From Pauling's abzyme concept to the new era of hydrolytic anti-DNA autoantibodies: a link to rational vaccine design? – A review

Author(s):  
Mirjana Pavlovic ◽  
Michelle Cavallo ◽  
Anna Kats ◽  
Alex Kotlarchyk ◽  
Hanqi Zhuang ◽  
...  
Author(s):  
Abhinay Sharma ◽  
Pooja Sanduja ◽  
Aparna Anand ◽  
Pooja Mahajan ◽  
Carlos A. Guzman ◽  
...  

AbstractInfectious diseases are one of the main grounds of death and disabilities in human beings globally. Lack of effective treatment and immunization for many deadly infectious diseases and emerging drug resistance in pathogens underlines the need to either develop new vaccines or sufficiently improve the effectiveness of currently available drugs and vaccines. In this review, we discuss the application of advanced tools like bioinformatics, genomics, proteomics and associated techniques for a rational vaccine design.


2006 ◽  
Vol 5 (4) ◽  
pp. 565-577 ◽  
Author(s):  
Emma L Beukema ◽  
Michael P Brown ◽  
John D Hayball

2020 ◽  
Author(s):  
Adam S. Dingens ◽  
Payal Pratap ◽  
Keara Malone ◽  
Sarah K. Hilton ◽  
Thomas Ketas ◽  
...  

AbstractMapping the epitope specificities of polyclonal serum is critical to rational vaccine design. However, most high-resolution mapping approaches involve isolating and characterizing individual monoclonal antibodies, which incompletely defines the full polyclonal response. Here we use two complementary approaches to directly map the specificities of the neutralizing and binding antibodies of polyclonal anti-HIV-1 sera from rabbits immunized with BG505 Env SOSIP trimers. To map the neutralizing specificity, we used mutational antigenic profiling to determine how all amino-acid mutations in Env affected viral neutralization. To map the binding specificity, we used electron microscopy polyclonal epitope mapping (EMPEM) to directly visualize the Fabs in serum bound to Env trimers. Mutational antigenic profiling showed that the dominant neutralizing specificities were the C3/V5 and/or 241/289 glycan hole epitopes, which were generally only a subset of the more diverse binding specificities mapped with EMPEM. Additional differences between binding and neutralization reflected antigenicity differences between virus and soluble Env trimer. Further, mutational antigenic profiling was able to refine epitope specificity in residue-level detail directly from sera, revealing subtle differences across rabbits. Together, mutational antigenic profiling and EMPEM allow for a holistic view of the binding and neutralizing specificity of polyclonal sera and could be used to finely evaluate and guide vaccine design.


Vaccines ◽  
2018 ◽  
Vol 6 (3) ◽  
pp. 58 ◽  
Author(s):  
Nicole Bouvier

For centuries, the development of vaccines to prevent infectious disease was an empirical process. From smallpox variolation in Song dynasty China, through the polysaccharide capsule vaccines developed in the 1970s, vaccines were made either from the pathogen itself, treated in some way to render it attenuated or non-infectious, or from a closely related non-pathogenic strain. In recent decades, new scientific knowledge and technologies have enabled rational vaccine design in a way that was unimaginable before. However, vaccines optimal against some infectious diseases, influenza among them, have remained elusive. This review will highlight the challenges that influenza viruses pose for rational vaccine design. In particular, it will consider the clinically beneficial endpoints, beyond complete sterilizing immunity, that have been achieved with vaccines against other infectious diseases, as well as the barriers to achieving similar success against influenza.


2019 ◽  
Vol 18 (9) ◽  
pp. 877-880
Author(s):  
Ekaterina Stepanova ◽  
Irina Isakova-Sivak ◽  
Larisa Rudenko

2020 ◽  
Vol 27 (5) ◽  
pp. 695-698 ◽  
Author(s):  
Dennis R. Burton ◽  
Laura M. Walker

Immunity ◽  
2010 ◽  
Vol 33 (4) ◽  
pp. 437-440 ◽  
Author(s):  
David A. D'Argenio ◽  
Christopher B. Wilson

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