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The presence of HLA-antibodies in recurrent miscarriage patients is associated with a reduced chance of a live birth

Henriette Svarre NielsenaCorresponding Author Informationemail addressemail address, Marian D. Witvlietb, Rudi Steffensenc, Geert W. Haasnootb, Els Goulmyb, Ole Bjarne Christiansenad, Frans Claasb

Received 16 March 2010; received in revised form 21 May 2010; accepted 23 May 2010. published online 16 June 2010.
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Abstract 

Anti-paternal HLA-antibodies are considered a harmless phenomenon during most pregnancies, whereas their role in recurrent miscarriage (RM) patients is disputed. In contrast to primary RM, patients with secondary RM have carried a fetus to term pregnancy prior to a series of miscarriages, which increases the chance that allogeneic fetal cells appear in the maternal circulation. This study investigates the frequency of HLA-antibodies in secondary RM, primary RM patients and parous controls and analyzes whether the presence of HLA-antibodies in early pregnancy is associated with pregnancy outcome. Sera from women with secondary RM (n=56), primary RM (n=13) and parous controls (n=24) were tested for HLA-antibodies using an ELISA assay and complement dependent cytotoxicity. Samples were taken at gestational week 4–5 in 62 (90%) of the patients. HLA-antibodies were significantly more frequent in secondary RM patients with a boy prior to the miscarriages (62%) compared to secondary RM patients with a firstborn girl (29%, p=0.03), primary RM patients (23%, p=0.02) and parous controls (25%, p=0.005). Forty-one percent of HLA-antibody positive pregnant RM patients had a live birth compared to 76% of HLA-antibody negative RM patients, p=0.006 (adjusted OR: 0.22 (0.07–0.68), p=0.008). In conclusion, HLA-antibodies are significantly more frequent in secondary RM patients with a firstborn boy than in other RM patients and controls. The presence of these antibodies in early pregnancy is associated with a reduced chance of a live birth. Further exploring this association may increase our understanding of maternal acceptance of the fetal allograft.

a The Fertility Clinic, University Hospital Copenhagen, Rigshospitalet, Fertility Clinic 4071, Blegdamsvej 9, DK-2100 Copenhagen, Denmark

b Department of Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, The Netherlands

c Department of Clinical Immunology, Aalborg Hospital, Aarhus University Hospital, Aalborg, Denmark

d Department of Obstetrics and Gynaecology, Aalborg Hospital, Aarhus University Hospital, Aalborg, Denmark

Corresponding Author InformationCorresponding author. Tel.: +45 35458486; fax: +45 35454946.

PII: S0165-0378(10)00101-4

doi:10.1016/j.jri.2010.05.006

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