Abstract
Preferential histoincompatible pregnancies and efficient fetal development by an active selective immune response of the female have to occur concomitantly in order to ensure the propagation of mammalian species. A compromise solution between phylogeny and ontogeny, with respect to transplantation antigens, would be the deviation of the maternal anti-fetal immune response towards an active protective reaction. To accomplish this the fetus will have to express during its development MHC-encoded molecules which, either because of their unique intrinsic molecular structure or because of their association with specific fetal membrane-associated products, will lead to different and mainly enhancing immunogenic interactions with the immune system of the mammalian female. Such interactions may be facilitated by a variety of regulatory products induced during pregnancy. A better understanding of the possibly unique way of immune response of females against 'modified self' antigens, as suggested above, may contribute to our understanding of a longstanding fact, namely, the increased frequency of autoimmune diseases in females.
| Original language | English |
|---|---|
| Pages (from-to) | 582-587 |
| Number of pages | 6 |
| Journal | Transplantation Proceedings |
| Volume | 12 |
| Issue number | 4 |
| State | Published - 1980 |
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