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Nikhil Prasad  Fact checked by:Thailand Medical News Team Aug 12, 2024  4 months, 1 week, 4 days, 2 hours, 28 minutes ago

Japanese study finds that COVID-19 infections and vaccines are inducing the emergence of atypical memory B cells!

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Japanese study finds that COVID-19 infections and vaccines are inducing the emergence of atypical memory B cells!
Nikhil Prasad  Fact checked by:Thailand Medical News Team Aug 12, 2024  4 months, 1 week, 4 days, 2 hours, 28 minutes ago
Medical News: In the battle against COVID-19, understanding the body's immune response is crucial. Researchers from various Japanese institutions, including Osaka University, have delved deep into the behavior of memory B cells, the guardians of immune memory, particularly in the context of SARS-CoV-2, the virus responsible for COVID-19. This Medical News report explores their groundbreaking findings on how these cells respond following mRNA vaccination or natural infection.


Japanese study finds that COVID-19 infections and vaccines are inducing
the emergence of atypical memory B cells!


Memory B Cells: The Body's Defense Memory
Memory B cells are a type of immune cell that "remembers" pathogens encountered by the body, enabling a faster and more effective response upon subsequent exposures. These cells are vital in ensuring long-term immunity, either through vaccination or after recovering from an infection. The study led by Osaka University researchers identified two main types of memory B cells: classical CD45RB+ and atypical CD45RBlo cells, which differ in their roles and responses to various infections.
 
Key Findings: The Dominance of Atypical Memory B Cells
The study revealed that following either mRNA vaccination or COVID-19 infection, the majority of SARS-CoV-2-specific memory B cells circulating in the blood were of the atypical CD45RBlo type. These atypical cells, characterized by their low expression of the CD45RB marker, formed a significant proportion of the body's immune response to the virus. In contrast, classical memory B cells, which express higher levels of CD45RB, were more prominent in bacterial infections, such as sepsis.
 
This distinction is crucial as it highlights how different pathogens can activate distinct subsets of memory B cells, tailoring the immune response to the specific threat. The findings also suggest that the CD45RBlo memory B cells play a pivotal role in producing antibodies that target the SARS-CoV-2 virus, contributing to long-term immunity.
 
Study Design: Analyzing Immune Responses
To arrive at these conclusions, the researchers conducted a comprehensive study involving various cohorts, including patients with severe COVID-19, individuals with bacterial sepsis, and healthcare workers who received the Pfizer-BioNTech mRNA vaccine. The study utilized advanced techniques like mass cytometry and CITE-seq to analyze the immune cells from these participants over time. This approach allowed the researchers to track changes in the populations of memory B cells and their activation states.
 
The analysis revealed that during COVID-19, there was a significant increase in atypical memory B cells, particularly those marked by the expression of CD11c and T-bet, two proteins associated with robust immune activation. This population of cells was not only prevalent during the acute phase of infection but also persisted after recovery, suggesting a long-lasting immune memory specific to SARS-CoV-2.
 
< ;strong>The Role of CD45RBlo Cells in Vaccination
Interestingly, the study found that following mRNA vaccination, similar patterns emerged. Atypical CD45RBlo memory B cells were the primary responders, expanding significantly after both the first and second doses of the vaccine. These cells were also found to be the main producers of antibodies that neutralize the virus, highlighting their critical role in vaccine-induced immunity.
 
The researchers noted that while classical memory B cells responded to bacterial infections, they did not show the same level of activation in response to SARS-CoV-2 or the mRNA vaccine. This finding underscores the specificity of the immune response and suggests that the body may prioritize different types of memory B cells depending on the nature of the pathogen.
 
Implications for Future Research and Vaccination Strategies
The discovery of the dominance of atypical CD45RBlo memory B cells in the immune response to SARS-CoV-2 has significant implications for future research and vaccine development. Understanding the mechanisms that drive the activation and maintenance of these cells could lead to more effective vaccines that offer longer-lasting protection against COVID-19.
 
Moreover, the study's findings could inform strategies for boosting immunity in individuals who have recovered from COVID-19 or who have received the vaccine. For instance, future vaccines might be designed to specifically target and enhance the response of these atypical memory B cells, thereby increasing their effectiveness.
 
Conclusion: A Step Forward in Immunology
In conclusion, the research conducted by the team from Osaka University and other collaborating institutions provides valuable insights into the immune response to SARS-CoV-2. By identifying the key role of atypical CD45RBlo memory B cells in both natural infection and vaccination, the study advances our understanding of how long-term immunity is established and maintained.
 
The findings, published in the peer-reviewed journal: Nature Communications, offer a promising avenue for the development of more effective vaccines and treatments for COVID-19.
https://www.nature.com/articles/s41467-024-50997-4
 
For the latest on COVID-19, keep on logging to Thailand Medical News.
 
Read Also:
https://www.thailandmedical.news/news/covid-19-infections-causes-reprogramming-of-leukocyte-metabolism-by-the-activation-of-certain-amino-acid-pathways
 
https://www.thailandmedical.news/news/study-discovers-that-sars-cov-2-mpro-protein-disarms-some-of-the-human-immune-responses-by-cleaving-nemo-an-immune-signaling-protein

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