Skip Navigation

This Article
Right arrow Full Text (PDF )
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by D'Hooghe, T.M.
Right arrow Articles by Bambra, C.S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by D'Hooghe, T.M.
Right arrow Articles by Bambra, C.S.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Human Reproduction, Vol. 10, No. 3, pp. 558-562, 1995
© 1995 European Society of Human Reproduction and Embryology


research-article

Immunology: Anti-endometrial lymphocytotoxicity and natural killer cell activity in baboons (Papio anubis and Papio cynocephalus) with endometriosis*

T.M. D'Hooghe1,2,5, J.-P.Y. Scheerlinck3, P.R. Koninckx2, J.A. Hill4 and C.S. Bambra1

1Department of Reproduction, Institute of Primate Research P.O. Box 24481, Nairobi, Kenya 2Department of Obstetrics and Gynecology, University Hospital Gasthuisberg B-3000 Leuven, Belgium 3Walter and Eliza Hall Institute for Medical Research Post Office, Royal Melbourne Hospital, Victoria 3050, Australia 4Fearing Research Laboratory 250 Longwood Avenue, Room 204, Boston, MA 02115, USA

Correspondence: 5To whom correspondence should be addressed at: Fearing Research Laboratory, Division of Reproductive Immunology, Department of Obstetrics, Gynecology and Reproductive Biology, Brigham and Women's Hospital, Harvard Medical School, 250 Longwood Avenue, SGMB 204, Boston, MA 02115, USA

This study was performed to test the hypothesis that anti-endometrial, lymphocyte-mediated cytotoxicity and natural killer (NK) activity are reduced in baboons with endometriosis when compared to animals with a normal pelvis. Lymphocyte-mediated cytotoxicity was determined in 28 baboons (15 with endometriosis, 13 with normal pelvis) and NK cell activity was evaluated in 42 baboons (31 with endometriosis, 11 with normal pelvis). Anti-endometrial lymphocyte-mediated cytotoxicity was determined by a 20 h assay with effector-target ratios of 50: 1 and 25: 1. The NK activity (K562 cell line as target) was simultaneously measured in all animals during a 4 h assay with effector:target ratios of 200: 1, 100: 1, 50: 1, 25: 1, 12: 1, 6: 1 and 3: 1. Statistical analysis was performed using analysis of variance, paired rank, Mann—Whitney, Kruskal—Wallis and Fisher exact tests where appropriate. Lymphocyte-mediated cytotoxicity was significantly lower (P < 0.025) in baboons with endometriosis (mean 5.9 ± 8.7 %, median 0%, range 0–26%) than in animals with a normal pelvis (mean 22.9 ± 23.0 %, median 7%, range 0–78 %). This difference could be explained by the absence of cytotoxicity in baboons with moderate to severe endometriosis, probably due to high spontaneous release of 51Cr from labelled target cells. When stricter criteria were used and only animals with a labelling index (maximal/spontaneous release) of ≥1.7 were analysed (n = 11), the anti-endometrial cytotoxicity was comparable between baboons with and without endometriosis. NK cell activity was also comparable in primates with and without endometriosis. In conclusion, no difference in lymphocyte-mediated cytotoxicity and NK cell activity was observed between baboons with and without endometriosis.

Key words: anti-endometrial/baboon (Papio anubis/P.cynocephalus/cytotoxicity/endometriosis/natural killer cell activity

*Presented at Serono Symposium ‘Immunobiology of Reproduction’, Boston, USA, August 26–29, 1993


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.