Derai R., Ennas O., Mamusa S., Pisano M. A., Carreras L., Rauseo A., Cervone S., Leggieri A., Pontonio M., Sturaro R., Quattrocchi F., Molinaro M., Trasatti M., Ferretti B., Labarile G., Baule G. M., Gentilini A., Spanu M. A., Fancellu A., Bianco P., Lione L., Massazza G., Bocchio G., Bosco E., Monachesi M., Carta G., Boschetti M., Ceresola E., Venier E., Calcaterra F., Cataldi F., Miola M., Manfrini S., Lai A., Locci B., Putzu D., Tanganelli I., Leonini M., Egger K., Marchiotto W., Vincis L., Orlandini V., Pilloni C., Farci R., Pelligra I., Renier G., Mameli M., Pala A., Devigus E., Fumagalli I., Lalli C., Leandri M., Agliani M., De Pascalis L., Malci F., De Ciocchis A., Diodati M. B., Macerola B., Davi S., Caccavale A., Brocato L., Pognant Gros M., Borla S., Lattanzi E., Piersanti C., Piersanti A., Spinelli I., Tuzzoli L., Tulini V., Quaranta G., Iorio V., Tirabovi M., De Terlizi C., Massarelli M. G., Venturi S., Travaglini A., Draghi P., Pomante P., Richiardi L., Clerico A., Bruno A., Cavallo Perin P., Ghigo E., Porta M., Scuntero P., Arcari R., Bertaina S., Bo S., Broglio F., Bruno G., Degiovanni M., Fornengo P., Grassi G., Inglese V., Maccario M., Maghenzani G., Marena S., Martina V., Passera P., Ruiu G., Tagliabue M., Zanone M., Monge M., Boffano G. M., Macri K., Maio P., Ozzello A., Pergolizzi E., Gaia D., Gennari P., Micali G., Rossetto E., Dalmazzo C., Oreglia M., Stefani T., Dossena C., Paglia P., Bosoni S., Romanelli T., Inchiostro S., Dauriz M., Bossi C. A., Meregalli G., Balini A., Berzi D., Filippini B., Crotto G., Paccagnella A., Orrasch M., Sambataro M., Citro T., Kiwanuka E., Bagolin E., Almoto B., Macchia A., Branca M. T., Filesi M., Candido R., Caroli E., Manca E., Petrucco A., Tommasi E., Jagodnik G., Baskar B., Daris N., Dal Col P., Pellegrini M. A., Tonutti L., Venturini G., Andreani M., Turchi F., Fedrighelli F., Martinelli G., Rongioletti R., Candidi M., Pais M., Moro E., Cervellino F., Sinisi R., Zampino A., Mingardi R., Lora L., Reitano R., Stocchiero C., Simoncini M., Mesturino C. A., Zen F., Di Pietro S., Scoponi C., Tilaro L., Pelliccioni S., Slongo R., Vita E., Garofalo A., Vitale F., Campanella B., Mastrilli V., Borrelli T., D'Avino A., and Perbellini A.
- Abstract
Background: Albuminuria has been classically considered a marker of kidney damage progression in diabetic patients and it is routinely assessed to monitor kidney function. However, the role of a mild GFR reduction on the development of stage ≥3 CKD has been less explored in type 1 diabetes mellitus (T1DM) patients. Aim of the present study was to evaluate the prognostic role of kidney disease measures, namely albuminuria and reduced GFR, on the development of stage ≥3 CKD in a large cohort of patients affected by T1DM. Methods: A total of 4284 patients affected by T1DM followed-up at 76 diabetes centers participating to the Italian Association of Clinical Diabetologists (Associazione Medici Diabetologi, AMD) initiative constitutes the study population. Urinary albumin excretion (ACR) and estimated GFR (eGFR) were retrieved and analyzed. The incidence of stage ≥3 CKD (eGFR < 60 mL/min/1.73 m2) or eGFR reduction > 30% from baseline was evaluated. Results: The mean estimated GFR was 98 ± 17 mL/min/1.73m2 and the proportion of patients with albuminuria was 15.3% (n = 654) at baseline. About 8% (n = 337) of patients developed one of the two renal endpoints during the 4-year follow-up period. Age, albuminuria (micro or macro) and baseline eGFR < 90 ml/min/m2 were independent risk factors for stage ≥3 CKD and renal function worsening. When compared to patients with eGFR > 90 ml/min/1.73m2 and normoalbuminuria, those with albuminuria at baseline had a 1.69 greater risk of reaching stage 3 CKD, while patients with mild eGFR reduction (i.e. eGFR between 90 and 60 mL/min/1.73 m2) show a 3.81 greater risk that rose to 8.24 for those patients with albuminuria and mild eGFR reduction at baseline. Conclusions: Albuminuria and eGFR reduction represent independent risk factors for incident stage ≥3 CKD in T1DM patients. The simultaneous occurrence of reduced eGFR and albuminuria have a synergistic effect on renal function worsening.
