Literature DB >> 28814660

Sustained immune tolerance induction in enzyme replacement therapy-treated CRIM-negative patients with infantile Pompe disease.

Zoheb B Kazi1, Ankit K Desai1, Kathryn L Berrier1, R Bradley Troxler2, Raymond Y Wang3, Omar A Abdul-Rahman4, Pranoot Tanpaiboon5, Nancy J Mendelsohn6, Eli Herskovitz7, David Kronn8, Michal Inbar-Feigenberg9, Catherine Ward-Melver10, Michelle Polan10, Punita Gupta11, Amy S Rosenberg12, Priya S Kishnani1.   

Abstract

BACKGROUND: Cross-reactive immunological material-negative (CRIM-negative) infantile Pompe disease (IPD) patients develop an immune response against enzyme replacement therapy (ERT) with alglucosidase alfa that nullifies ERT efficacy. Prophylactic immune tolerance induction (ITI) with rituximab, methotrexate, and IVIG successfully prevents development of deleterious rhGAA IgG antibodies; however, safety, likelihood of success, and long-term efficacy of ITI in a larger cohort remain unknown.
METHODS: Clinical data were analyzed for 19 CRIM-negative IPD patients who received ITI with rituximab, methotrexate, and IVIG in the ERT-naive setting (ERT+ITI) and compared to a historical cohort of 10 CRIM-negative IPD patients on ERT monotherapy.
RESULTS: ITI was safely tolerated, although infections were reported in 4 patients. Fourteen (74%) ERT+ITI patients were alive, with a median age of 44.2 months at their final assessment. The eldest survivor was 103.9 months old, with 100.2 months of follow-up after initiation of ERT+ITI. Death (n = 5) occurred at a median age of 29.2 months and was unrelated to the administration of ITI. Fifteen patients either did not seroconvert (n = 8) or maintained low titers (n = 7; defined as titers of ≤6,400 throughout the course of ERT) following ERT+ITI. Only one patient developed high and sustained antibody titers (defined as titers of ≥51,200 at or beyond 6 months on ERT). Left ventricular mass index (LVMI) decreased from a median of 248.5 g/m2 at baseline to 76.8 g/m2 at a median time from ERT+ITI initiation to 59 weeks. ERT+ITI significantly improved overall survival (P = 0.001), eliminated/reduced antibodies at values of ≤6,400 at week 52 on ERT (P = 0.0004), and improved LVMI at week 52 on ERT (P = 0.02) when compared with ERT monotherapy.
CONCLUSION: Evidence from this international cohort of CRIM-negative IPD patients further supports the safety, feasibility, and efficacy of ITI in the prevention of immune responses to ERT. TRIAL REGISTRATION: Clinicaltrials.gov NCT01665326. FUNDING: This research was supported in part by the Lysosomal Disease Network, a part of NIH Rare Diseases Clinical Research Network, and by a grant from Genzyme, a Sanofi company.

Entities:  

Keywords:  Genetics; Immunology

Year:  2017        PMID: 28814660      PMCID: PMC5621909          DOI: 10.1172/jci.insight.94328

Source DB:  PubMed          Journal:  JCI Insight        ISSN: 2379-3708


  37 in total

1.  A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease.

Authors:  Priya S Kishnani; Wuh-Liang Hwu; Hanna Mandel; Marc Nicolino; Florence Yong; Deyanira Corzo
Journal:  J Pediatr       Date:  2006-05       Impact factor: 4.406

2.  BAFF blockade prevents anti-drug antibody formation in a mouse model of Pompe disease.

Authors:  Phillip A Doerfler; Sushrusha Nayak; Roland W Herzog; Laurence Morel; Barry J Byrne
Journal:  Clin Immunol       Date:  2015-04-01       Impact factor: 3.969

Review 3.  Intravenous immunoglobulin therapy: how does IgG modulate the immune system?

Authors:  Inessa Schwab; Falk Nimmerjahn
Journal:  Nat Rev Immunol       Date:  2013-02-15       Impact factor: 53.106

4.  Durable and sustained immune tolerance to ERT in Pompe disease with entrenched immune responses.

Authors:  Zoheb B Kazi; Sean N Prater; Joyce A Kobori; David Viskochil; Carrie Bailey; Renuka Gera; David W Stockton; Paul McIntosh; Amy S Rosenberg; Priya S Kishnani
Journal:  JCI Insight       Date:  2016-07-21

5.  Immunogenicity of granulocyte-macrophage colony-stimulating factor (GM-CSF) products in patients undergoing combination therapy with GM-CSF.

Authors:  M Wadhwa; A L Skog; C Bird; P Ragnhammar; M Lilljefors; R Gaines-Das; H Mellstedt; R Thorpe
Journal:  Clin Cancer Res       Date:  1999-06       Impact factor: 12.531

6.  Influence of immunogenicity on the long-term efficacy of infliximab in Crohn's disease.

Authors:  Filip Baert; Maja Noman; Severine Vermeire; Gert Van Assche; Geert D' Haens; An Carbonez; Paul Rutgeerts
Journal:  N Engl J Med       Date:  2003-02-13       Impact factor: 91.245

7.  Predicting cross-reactive immunological material (CRIM) status in Pompe disease using GAA mutations: lessons learned from 10 years of clinical laboratory testing experience.

