Sergio Abrignani

ORCID: 0000-0002-0794-3285
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About
Contact & Profiles
Research Areas
  • Hepatitis C virus research
  • Immune Cell Function and Interaction
  • T-cell and B-cell Immunology
  • Hepatitis B Virus Studies
  • Immunotherapy and Immune Responses
  • Monoclonal and Polyclonal Antibodies Research
  • Systemic Lupus Erythematosus Research
  • SARS-CoV-2 and COVID-19 Research
  • Liver Disease Diagnosis and Treatment
  • COVID-19 Clinical Research Studies
  • PARP inhibition in cancer therapy
  • MicroRNA in disease regulation
  • Cancer Immunotherapy and Biomarkers
  • Glycosylation and Glycoproteins Research
  • HIV Research and Treatment
  • Colorectal Cancer Treatments and Studies
  • Immunodeficiency and Autoimmune Disorders
  • CAR-T cell therapy research
  • Cancer-related molecular mechanisms research
  • Diabetes and associated disorders
  • Inflammatory Bowel Disease
  • Animal Virus Infections Studies
  • RNA modifications and cancer
  • Liver Diseases and Immunity
  • IL-33, ST2, and ILC Pathways

Istituto Nazionale Genetica Molecolare
2015-2024

University of Milan
2015-2024

Ospedale Maggiore
2011-2023

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
2011-2023

Ospedale San Giuseppe
2022

MultiMedica
2022

University of Milano-Bicocca
2015-2019

Policlinico Tor Vergata
2015-2017

Istituti di Ricovero e Cura a Carattere Scientifico
2015-2016

Science for Life Laboratory
2015

Chronic hepatitis C virus (HCV) infection occurs in about 3 percent of the world's population and is a major cause liver disease. HCV also associated with cryoglobulinemia, B lymphocyte proliferative disorder. Virus tropism controversial, mechanisms cell entry remain unknown. The envelope protein E2 binds human CD81, tetraspanin expressed on various types including hepatocytes lymphocytes. Binding was mapped to extracellular loop CD81. Recombinant molecules containing this bound antibodies...

10.1126/science.282.5390.938 article EN Science 1998-10-30

We investigated whether human resting T cells could be activated to proliferate and display effector function in the absence of cell receptor occupancy. report that combination interleukin 2 (IL-2), tumor necrosis factor alpha, IL-6 highly purified naive (CD45RA+) memory (CD45RO+) CD4+ proliferate. Under this condition, also as measured by lymphokine synthesis help for immunoglobulin production B cells. This novel Ag-independent pathway activation may play an important role vivo recruiting...

10.1084/jem.180.3.1159 article EN The Journal of Experimental Medicine 1994-09-01
H.G. Stunnenberg Martin Hirst Sergio Abrignani David J. Adams Melanie de Almeida and 95 more Lucia Altucci Viren Amin Ido Amit Stylianos E. Antonarakis Samuel Aparício Takahiro Arima Laura Arrigoni Rob J.W. Arts Vahid Asnafi Manel Esteller Jae‐Bum Bae Kevin Baßler Stephan Beck Benjamin E. Berkman B Bernstein Mikhail Bilenky Adrian Bird Christoph Bock Bernhard O. Boehm Guillaume Bourque Charles E. Breeze Benedikt Brors David Bujold Oliver S. Burren Marion J.G. Bussemakers Adam S. Butterworth Elı́as Campo Enrique Carrillo de Santa Pau Lisa H. Chadwick Kui Ming Chan Wei Chen Tom H. Cheung Luca Chiapperino Nam‐Kyong Choi Ho‐Ryun Chung Laura Clarke Joseph M. Connors Philippe Cronet John Danesh Manolis Dermitzakis Gerard Drewes Pawel Durek Stephanie O. M. Dyke Tomasz Dyląg Connie J. Eaves Peter Ebert Roland Eils Roland Eils Catherine Ennis Tariq Enver Elise A. Feingold Bärbel Felder Anne C. Ferguson‐Smith Jude Fitzgibbon Paul Flicek Roger Foo Peter Fraser Mattia Frontini Eileen E. M. Furlong Sitanshu Gakkhar Nina Gasparoni Gilles Gasparoni Daniel H. Geschwind Petar Glažar Thomas Graf Frank Grosveld Xin‐Yuan Guan Roderic Guigó Marta Gut Alf Hamann Bok-Ghee Han R. Alan Harris Simon Heath Kristian Helin Jan G. Hengstler Alireza Heravi‐Moussavi Karl Herrup Steven Hill Jason A. Hilton Benjamin C. Hitz Bernhard Horsthemke Ming Hu Joo-Yeon Hwang Nancy Y. Ip Takashi Ito Biola M. Javierre Sasa Jenko Thomas Jenuwein Yann Joly Steven J.M. Jones Yae Kanai Hee Gyung Kang Aly Karsan Alexandra K. Kiemer Song Cheol Kim

10.1016/j.cell.2016.11.007 article EN publisher-specific-oa Cell 2016-11-01

The immune response against hepatitis C virus (HCV) is rarely effective at clearing the virus, resulting in ∼170 million chronic HCV infections worldwide. Here we report that ligation of an receptor (CD81) inhibits natural killer (NK) cells. Cross-linking CD81 by major envelope protein (HCV-E2) or anti-CD81 antibodies blocks NK cell activation, cytokine production, cytotoxic granule release, and proliferation. This inhibitory effect was observed using both activated resting Conversely, on...

