{"title":"RH genetic variation and the impact for typing and personalized transfusion strategies: a narrative review","authors":"Margaret A. Keller","doi":"10.21037/aob-22-6","DOIUrl":"https://doi.org/10.21037/aob-22-6","url":null,"abstract":"","PeriodicalId":72211,"journal":{"name":"Annals of blood","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44997318","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
C. Hyland, Helen O'Brien, E. McGowan, A. Perros, R. Flower, G. Lopez, G. Gardener
{"title":"The power of digital PCR in fetal blood group genotyping: a review","authors":"C. Hyland, Helen O'Brien, E. McGowan, A. Perros, R. Flower, G. Lopez, G. Gardener","doi":"10.21037/aob-22-4","DOIUrl":"https://doi.org/10.21037/aob-22-4","url":null,"abstract":"","PeriodicalId":72211,"journal":{"name":"Annals of blood","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46785752","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Stefano Tigano, Chiara Vitiello, M. D’Alesio, F. Sanfilippo, M. Astuto, A. Arcadipane, G. Martucci
{"title":"Transfusion management during extracorporeal membrane oxygenation for extended indications: a narrative review","authors":"Stefano Tigano, Chiara Vitiello, M. D’Alesio, F. Sanfilippo, M. Astuto, A. Arcadipane, G. Martucci","doi":"10.21037/aob-21-81","DOIUrl":"https://doi.org/10.21037/aob-21-81","url":null,"abstract":"","PeriodicalId":72211,"journal":{"name":"Annals of blood","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47785026","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Molecular typing of blood group genes in diagnostics","authors":"L. Castilho","doi":"10.21037/AOB-20-73","DOIUrl":"https://doi.org/10.21037/AOB-20-73","url":null,"abstract":": The molecular basis associated with the expression of all blood group antigens in the 43 blood group systems recognized by the International Society of Blood Transfusion (ISBT) was established and most are due to single nucleotide variations (SNVs). This allowed the development of a plethora of DNA tests to predict blood group antigens. Molecular typing of blood group genes in diagnostics facilitates the resolution of clinical problems that cannot be addressed by hemagglutination. They are useful to determine antigen types for which there is no typing reagents; to type patients who have been recently transfused or with warm auto antibodies; for definition of blood group variants; in prenatal testing; to search for rare blood types and to increase the reliability of repositories of antigen negative red blood cells (RBCs) for transfusion. This review summarizes the employment of molecular blood group typing and its benefits in diagnostics, especially in transfusion medicine and in maternal-fetal medicine. Advances in molecular methods have enabled the implementation of blood group genotyping in clinical laboratories changing work practices and revolutionizing the way transfusion is managed. The strength of next generation sequencing (NGS) of whole genomes or exomes or by targeting the specific blood group loci combined with pretransfusion serologic testing will enhance immunohematology in daily transfusion practice.","PeriodicalId":72211,"journal":{"name":"Annals of blood","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42490279","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Serena Ekman, R. Flower, S. Mahler, Alison Gould, R. Barnard, C. Hyland, Martina L. Jones, A. Malde, Xuan T Bui
{"title":"In silico molecular dynamics of human glycophorin A (GPA) extracellular structure","authors":"Serena Ekman, R. Flower, S. Mahler, Alison Gould, R. Barnard, C. Hyland, Martina L. Jones, A. Malde, Xuan T Bui","doi":"10.21037/AOB-20-51","DOIUrl":"https://doi.org/10.21037/AOB-20-51","url":null,"abstract":"Background: Glycophorin A (GPA) is one of two glycoproteins found on the surface of human red blood cells (RBCs) that constitute the MNS blood group system. The structure of GPA’s extracellular domain is unknown despite previous attempts using X-ray crystallography and NMR spectroscopy. As a result, there is a knowledge gap regarding antigen presentation. This hinders the production of monoclonal antibodies (mAbs) against MNS antigens. Methods: In silico modelling techniques including homology modelling and ab initio predictions were implemented to develop a proposed structure for the monomeric form of the GPA extracellular domain. Developed structures were then subjected to molecular dynamics (MD) simulations. Results: The results obtained indicated that the monomeric extracellular domain of GPA is most likely intrinsically disordered, with the exception of a β -hairpin-like structure spanning the exon 3–4 junction. Further analysis showed this β -hairpin-like structure was not observed when starting from an extended or cyclical peptide structure within the time-scale used in the MD simulation study, suggesting that linear or cyclical peptide fragments of this region are unsuitable representations for the purposes of antigen presentation. Lastly, of the MNS antigens produced by single amino acid variations found in the exon 3–4 junction, only the ERIK antigen (p.Gly78Arg; MNS37) was found to alter the β -hairpin-like structure. Conclusions: The monomer of the extracellular domain of GPA has a high level of disorder, with the exception of the antigenic exon 3–4 junction, which adopts a β -hairpin-like structure. Our work suggests that linear peptides and expression of the monomeric form of GPA might be of limited use for immunisation or screening processes used in antibody identification. Further understanding of the antigenic determinants of GPA will require a more sophisticated combination of laboratory and computational approaches, as well as consideration of possible structural changes as a result of dimerisation.","PeriodicalId":72211,"journal":{"name":"Annals of blood","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46474761","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Performance evaluation of two supplemental confirmatory assays of hepatitis C virus antibody","authors":"Li Zhang, Yi Zha, Li Shi, Y. Qiu","doi":"10.21037/AOB-20-67","DOIUrl":"https://doi.org/10.21037/AOB-20-67","url":null,"abstract":"Background: The overall relative change in Hepatitis C virus (HCV) reporting incidences was 1.16 in China recently, which exhibited increasing trend in most provinces. Screening tests for HCV antibodies are prone to generate higher false positivity in low-risk populations. The aim of this study was to compare the performance of two HCV supplemental confirmatory assays CWT (Wantai Biological Pharmaceutical Co., Ltd, Beijing, China) and RIBA HCV 3.0 SIA (RIBA 3.0). Methods: We selected 530 reactive specimens identified by two rounds of anti-HCV enzyme-linked immunosorbent assays (EIA) to carry out CWT and RIBA 3.0 supplemental tests simultaneously. Then the parallel testing results were evaluated as positive, indeterminate and negative, and made comparative analysis. Results: There were 182 and 160 confirmed positive samples for CWT and RIBA 3.0 respectively, of which 128 (24.2%) cases were common positive. the positive rate of CWT (34.3%) was significantly higher than RIBA 3.0 (30.2%) (P<0.01). And the common negative and indeterminate specimens were 156 (29.4%) and 53 (10%). The remaining 193 (36.4%) specimens had inconsistent results. The 182 CWT positive specimens included 35 indeterminate specimens (22%, 35/164) and 18 negative specimens (8.7%, 18/206) of RIBA 3.0. The diagnostic results of RIBA 3.0 and CWT supplementary assays were generally consistent (kappa =0.445, P<0.01). Conclusions: This study suggested that RIBA 3.0 and CWT each had its own genetic sequences of target peptides on HCV confirmatory tests and the latter might be more applicable for China’s current HCV epidemic strains. The number of positive cases confirmed by CWT is higher than that of RIBA 3.0, which corroborates this.","PeriodicalId":72211,"journal":{"name":"Annals of blood","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49246568","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}