{Reference Type}: Journal Article
{Title}: Effect of antimetabolite regimen on cellular and humoral immune response to SARS-COV-2 vaccination in solid organ transplant recipients.
{Author}: Capone M;Vanni A;Salvati L;Lamacchia G;Mazzoni A;Maggi L;Cosmi L;Liotta F;Romagnani P;Cirillo L;Buti E;Terlizzi V;Azzari C;Citera F;Barbati F;Rossolini GM;Bresci S;Borchi B;Cavallo A;Mencarini J;Francalanci E;Kiros ST;Bartoloni A;Annunziato F;
{Journal}: Immunol Lett
{Volume}: 268
{Issue}: 0
{Year}: 2024 Aug 19
{Factor}: 4.23
{DOI}: 10.1016/j.imlet.2024.106886
{Abstract}: <B>OBJECTIVE: </B>Novel mRNA-based vaccines have been proven to be powerful tools in combating the global pandemic caused by SARS-CoV-2 protecting individuals, especially the immunocompromised, from COVID-19. Still, it remains largely unknown how solid organ transplant and different immunosuppressive medications affect development of vaccine-induced immunity.<BR><B>METHODS: </B>In this work, we monitored humoral and cellular memory responses after mRNA SARS-CoV-2 two-doses and booster doses vaccination in cystic fibrosis lung transplanted patients (CFT) and compared them with both cystic fibrosis patients without lung transplant (CF) and with kidney transplant recipients (KT). In particular, we investigated the effects of immunosuppressive regimens on immune memory to SARS-CoV-2 after mRNA SARS-CoV-2 vaccine in transplanted patients.<BR><B>RESULTS: </B>Our results showed that immunocompromised transplanted patients displayed a weak cellular and humoral memory to SARS-CoV-2 mRNA vaccination. In addition, obtained data clearly demonstrate that immunosuppressive therapy regimen including antimetabolites, further reduces patients' ability to respond to vaccination at both humoral and cell-mediated level. Notably, patient treated with antimetabolites showed a lower humoral and cellular response also after a booster dose vaccination.<BR><B>CONCLUSIONS: </B>These results, even if obtained on a small patient's cohort, question whether immunocompromised patients need interventions to improve vaccine SARS-CoV-2 mRNA vaccine response such as additional jab or modulation of immunosuppressive therapy.