10.1084/jem.20011124 article EN The Journal of Experimental Medicine 2001-12-31

The high-throughput analysis of microRNAs (miRNAs) circulating within the blood healthy and diseased individuals is an active area biomarker research. Whereas quantitative real-time reverse transcription polymerase chain reaction (qPCR)-based methods are widely used, it yet unresolved how data should be normalized. Here, we show that a combination different algorithms results in identification candidate reference miRNAs can exploited as normalizers, both discovery validation phases. Using...

10.1093/bib/bbv056 article EN Briefings in Bioinformatics 2015-08-03

Hepatitis C virus (HCV) is a major cause of chronic hepatitis. The does not replicate efficiently in cell cultures, and it therefore difficult to assess infection-neutralizing antibodies evaluate protective immunity vitro. To study the binding HCV envelope cell-surface receptors, we developed an assay specific recombinant proteins human cells neutralization thereof. expressed various systems were incubated with cells, was assessed by flow cytometry using anti-envelope antibodies. Envelope...

10.1073/pnas.93.5.1759 article EN Proceedings of the National Academy of Sciences 1996-03-05

Regulatory T (TR) cells consist of phenotypically and functionally distinct CD4+ CD8+ cell subsets engaged both in maintaining self-tolerance preventing anti–non-self effector responses (microbial, tumor, transplant, so on) that may be harmful to the host. Here we propose proinflammatory function virus-specific memory CCR7–CD8+ cells, which are massively recruited liver, inefficient (in terms IFN-γ production) patients with chronic hepatitis C virus (HCV) infection because concomitant...

10.1172/jci200420515 article EN Journal of Clinical Investigation 2004-04-01

Infection with hepatitis C virus (HCV), a leading cause of chronic liver diseases, can associate B lymphocyte proliferative disorders, such as mixed cryoglobulinemia and non-Hodgkin lymphoma. The major envelope protein HCV (HCV-E2) binds, high affinity CD81, tetraspanin expressed on several cell types. Here, we show that engagement CD81 human cells by combination HCV-E2 an anti-CD81 mAb triggers the JNK pathway leads to preferential proliferation naïve (CD27 - ) subset. In parallel, have...

10.1073/pnas.0509402102 article EN Proceedings of the National Academy of Sciences 2005-12-09

The adult liver is an organ without constitutive lymphoid components. Therefore, any intrahepatic T cell found in chronic hepatitis should have migrated to the after infection and inflammation. Because of little information available on differences between peripheral cells, we used recombinant proteins C virus (HCV) establish specific lines clones from biopsies patients with compared them those present blood mononuclear cells (PBMC). We that protein nonstructural 4 (NS4) was able stimulate...

10.1084/jem.178.1.17 article EN The Journal of Experimental Medicine 1993-07-01

Invariant natural killer T (NKT) cells are a highly conserved subset of lymphocytes expressing semi-invariant cell receptor (TCR), which is restricted to CD1d and specific for the glycosphingolipid antigen α-galactosylceramide. Their ability secrete variety cytokines, in turn modulate activation both innate acquired immune responses, suggests that invariant NKT exert regulatory role mainly via indirect mechanisms. A relevant question whether can directly help B cells. We document here human...

10.1084/jem.20021616 article EN The Journal of Experimental Medicine 2003-04-14

Invariant natural killer T (iNKT) cells are innate-like lymphocytes recognizing CD1d-restricted glycolipid antigens, such as alpha-galactosylceramide (alphaGC). We assessed whether iNKT help B lymphocyte responses and found that mice immunized with proteins alphaGC develop antibody titers 1-2 logs higher than those induced by alone. Activation of enhances protection against infections influenza elicits frequencies memory to booster immunizations. Protein vaccination alphaGC, but not...

10.1073/pnas.0700191104 article EN Proceedings of the National Academy of Sciences 2007-02-28

Hepatitis C virus (HCV) is a major human pathogen causing chronic liver disease. We have recently found that the large extracellular loop (LEL) of CD81 binds HCV. This finding prompted us to assess structure-function features HCV-CD81 interaction by using recombinant E2 protein and soluble form LEL. HCV-E2 LEL with K d 1.8 nM; can mediate attachment on hepatocytes; engagement mediates internalization only 30% molecules even after 12 h; four cysteines two disulfide bridges, integrity which...

10.1128/jvi.74.10.4824-4830.2000 article EN Journal of Virology 2000-05-15
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