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Expression of Human T‐cell Lymphotropic Virus Type‐1 Gene Products in the Short‐term Cultured Skin Tissues of an Adult T‐cell Leukemia/Lymphoma Patient with Cutaneous Manifestations
Author(s) -
Setoyama Mitsuru,
Katahira Yoshihiko,
Hamada Tetsu,
Tashiro Masaaki,
Yashiki Shinji,
Tanaka Yuetsu,
Tozawa Hideki,
Sonoda Shunro
Publication year - 1992
Publication title -
the journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.9
H-Index - 65
eISSN - 1346-8138
pISSN - 0385-2407
DOI - 10.1111/j.1346-8138.1992.tb03196.x
Subject(s) - immunofluorescence , leukemia , antigen , virology , biology , human t lymphotropic virus 1 , lymphoma , pathology , dermis , monoclonal antibody , antibody , virus , human skin , t cell leukemia , immunology , medicine , genetics
Adult T‐cell leukemia/lymphoma (ATLL) is recognized as a disease etiologically associated with human T lymphotropic virus type‐1 (HTLV‐1) infection, but, neither viral replication nor specific virus antigen expression have been detected on ATLL cells distributed in organs, including skin. To examine the latent expression of HTLV‐1 in the cutaneous lesions of ATLL patients, we cultured the lesional skin tissues in vitro and applied immunofluorescence staining with mouse monoclonal antibodies Lt‐4, GIN‐14, and F10, which react with p40 tax , p19 and gp21, respectively. We recognized HTLV‐1 specific antigens on clustered ATLL cells only in the deeper dermis of the skin after 24 hrs cultivation of the lesional skin tissue from an ATLL patient in RPMI‐1640 medium supplemented with 20% fetal calf serum. In the electron microscope, we observed HTLV‐1 like particles, 80–140 nm in diameter with envelope and core structures, in the same tissue specimen. These findings suggest that HTLV‐1 gene products may be expressed in the skin lesions of ATLL patients and involved in the pathogenesis of skin eruptions in cutaneous type ATLLs. To our knowledge, this is the first report that envisages the potency of intracutaneous HTLV‐1 expression in vivo .