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Antibody Response to a Fourth Dose of SARS-CoV-2 Vaccine in Solid Organ Transplant Recipients: An Update

Mitchell, Jonathan; Alejo, Jennifer L; Chiang, Teresa P Y; Kim, Jake; Chang, Amy; Abedon, Aura T; Avery, Robin K; Tobian, Aaron A R; Massie, Allan B; Levan, Macey L; Warren, Daniel S; Garonzik-Wang, Jacqueline M; Segev, Dorry L; Werbel, William A
PMID: 35426888
ISSN: 1534-6080
CID: 5204472

Heterologous Ad.26.COV2.S versus homologous BNT162b2/mRNA-1273 as a third dose in solid organ transplant recipients seronegative after two-dose mRNA vaccination

Chiang, Teresa Py; Alejo, Jennifer L; Mitchell, Jonathan; Kim, Jake D; Abedon, Aura T; Karaba, Andrew H; Thomas, Letitia; Levan, Macey L; Garonzik-Wang, Jacqueline M; Avery, Robin K; Pekosz, Andrew; Clarke, William A; Warren, Daniel S; Tobian, Aaron A R; Massie, Allan B; Segev, Dorry L; Werbel, William A
Heterologous vaccination ("mixing platforms") for the third (D3) dose of SARS-CoV-2 vaccine is a potential strategy to improve antibody responses in solid organ transplant recipients (SOTRs), but data are mixed regarding potential differential immunogenicity. We assessed for differences in immunogenicity and tolerability of homologous (BNT162b2 or mRNA-1273; D3-mRNA) versus heterologous (Ad.26.COV2.S; D3-JJ) D3 among 377 SARS-CoV-2-infection naïve SOTRs who remained seronegative after two mRNA vaccines. We measured anti-spike titers and used weighted Poisson regression to evaluate seroconversion and development of high-titers, comparing D3-JJ to D3-mRNA, at 1-, 3-, and 6 month post-D3. 1-month post-D3, seroconversion (63% vs. 52%, p = .3) and development of high-titers (29% vs. 25%, p = .7) were comparable between D3-JJ and D3-mRNA recipients. 3 month post-D3, D3-JJ recipients were 1.4-fold more likely to seroconvert (80% vs. 57%, weighted incidence-rate-ratio: wIRR = 1.10 1.401.77 , p = .006) but not more likely to develop high-titers (27% vs. 22%, wIRR = 0.44 0.921.93 , p = .8). 6 month post-D3, D3-JJ recipients were 1.41-fold more likely to seroconvert (88% vs. 59%, wIRR = 1.04 1.411.93 , p = .029) and 2.63-fold more likely to develop high-titers (59% vs. 21%, wIRR = 1.38 2.635.00 , p = .003). There was no differential signal in alloimmune events or reactogenicity between platforms. SOTRs without antibody response after two mRNA vaccines may derive benefit from heterologous Ad.26.COV2.S D3.
PMID: 35429211
ISSN: 1600-6143
CID: 5204552

Quantifying excess deaths among solid organ transplant recipients in the COVID-19 era

Massie, Allan B; Werbel, William A; Avery, Robin K; Po-Yu Chiang, Teresa; Snyder, Jon J; Segev, Dorry L
Estimating the total coronavirus disease 2019 (COVID-19) mortality burden of solid organ transplant recipients (SOTRs), both directly through COVID-19 infection and indirectly through other impacts on the healthcare system and society, is critical for understanding the disease's impact on the SOTR population. Using SRTR data, we modeled expected mortality risk per month pre-COVID (January 2015-February 2020) for kidney/liver/heart/lung SOTRs, and compared monthly COVID-era deaths (March 2020-March 2021) to expected rates, overall and among subgroups. Deaths above expected rates were designated "excess deaths." Between March 2020 and March 2021, there were 3739/827/265/252 excess deaths among kidney/liver/heart/lung SOTRs, respectively, representing a 41.2%/27.4%/18.5%/15.0% increase above expected deaths. 93.0% of excess deaths occurred in patients age≥50. The observed:expected ratio was highest among Hispanic SOTRs (1.82) and lowest among White SOTRs (1.20); 56.0% of excess deaths occurred among Black or Hispanic SOTRs. 64.7% of excess deaths occurred among patients who had survived ≥5 years post-transplant. Excess deaths peaked in January 2021; geographic distribution of excess deaths broadly mirrored COVID-19 incidence. COVID-19 likely caused over 5000 excess deaths among SOTRs in the US in a 13-month period, representing 1 in 75 SOTRs and a substantial proportion of all deaths among SOTRs during this time. SOTRs will remain at elevated mortality risk until the COVID-19 pandemic can be controlled.
PMID: 35294799
ISSN: 1600-6143
CID: 5200282

