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The Journal of Immunology, 1999, 162: 3350-3355.
Copyright © 1999 by The American Association of Immunologists

Enumeration of Antigen-Presenting Cells in Mice Infected with Sendai Virus1

Edward J. Usherwood*, Twala L. Hogg* and David L. Woodland2,*,{dagger}

* Department of Immunology, St. Jude Children’s Research Hospital, Memphis, TN 38105; and {dagger} Department of Pathology, University of Tennessee Medical Center, Memphis, TN 38163

Substantial progress has been made in understanding Ag presentation to T cells; however, relatively little is known about the location and frequency of cells presenting viral Ags during a viral infection. Here, we took advantage of a highly sensitive system using lacZ-inducible T cell hybridomas to enumerate APCs during the course of respiratory Sendai virus infection in mice. Using lacZ-inducible T cell hybridomas specific for the immunodominant hemagglutinin-neuraminidase HN421–436/I-Ab and nucleoprotein NP324–332/Kb epitopes, we detected APCs in draining mediastinal lymph nodes (MLNs), in cervical lymph nodes, and also in the spleen. HN421–436/I-Ab- and NP324–332/Kb-presenting cells were readily detectable between days 3 and 9 postinfection, with more APCs present in the MLN than in the cervical lymph nodes. Interestingly, no infectious virus was detected in lymphoid tissue beyond day 6, suggesting that a depot of noninfectious viral Ag survives, in some form, for 2–3 days after viral clearance. Fractionation of the MLN demonstrated that APC frequency was enriched in dendritic cells and macrophages but depleted in the B cell population, suggesting that B cells do not form a large population of APCs during the primary response to this virus.




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