Important note: Information in this article was accurate in 1993. The state of the art may have changed since the publication date.
An HTLV-I vaccine: why, how, for whom?
AIDS Res Hum Retroviruses. 1993 May;9(5):381-6. Unique Identifier : AIDSLINE MED/93305376 de The G; Bomford R; Unite d'Epidemiologie des Virus Oncogenes, Institut Pasteur,; Paris, France.
Abstract:
Endemic infection with the human T cell leukemia/lymphoma viruses I and II (HTLV-I/II) is now recognized to be worldwide, and is becoming epidemic among intravenous drug abusers (IVDAs) in the United States and Europe. The number of people around the world infected with HTLV-I can be estimated as between 10 and 20 million (Table 1). HTLV-I causes a rapidly progressing adult T cell leukemia/lymphoma (ATLL), and an incurable progressive neuromyelopathy named tropical spastic paraparesis/HTLV-I-associated myelopathy (TSP/HAM), as well as a number of less well-studied syndromes. There is evidence that coinfection with HTLV-I or -II accelerates progression to AIDS. The cumulative lifetime risk of developing ATLL or TSP/HAM is around 5%, which, in terms of the induction of serious diseases, places HTLV-I in the same category of viruses for which efficient vaccines are made and used. Furthermore, there are factors favoring the feasibility of a vaccine against HTLV-I, in that the virus displays relatively low antigenic variability, natural immunity occurs in humans, and experimental vaccination with the envelope (Env) antigen is successful in animal models. A vaccine against HTLV-I would be of significant public health value in the fields of oncology, neurology, and AIDS, and it would serve as a pathfinder for a vaccine against HIV.
Keywords: Adult Animal AIDS Vaccines/ISOLATION & PURIF Disease Models, Animal Female Human HTLV-I/*IMMUNOLOGY HTLV-I Infections/EPIDEMIOLOGY/PREVENTION & CONTROL/TRANSMISSION HTLV-II/IMMUNOLOGY Pregnancy Support, Non-U.S. Gov't Viral Vaccines/ISOLATION & PURIF/*PHARMACOLOGY JOURNAL ARTICLE REVIEW REVIEW, TUTORIAL 931030
M93A0729
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