Low fecal rotavirus vaccine virus shedding is significantly associated with non-secretor histo-blood group antigen phenotype among infants in northern Pretoria, South Africa

Vaccine ◽  
2020 ◽  
Vol 38 (52) ◽  
pp. 8260-8263
Author(s):  
Cliff A. Magwira ◽  
Lerato P. Kgosana ◽  
Mathew D. Esona ◽  
Mapaseka L. Seheri
2018 ◽  
Vol 69 (8) ◽  
pp. 1313-1319 ◽  
Author(s):  
Louisa Pollock ◽  
Aisleen Bennett ◽  
Khuzwayo C Jere ◽  
Queen Dube ◽  
Jonathan Mandolo ◽  
...  

Abstract Background Histo–blood group antigen (HBGA) Lewis/secretor phenotypes predict genotype-specific susceptibility to rotavirus gastroenteritis (RVGE). We tested the hypothesis that nonsecretor/Lewis-negative phenotype leads to reduced vaccine take and lower clinical protection following vaccination with G1P[8] rotavirus vaccine (RV1) in Malawian infants Methods A cohort study recruited infants receiving RV1 at age 6 and 10 weeks. HBGA phenotype was determined by salivary enzyme-linked immunosorbent assay (ELISA). RV1 vaccine virus shedding was detected by quantitative real-time polymerase chain reaction (qRT-PCR) in stool collected on alternate days for 10 days post-immunization. Plasma rotavirus–specific immunoglobulin A was determined by ELISA pre- and post-immunization. In a case-control study, HBGA phenotype distribution was compared between RV1-vaccinated infants with RVGE and 1:1 age-matched community controls. Rotavirus genotype was determined by RT-PCR. Results In 202 cohort participants, neither overall vaccine virus fecal shedding nor seroconversion differed by HBGA phenotype. In 238 case-control infants, nonsecretor phenotype was less common in infants with clinical vaccine failure (odds ratio [OR], 0.39; 95% confidence interval [CI], 0.20–0.75). Nonsecretor phenotype was less common in infants with P[8] RVGE (OR, 0.12; 95% CI, 0.03–0.50) and P[4] RVGE (OR, 0.17; 95% CI, 0.04–0.75). Lewis-negative phenotype was more common in infants with P[6] RVGE (OR, 3.2; 95% CI, 1.4–7.2). Conclusions Nonsecretor phenotype was associated with reduced risk of rotavirus vaccine failure. There was no significant association between HBGA phenotype and vaccine take. These data refute the hypothesis that high prevalence of nonsecretor/Lewis-negative phenotypes contributes to lower rotavirus vaccine effectiveness in Malawi.


2015 ◽  
Vol 34 (3) ◽  
pp. 326-328 ◽  
Author(s):  
Jérôme Kaplon ◽  
Guilhem Cros ◽  
Katia Ambert-Balay ◽  
Marianne Leruez-Ville ◽  
Maryline Chomton ◽  
...  

2017 ◽  
Vol 215 (5) ◽  
pp. 786-789 ◽  
Author(s):  
Abdul Momin Kazi ◽  
Margaret M. Cortese ◽  
Ying Yu ◽  
Benjamin Lopman ◽  
Ardythe L. Morrow ◽  
...  

2018 ◽  
Vol 217 (9) ◽  
pp. 1399-1407 ◽  
Author(s):  
Benjamin Lee ◽  
Dorothy M Dickson ◽  
Allan C deCamp ◽  
E Ross Colgate ◽  
Sean A Diehl ◽  
...  

Vox Sanguinis ◽  
1961 ◽  
Vol 6 (2) ◽  
pp. 151-156 ◽  
Author(s):  
B. P. L. Moore ◽  
P. H. Newstead ◽  
Joanne Johnson

Vaccines ◽  
2020 ◽  
Vol 9 (1) ◽  
pp. 4
Author(s):  
Janika Wolff ◽  
Tom Moritz ◽  
Kore Schlottau ◽  
Donata Hoffmann ◽  
Martin Beer ◽  
...  

Capripox virus (CaPV)-induced diseases (lumpy skin disease, sheeppox, goatpox) are described as the most serious pox diseases of livestock animals, and therefore are listed as notifiable diseases under guidelines of the World Organisation for Animal Health (OIE). Until now, only live-attenuated vaccines are commercially available for the control of CaPV. Due to numerous potential problems after vaccination (e.g., loss of the disease-free status of the respective country, the possibility of vaccine virus shedding and transmission as well as the risk of recombination with field strains during natural outbreaks), the use of these vaccines must be considered carefully and is not recommended in CaPV-free countries. Therefore, innocuous and efficacious inactivated vaccines against CaPV would provide a great tool for control of these diseases. Unfortunately, most inactivated Capripox vaccines were reported as insufficient and protection seemed to be only short-lived. Nevertheless, a few studies dealing with inactivated vaccines against CaPV are published, giving evidence for good clinical protection against CaPV-infections. In our studies, a low molecular weight copolymer-adjuvanted vaccine formulation was able to induce sterile immunity in the respective animals after severe challenge infection. Our findings strongly support the possibility of useful inactivated vaccines against CaPV-infections, and indicate a marked impact of the chosen adjuvant for the level of protection.


Vox Sanguinis ◽  
1966 ◽  
Vol 11 (2) ◽  
pp. 157-169
Author(s):  
M.N. Metaxas ◽  
M. Metaxas-Bühler ◽  
J. Romanski

Vox Sanguinis ◽  
1967 ◽  
Vol 13 (2) ◽  
pp. 165-170
Author(s):  
L. Kornstad ◽  
M. Kout ◽  
A.M. Heier Larsen ◽  
H. Ørjasaeter

Nature ◽  
1963 ◽  
Vol 198 (4881) ◽  
pp. 697-698 ◽  
Author(s):  
JAMES F. MOHN ◽  
REGINALD M. LAMBERT ◽  
CHESTER M. ZMIJEWSKI

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