Key result
Two mRNA-1273 vaccine doses elicit immune responses in ~90% of heart and liver transplant recipients.
Why the study?
Impaired immune response after SARS-CoV-2 vaccination had been observed in solid organ recipients, but most studies had not assessed cellular responses in liver and heart transplant recipients.
Does the mRNA-1273 SARS-CoV-2 vaccine induce humoral and cellular immune responses in liver and heart transplant recipients?
Cohort (n=104)
Does the mRNA-1273 SARS-CoV-2 vaccine induce humoral and cellular immune responses in liver and heart transplant recipients?
The mRNA-1273 vaccine induces a robust humoral or cellular immune response in 90% of heart and liver transplant recipients, though hypogammaglobulinemia and recent transplantation are associated with unresponsiveness.
May inform vaccination decisions in transplant recipients; leaves open optimal regimens for reduced responders.
Recently published studies have found an impaired immune response after SARS-CoV-2 vaccination in solid organ recipients. However, most of these studies have not assessed immune cellular responses in liver and heart transplant recipients. We prospectively studied heart and liver transplant recipients eligible for SARS-CoV-2 vaccination. Patients with past history of SARS-CoV-2 infection or SARS-CoV-2 detectable antibodies (IgM or IgG) were excluded. We assessed IgM/IgG antibodies and ELISpot against the S protein 4 weeks after receiving the second dose of the mRNA-1273 (Moderna) vaccine. Side effects, troponin I, liver tests and anti-HLA donor-specific antibodies (DSA) were also assessed. A total of 58 liver and 46 heart recipients received two doses of mRNA-1273 vaccine. Median time from transplantation to vaccination was 5.4 years (IQR 0.3-27). Sixty-four percent of the patients developed SARS-CoV-2 IgM/IgG antibodies and 79% S-ELISpot positivity. Ninety percent of recipients developed either humoral or cellular response (87% in heart recipients and 93% in liver recipients). Factors associated with vaccine unresponsiveness were hypogammaglobulinemia and vaccination during the first year after transplantation. Local and systemic side effects were mild or moderate, and none presented DSA or graft dysfunction after vaccination. Ninety percent of our patients did develop humoral or cellular responses to mRNA-1273 vaccine. Factors associated with vaccine unresponsiveness were hypogammaglobulinemia and vaccination during the first year after transplantation, highlighting the need to further protect these patients.
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Herrera et al. (2021) conducted a cohort in Heart and liver transplant recipients (n=104). mRNA-1273 SARS-CoV-2 vaccine was evaluated on Humoral or cellular immune response (IgM/IgG antibodies and S-ELISpot positivity). Two doses of the mRNA-1273 vaccine elicited a humoral or cellular immune response in 90% of heart and liver transplant recipients, though hypogammaglobulinemia and recent transplant reduced response.
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