Outcome of autoimmune cytopenia after hematopoietic cell transplantation in primary immunodeficiency - 05/08/20
, Sabeena Selvarajah, FRACP a, Angela Deya-Martinez, PhD a, Peter McNaughton, FRACP a, Ali Sobh, PhD a, Sheila Waugh, PhD c, Shirelle Burton-Fanning, PhD b, Lisa Newton, BSc c, Julie Gandy, BSc c, Zohreh Nademi, PhD a, d, Stephen Owens, PhD a, Eleri Williams, MD a, Marieke Emonts, PhD a, d, Terry Flood, MD a, Andrew Cant, MD a, d, Mario Abinun, MD a, c, Sophie Hambleton, PhD a, d, Andrew R. Gennery, MD a, d, Mary Slatter, MD a, dAbstract |
Background |
Post hematopoietic cell transplantation (HCT) autoimmune cytopenia (AIC) is a potentially life-threatening complication, but studies focusing on large cohorts of patients transplanted for primary immunodeficiency are lacking.
Objectives |
This study sought to determine the incidence, risk factors, and outcomes of post-HCT AIC and B-lymphocyte function following rituximab.
Methods |
We retrospectively studied 502 children with primary immunodeficiency who were transplanted at our center between 1987 and 2018.
Results |
Thirty-six patients (9%) developed post-HCT AIC, with a median onset of 6.5 months post-HCT. On univariate analysis, pre-HCT AIC, mismatched donor, alemtuzumab, anti-thymocyte antiglobulin, and acute and chronic graft versus host disease were significantly associated with post-HCT AIC. After multivariate analysis, alemtuzumab (subdistribution hazard ratio, 9.0; 95% CI, 1.50-54.0; P = .02) was independently associated with post-HCT AIC. Corticosteroid and high-dose intravenous immunoglobulin achieved remission in 50% (n = 18), additional rituximab led to remission in 25% (n = 9), and the remaining 25% were treated with a combination of various modalities including sirolimus (n = 5), bortezomib (n = 3), mycophenolate mofetil (n = 2), splenectomy (n = 2), and second HCT (n = 3). The mortality of post-HCT AIC reduced from 25% (4 of 16) prior to 2011 to 5% (1 of 20) after 2011. The median follow-up of 5.8 years (range, 0.4 to 29.1 years) showed that 26 of 30 survivors (87%) were in complete remission, and 4 were in remission with ongoing sirolimus and low-dose steroids. Of the 17 who received rituximab, 7 had B-lymphocyte recovery, 5 had persistent low B-lymphocyte count and remained on intravenous immunoglobulin replacement, 2 had second HCT, and 3 died.
Conclusions |
The frequency of post HCT AIC in our cohort was 9%, and the most significant risk factors for its occurrence were the presence of graft versus host disease and the use of alemtuzumab.
Il testo completo di questo articolo è disponibile in PDF.Graphical abstract |
Key words : primary immunodeficiency, posttransplant autoimmune cytopenia, pediatrics
Abbreviations used : AIC, AIHA, AIN, ATG, GvHD, HCT, ITP, IVIg, PID, SCID, TRM
Mappa
| Disclosure of potential conflict of interest: The authors declare that they have no relevant conflicts of interest. |
Vol 146 - N° 2
P. 406-416 - Agosto 2020 Ritorno al numero
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