Multiple sclerosis (MS) is a debilitating neurological disease that has been classified as an immune-mediated attack on myelin, the protective sheath of nerves. Some aspects of its pathogenesis are still unclear; nevertheless, it is generally established that viral infections influence the course of the disease. Cytomegalovirus (CMV) is a major pathogen involved in alterations of the immune system, including the expansion of highly differentiated cytotoxic CD8+ T cells and the accumulation of adaptive natural killer (NK) cells expressing high levels of the NKG2C receptor. In this study, we evaluated the impact of latent CMV infection on MS patients through the characterization of peripheral NK cells, CD8+ T cells, and NKT-like cells using flow cytometry. We evaluated the associations between immune cell profiles and clinical features such as MS duration and MS progression, evaluated using the Expanded Disability Status Scale (EDSS). We showed that NK cells, CD8+ T cells, and NKT-like cells had an altered phenotype in CMV-infected MS patients and displayed high levels of the NKG2C receptor. Moreover, in MS patients, increased NKG2C expression levels were found to be associated with higher EDSS scores. Overall, these results support the hypothesis that CMV infection imprints the immune system by modifying the phenotype and receptor repertoire of NK and CD8+ T cells, suggesting a detrimental role of CMV on MS progression.

The impact of Cytomegalovirus infection on natural killer and CD8+ t cell phenotype in multiple sclerosis / Perri, Valentina; Zingaropoli, Maria Antonella; Pasculli, Patrizia; Ciccone, Federica; Tartaglia, Matteo; Baione, Viola; Malimpensa, Leonardo; Ferrazzano, Gina; Mastroianni, Claudio Maria; Conte, Antonella; Ciardi, Maria Rosa. - In: BIOLOGY. - ISSN 2079-7737. - 13:3(2024), pp. 1-14. [10.3390/biology13030154]

The impact of Cytomegalovirus infection on natural killer and CD8+ t cell phenotype in multiple sclerosis

Pasculli, Patrizia;Ciccone, Federica;Tartaglia, Matteo;Baione, Viola;Malimpensa, Leonardo;Ferrazzano, Gina;Mastroianni, Claudio Maria;Conte, Antonella;Ciardi, Maria Rosa
2024

Abstract

Multiple sclerosis (MS) is a debilitating neurological disease that has been classified as an immune-mediated attack on myelin, the protective sheath of nerves. Some aspects of its pathogenesis are still unclear; nevertheless, it is generally established that viral infections influence the course of the disease. Cytomegalovirus (CMV) is a major pathogen involved in alterations of the immune system, including the expansion of highly differentiated cytotoxic CD8+ T cells and the accumulation of adaptive natural killer (NK) cells expressing high levels of the NKG2C receptor. In this study, we evaluated the impact of latent CMV infection on MS patients through the characterization of peripheral NK cells, CD8+ T cells, and NKT-like cells using flow cytometry. We evaluated the associations between immune cell profiles and clinical features such as MS duration and MS progression, evaluated using the Expanded Disability Status Scale (EDSS). We showed that NK cells, CD8+ T cells, and NKT-like cells had an altered phenotype in CMV-infected MS patients and displayed high levels of the NKG2C receptor. Moreover, in MS patients, increased NKG2C expression levels were found to be associated with higher EDSS scores. Overall, these results support the hypothesis that CMV infection imprints the immune system by modifying the phenotype and receptor repertoire of NK and CD8+ T cells, suggesting a detrimental role of CMV on MS progression.
2024
cytomegalovirus; multiple sclerosis; nk cells; cd8+ t cells; nkt-like cells; nkg2c; flow cytometry
01 Pubblicazione su rivista::01a Articolo in rivista
The impact of Cytomegalovirus infection on natural killer and CD8+ t cell phenotype in multiple sclerosis / Perri, Valentina; Zingaropoli, Maria Antonella; Pasculli, Patrizia; Ciccone, Federica; Tartaglia, Matteo; Baione, Viola; Malimpensa, Leonardo; Ferrazzano, Gina; Mastroianni, Claudio Maria; Conte, Antonella; Ciardi, Maria Rosa. - In: BIOLOGY. - ISSN 2079-7737. - 13:3(2024), pp. 1-14. [10.3390/biology13030154]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1714738
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