Comparative T-cell responses during pregnancy in large animals and humans

Citation
Ent. Meeusen et al., Comparative T-cell responses during pregnancy in large animals and humans, AM J REPROD, 46(2), 2001, pp. 169-179
Citations number
63
Categorie Soggetti
Immunology
Journal title
AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY
ISSN journal
10467408 → ACNP
Volume
46
Issue
2
Year of publication
2001
Pages
169 - 179
Database
ISI
SICI code
1046-7408(200108)46:2<169:CTRDPI>2.0.ZU;2-Q
Abstract
PROBLEM: Placentation in different large animal species shows a remarkable diversity in the level of trophoblast invasion into the maternal endometria l tissues. We wish to determine the influence of implantation on T-cell res ponses during pregnancy. METHOD OF STUDY: Review of the literature and current data. RESULTS: alpha beta -TCR (+) T cells are only prominent during early pregnancy in species with relatively non-invasive placentation (pig and horse) but are rapidly d ownregulated in species with more invasive placentae. gamma delta -TCR (+) T cells are prominent in species with moderate trophoblast invasion (rumina nts) where they increase dramatically during mid and late pregnancy. gamma delta -TCR (+) T cells remain prominent during late gestation in species wi th highly invasive placentation (humans) and, in addition, a distinct gamma delta T-cell population is present in first trimester decidua where it may play a regulatory role in controlling natural killer cell activity. The ga mma delta -TCR (+) population present in both ruminants and humans shows la rge granular morphology and contains antimicrobial proteins, suggesting the ir function may be to protect the uterine environment from infection during pregnancy and parturition. CONCLUSION: The comparative analysis of T-cell responses during pregnancy i n different large animal species supports an increasing role for cells of t he innate immune response (NK and gamma delta T cells) and a downregulation of the adaptive immune response with increasingly invasive placentation.