Document 0152 DOCN M95A0152 TI Human T cell lymphotropic virus: necessity for and feasibility of a vaccine. DT 9510 AU de The G; Bomford R; Kazanji M; Ibrahim F; Departement des Retrovirus, Institut Pasteur, Paris, France. SO Ciba Found Symp. 1994;187:47-55; discussion 55-60. Unique Identifier : AIDSLINE MED/95317149 AB Human T cell lymphotropic virus types I and II (HTLV-I/II) are endemic in certain areas of the world. They cause two life-threatening diseases, adult T cell leukaemia/lymphoma and tropical spastic paraparesis. A vaccine is needed because in developing countries there are no other feasible preventive interventions against these diseases and in Western countries intravenous drug users at high risk for HTLV-I and HTLV-II infections and the health workers in contact with such populations must be protected. We have developed a rat model in which we observed variations of susceptibility to viral infection between inbred strains, the most susceptible being the Fischer F344, and the possibility of viral latency in the nervous system. We have prepared a recombinant adenovirus vector that expresses the HTLV-I envelope glycoprotein env in HeLa cells. A target human population in French Guyana, in which the prevalence rate reaches 5.6% in one ethnic group (Bonis), has been identified for possible intervention. DE Disease Models, Animal Feasibility Studies Human HTLV-I/*IMMUNOLOGY HTLV-I Infections/*PREVENTION & CONTROL HTLV-II/*IMMUNOLOGY HTLV-II Infections/*PREVENTION & CONTROL Leukemia-Lymphoma, T-Cell, Acute, HTLV-I-Associated/PREVENTION & CONTROL Paraparesis, Tropical Spastic/PREVENTION & CONTROL Support, Non-U.S. Gov't Vaccines, Synthetic/*THERAPEUTIC USE Viral Vaccines/*THERAPEUTIC USE JOURNAL ARTICLE REVIEW REVIEW, TUTORIAL SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).