Abstract
Factors involved in pregnancy failure due to abnormal fetomaternal tolerance are poorly understood. Here we describe distinct defects in placenta formation and subsequent pregnancy loss solely dependent on the activation of the complement alternative pathway and the effector mechanisms provided by the maternal C3. Surprisingly, this effect is independent of other complement activation pathways and of the effector mechanisms provided by other complement components. These findings provide significant insight into the role of the innate immune system in human pregnancy failure, a frequent clinical outcome.
Original language | English |
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Pages (from-to) | 813-822 |
Number of pages | 10 |
Journal | Immunity |
Volume | 19 |
Issue number | 6 |
DOIs | |
State | Published - Dec 2003 |