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Deficient Generation of Spike-Specific Long-Lived Plasma Cells in the Bone Marrow After Severe Acute Respiratory Syndrome Coronavirus 2 Infection.

Zahra R TehraniParham HabibzadehRobin FlinkoHegang ChenAbdolrahim AbbasiJean A YaredStanca M CiupeGeorge K LewisMohammad M Sajadi
Published in: The Journal of infectious diseases (2024)
Generation of a stable long-lived plasma cell (LLPC) population is the sine qua non of durable antibody responses after vaccination or infection. We studied 20 individuals with a prior coronavirus disease 2019 infection and characterized the antibody response using bone marrow aspiration and plasma samples. We noted deficient generation of spike-specific LLPCs in the bone marrow after severe acute respiratory syndrome coronavirus 2 infection. Furthermore, while the regression model explained 98% of the observed variance in anti-tetanus immunoglobulin G levels based on LLPC enzyme-linked immunospot assay, we were unable to fit the same model with anti-spike antibodies, again pointing to the lack of LLPC contribution to circulating anti-spike antibodies.
Keyphrases
  • respiratory syndrome coronavirus
  • bone marrow
  • coronavirus disease
  • sars cov
  • mesenchymal stem cells
  • induced apoptosis
  • single cell
  • high throughput
  • ultrasound guided
  • cell cycle arrest
  • pi k akt
  • solid state