Abstract
To determine whether non-secretion of blood group antigens is associated with respiratory virus diseases. Study of secretor status in patients with respiratory virus diseases determined by an enzyme linked immunosorbent assay (ELISA) developed to identify Lewis (Le) blood group antigen phenotypes (Le(a) non-secretor; Le(b) secretor). Patients aged 1 month to 90 years in hospital with respiratory virus diseases (584 nasal specimens). Criteria for validation of ELISA (congruence between results on ELISA testing of 1155 saliva samples from a previous study and previously established results on haemagglutination inhibition (HAI) testing, proportions of Le(a), Le(b), and Le- phenotypes in 872 samples of nasal washings from a previous study compared with the normal population). Secretor status of patients determined by ELISA and viruses isolated. Agreement between HAI and ELISA for 1155 saliva samples was 97%. Lewis antigens were detected by ELISA in 854 (97.9%) of nasal washings (Le(a) 233 (26.7%), Le(b) 621 (71.2%), and Le- 18 (2.1%)) in proportions predicted for a northern European population. Secretors were significantly overrepresented among patients from whom influenza viruses A and B (55/64, 86%; p less than 0.025), rhinoviruses (63/72, 88%; p less than 0.01), respiratory syncytial virus (97/109, 89%; p less than 0.0005), and echoviruses (44/44, p less than 0.0005) had been isolated compared with the distribution of secretors in the local population. Secretion of blood group antigens is associated with respiratory virus diseases.
MeSH Terms
Adolescent
Adult
Aged
Aged, 80 and over
Child
Child, Preschool
Enzyme-Linked Immunosorbent Assay
Humans
Infant
Isoantigens/analysis
Lewis Blood Group Antigens/genetics,immunology
Middle Aged
Respiratory Tract Infections/blood,immunology
Saliva/chemistry,immunology
Virus Diseases/blood,immunology
Chemicals
Isoantigens
Lewis Blood Group Antigens
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Raza M W
Department of Medical Microbiology, University of Edinburgh Medical School.
Blackwell C C
Molyneaux P
James V S
Ogilvie M M
Inglis J M
Weir D M
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