Document 0402 DOCN M9610402 TI A nonlethal rat parvovirus infection suppresses rat T lymphocyte effector functions. DT 9601 AU McKisic MD; Paturzo FX; Gaertner DJ; Jacoby RO; Smith AL; Section of Comparative Medicine, Yale School of Medicine, New; Haven, CT 06520-8016, USA. SO J Immunol. 1995 Oct 15;155(8):3979-86. Unique Identifier : AIDSLINE MED/96003439 AB Inoculation of the UMass strain of rat virus (RV-UMass) into adult immunocompetent rats results in a prolonged subclinical infection that is resolved in 4 to 8 wk. Co-labeling studies, using in situ hybridization (ISH) and immunohistochemistry (IHC), confirmed that RV-UMass was lymphocytotropic and capable of infecting CD4+ and CD8+ T cells as well as B cells. ISH studies also revealed that virus replication was restricted in unstimulated cells but was productive in concanavalin A-stimulated lymphocytes. A corollary of productive infection of lymphocytes was the suppression of lymphocyte functions. Although RV-UMass did not appear to induce phenotypic changes during the course of infection, cells from infected rats had diminished proliferation and cytolytic responses. Both peripheral and mesenteric lymph node cells exhibited only partial recovery of their proliferative and cytolytic capacities one month after infection. Furthermore, RV-UMass-infected tissue culture maintained alloreactive CD4+ T cells in vitro, and a nonlethal infection of this T cell line inhibited Ag- and IL-2-induced proliferation. Because parvoviruses are widespread among laboratory rodents, these findings emphasize the importance of identifying and excluding parvovirus infection in rodents and in cultures of rat T lymphocytes. DE Animal Cell Line Cytotoxicity, Immunologic CD4-Positive T-Lymphocytes/IMMUNOLOGY CD8-Positive T-Lymphocytes/IMMUNOLOGY Disease Susceptibility *Immune Tolerance Lymphocyte Transformation Parvoviridae Infections/*IMMUNOLOGY Parvovirus/*IMMUNOLOGY Phenotype Rats Rats, Inbred Lew Rats, Inbred WF Species Specificity Support, Non-U.S. Gov't Support, U.S. Gov't, P.H.S. T-Lymphocyte Subsets/*IMMUNOLOGY JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).