3.8 Article

Effects of Sirolimus Treatment on Fetal Hemoglobin Production and Response to SARS-CoV-2 Vaccination: A Case Report Study

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HEMATOLOGY REPORTS
卷 15, 期 3, 页码 432-439

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MDPI
DOI: 10.3390/hematolrep15030044

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beta-thalassemia; sirolimus; SARS-CoV-2; vaccine; immunity

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In this study, a representative clinical case showed that sirolimus monotherapy in fi-thalassemia patients induced an increase in fetal hemoglobin but did not prevent the production of anti-SARS-CoV-2 IgG. Further studies are needed to confirm the safety and potential positive effects of sirolimus on the humoral response to anti-SARS-CoV-2 vaccination in fi-thalassemia patients. This study may also be of interest to a broader population receiving sirolimus treatment for various pathologies.
The beta-thalassemias are a group of monogenic hereditary hematological disorders caused by deletions and/or mutations of the beta-globin gene, leading to low or absent production of adult hemoglobin (HbA). For fi-thalassemia, sirolimus has been under clinical consideration in two trials (NCT03877809 and NCT04247750). A reduced immune response to anti-SARS-CoV-2 vaccination has been reported in organ recipient patients treated with the immunosuppressant sirolimus. Therefore, there was some concern regarding the fact that monotherapy with sirolimus would reduce the antibody response after SARS-CoV-2 vaccination. In the representative clinical case reported in this study, sirolimus treatment induced the expected increase of fetal hemoglobin (HbF) but did not prevent the production of anti-SARS-CoV-2 IgG after vaccination with mRNA-1273 (Moderna). In our opinion, this case report should stimulate further studies on fi-thalassemia patients under sirolimus monotherapy in order to confirm the safety (or even the positive effects) of sirolimus with respect to the humoral response to anti-SARS-CoV-2 vaccination. In addition, considering the extensive use of sirolimus for the treatment of other human pathologies (for instance, in organ transplantation, systemic lupus erythematosus, autoimmune cytopenia, and lymphangioleiomyomatosis), this case report study might be of general interest, as large numbers of patients are currently under sirolimus treatment.

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