Chiara Villa

ORCID: 0000-0002-1667-5892
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Research Areas
  • Virus-based gene therapy research
  • CRISPR and Genetic Engineering
  • Atherosclerosis and Cardiovascular Diseases
  • Cell Adhesion Molecules Research
  • HIV Research and Treatment
  • Chemokine receptors and signaling
  • HIV/AIDS drug development and treatment
  • Protein Degradation and Inhibitors
  • Lymphoma Diagnosis and Treatment
  • Eosinophilic Disorders and Syndromes
  • Ubiquitin and proteasome pathways
  • HIV/AIDS Research and Interventions
  • Viral Infections and Immunology Research
  • Chronic Lymphocytic Leukemia Research
  • Ocular Infections and Treatments
  • Acute Ischemic Stroke Management
  • Cardiovascular Health and Disease Prevention
  • Extracellular vesicles in disease
  • Bacteriophages and microbial interactions
  • Acute Myeloid Leukemia Research
  • Ocular Surface and Contact Lens
  • Acute Lymphoblastic Leukemia research
  • Respiratory viral infections research
  • Immune cells in cancer
  • Glaucoma and retinal disorders

IRCCS Ospedale San Raffaele
2022-2025

Vita-Salute San Raffaele University
2000-2025

San Raffaele University of Rome
2011-2023

Nestlé (Switzerland)
2015

Ruhr University Bochum
2000

The SDF-1 3'A allelic polymorphism has been reported to influence either positively or negatively the progression of human immunodeficiency virus type 1 (HIV-1) disease. Therefore, genotype 729 HIV-1-infected individuals pooled from 3 distinct cohorts was determined. A statistically nonsignificant association between SDF1-3'A/3'A and accelerated disease evident among seroconverters (n=319), but a striking correlation decreased survival after diagnosis AIDS according 1993 definition loss...

10.1086/315650 article EN The Journal of Infectious Diseases 2000-07-01

ABSTRACT Extracellular vesicles (EVs) are crucial for intercellular communication and found in various biological fluids. The identification immunophenotyping of such small particles continue to pose significant challenges. Here, we have developed a workflow the optimisation next‐generation panel in‐depth circulating plasma EVs using spectral flow cytometry. Our data collection followed multistep phase both instrument setup 21‐colour design, thus maximising fluorescent signal recovery. This...

10.1002/jex2.70045 article EN cc-by-nc-nd Journal of Extracellular Biology 2025-04-01

We explored the relation between blood concentrations of monocyte/lymphocyte subsets and carotid artery plaque macrophage content, measured by positron emission tomography (PET) with 11C-PK11195.In 9 patients plaques we performed 11C-PK11195-PET/computed angiography imaging measurement absolute frequencies circulating monocytes T-cell subsets. Plaque standardized uptake value (SUV) for 11C-PK11195 was negatively correlated total (r = -0.58, p 0.05) CD14++CD16-HLA-DR+ classical subset -0.82,...

10.1016/j.ijcha.2018.09.005 article EN cc-by-nc-nd IJC Heart & Vasculature 2018-09-25

The purpose of this study was to develop a novel, objective, and semiautomated method quantify conjunctival redness by correlating measured with standard clinical symptom scales inflammatory cell infiltration.Eleven outpatients presenting mild severe hyperemia were included in the study. Clinical examination patient history; visual analogue score (VAS) for ocular symptoms; 25-item National Eye Institute Visual Function Questionnaire (NEI-VFQ 25) quality life/vision; photographs anterior...

10.1167/iovs.15-17105 article EN Investigative Ophthalmology & Visual Science 2015-11-03

Summary. The purging efficacy of the Miltenyi sorting system was evaluated by qualitative and TaqMan quantitative polymerase chain reaction (PCR) in myeloma patients, using immunoglobulin genes. After small‐scale selection, PCR showed that 6 12 leukaphereses cells were no longer detectable. Envisaging a possible clinical application, from three patients underwent large‐scale selection. Qualitative still Quantitative PCR, performed two tumour depletion of␣1 2 logs respectively. Although...

10.1046/j.1365-2141.2002.03448.x article EN British Journal of Haematology 2002-05-19

We describe a multi-step high-dimensional (HD) flow cytometry workflow for the deep phenotypic characterization of T cells infiltrating metastatic tumor lesions in liver, particularly derived from colorectal cancer (CRC-LM). First, we applied novel cytometer setting approach based on single positive rather than fluorescent beads, resulting optimal sensitivity when compared with previously published protocols. Second, set up 26-color antibody panel designed to assess functional state both...

10.26508/lsa.202101316 article EN cc-by Life Science Alliance 2022-06-03

Recombinant MVAs (rMVAs) are widely used both in basic and clinical research. Our previously developed Red-to-Green Gene Swapping Method (RGGSM), a cytometry-based Cell-Sorting protocol, revolves around the transient expression of green fluorescent cytoplasmic marker, to subsequently obtain purified untagged rMVA upon loss that marker by site-specific recombination. The standard RGSSM is quite costly terms bench work, reagents, Sorting Facility fees. Although faster than other methods...

10.1186/s12967-023-04353-7 article EN cc-by Journal of Translational Medicine 2023-07-23

Extracellular vesicles (EVs) released by mesenchymal stromal cells (MSCs) contain a set of microRNAs with regenerative and anti-inflammatory roles. Therefore, purified MSC-EVs are envisioned as next-generation therapeutic option for wide array diseases. In this protocol, we report the strategy successfully sorting EVs from supernatant adipose-derived MSCs (ASCs), often used in orthopedics medicine applications. First, described sample preparation, focusing on EV isolation labeling steps...

