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From the Institute of Neuropathology,* University Hospital of Zürich, Zürich, Switzerland; the Institute of Experimental Immunology,
University Hospital of Zürich, Zürich, Switzerland; the Institute of Internal Medicine,
University Hospital of Zürich, Section of Clinical Immunology, Zürich, Switzerland; and the Institute of Genetics,
University of Cologne, Cologne, Germany
Prion pathogenesis following oral exposure is thought to involve gut-associated lymphatic tissue, which includes Peyers patches (PPs) and M cells. Recruitment of activated B lymphocytes to PPs requires
4ß7 integrin; PPs of ß7-/- mice are normal in number but are atrophic and almost entirely devoid of B cells. Here we report that minimal infectious dose and disease incubation after oral exposure to logarithmic dilutions of prion inoculum were similar in ß7-/- and wild-type mice, and PPs of both ß7-/- and wild-type mice contained 34 log LD50/g prion infectivity
125 days after challenge. Despite marked reduction of B cells, M cells were present in ß7-/- mice. In contrast, mice deficient in both tumor necrosis factor and lymphotoxin-
(TNF
-/- x LT
-/-) or in lymphocytes (RAG-1-/-, µMT), in which numbers of PPs are reduced in number, were highly resistant to oral challenge, and their intestines were virtually devoid of prion infectivity at all times after challenge. Therefore, lymphoreticular requirements for enteric and for intraperitoneal uptake of prions differ from each other. Although susceptibility to prion infection following oral challenge correlates with the number of PPs, it is remarkably independent of the number of PP-associated lymphocytes.
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