Document 0662 DOCN M9650662 TI T-cell mediated rejection of gene-modified HIV-specific cytotoxic T lymphocytes in HIV-infected patients [see comments] DT 9605 AU Riddell SR; Elliott M; Lewinsohn DA; Gilbert MJ; Wilson L; Manley SA; Lupton SD; Overell RW; Reynolds TC; Corey L; Greenberg PD; Fred Hutchinson Cancer Research Center, Seattle, Washington; 98104, USA. SO Nat Med. 1996 Feb;2(2):216-23. Unique Identifier : AIDSLINE MED/96160371 CM Comment in: Nat Med 1996 Feb;2(2):165-7 AB The introduction and expression of genes in somatic cells is an innovative therapy for correcting genetic deficiency diseases and augmenting immune function. A potential obstacle to gene therapy is the elimination of such gene-modified cells by an immune response to novel protein products of the introduced genes. We are conducting an immunotherapy trial in which individuals seropositive for human immunodeficiency virus (HIV) receive CD8+ HIV-specific cytotoxic T cells modified by retroviral transduction to express a gene permitting positive and negative selection. However, five of six subjects developed cytotoxic T-lymphocyte responses specific for the novel protein and eliminated the transduced cytotoxic T cells. The rejection of genetically modified cells by these immunocompromised hosts suggests that strategies to render gene-modified cells less susceptible to host immune surveillance will be required for successful gene therapy of immunocompetent hosts. DE Antigen Presentation Base Sequence *Cytotoxicity, Immunologic CD8-Positive T-Lymphocytes/*IMMUNOLOGY/TRANSPLANTATION Histocompatibility Antigens Class I/IMMUNOLOGY Human HIV Antigens/*IMMUNOLOGY HIV Infections/IMMUNOLOGY/*THERAPY *Immunotherapy, Adoptive Molecular Sequence Data Support, Non-U.S. Gov't Support, U.S. Gov't, P.H.S. CLINICAL TRIAL JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).