Document 0714 DOCN M9440714 TI Effects of CD45 on NF-kappa B. Implications for replication of HIV-1. DT 9404 AU Baur A; Garber S; Peterlin BM; Howard Hughes Medical Institute, University of California at San; Francisco 94143-0724. SO J Immunol. 1994 Feb 1;152(3):976-83. Unique Identifier : AIDSLINE MED/94132650 AB Increased levels of replication of the HIV type 1 are observed after the activation of infected T cells through the TCR. However, anti-CD45 antibodies inhibit these effects in cells from infected individuals. In this study, we examined interrelationships between CD45 and HIV-1 further. We measured effects on the HIV-1 LTR in T cell lines that were stimulated with antibodies against CD45 and in those that lacked the expression of CD45 on their surfaces. First, anti-CD45 antibodies did not affect basal but decreased activated levels of expression from the HIV-1 LTR. Second, T cells, which lack CD45 and cannot signal via the TCR, supported higher levels of viral replication and gene expression. This was due to the presence of active NF-kappa B complexes in the nucleus of CD45- T cells. Additionally, infected T cells displayed lower levels of CD45 on their surfaces. Thus, CD45 plays an active role in the physiology of T cells and in the replication of HIV-1. DE Antigens, CD45/*PHYSIOLOGY Cell Nucleus/METABOLISM *Gene Expression Regulation, Viral Human HIV/*GROWTH & DEVELOPMENT HIV Infections/*IMMUNOLOGY HIV Long Terminal Repeat In Vitro NF-kappa B/*PHYSIOLOGY Receptors, Antigen, T-Cell/PHYSIOLOGY RNA, Messenger/GENETICS Support, Non-U.S. Gov't Tumor Cells, Cultured T4 Lymphocytes/IMMUNOLOGY/*MICROBIOLOGY Virus Replication JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).