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Department of Clinical Sciences1 , Section for Comparative Physiology and Medicine; Department of Clinical Sciences2 and Department of Anatomy and Physiology3 , Swedish University of Agricultural Sciences, PO Box 7018, S-750 07 Uppsala, Sweden
Correspondence
Robert Jonasson
Robert.Jonasson{at}kv.slu.se
Received 24 January 2006
Accepted 27 March 2006
+ CD4 cells and 
T cells at days 4 and 14 post-inoculation. In addition, an increase in CD4+ CD8
+ cells and CD8
+ CD8ß+ cells was observed at days 4 and 14 post-inoculation in animals that developed dysentery. During clinical signs of dysentery, the acute-phase protein serum amyloid A was increased. There was a two- to threefold increase in both neutrophils and monocytes during signs of dysentery and at the beginning of the recovery period. The numbers of CD8
+ CD8ß CD4, CD45RA lymphocytes also increased during the dysentery period. Circulating CD21+ cells and CD21+ CD45RA cells decreased at the end of the incubation period, during signs of dysentery and at the beginning of the recovery period. The dysentery-affected animals developed antibodies to B. hyodysenteriae-specific antigens (
16 kDa and
30 kDa) from the first day of recovery, and 
T cells showed an increase during the recovery period. In comparison with pre-inoculation, increased numbers of monocytes, neutrophils, CD8
+ CD8ß CD4 lymphocytes and CD45RA lymphocytes were observed during clinical dysentery. Increased numbers of neutrophils, 
T cells and specific antibodies were seen during the recovery period.
Abbreviations: PE, phycoerythrin; SAA, serum amyloid A.
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