| Literature DB >> 30195746 |
Deanna L Kelly1, Xin Li2, Catherine Kilday1, Stephanie Feldman1, Sarah Clark2, Fang Liu1, Robert W Buchanan1, Leonardo H Tonelli3.
Abstract
Immunological abnormalities are increasingly reported in people with schizophrenia, but no clear functional biomarkers associated with genetic correlates of the disease have been found. Regulatory T cells (Tregs) are key immunoregulatory cells involved in the control of inflammatory processes and their functions are directly related to the human leucocyte antigen (HLA) gene, which has been implicated in schizophrenia genetic studies. However, there is a lack of studies reporting Treg status in people with schizophrenia. In the current study, the proportion of circulating Tregs was examined using flow cytometry in 26 medicated participants with schizophrenia and 17 healthy controls. Psychiatric symptoms and cognitive function were evaluated using the Scale for the Assessment of Negative Symptoms, the Brief Psychiatric Rating Scale, and the MATRICS Consensus Cognitive Battery. The proportion of Tregs was found to be significantly greater in the schizophrenia group compared to healthy controls. No differences were observed in total lymphocyte counts or CD3+ and CD4+ T cells, confirming a specific effect for Tregs. Elevated Tregs in schizophrenia correlated with fewer negative symptoms, a core domain of the illness. These results suggest that Tregs may contribute to improved negative symptoms in schizophrenia, possibly by counteracting on-going inflammatory processes.Entities:
Keywords: Blood biomarkers; CD4 cells; Cognition; Foxp3; Lymphocytes; MHC locus; Schizophrenia biomarkers
Mesh:
Substances:
Year: 2018 PMID: 30195746 PMCID: PMC6207456 DOI: 10.1016/j.psychres.2018.09.006
Source DB: PubMed Journal: Psychiatry Res ISSN: 0165-1781 Impact factor: 3.222