- Published
- 2018
43. HLA allele frequencies and susceptibility to COVID-19 in a group of 99 Italian patients
- Author
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Novelli, A., Andreani, M., Biancolella, M., Liberatoscioli, L., Passarelli, C., Colona, V. L., Rogliani, P., Leonardis, F., Campana, A., Carsetti, R., Andreoni, M., Bernardini, S., Novelli, G., Locatelli, Franco, Locatelli F. (ORCID:0000-0002-7976-3654), Novelli, A., Andreani, M., Biancolella, M., Liberatoscioli, L., Passarelli, C., Colona, V. L., Rogliani, P., Leonardis, F., Campana, A., Carsetti, R., Andreoni, M., Bernardini, S., Novelli, G., Locatelli, Franco, and Locatelli F. (ORCID:0000-0002-7976-3654)
- Abstract
With the aim to individuate alleles that may reflect a higher susceptibility to the disease, in the present study we analyzed the HLA allele frequency distribution in a group of 99 Italian patients affected by a severe or extremely severe form of COVID-19. After the application of Bonferroni's correction for multiple tests, a significant association was found for HLA-DRB1*15:01, -DQB1*06:02 and -B*27:07, after comparing the results to a reference group of 1017 Italian individuals, previously typed in our laboratory. The increased frequencies observed may contribute to identify potential markers of susceptibility to the disease, although controversial results on the role of single HLA alleles in COVID-19 patients have been recently reported.
- Published
- 2020
44. Human leucocyte antigen diversity: A biological gift to escape infections, no longer a barrier for haploidentical Hemopoietic Stem Cell Transplantation
- Author
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Andreani, M., Gaspari, S., Locatelli, Franco, Locatelli F. (ORCID:0000-0002-7976-3654), Andreani, M., Gaspari, S., Locatelli, Franco, and Locatelli F. (ORCID:0000-0002-7976-3654)
- Abstract
Since the beginning of life, every multicellular organism appeared to have a complex innate immune system although the adaptive immune system, centred on lymphocytes bearing antigen receptors generated by somatic recombination, arose in jawed fish approximately 500 million years ago. The major histocompatibility complex MHC, named the Human leucocyte antigen (HLA) system in humans, represents a vital function structure in the organism by presenting pathogen-derived peptides to T cells as the main initial step of the adaptive immune response. The huge level of polymorphism observed in HLA genes definitely reflects selection, favouring heterozygosity at the individual or population level, in a pathogen-rich environment, although many are located in introns or in exons that do not code for the antigen-biding site of the HLA. Over the past three decades, the extent of allelic diversity at HLA loci has been well characterized using high-resolution HLA-DNA typing and the number of new HLA alleles, produced through next-generation sequencing methods, is even more rapidly increasing. The level of the HLA system polymorphism represents an obstacle to the search of potential compatible donors for patients affected by haematological disease proposed for a hematopoietic stem cell transplant (HSCT). Data reported in literature clearly show that antigenic and/or allelic mismatches between related or unrelated donors and patients influences the successful HSCT outcome. However, the recent development of the new transplant strategy based on the choice of haploidentical donors for HSCT is questioning the role of HLA compatibility, since the great HLA disparities present do not worsen the overall clinical outcome. Nowadays, NGS has contributed to define at allelic levels the HLA polymorphism and solve potential ambiguities. However, HLA functions and tissue typing probably need to be further investigated in the next future, to understand the reasons why in haploidentical transplants
- Published
- 2020
45. Efficacy of third-party chimeric antigen receptor modified peripheral blood natural killer cells for adoptive cell therapy of B-cell precursor acute lymphoblastic leukemia
- Author
