Protective heterologous antiviral immunity and enhanced immunopathogenesis mediated by memory T cell populations
UMass Chan AffiliationsDepartment of Pathology
Program in Immunology/Virology
Graduate School of Biomedical Sciences
KeywordsAdipose Tissue; Animals; Female; Immunization; *Immunologic Memory; Interferon Type II; Lymphocytic choriomeningitis virus; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Muromegalovirus; Necrosis; Phenotype; Pichinde virus; T-Lymphocytes; T-Lymphocytes, Cytotoxic; Vaccinia virus; Virus Diseases; Viruses
Medicine and Health Sciences
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AbstractA basic principle of immunology is that prior immunity results in complete protection against a homologous agent. In this study, we show that memory T cells specific to unrelated viruses may alter the host's primary immune response to a second virus. Studies with a panel of heterologous viruses, including lymphocytic choriomeningitis (LCMV), Pichinde (PV), vaccinia (VV), and murine cytomegalo (MCMV) viruses showed that prior immunity with one of these viruses in many cases enhanced clearance of a second unrelated virus early in infection. Such protective immunity was common, but it depended on the virus sequence and was not necessarily reciprocal. Cell transfer studies showed that both CD4 and CD8 T cell populations from LCMV-immune mice were required to transfer protective immunity to naive hosts challenged with PV or VV. In the case of LCMV-immune versus naive mice challenged with VV, there was an enhanced early recruitment of memory phenotype interferon (IFN) gamma-secreting CD4(+) and CD8(+) cells into the peritoneal cavity and increased IFN-gamma levels in this initial site of virus replication. Studies with IFN-gamma receptor knockout mice confirmed a role for IFN-gamma in mediating the protective effect by LCMV-immune T cell populations when mice were challenged with VV but not PV. In some virus sequences memory cell populations, although clearing the challenge virus more rapidly, elicited enhanced IFN-gamma-dependent immunopathogenesis in the form of acute fatty necrosis. These results indicate that how a host responds to an infectious agent is a function of its history of previous infections and their influence on the memory T cell pool.
J Exp Med. 1998 Nov 2;188(9):1705-15.
Permanent Link to this Itemhttp://hdl.handle.net/20.500.14038/32523
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