BASIC SCIENCE: PDF OnlyAdoptive Immunotherapy of Feline Leukemia Virus Infection Using Autologous Lymph Node LymphocytesBlakeslee, James*; Noll, Greg*; Olsen, Richard*; Triozzi, Pierre L.*†Author Information *College of Veterinary Medicine and †James Cancer Hospital and Research Institute, The Ohio State University, Columbus, Ohio, U.S.A. Address correspondence and reprint requests to Pierre L. Triozzi, Division of Hematology and Oncology, The Ohio State University, 410 West 10th Avenue, Columbus, OH 43210, U.S.A. Manuscript received December 9, 1996; accepted November 24, 1997. Journal of Acquired Immune Deficiency Syndromes & Human Retrovirology: May 1, 1998 - Volume 18 - Issue 1 - p 1-6 Free Abstract Adoptive immunotherapy using autologous cells expanded ex vivo from lymph nodes was examined in cats infected with the retrovirus feline leukemia virus (FeLV). Cells were obtained from popliteal lymph nodes from 18 FeLV-antigenpositive cats without complications; a mean of 6.2 × 107 cells were obtained. Lymph node cells were cultured with 600 IU/ml interleukin-2 (IL-2) for 7 days. Cells expanded 0.8- to 11-fold (mean, 2.7; median, 2.4); were 80% ± 8.0% CD3+, 29% ±8.1% CD4+, and 41% ± 7.0% CD8+, and exhibited cytolytic activity against FeLV-transformed FL74 cells. Sixteen cats received a single intravenous infusion of 0.13 to 3.9 × 108 cells. Cell infusion was well tolerated; fever developed approximately 1 hour postinfusion. Clinical activity, antiviral activity, or both was observed in 10 cats. Nine cats had clinical responses with improvement in weight, activity, appearance, or a combination of these that began 2 to 4 weeks after cell infusion and that lasted for up to 13 or more months. FeLV antigen became undetectable in 4 cats. These results indicate that adoptive immunotherapy using autologous lymph node cells, activated and expanded ex vivo in short-term cultures with low concentrations of IL-2, can modulate the course of a retroviral infection. © Lippincott-Raven Publishers.