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Quintarelli, C., Sivori, S., Caruso, S., Carlomagno, S., Falco, M., Boffa, I., Orlando, D., Guercio, M., Abbaszadeh, Z., Sinibaldi, M., Di Cecca, S., Camera, A., Cembrola, B., Pitisci, A., Andreani, M., Vinti, L., Gattari, S., Del Bufalo, F., Algeri, M., Li Pira, G., Moseley, A., De Angelis, B., Moretta, L., Locatelli, Franco, Locatelli F. (ORCID:0000-0002-7976-3654), Quintarelli, C., Sivori, S., Caruso, S., Carlomagno, S., Falco, M., Boffa, I., Orlando, D., Guercio, M., Abbaszadeh, Z., Sinibaldi, M., Di Cecca, S., Camera, A., Cembrola, B., Pitisci, A., Andreani, M., Vinti, L., Gattari, S., Del Bufalo, F., Algeri, M., Li Pira, G., Moseley, A., De Angelis, B., Moretta, L., Locatelli, Franco, and Locatelli F. (ORCID:0000-0002-7976-3654)
- Abstract
We developed an innovative and efficient, feeder-free culture method to genetically modify and expand peripheral blood-derived NK cells with high proliferative capacity, while preserving the responsiveness of their native activating receptors. Activated peripheral blood NK cells were efficiently transduced by a retroviral vector, carrying a second-generation CAR targeting CD19. CAR expression was demonstrated across the different NK-cell subsets. CAR.CD19-NK cells display higher antileukemic activity toward CD19+ cell lines and primary blasts obtained from patients with B-cell precursor ALL compared with unmodified NK cells. In vivo animal model data showed that the antileukemia activity of CAR.CD19-NK cell is superimposable to that of CAR-T cells, with a lower xenograft toxicity profile. These data support the feasibility of generating feeder-free expanded, genetically modified peripheral blood NK cells for effective “off-the-shelf” immuno-gene-therapy, while their innate alloreactivity can be safely harnessed to potentiate allogeneic cell therapy.
- Published
- 2020
46. Characterization of the novel HLA-DPA1*01:03:19 allele by sequencing-based typing
- Author
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Cargou, M., Andreani, M., Locatelli, Franco, Blouin, L., Visentin, J., Locatelli F. (ORCID:0000-0002-7976-3654), Cargou, M., Andreani, M., Locatelli, Franco, Blouin, L., Visentin, J., and Locatelli F. (ORCID:0000-0002-7976-3654)
- Abstract
HLA-DPA1*01:03:19 differs from DPA1*01:03:01:02 by one nucleotide substitution in codon 190 in exon 4.
- Published
- 2020
47. Fluid Circulation Along an Oceanic Detachment Fault: Insights From Fluid Inclusions in Silicified Brecciated Fault Rocks (Mid‐Atlantic Ridge at 13°20′N)
- Author
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Verlaguet, A., primary, Bonnemains, D., additional, Mével, C., additional, Escartín, J., additional, Andreani, M., additional, Bourdelle, F., additional, Boiron, M‐C., additional, and Chavagnac, V., additional
- Published
- 2021
- Full Text
- View/download PDF
48. Recipient mHag-HA1 disparity and aGVHD in thalassemic-transplanted patients
- Author
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Nesci, S, Buffi, O, Iliescu, A, Andreani, M, and Lucarelli, G
- Published
- 2003
- Full Text
- View/download PDF
49. 16th IHIW: Analysis of HLA Population Data, with updated results for 1996 to 2012 workshop data (AHPD project report)
- Author
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Riccio, M. E., Buhler, S., Nunes, J. M., Vangenot, C., Cuénod, M., Currat, M., Di, D., Andreani, M., Boldyreva, M., Chambers, G., Chernova, M., Chiaroni, J., Darke, C., Di Cristofaro, J., Dubois, V., Dunn, P., Edinur, H. A., Elamin, N., Eliaou, J.-F., Grubic, Z., Jaatinen, T., Kanga, U., Kervaire, B., Kolesar, L., Kunachiwa, W., Lokki, M. L., Mehra, N., Nicoloso, G., Paakkanen, R., Voniatis, Papaioannou D., Papasteriades, C., Poli, F., Richard, L., Alonso, Romón I., Slavčev, A., Sulcebe, G., Suslova, T., Testi, M., Tiercy, J.-M., Varnavidou, A., Vidan-Jeras, B., Wennerström, A., and Sanchez-Mazas, A.
- Published
- 2013
- Full Text
- View/download PDF
50. Fate of chronic myeloid leukemia patients treated with allogeneic bone marrow transplantation or chemotherapy and/or interferon at a single center: long-term results
- Author
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Gaziev, D, Galimberti, M, Polchi, P, Angelucci, E, Giardini, C, Baronciani, D, Andreani, M, Persini, B, Erer, B, Sodani, P, Manna, M, Nicolini, G, Visani, G, and Lucarelli, G
- Published
- 2002
- Full Text
- View/download PDF
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