One way messenger RNA (mRNA) vaccines provide robust protection against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is by creating memory B cells that can detect the spike protein. Previous work has shown that the COVID-19 vaccine induces a robust germinal center response.
When there is antigenic stimulation, naive B cells can differentiate into plasmablasts with low-affinity antibodies or with the use of lymphoid structures known as germinal centers, naive B cells can gain affinity-enhancing somatic hypermutations that later differentiate into memory B cells and long-lived bone marrow plasma cells. However, whether the vaccine-induced germinal center response is the underlying cause for the increase in affinity-matured bone marrow-resident plasma cells after immunization remains under investigation.
A new study published in the preprint bioRxiv* server suggests vaccination helps to inflate the number of somatic hypermutations acquired by B cells. The increase in somatic hypermutations allows for an accumulation of highly matured bone marrow plasma cells.
Their results can provide a basis to understanding how mRNA vaccines can elicit strong antibody responses against viruses and apply this to other viral infections such as influenza, malaria, and HIV.
Antigen GC B-cell response six months after vaccination
The researchers followed up with participants of a previous study who had received both doses of the Pfizer-BioNTech mRNA COVID-19 vaccine to measure their immune levels.
After 29 weeks from the primary vaccination, the team collected blood samples, fine needle aspirates of the draining axillary lymph nodes, and bone marrow specimens. All participants had no previous exposure or SARS-CoV-2 infection.
The researchers found germinal center B cells in all 15 participants who allowed for fine-needle aspirates. About 14 participants who had fine-needle aspirates collected before week 29 showed a range of SARS-CoV-2-spike protein binding antigen-specific germinal center B cell responses.
Ten of the 15 participants with fine-needle aspirate samples showed signs of spike protein-binding germinal center B cells. The findings indicate more than half of participants had an antigen-specific germinal center B cell response six months after immunization.
Antigen-specific bone marrow plasma cells found after immunization
The researchers collected bone marrow specimens from participants 29 weeks after vaccination to measure bone marrow plasma cells.
They measured the amount of IgG and IgA antibodies secreted from bone marrow plasma cells and compared the levels to those secreted for the flu virus, SARS-CoV-2 spike protein, or the tetanus-diphtheria vaccine.
About 11 participants who received either the flu or tetanus shot showed detectable influenza- and tetanus-diphtheria vaccine-specific IgG-secreting bone marrow plasma cells. When exposed to the SARS-CoV-2 spike protein, 9 of 11 participants showed a response in the form of SARS-CoV-2 S-binding IgG secreting bone marrow plasma cells.
However, IgA-secreting bone marrow plasma cells specific for the SARS-CoV-2 spike protein were below the detection level.
Every participant showed IgG antibodies specific for the spike protein and circulating spike protein-specific memory B cells 29 weeks after immunization. People who were vaccinated but had a prior COVID-19 infection showed significantly higher anti-S IgG titers 5 and 29 weeks after vaccination.
IgG antibodies did decrease after a peak stemming from the second vaccination. Still, they continued to show detectable levels six months after vaccination.
Additionally, all vaccinated participants had memory B cells specifically targeting the spike protein. The median frequency for CD19+ circulating B cells was 0.23%, indicating a robust and enduring humoral response.
Somatic hypermutations accumulate and help with differentiation
The researchers tracked more than 1,500 vaccine-induced B cell clones to observe for any changes over time. There they found a gradual accumulation of somatic hypermutations with germinal center B cell compartments.
The buildup of somatic hypermutations pivoted B germinal center B cells to lymph node plasma cells in the lymph node and eventually into mature bone marrow plasma cells.
The number of mature bone marrow plasma cells is associated with SARS-CoV-2 antibody levels. More maturation of bone marrow plasma cells was observed 6 months after vaccination rather than 2 weeks after.
bioRxiv publishes preliminary scientific reports that are not peer-reviewed and, therefore, should not be regarded as conclusive, guide clinical practice/health-related behavior, or treated as established information.
- Kim W, et al. (2021). Germinal centre-driven maturation of B cell response to SARS-CoV-2 vaccination. bioRxiv. Doi: https://doi.org/10.1101/2021.10.31.466651, https://www.biorxiv.org/content/10.1101/2021.10.31.466651v1
Posted in: Medical Research News | Disease/Infection News
Tags: Antibodies, Antibody, Antigen, B Cell, Blood, Bone, Bone Marrow, CD3, Cell, Coronavirus, Coronavirus Disease COVID-19, Cytometry, Diphtheria, Flow Cytometry, Flu, Frequency, HIV, Immunization, Immunoglobulin, Influenza, Lymph Node, Lymph Nodes, Malaria, Protein, Respiratory, RNA, SARS, SARS-CoV-2, Severe Acute Respiratory, Severe Acute Respiratory Syndrome, Spike Protein, Syndrome, Tetanus, Vaccine, Virus
Jocelyn Solis-Moreira graduated with a Bachelor's in Integrative Neuroscience, where she then pursued graduate research looking at the long-term effects of adolescent binge drinking on the brain's neurochemistry in adulthood.
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