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Sars-Cov-2 Vaccination in the First Year after Hematopoietic Cell Transplant or Chimeric Antigen Receptor T Cell Therapy: A CIBMTR and BMT CTN Study
We previously reported the immunogenicity of SARS-CoV-2 vaccination within the first year after allogeneic hematopoietic cell transplant (HCT) from CIBMTR SC21-07/BMT CTN 2101. We herein report updated results from the full allogeneic HCT cohort in addition to the autologous HCT and CAR-T cell thera...
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Published in: | Transplantation and cellular therapy 2024-02, Vol.30 (2), p.S82-S83 |
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Online Access: | Get full text |
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Summary: | We previously reported the immunogenicity of SARS-CoV-2 vaccination within the first year after allogeneic hematopoietic cell transplant (HCT) from CIBMTR SC21-07/BMT CTN 2101. We herein report updated results from the full allogeneic HCT cohort in addition to the autologous HCT and CAR-T cell therapy cohorts.
We conducted a prospective multicenter study of individuals who initiated SARS-CoV-2 vaccinations within 12 months of allogenic HCT, autologous HCT, or CAR-T cell therapy. We obtained blood prior to and after each vaccine dose for up to 4 vaccine doses, with an end-of-study sample 7 to 9 months after enrollment. We tested for SARS-CoV-2 spike protein (anti-S) IgG; nucleocapsid protein (anti-N) IgG; and neutralizing antibodies for Wuhan D614G, Delta B.1.617.2, and Omicron B.1.1.529 strains in all participants (LabCorp), in addition to SARS-CoV-2-specific T-cell receptors (TCRs) in a subgroup (n=151; Adaptive Biotech). We established a relevant threshold for immunogenicity assessment using receiver operating characteristic curves to determine the anti-S IgG threshold predictive of median neutralizing antibody levels (≥5274 ID50) achieved in a non-immunocompromised cohort vaccinated with two doses of mRNA-1273. We compared the proportion of participants with anti-S IgG titers above this threshold among those initiating vaccination |
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ISSN: | 2666-6367 2666-6367 |
DOI: | 10.1016/j.jtct.2023.12.134 |