19 research outputs found
Is there a relationship between anti-HPA-1a concentration and severity of neonatal alloimmune thrombocytopenia?
Deletion of the dominant autoantigen in NZB mice with autoimmune hemolytic anemia : Effects on autoantibody and T-helper responses
Peer reviewedPublisher PD
Routine Antenatal Anti-D Prophylaxis in Women Who Are Rh(D) Negative: Meta-Analyses Adjusted for Differences in Study Design and Quality
Background: To estimate the effectiveness of routine antenatal anti-D prophylaxis for preventing sensitisation in pregnant Rhesus negative women, and to explore whether this depends on the treatment regimen adopted. Methods: Ten studies identified in a previous systematic literature search were included. Potential sources of bias were systematically identified using bias checklists, and their impact and uncertainty were quantified using expert opinion. Study results were adjusted for biases and combined, first in a random-effects meta-analysis and then in a random-effects metaregression analysis. Results: In a conventional meta-analysis, the pooled odds ratio for sensitisation was estimated as 0.25 (95 % CI 0.18, 0.36), comparing routine antenatal anti-D prophylaxis to control, with some heterogeneity (I 2 = 19%). However, this naĆÆve analysis ignores substantial differences in study quality and design. After adjusting for these, the pooled odds ratio for sensitisation was estimated as 0.31 (95 % CI 0.17, 0.56), with no evidence of heterogeneity (I 2 = 0%). A meta-regression analysis wa
Combination peptide immunotherapy suppresses antibody and helper T cell responses to the RhD protein in HLA-transgenic mice
Funding This work was supported by grants from the Scottish National Blood Transfusion Service and the Wellcome Trust, UK (058766).Peer reviewedPublisher PD
W1208 No Significant Transfer of Certolizumab Pegol Compared With IgG in the Perfused Human Placenta In Vitro
Combination peptide immunotherapy suppresses antibody and helper T cell responses to the major human platelet autoantigen GPIIb/IIIa in HLA-transgenic mice
The study was funded by grants from the Medical Research Council (UK) Confidence in Concept, the Scottish National Blood Transfusion Service and the Wellcome Trust (UK). Acknowledgments We would like to acknowledge the assistance of Iain Fraser Cytometry Centre at the University of Aberdeen.Peer reviewedPublisher PD