| Literature DB >> 33074247 |
Kenta Tezuka1, Naoki Fuchi2, Kazu Okuma1, Takashi Tsukiyama2, Shoko Miura2, Yuri Hasegawa2, Ai Nagata2, Nahoko Komatsu2, Hiroo Hasegawa3, Daisuke Sasaki3, Eita Sasaki1, Takuo Mizukami1, Madoka Kuramitsu1, Sahoko Matsuoka1, Katsunori Yanagihara3, Kiyonori Miura2, Isao Hamaguchi1.
Abstract
Human T cell leukemia virus type 1 (HTLV-1) is mainly transmitted vertically through breast milk. The rate of mother-to-child transmission (MTCT) through formula feeding, although significantly lower than through breastfeeding, is approximately 2.4%-3.6%, suggesting the possibility of alternative transmission routes. MTCT of HTLV-1 might occur through the uterus, birth canal, or placental tissues; the latter is known as transplacental transmission. Here, we found that HTLV-1 proviral DNA was present in the placental villous tissues of the fetuses of nearly half of pregnant carriers and in a small number of cord blood samples. An RNA ISH assay showed that HTLV-1-expressing cells were present in nearly all subjects with HTLV-1-positive placental villous tissues, and their frequency was significantly higher in subjects with HTLV-1-positive cord blood samples. Furthermore, placental villous trophoblasts expressed HTLV-1 receptors and showed increased susceptibility to HTLV-1 infection. In addition, HTLV-1-infected trophoblasts expressed high levels of viral antigens and promoted the de novo infection of target T cells in a humanized mouse model. In summary, during pregnancy of HTLV-1 carriers, HTLV-1 was highly expressed in placental villous tissues, and villous trophoblasts showed high HTLV-1 sensitivity, suggesting that MTCT of HTLV-1 occurs through the placenta.Entities:
Keywords: Epidemiology; Infectious disease; Virology
Year: 2020 PMID: 33074247 PMCID: PMC7598071 DOI: 10.1172/JCI135525
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808