TY - JOUR
T1 - ABO blood group and COVID-19
T2 - a review on behalf of the ISBT COVID-19 Working Group
AU - the ISBT COVID-19 Working Group
AU - Goel, Ruchika
AU - Bloch, Evan M.
AU - Pirenne, France
AU - Al-Riyami, Arwa Z.
AU - Crowe, Elizabeth
AU - Dau, Laetitia
AU - Land, Kevin
AU - Townsend, Mary
AU - Jecko, Thachil
AU - Rahimi-Levene, Naomi
AU - Patidar, Gopal
AU - Josephson, Cassandra D.
AU - Arora, Satyam
AU - Vermeulen, Marion
AU - Vrielink, Hans
AU - Montemayor, Celina
AU - Oreh, Adaeze
AU - Hindawi, S.
AU - van den Berg, Karin
AU - Serrano, Katherine
AU - So-Osman, Cynthia
AU - Wood, Erica
AU - Devine, D. V.
AU - Spitalnik, Steven L.
N1 - Funding Information:
EMB’s effort is supported in part by the National Institutes of Health (K23 HL151826). SLS’s effort is supported in part by the National Institutes of Health (R01 HL133049, R01 HL139489, R01 HL148151 and N26819 HB00003R).
Publisher Copyright:
© 2021 International Society of Blood Transfusion
PY - 2021/9
Y1 - 2021/9
N2 - Growing evidence suggests that ABO blood group may play a role in the immunopathogenesis of SARS-CoV-2 infection, with group O individuals less likely to test positive and group A conferring a higher susceptibility to infection and propensity to severe disease. The level of evidence supporting an association between ABO type and SARS-CoV-2/COVID-19 ranges from small observational studies, to genome-wide-association-analyses and country-level meta-regression analyses. ABO blood group antigens are oligosaccharides expressed on red cells and other tissues (notably endothelium). There are several hypotheses to explain the differences in SARS-CoV-2 infection by ABO type. For example, anti-A and/or anti-B antibodies (e.g. present in group O individuals) could bind to corresponding antigens on the viral envelope and contribute to viral neutralization, thereby preventing target cell infection. The SARS-CoV-2 virus and SARS-CoV spike (S) proteins may be bound by anti-A isoagglutinins (e.g. present in group O and group B individuals), which may block interactions between virus and angiotensin-converting-enzyme-2-receptor, thereby preventing entry into lung epithelial cells. ABO type-associated variations in angiotensin-converting enzyme-1 activity and levels of von Willebrand factor (VWF) and factor VIII could also influence adverse outcomes, notably in group A individuals who express high VWF levels. In conclusion, group O may be associated with a lower risk of SARS-CoV-2 infection and group A may be associated with a higher risk of SARS-CoV-2 infection along with severe disease. However, prospective and mechanistic studies are needed to verify several of the proposed associations. Based on the strength of available studies, there are insufficient data for guiding policy in this regard.
AB - Growing evidence suggests that ABO blood group may play a role in the immunopathogenesis of SARS-CoV-2 infection, with group O individuals less likely to test positive and group A conferring a higher susceptibility to infection and propensity to severe disease. The level of evidence supporting an association between ABO type and SARS-CoV-2/COVID-19 ranges from small observational studies, to genome-wide-association-analyses and country-level meta-regression analyses. ABO blood group antigens are oligosaccharides expressed on red cells and other tissues (notably endothelium). There are several hypotheses to explain the differences in SARS-CoV-2 infection by ABO type. For example, anti-A and/or anti-B antibodies (e.g. present in group O individuals) could bind to corresponding antigens on the viral envelope and contribute to viral neutralization, thereby preventing target cell infection. The SARS-CoV-2 virus and SARS-CoV spike (S) proteins may be bound by anti-A isoagglutinins (e.g. present in group O and group B individuals), which may block interactions between virus and angiotensin-converting-enzyme-2-receptor, thereby preventing entry into lung epithelial cells. ABO type-associated variations in angiotensin-converting enzyme-1 activity and levels of von Willebrand factor (VWF) and factor VIII could also influence adverse outcomes, notably in group A individuals who express high VWF levels. In conclusion, group O may be associated with a lower risk of SARS-CoV-2 infection and group A may be associated with a higher risk of SARS-CoV-2 infection along with severe disease. However, prospective and mechanistic studies are needed to verify several of the proposed associations. Based on the strength of available studies, there are insufficient data for guiding policy in this regard.
KW - ABO blood groups
KW - COVID-19
KW - SARS-CoV-2
KW - disease severity
KW - disease susceptibility
UR - http://www.scopus.com/inward/record.url?scp=85100858506&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85100858506&partnerID=8YFLogxK
U2 - 10.1111/vox.13076
DO - 10.1111/vox.13076
M3 - Review article
C2 - 33578447
AN - SCOPUS:85100858506
SN - 0042-9007
VL - 116
SP - 849
EP - 861
JO - Vox Sanguinis
JF - Vox Sanguinis
IS - 8
ER -