2016
DOI: 10.1182/blood-2016-09-739433
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Screening transplant donors for HTLV-1 and -2

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Cited by 40 publications
(23 citation statements)
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“…Adult T‐cell leukemia/lymphoma (ATLL) is a rare and extremely aggressive T‐cell neoplasm with a dismal prognosis. The disease is caused by the retrovirus human T‐cell leukemia virus type 1 (HTLV‐1), which is endemic in southwestern Japan, sub‐Saharan Africa, South America, the Caribbean region, and certain areas in the Middle East and Australia . HTLV‐1 is also prevalent at low levels in the United States .…”
Section: Introductionmentioning
confidence: 99%
“…Adult T‐cell leukemia/lymphoma (ATLL) is a rare and extremely aggressive T‐cell neoplasm with a dismal prognosis. The disease is caused by the retrovirus human T‐cell leukemia virus type 1 (HTLV‐1), which is endemic in southwestern Japan, sub‐Saharan Africa, South America, the Caribbean region, and certain areas in the Middle East and Australia . HTLV‐1 is also prevalent at low levels in the United States .…”
Section: Introductionmentioning
confidence: 99%
“…Human T-cell leukemia virus type 1 (HTLV-1) and -2 (HTLV-2) belong to the Primate T Lymphotropic Virus group (PTLV), sharing common epidemiological and biological properties, and in particular T-lymphocytes tropism [ 1 ]. Isolated in 1980, HTLV-1 is the causative agent of adult T-cell leukemia/lymphoma (ATL) [ 2 ] and tropical spastic paraparesis/HTLV-1-associated myelopathy (TSP/HAM) [ 3 ].…”
Section: Introductionmentioning
confidence: 99%
“…Of note, the Global Virus Network Task Force on HTLV-1 recommends that transplant societies should make extensive use of screening assays and should instruct donors and recipients about HTLV-1/2 infection, transmission, and disease prevention, as high rates of ATLL and HAM have been detected in HTLV-1-infected patients after organ transplantation ( Gallo et al 2016 ).…”
mentioning
confidence: 99%