TY - JOUR A1 - Lérias, Joana A1 - Paraschoudi, Georgia A1 - Silva, Ines A1 - Martins, João A1 - Sousa, Eric de A1 - Condeço, Carolina A1 - Figueiredo, Nuno A1 - Carvalho, Carlos A1 - Dodoo, Ernest A1 - Jäger, Elke A1 - Rao, Martin A1 - Maeurer, Markus T1 - Clinically relevant immune responses against Cytomegalovirus : implications for precision medicine T2 - International journal of molecular sciences N2 - Immune responses to human cytomegalovirus (CMV) can be used to assess immune fitness in an individual. Further to its clinical significance in posttransplantation settings, emerging clinical and translational studies provide examples of immune correlates of protection pertaining to anti-CMV immune responses in the context of cancer or infectious diseases, e.g., tuberculosis. In this viewpoint, we provide a brief overview about CMV-directed immune reactivity and immune fitness in a clinical context and incorporate some of our own findings obtained from peripheral blood or tumour-infiltrating lymphocytes (TIL) from patients with advanced cancer. Observations in patients with solid cancers whose lesions contain both CMV and tumour antigen-specific T-cell subsets are highlighted, due to a possible CMV-associated "bystander" effect in amplifying local inflammation and subsequent tumour rejection. The role of tumour-associated antibodies recognising diverse CMV-derived epitopes is also discussed in light of anti-cancer immune responses. We discuss here the use of anti-CMV immune responses as a theranostic tool—combining immunodiagnostics with a personalised therapeutic potential—to improve treatment outcomes in oncological indications. KW - cytomegalovirus KW - immune responses KW - interferon gamma KW - antibodies KW - cancer KW - immunotherapy KW - T cells Y1 - 2019 UR - http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/50125 UR - https://nbn-resolving.org/urn:nbn:de:hebis:30:3-501257 SN - 1422-0067 SN - 1661-6596 N1 - This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0). VL - 20 IS - 8, Art. 1986 SP - 1 EP - 13 PB - Molecular Diversity Preservation International CY - Basel ER -