Waites G T, Whyte A
Clin Exp Immunol. 1987 Mar;67(3):467-76.
Bovine type II collagen administered to non-pregnant female DBA/1 mice caused arthritis in 55% of animals with a mean onset time of 70 days following immunization. Of collagen-treated females subsequently becoming syngeneically pregnant before the onset of arthritis, all developed the disease within 10 days of parturition, representing an earlier onset, compared to non-pregnant females, of 41 days. This earlier onset also occurred in females with an allogenic pregnancy, but did not occur in females resorbing their fetuses (only syngeneic pregnancies were examined). In females with arthritis at the time of conception a significant remission was observed during pregnancy followed by exacerbation post-partum. This sequence of remissions during pregnancy and exacerbations post-partum occurred with each pregnancy (parties of up to four studied). The treatment of multiparous females with collagen demonstrated that pregnancy does not provide long-term protection against the development or progression of arthritis, as such females were equally susceptible to post-partum onset of collagen-induced arthritis (CIA) and the remissions and exacerbations described above. The modifying effect of pregnancy on CIA in mice is complex and does not appear to be the result of a single pregnancy-associated phenomenon.
给未怀孕的雌性DBA/1小鼠注射牛II型胶原后,55%的动物发生了关节炎,免疫后平均发病时间为70天。在关节炎发病前同基因怀孕的胶原处理雌性小鼠中,所有小鼠在分娩后10天内都患上了这种疾病,与未怀孕的雌性小鼠相比,发病时间提前了41天。这种提前发病在异基因怀孕的雌性小鼠中也会出现,但在吸收胎儿的雌性小鼠中不会出现(仅研究了同基因怀孕情况)。在怀孕时患有关节炎的雌性小鼠中,怀孕期间观察到明显缓解,产后病情加重。每次怀孕(研究了多达四次分娩)都会出现这种怀孕期间缓解和产后加重的情况。用胶原处理经产雌性小鼠表明,怀孕并不能长期预防关节炎的发生或进展,因为这类雌性小鼠同样易患产后胶原诱导性关节炎(CIA)以及上述的缓解和加重情况。怀孕对小鼠CIA的调节作用很复杂,似乎不是单一的与怀孕相关现象的结果。