Collagen-induced arthritis is a well-established model of chronic inflammat
ory arthritis. We here introduce a development of this model which combines
the benefits of adoptive transfer and sequential relapse, DBA/1 x B10.Q F1
hybrid mice were immunised with bovine type II collagen, and those which d
eveloped a sufficiently high level of arthritis served as donors of spleen
cells transferred into BALB/c SCID hosts. After boosting with 500 mu g coll
agen, the development of host arthritis was monitored over a period of up t
o 256 days, during which up to three successive peaks were detected. In com
parison with bovine collagen, mouse collagen used for boosting induced a lo
wer initial peak but higher relapses, As expected, the transferred disease
was more uniform than the freshly induced one. Previous information suggest
s that a shifting cytokine balance between protective and aggressive T cell
s may account for the relapse and remission. This study provides a model of
relapsing polyarthritis, obtained with normal immunocytes boosted with a w
ell-defined protein antigen in animals not themselves treated with adjuvant
, As such it is relevant to the etiology of inflammatory arthritis in man,
and, if further developed, could be of value for testing new therapeutic st
rategies.