Deficient Generation of Spike-Specific Long-Lived Plasma Cells in the Bone Marrow After Severe Acute Respiratory Syndrome Coronavirus 2 Infection
dc.contributor.author | Tehrani, Zahra R. | en |
dc.contributor.author | Habibzadeh, Parham | en |
dc.contributor.author | Flinko, Robin | en |
dc.contributor.author | Chen, Hegang | en |
dc.contributor.author | Abbasi, Abdolrahim | en |
dc.contributor.author | Yared, Jean A. | en |
dc.contributor.author | Ciupe, Stanca M. | en |
dc.contributor.author | Lewis, George K. | en |
dc.contributor.author | Sajadi, Mohammad M. | en |
dc.date.accessioned | 2025-01-09T14:57:24Z | en |
dc.date.available | 2025-01-09T14:57:24Z | en |
dc.date.issued | 2024-02-14 | en |
dc.description.abstract | 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. | en |
dc.description.version | Published version | en |
dc.format.mimetype | application/pdf | en |
dc.identifier.doi | https://doi.org/10.1093/infdis/jiad603 | en |
dc.identifier.eissn | 1537-6613 | en |
dc.identifier.issn | 0022-1899 | en |
dc.identifier.issue | 1 | en |
dc.identifier.orcid | Ciupe, Mihaela [0000-0002-5386-6946] | en |
dc.identifier.other | 7606721 (PII) | en |
dc.identifier.pmid | 38365441 | en |
dc.identifier.uri | https://hdl.handle.net/10919/124004 | en |
dc.identifier.volume | 230 | en |
dc.language.iso | en | en |
dc.publisher | Oxford University Press | en |
dc.relation.uri | https://www.ncbi.nlm.nih.gov/pubmed/38365441 | en |
dc.rights | Creative Commons Attribution 4.0 International | en |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | en |
dc.subject | COVID-19 | en |
dc.subject | SARS-CoV-2 | en |
dc.subject | humoral immunity | en |
dc.subject | immunological memory | en |
dc.subject | plasma cells | en |
dc.subject.mesh | Humans | en |
dc.subject.mesh | COVID-19 | en |
dc.subject.mesh | Plasma Cells | en |
dc.subject.mesh | Spike Glycoprotein, Coronavirus | en |
dc.subject.mesh | Antibodies, Viral | en |
dc.subject.mesh | SARS-CoV-2 | en |
dc.subject.mesh | Male | en |
dc.subject.mesh | Middle Aged | en |
dc.subject.mesh | Female | en |
dc.subject.mesh | Bone Marrow | en |
dc.subject.mesh | Adult | en |
dc.subject.mesh | Immunoglobulin G | en |
dc.subject.mesh | Aged | en |
dc.title | Deficient Generation of Spike-Specific Long-Lived Plasma Cells in the Bone Marrow After Severe Acute Respiratory Syndrome Coronavirus 2 Infection | en |
dc.title.serial | The Journal of Infectious Diseases | en |
dc.type | Article - Refereed | en |
dc.type.dcmitype | Text | en |
dc.type.other | Journal Article | en |
dcterms.dateAccepted | 2024-01-02 | en |
pubs.organisational-group | Virginia Tech | en |
pubs.organisational-group | Virginia Tech/Science | en |
pubs.organisational-group | Virginia Tech/Science/Mathematics | en |
pubs.organisational-group | Virginia Tech/All T&R Faculty | en |
pubs.organisational-group | Virginia Tech/Science/COS T&R Faculty | en |