PMID- 35905658 OWN - NLM STAT- MEDLINE DCOM- 20220919 LR - 20220927 IS - 1872-7603 (Electronic) IS - 0165-0378 (Linking) VI - 153 DP - 2022 Sep TI - Soluble HLA-G blood levels are not increased during ongoing pregnancy in women with a history of recurrent pregnancy loss. PG - 103665 LID - S0165-0378(22)00194-2 [pii] LID - 10.1016/j.jri.2022.103665 [doi] AB - Recurrent pregnancy loss (RPL) affects 1-2 % of couples who are trying to conceive. At some point, some couples do maintain a healthy pregnancy to term, but the underlying mechanism of RPL remains elusive. Human leukocyte antigen (HLA)-G is an immune modulatory molecule. Our group previously showed increased HLA-G levels in the decidua of term pregnancies after RPL, while other studies showed reduced soluble HLA-G (sHLA-G) blood levels in women with RPL. This led us to investigate sHLA-G levels in blood of women with RPL who had either a subsequent pregnancy loss (RPL-pregnancy loss) or a healthy term pregnancy (RPL-live birth), and compare these to healthy control pregnancies and non-pregnant controls. Soluble HLA-G concentrations were quantified by ELISA. Women with healthy term pregnancy had increased sHLA-G levels compared to non-pregnant controls. In contrast, RPL-live birth women at term did not have increased blood sHLA-G levels. Soluble HLA-G levels remained stable between first and third trimester. Interestingly, when comparing first trimester samples of RPL-live birth to RPL-pregnancy loss, sHLA-G levels also did not significantly differ. High sHLA-G levels in blood seem not to be crucial for an ongoing healthy pregnancy after RPL. However, since it was previously shown that women with RPL-live birth have increased HLA-G levels in term decidua compared to control pregnancies, the current data suggest that local and systemic immune regulation are not necessarily in concert. Further study of the contribution of fetus-derived HLA-G and HLA-G of maternal origin may provide more insight in the pathophysiology of RPL. CI - Copyright (c) 2022 The Authors. Published by Elsevier B.V. All rights reserved. FAU - Krop, J AU - Krop J AD - Department of Immunology, Leiden University Medical Centre, Leiden, the Netherlands. FAU - Van Der Keur, C AU - Van Der Keur C AD - Department of Immunology, Leiden University Medical Centre, Leiden, the Netherlands. FAU - Kapsenberg, J M AU - Kapsenberg JM AD - Department of Immunology, Leiden University Medical Centre, Leiden, the Netherlands. FAU - Den Hollander, F AU - Den Hollander F AD - Department of Immunology, Leiden University Medical Centre, Leiden, the Netherlands. FAU - Van Der Hoorn, M L P AU - Van Der Hoorn MLP AD - Department of Obstetrics, Leiden University Medical Centre, Leiden, the Netherlands. FAU - Heidt, S AU - Heidt S AD - Department of Immunology, Leiden University Medical Centre, Leiden, the Netherlands. FAU - Claas, F H J AU - Claas FHJ AD - Department of Immunology, Leiden University Medical Centre, Leiden, the Netherlands. FAU - Eikmans, M AU - Eikmans M AD - Department of Immunology, Leiden University Medical Centre, Leiden, the Netherlands. Electronic address: m.eikmans@lumc.nl. LA - eng PT - Journal Article DEP - 20220720 PL - Ireland TA - J Reprod Immunol JT - Journal of reproductive immunology JID - 8001906 RN - 0 (HLA-G Antigens) SB - IM MH - *Abortion, Habitual MH - Female MH - Fetus MH - *HLA-G Antigens MH - Humans MH - Pregnancy MH - Pregnancy Trimester, First MH - Pregnancy Trimester, Third OTO - NOTNLM OT - BMI OT - HLA-G polymorphisms OT - RPL with subsequent ongoing pregnancy OT - Recurrent Pregnancy Loss OT - Soluble HLA-G EDAT- 2022/07/30 06:00 MHDA- 2022/09/20 06:00 CRDT- 2022/07/29 18:23 PHST- 2022/01/13 00:00 [received] PHST- 2022/05/30 00:00 [revised] PHST- 2022/07/11 00:00 [accepted] PHST- 2022/07/30 06:00 [pubmed] PHST- 2022/09/20 06:00 [medline] PHST- 2022/07/29 18:23 [entrez] AID - S0165-0378(22)00194-2 [pii] AID - 10.1016/j.jri.2022.103665 [doi] PST - ppublish SO - J Reprod Immunol. 2022 Sep;153:103665. doi: 10.1016/j.jri.2022.103665. Epub 2022 Jul 20.