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Updated: May 11, 2025

In Vitro and In Vivo Assessment of T, B and Myeloid Cells Suppressive Activity and Humoral Responses from Transplant Recipients
Published on: August 12, 2017
mRNA-1273 COVID-19 vaccine induces CD4+ T-cell responses among solid organ transplant recipients
Bethany Girard1, Amparo L Figueroa1, Stephen C De Rosa2
1Moderna, Inc., Cambridge, MA, United States.
Background:
Cell-mediated immunity may provide durable protection against severe COVID-19, including among solid organ transplant recipients (SOTRs). This exploratory analysis in the open-label phase 3b trial evaluated cell-mediated immunity of mRNA-1273 in a subset of participants (59 kidney and 33 liver SOTRs; 12 immunocompetent participants).
Methods:
In Part A, SOTRs received three 100-µg doses of mRNA-1273; immunocompetent participants received two doses. In Part B, an additional 100-µg dose was offered ≥4 months after the primary series. SARS-CoV-2 spike (S) protein-specific T-cell responses were measured by intracellular cytokine staining and polyfunctionality analyses.
Results:
The primary series and additional dose of mRNA-1273 induced S protein-specific CD4+ T-cell responses exhibiting a Th-1-biased profile in both SOTRs and immunocompetent participants; however, response rates and magnitudes were lower among SOTRs. S protein-specific Th-2 CD4+ T-cell responses were below those observed for Th-1; CD8+ T-cell responses were not as robust among SOTRs compared with immunocompetent participants. Kidney SOTRs received multiple immunosuppressants and had lower cell-mediated immunity responses than liver SOTRs. Polyfunctional responses exhibited Th-1 cytokine signatures with ≤5 functional markers reported in SOTRs and immunocompetent participants.
Conclusion:
Overall, a three-dose mRNA-1273 primary series elicited Th-1-biased CD4+ T-cell responses among SOTRs that were improved with an additional dose.
Clinical Trial Registration:
https://beta.clinicaltrials.gov/study/NCT04860297?term=NCT04860297%20&rank=1, identifier NCT04860297.
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