{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,1]],"date-time":"2026-09-01T02:09:26Z","timestamp":1788228566082,"version":"build-2803163510"},"reference-count":40,"publisher":"Rockefeller University Press","issue":"11","content-domain":{"domain":["rupress.org"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2010,10,25]]},"abstract":"<jats:p>Recently, several cases of fatal lymphocytic choriomeningitis virus (LCMV) infection occurred in transplant recipients being treated with the immunosuppressive calcineurin inhibitor FK506. These findings were surprising because LCMV is a noncytolytic virus. To understand how a noncytolytic virus can cause disease under conditions of immunosuppression, we used the mouse LCMV model and found that, similar to the observations in human transplant recipients, LCMV infection of FK506-treated mice resulted in a lethal disease characterized by viremia, lack of seroconversion, and minimal lymphocytic infiltrates in the tissues. However, despite the apparent absence of an antiviral immune response, this disease was orchestrated by virus-specific T cells. FK506 did not prevent the generation and proliferation of LCMV-specific T cells but instead altered their differentiation so that these effector T cells lost the ability to control virus but were still capable of mediating disease. These pathogenic T cells initiated a cytokine storm characterized by high levels of tumor necrosis factor (TNF) and interleukin 6 (IL-6), and depletion of T cells or blockade of these inflammatory cytokines prevented the lethal disease. Our study shows that inhibiting calcineurin can generate pathogenic T cells and indicates that T cell\u2013mediated viral disease can occur even under conditions of immunosuppression. Furthermore, we identify a potential strategy (blockade of TNF and IL-6) for treatment of transplant recipients who have acute complications of viral infection.<\/jats:p>","DOI":"10.1084\/jem.20100124","type":"journal-article","created":{"date-parts":[[2010,10,5]],"date-time":"2010-10-05T03:23:38Z","timestamp":1286249018000},"page":"2355-2367","update-policy":"https:\/\/doi.org\/10.1084\/jem.crossmarkpolicy","source":"Crossref","is-referenced-by-count":36,"title":["Pathogenic virus-specific T cells cause disease during treatment with the calcineurin inhibitor FK506: implications for transplantation"],"prefix":"10.1084","volume":"207","author":[{"given":"Koichi","family":"Araki","sequence":"first","affiliation":[{"name":"Emory Vaccine Center 1 , 2 , 3 , 4 , 5 , and 6"},{"name":"Department of Microbiology and Immunology 1 , 2 , 3 , 4 , 5 , and 6"},{"name":"Emory Transplant Center 1 , 2 , 3 , 4 , 5 , and 6"},{"name":"Department of Surgery 1 , 2 , 3 , 4 , 5 , and 6"},{"name":"Department of 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