scholarly journals Glycosylation and serological reactivity of an expression-enhanced SARS-CoV-2 viral spike mimetic

2021 ◽  
pp. 167332
Author(s):  
Himanshi Chawla ◽  
Sian E. Jossi ◽  
Sian E. Faustini ◽  
Firdaus Samsudin ◽  
Joel D. Allen ◽  
...  
Author(s):  
N. K Chakraborty ◽  
Y. S. Ahlawat ◽  
A. Varma ◽  
K. J. Chandra ◽  
S. Ramapandu ◽  
...  

Author(s):  
Iheanyi O. Okonko ◽  
Tochi I. Cookey ◽  
Sofiat Adewuyi-Oseni ◽  
Amaka M. Awanye

Aim: This study reports on the detection of Treponema pallidum (syphilis) antibodies in HIV infected patients in Port Harcourt, Nigeria. Screening for syphilis was carried out to determine the prevalence levels of these infections, as biological markers of risk, modes, and time functions of their transmission. Study Design: Cross-sectional study. Place and Duration of Study: University of Port Harcourt Teaching Hospital (UPTH) and O.B. Lulu Briggs Medical Centre, University of Port Harcourt, both in Port Harcourt, Nigeria, between August 2012 and July 2015. Methods: A total of 100 HIV-infected individuals and 100 sexually-active attendees were recruited for this study. Samples of blood were collected and re-screened for the presence of HIV antibodies using the Determine HIV-1/2 (Alere), HIV ½ Stat-Pak (Chembio), and HIV-1/2/P24/O ELISA kit (Dia.Pro). The same set of samples were screened for Treponema pallidum specific antibodies using the syphilis Ultra Rapid Test Strip (ACON(R), USA) and syphilis rapid strips (Global, USA) following the respective manufacturer's instructions. Results: Among the 200 samples, serological reactivity was detected for syphilis in 3(1.5%). The incidence of syphilis was higher in males (2.0%) than in females (1.0%). Age, sex, and locality did not significantly (P>0.05) influence the rate of syphilis. Conclusion: This study further confirms the presence of syphilis among the population studied. Routine screening of Syphilis among patients is therefore advocated.


2010 ◽  
Vol 143 (2-4) ◽  
pp. 384-388 ◽  
Author(s):  
Rebecca J. Grant ◽  
Karen L. Kelley ◽  
James E. Maruniak ◽  
Alejandra Garcia-Maruniak ◽  
Tom Barrett ◽  
...  

2005 ◽  
Vol 244 (1) ◽  
pp. 47-52 ◽  
Author(s):  
Maria Helena Villas-Boas ◽  
Robin Wait ◽  
Rosana B. Silva ◽  
Marcio L. Rodrigues ◽  
Eliana Barreto-Bergter

1994 ◽  
Vol 89 (suppl 2) ◽  
pp. 13-15 ◽  
Author(s):  
W. Roeffen ◽  
T. Lensen ◽  
B. Mulder ◽  
K. Teelen ◽  
R. Sauerwein ◽  
...  

2008 ◽  
Vol 41 (2) ◽  
pp. 135-141 ◽  
Author(s):  
Adriano Gomes-Silva ◽  
Maria Aparecida Souza ◽  
Sandra Regina Afonso-Cardoso ◽  
Lívia Resende Andrade ◽  
Reynaldo Dietze ◽  
...  

Total antigen from Leishmania (Leishmania) amazonensis and isolates from the Leishmania braziliensis complex, along with their respective antigenic fractions obtained by affinity chromatography on concanavalin-A-Sepharose and jacalin-agarose columns evaluated using immunoenzymatic ELISA assay. For this, serum samples from 229 patients were used, grouped as American tegmental leishmaniasis (nº=58), visceral leishmaniasis (nº=28), Chagas disease (nº=49), malaria (nº=32), tuberculosis (nº=13) and healthy volunteers (nº=49). Samples from American tegmentary leishmaniasis showed higher reactivity with antigens isolated from the Leishmania braziliensis complex than with antigens from Leishmania amazonensis (p<0.001). ELISA assays showed a sensitivity range from 60% to 95% with antigens isolated from the Leishmania braziliensis complex. There was marked nonspecific reactivity among serum samples with the use of antigenic fractions binding with concanavalin-A and jacalin from both Leishmania complexes, in comparison with other antigens (p<0.001). The results presented in this study suggest that the use of homologous antigens increases the efficiency of anti-Leishmania immunoglobulin detection, which may be very valuable for diagnostic purposes.


2016 ◽  
Vol 189 ◽  
pp. 15-23 ◽  
Author(s):  
Gian Luca Autorino ◽  
Claudia Eleni ◽  
Giuseppe Manna ◽  
Raffaele Frontoso ◽  
Roberto Nardini ◽  
...  

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