Sibylle Schneider-Schaulies, Stefan Niewiesk, Jurgen Schneider-Schaulies and Volker Ter Meulen Pages 163 - 181 ( 19 )
A profound, transient suppression of immune functions during and after the acute infection is the major cause of more than one million cases of infant deaths associated with measles worldwide. Concommittant with the generation of an efficient measles virus (MV) specific immunity, immune responses towards other pathogens are strongly impaired and provide the basis for the establishment and severe course of opportunistic infections. The molecular basis for MV-induced immunosuppression has not been resolved as yet. Similar to other immunosuppressive viruses, MV is lymphotropic and viral nucleic acid and proteins are detectable in peripheral blood mononuclear cells (PBMC). It is considered central to MV-induced immunosuppression that PBMC isolated from patients largely fail to proliferate in response to antigen specific and polyclonal stimulation. The low abundancy of MV-infected PBMC suggests that MV-induced immunosuppression is not directly caused by infection-mediated cell loss or fusion, but rather by indirect mechanisms such as deregulation of cytokines or surface contact-mediated signaling which may lead to apoptosis or impair the proliferative response of uninfected PBMC. Evidence for a role of any of these mechanisms was obtained in vitro, however, much has still to be learned about the tropism of MV and its interactions with particular host cells such as dendritic cells in vivo.
Measles Virus Induced Immunosuppression, Targets and Effector Mechanisms, peripheral blood mononuclear cells, THE VIRUS, ACUTE MEASLES, MV-induced Cell Death, Aberrant Homing, Leukopenia, MV F protein, Antigen-Presenting Cells
Institute for Virology and Immunobiology, University of Wurzburg, Versbacher Str. 7, D-97078 Wurzburg, Germany.