scholarly journals B-Cell Memory Responses to Variant Viral Antigens

Viruses ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 565
Author(s):  
Harry N. White

A central feature of vertebrate immune systems is the ability to form antigen-specific immune memory in response to microbial challenge and so provide protection against future infection. In conflict with this process is the ability that many viruses have to mutate their antigens to escape infection- or vaccine-induced antibody memory responses. Mutable viruses such as dengue virus, influenza virus and of course coronavirus have a major global health impact, exacerbated by this ability to evade immune responses through mutation. There have been several outstanding recent studies on B-cell memory that also shed light on the potential and limitations of antibody memory to protect against viral antigen variation, and so promise to inform new strategies for vaccine design. For the purposes of this review, the current understanding of the different memory B-cell (MBC) populations, and their potential to recognize mutant antigens, will be described prior to some examples from antibody responses against the highly mutable RNA based flaviviruses, influenza virus and SARS-CoV-2.

Vaccine ◽  
2010 ◽  
Vol 28 (10) ◽  
pp. 2186-2194 ◽  
Author(s):  
Hye Mee Joo ◽  
Yuxia He ◽  
Aarthi Sundararajan ◽  
Lifang Huan ◽  
Mark Y. Sangster

Author(s):  
Fan Yang ◽  
Sandra C. A. Nielsen ◽  
Ramona A. Hoh ◽  
Ji-Yeun Lee ◽  
Tho D. Pham ◽  
...  

AbstractVaccination and infection promote the formation, tissue distribution, and clonal evolution of B cells encoding humoral immune memory. We evaluated convergent antigen-specific antibody genes of similar sequences shared between individuals in pediatric and adult blood, and deceased organ donor tissues. B cell memory varied for different pathogens. Polysaccharide antigen-specific clones were not exclusive to the spleen. Adults’ convergent clones often express mutated IgM or IgD in blood and are class-switched in lymphoid tissues; in contrast, children have abundant class-switched convergent clones in blood. Consistent with serological reports, pre-pandemic children had class-switched convergent clones to SARS-CoV-2, enriched in cross-reactive clones for seasonal coronaviruses, while adults showed few such clones in blood or lymphoid tissues. These results extend age-related and anatomical mapping of human humoral pathogen-specific immunity.One Sentence SummaryChildren have elevated frequencies of pathogen-specific class-switched memory B cells, including SARS-CoV-2-binding clones.


Science ◽  
2021 ◽  
pp. eabf6648
Author(s):  
Fan Yang ◽  
Sandra C. A. Nielsen ◽  
Ramona A. Hoh ◽  
Katharina Röltgen ◽  
Oliver Fabian Wirz ◽  
...  

Vaccination and infection promote the formation, tissue distribution, and clonal evolution of B cells, which encode humoral immune memory. We evaluated convergent antigen-specific antibody genes of similar sequences shared between individuals in pediatric and adult blood, and deceased organ donor tissues. B cell memory varied for different pathogens. Polysaccharide antigen-specific clones were not exclusive to the spleen. Adults had higher clone frequencies and greater class-switching in lymphoid tissues than blood, while pediatric blood had abundant class-switched convergent clones. Consistent with reported serology, pre-pandemic children had class-switched convergent clones to SARS-CoV-2 with weak cross-reactivity to other coronaviruses, while adult blood or tissues showed few such clones. The results highlight the prominence of early childhood B cell clonal expansions and cross-reactivity for future responses to novel pathogens.


2016 ◽  
Vol 35 (4) ◽  
pp. 491-499 ◽  
Author(s):  
Simon Urschel ◽  
Lauren A. Ryan ◽  
Ingrid M. Larsen ◽  
Kimberley Biffis ◽  
I. Esme Dijke ◽  
...  

Nature ◽  
1988 ◽  
Vol 336 (6194) ◽  
pp. 70-73 ◽  
Author(s):  
David Gray ◽  
Helena Skarvall
Keyword(s):  
B Cell ◽  

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