Effect of Mycophenolate Mofetil Dosing on Antibody Response to SARS-CoV-2 Vaccination in Heart and Lung Transplant Recipients

Mitchell, Jonathan; Chiang, Teresa P-Y; Alejo, Jennifer L; Chang, Amy; Abedon, Aura T; Avery, Robin K; Tobian, Aaron A R; Massie, Allan B; Levan, Macey L; Warren, Daniel S; Garonzik-Wang, Jacqueline M; Segev, Dorry L; Werbel, William A
PMID: 35250006
ISSN: 1534-6080
CID: 5185292

Improved Antibody Response After a Fifth Dose of a SARS-CoV-2 Vaccine in Solid Organ Transplant Recipients: A Case Series

Abedon, Aura T; Teles, Mayan S; Alejo, Jennifer L; Kim, Jake D; Mitchell, Jonathan; Chiang, Teresa P Y; Avery, Robin K; Tobian, Aaron A R; Levan, Macey L; Warren, Daniel S; Massie, Allan B; Garonzik-Wang, Jacqueline M; Segev, Dorry L; Werbel, William A
PMID: 35175241
ISSN: 1534-6080
CID: 5185272

Humoral and Cellular Immune Response to a Third Dose of SARS-CoV-2 Vaccine in Kidney Transplant Recipients Taking Belatacept

Mitchell, Jonathan; Kim, Jake; Alejo, Jennifer L; Chiang, Teresa P-Y; Karaba, Andrew H; Blankson, Joel N; Aytenfisu, Tihitina Y; Chang, Amy; Abedon, Aura T; Avery, Robin K; Tobian, Aaron A; Massie, Allan B; Levan, Macey L; Warren, Daniel S; Garonzik-Wang, Jacqueline M; Segev, Dorry L; Werbel, William A
PMID: 35289776
ISSN: 1534-6080
CID: 5185302

Don't Stop Thinking About Tomorrow: Ascertainment Bias in Pre-post Design Transplant Registry Studies [Editorial]

Motter, Jennifer D; Segev, Dorry L; Massie, Allan B
PMID: 35112490
ISSN: 1600-6143
CID: 5151902

Prevalence and Durability of SARS-CoV-2 Antibodies Among Unvaccinated US Adults by History of COVID-19

Alejo, Jennifer L; Mitchell, Jonathan; Chang, Amy; Chiang, Teresa P Y; Massie, Allan B; Segev, Dorry L; Makary, Martin A
PMID: 35113143
ISSN: 1538-3598
CID: 5151912

The effect of the cystic fibrosis care center on outcomes after lung transplantation for cystic fibrosis

Bush, Errol L; Krishnan, Aravind; Chidi, Alexis P; Nolley, Eric; Agbor-Enoh, Sean; West, Natalie E; Tallarico, Erin; Orens, Jonathan B; Ha, Jinny; Shah, Pali D; Ramos, Kathleen J; Segev, Dorry; Massie, Allan; Higgins, Robert Sd; Merlo, Christian A
BACKGROUND:The purpose of this study was to evaluate outcomes in people with cystic fibrosis (CF) who underwent lung transplant (LT) at a transplant center with an accredited Cystic Fibrosis Care Center (CFCC) in the United States. METHODS:We reviewed the Scientific Registry of Transplant Recipients for all adult patients with CF who received a first-time LT from 2005 to 2018. The primary outcome was graft failure. Unadjusted Kaplan-Meier analysis and adjusted multilevel Cox proportional hazards models were used to evaluate outcomes in CF patients undergoing lung transplantation at a CFCC. RESULTS:2,573 patients with CF underwent a first time LT during the study period. Of the 68 lung transplantation centers, 50 were CFCCs (73.5%). After adjustment for potential confounders, patients who underwent lung transplantation at a hospital with an accredited CFCC had a 33% reduction in risk of death or re-transplantation compared to those transplanted at a hospital without an accredited CFCC (HR: 0.67, 95% CI: 0.56-0.82, p < 0.001). CONCLUSIONS:People with CF who undergo LT at a transplant center with a CFCC have improved graft survival and decreased need for re-transplantation compared to those who undergo LT at a non-CFCC, independent of volume.
PMID: 34930671
ISSN: 1557-3117
CID: 5127822

Temporary hold of mycophenolate augments humoral response to SARS-CoV-2 vaccination in patients with rheumatic and musculoskeletal diseases: a case series [Letter]

Connolly, Caoilfhionn M; Chiang, Teresa Po-Yu; Boyarsky, Brian J; Ruddy, Jake A; Teles, Mayan; Alejo, Jennifer L; Massie, Allan; Werbel, William A; Shah, Ami A; Christopher-Stine, Lisa; Garonzik-Wang, Jacqueline; Segev, Dorry L; Paik, Julie J
PMID: 34556484
ISSN: 1468-2060
CID: 5127672