Rapid dissemination of human T-lymphotropic virus type 1 during primary infection in transplant recipients. Issue 1 (December 2016)

• Record Type: Journal Article
• Authors: Cook, Lucy; Melamed, Anat; Demontis, Maria; Laydon, Daniel; Fox, James; Tosswill, Jennifer; Freitas, Declan; Price, Ashley; Medcalf, James; Martin, Fabiola; Neuberger, James; Bangham, Charles; Taylor, Graham
• Is Part Of: Retrovirology. Volume 13:Issue 1(2016)
• Page Start: 1
• Page End: 9
• Publication Date: 2016-12
• Subjects: HTLV-1 -- Proviral load -- Clonality -- 2LTR DNA circles -- Organ transplantation -- Raltegravir -- Zidovudine; Retroviruses -- Periodicals; 579.2569
• DOI: 10.1186/s12977-015-0236-7
• Languages: English
• ISSNs: 1742-4690

Abstract

Abstract Background Human T-lymphotropic virus type 1 (HTLV-1) infects an estimated 10 million persons globally with transmission resulting in lifelong infection. Disease, linked to high proviral load, occurs in a minority. In established infection HTLV-1 replicates through infectious spread and clonal expansion of infected lymphocytes. Little is known about acute HTLV-1 infection. The kinetics of early HTLV-1 infection, following transplantation-acquired infection in three recipients from one HTLV-1 infected donor, is reported. The recipients were treated with two HTLV-1 enzyme inhibitors 3 weeks post exposure following the detection of HTLV-1 provirus at low level in each recipient. HTLV-1 infection was serially monitored by serology, quantification of proviral load and HTLV-1 2LTR DNA circles and by HTLV-1 unique integration site analysis. Results HTLV-1 antibodies were first detected 16–39 days post-transplantation. HTLV-1 provirus was detected by PCR on day 16–23 and increased by 2–3 log by day 38–45 with a peak proviral doubling time of 1.4 days, after which steady state was reached. The rapid proviral load expansion was associated with high frequency of HTLV-1 2LTR DNA circles. The number of HTLV-1 unique integration sites was high compared with established HTLV-1 infection. Clonal expansion of infected cells was detected as early as day 37 with high initial oligoclonality index, consistent with early mitotic proliferation. Conclusions In recipients infected through organ transplantation HTLV-1 disseminated rapidly despite early anti-HTLV-1 treatment. Proviral load set point was reached within 6 weeks. Seroconversion was not delayed. Unique integration site analysis and HTLV-1 2LTR DNA circles indicated early clonal expansion and high rate of infectious spread.