10.3791/67232 article EN Journal of Visualized Experiments 2024-10-11
Chu Jin Jianguo Li Carolina Ceballos‐Diaz Todd E. Golde Domenico Pratic and 95 more Marie Sarazin Guillaume Doroth É E Leonardo Cruz de Souza Pièrre Aucouturier Andrew Coogan Barbora Schutov Susanne Husung Karolina Furczyk Bernhard T. Baune Peter Kropp Johannes Thome Yvette I. Sheline Marcus E. Raichle Phillip F. Giannopoulos Yash B. Joshi Margaret Sperow Jinguo Li Lynn G. Kirby David Baglietto‐Vargas Rodrigo Medeiros Hilda Martínez‐Coria Frank M. LaFerla Kim Y. Green Jose F. Abisambra Umesh K. Jinwal Yoshinari Miyata Justin Rogers Laura J. Blair Xiaokai Li Sandlin P. Seguin Li Wang Ying Jin Justin Bacon Sarah Brady Matthew E. Cockman Chantal Guidi Juan Zhang John Koren Zapporah T. Young Christopher Atkins Bo Zhang Lisa Y. Lawson Edwin J. Weeber Jeff Rey Leonid Brodsky Jason E. Gestwicki Chad A. Dickey Giovanna Zamboni Gordon Wilcock Gwenaëlle Douaud Erin Drazich Ellen McCulloch Nicola Filippini Irene Tracey J.C. Brooks Stephen M. Smith M. Webster Jenkinson Clare E. Mackay Daniela Galimberti Chiara Fenoglio María Serpente Chiara Villa R Bonsi Andrea Arighi Giorgio Fumagalli Roberto Del Bo Amalia C. Bruni Maria Anfossi Alessandra Clodomiro Chiara Cupidi Benedetta Nacmias Sandro Sorbi Irene Piaceri Silvia Bagnoli Valentina Bessi Alessandra Marcone Chiara Cerami Stefano Cappa Massimo Filippi Federica Agosta Giuseppe Magnani Gıancarlo Comı M. Franceschi Innocenzo Rainero M. T. Giordana Elisa Rubino Patrizia Ferrero Ekaterina Rogaeva Zhengrui Xi Annamaria Confaloni Paola Piscopo Giuseppe Bruno Giuseppina Talarico Annachiara Cagnin Francesca Clerici

10.1016/s0006-3223(13)00653-7 article EN Biological Psychiatry 2013-08-09

Abstract Background Recombinant MVAs (rMVAs) are widely used both in basic and clinical research. Our previously developed Red-to-Green Gene Swapping Method (RGGSM), a cytometry-based Cell-Sorting protocol, revolves around the transient expression of green fluorescent cytoplasmic marker, to subsequently obtain purified untagged rMVA upon loss that marker by site-specific recombination. The standard RGSSM is quite costly terms bench work, reagents, Sorting Facility fees. Although faster than...

10.21203/rs.3.rs-3071499/v1 preprint EN cc-by Research Square (Research Square) 2023-06-28
Qiaoli Li Koen van de Wetering Jouni Uitto Mehmet M. Altintas Jochen Reiser and 95 more Moritz Lux Alexander Blaut Nuru Eltrich Andrei Bideak Martin Müller John Michael Hoppe Hermann‐Josef Gröne Massimo Locati Volker Vielhauer Masanori Hara Kazuhiko Oohara Dao‐Fu Dai Helen Liapis Stephen N. Greenhalgh Kylie Matchett Richard Taylor Katherine Huang John Li Koy Saeteurn Mhairi Donnelly Eilidh Simpson Joshua L. Pollack Amha Atakilit Kenneth GL Simpson Jacquelyn J. Maher John P. Iredale Dean Sheppard Neil C. Henderson Guomin Xie Shi Yin Zhenzhen Zhang Dan Qi Xia Wang Donghwan Kim Tomoki Yagai Chad Brocker Yan Wang Frank González Hua Wang Aijuan Qu Ashley M. Woodward Sylvain Lehoux Flavio Mantelli Antonio Di Zazzo Inka Brockhausen Stefano Bonini Pablo Argüeso Max Vaickus Terry Hsieh Ekaterina Kintsurashvili Jiyoun Kim Daniel Kirsch George Kasotakis Daniel G. Remick Hirokazu Kameyama Kenji Uchimura Taro Yamashita Kaori Kuwabara Mineyuki Mizuguchi Shang‐Cheng Hung Keiichiro Okuhira Tomohiro Masuda Tomoki Kosugi Takashi Ohgita Hiroyuki Saito Yukio Ando Kazuchika Nishitsuji Fabian P.S. Yu Benjamin S. Sajdak Jakub Sikora Alexander E Salmon Murtaza S. Nagree Ji Rí Gurka Iris S. Kassem Daniel M. Lipinski Joseph Carroll Jeffrey A. Medin Andrea Farini Aoife Gowran Pamela Bella Clementina Sitzia Alessandro Scopece Elisa Castiglioni Davide Rovina Patrizia Nigro Chiara Villa Francesco Fortunato Giacomo P. Comi Giuseppina Milano Giulio Pompilio Yvan Torrente Elisabetta Gazzerro Serena Baratto Stefania Assereto Sımona Baldassari

10.1016/s0002-9440(18)31128-3 article EN publisher-specific-oa American Journal Of Pathology 2019-01-18
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