The Impact of Cytomegalovirus Infection on Natural Killer and CD8+ T Cell Phenotype in Multiple Sclerosis

Author:

Perri Valentina1,Zingaropoli Maria Antonella1ORCID,Pasculli Patrizia1ORCID,Ciccone Federica1,Tartaglia Matteo2,Baione Viola2,Malimpensa Leonardo3,Ferrazzano Gina2,Mastroianni Claudio Maria1ORCID,Conte Antonella23ORCID,Ciardi Maria Rosa1

Affiliation:

1. Department of Public Health and Infectious Diseases, Sapienza University of Rome, 00185 Rome, Italy

2. Department of Human Neurosciences, Sapienza University of Rome, 00185 Rome, Italy

3. IRCCS Neuromed, 86077 Pozzilli, Italy

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.

Publisher

MDPI AG

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