Document 0415 DOCN M9490415 TI Murine AIDS is an antigen-driven disease: requirements for major histocompatibility complex class II expression and CD4+ T cells. DT 9411 AU Giese NA; Giese T; Morse HC 3rd; Laboratory of Immunopathology, National Institute of Allergy and; Infectious Diseases, Bethesda, Maryland 20892. SO J Virol. 1994 Sep;68(9):5819-24. Unique Identifier : AIDSLINE MED/94335098 AB Murine AIDS (MAIDS) is a complex syndrome of lymphoproliferation and immunodeficiency induced by a replication-defective murine leukemia virus (BM5def) that encodes Pr60gag as its only product. It has been suggested that the gag polyprotein is responsible for vigorous antigenic stimulation of CD4+ T cells and generalized secondary activation of the immune system. This model was tested first by infecting mice (C2K/O) that lack class II major histocompatibility complex molecules required for presentation of antigens to CD4+ T cells. C2K/O mice expressed BM5def at high levels but did not develop MAIDS either when unmanipulated or following transfer of CD4+ T cells. Second, B6 mice reconstituted with C2K/O bone marrow cells had normal frequencies of B cells (class II negative) and CD4+ cells and expressed high levels of BM5def transcripts but did not develop MAIDS; however, MAIDS developed in class II-competent nu/nu mice reconstituted with CD4+ T cells and in C2K/O mice reconstituted with B6 bone marrow to give class II-positive B cells and with purified CD4+ T cells. These results indicate that induction of MAIDS by BM5def is antigen driven and is dependent on expression of major histocompatibility complex class II molecules on antigen-presenting cells and the presence of CD4+ T cells. DE Animal Antigens, Surface/ANALYSIS Base Sequence DNA Primers/CHEMISTRY Histocompatibility Antigens Class II/*IMMUNOLOGY Leukemia Viruses, Murine/GROWTH & DEVELOPMENT/IMMUNOLOGY/ *PATHOGENICITY Lymphocyte Transformation Membrane Glycoproteins/ANALYSIS Mice Mice, Inbred C57BL Mice, Nude Molecular Sequence Data Murine Acquired Immunodeficiency Syndrome/*IMMUNOLOGY Mutagenesis, Site-Directed Structure-Activity Relationship Support, Non-U.S. Gov't Support, U.S. Gov't, P.H.S. T-Lymphocyte Subsets/IMMUNOLOGY T4 Lymphocytes/*IMMUNOLOGY JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).