Authors:  Deeksha S Bali; Jennifer L Goldstein; Suhrad Banugaria; Jian Dai; Joanne Mackey; Catherine Rehder; Priya S Kishnani
Journal:  Am J Med Genet C Semin Med Genet       Date:  2012-01-17       Impact factor: 3.908

8.  B-Cell depletion and immunomodulation before initiation of enzyme replacement therapy blocks the immune response to acid alpha-glucosidase in infantile-onset Pompe disease.

Authors:  Melissa E Elder; Sushrusha Nayak; Shelley W Collins; Lee Ann Lawson; Jeffry S Kelley; Roland W Herzog; Renee F Modica; Judy Lew; Robert M Lawrence; Barry J Byrne
Journal:  J Pediatr       Date:  2013-04-16       Impact factor: 4.406

9.  The impact of antibodies on clinical outcomes in diseases treated with therapeutic protein: lessons learned from infantile Pompe disease.

Authors:  Suhrad G Banugaria; Sean N Prater; Yiu-Ki Ng; Joyce A Kobori; Richard S Finkel; Roger L Ladda; Yuan-Tsong Chen; Amy S Rosenberg; Priya S Kishnani
Journal:  Genet Med       Date:  2011-08       Impact factor: 8.822

10.  CRIM-negative infantile Pompe disease: characterization of immune responses in patients treated with ERT monotherapy.

Authors:  Kathryn L Berrier; Zoheb B Kazi; Sean N Prater; Deeksha S Bali; Jennifer Goldstein; Mihaela C Stefanescu; Catherine W Rehder; Eleanor G Botha; Carolyn Ellaway; Kaustuv Bhattacharya; Anna Tylki-Szymanska; Nesrin Karabul; Amy S Rosenberg; Priya S Kishnani
Journal:  Genet Med       Date:  2015-03-05       Impact factor: 8.822

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  21 in total

Review 1.  Challenges in treating Pompe disease: an industry perspective.

Authors:  Hung V Do; Richie Khanna; Russell Gotschall
Journal:  Ann Transl Med       Date:  2019-07

Review 2.  Immunological challenges and approaches to immunomodulation in Pompe disease: a literature review.

Authors:  Ankit K Desai; Cindy Li; Amy S Rosenberg; Priya S Kishnani
Journal:  Ann Transl Med       Date:  2019-07

Review 3.  Effects of Enzyme Replacement Therapy and Antidrug Antibodies in Patients with Fabry Disease.

Authors:  Malte Lenders; Eva Brand
Journal:  J Am Soc Nephrol       Date:  2018-08-09       Impact factor: 10.121

4.  HLA- and genotype-based risk assessment model to identify infantile onset pompe disease patients at high-risk of developing significant anti-drug antibodies (ADA).

Authors:  A S De Groot; Z B Kazi; R F Martin; F E Terry; A K Desai; W D Martin; P S Kishnani
Journal:  Clin Immunol       Date:  2019-01-31       Impact factor: 3.969

Review 5.  Emptying the stores: lysosomal diseases and therapeutic strategies.

Authors:  Frances M Platt
Journal:  Nat Rev Drug Discov       Date:  2017-11-17       Impact factor: 84.694

Review 6.  Long-term outcome and unmet needs in infantile-onset Pompe disease.

Authors:  Andreas Hahn; Anne Schänzer
Journal:  Ann Transl Med       Date:  2019-07

7.  Systemic Delivery of AAVB1-GAA Clears Glycogen and Prolongs Survival in a Mouse Model of Pompe Disease.

Authors:  Allison M Keeler; Marina Zieger; Sophia H Todeasa; Angela L McCall; Jennifer C Gifford; Samantha Birsak; Sourav R Choudhury; Barry J Byrne; Miguel Sena-Esteves; Mai K ElMallah
Journal:  Hum Gene Ther       Date:  2018-07-25       Impact factor: 5.695

8.  Pulmonary outcome measures in long-term survivors of infantile Pompe disease on enzyme replacement therapy: A case series.

Authors:  Mai K ElMallah; Ankit K Desai; Erica B Nading; Stephanie DeArmey; Richard M Kravitz; Priya S Kishnani
Journal:  Pediatr Pulmonol       Date:  2020-01-03

9.  B cell-activating factor modulates the factor VIII immune response in hemophilia A.

Authors:  Bhavya S Doshi; Jyoti Rana; Giancarlo Castaman; Mostafa A Shaheen; Radoslaw Kaczmarek; John Ss Butterfield; Shannon L Meeks; Cindy Leissinger; Moanaro Biswas; Valder R Arruda
Journal:  J Clin Invest       Date:  2021-04-15       Impact factor: 14.808

10.  Immune Tolerance-Adjusted Personalized Immunogenicity Prediction for Pompe Disease.

Authors:  Anne S De Groot; Ankit K Desai; Sandra Lelias; S M Shahjahan Miah; Frances E Terry; Sundos Khan; Cindy Li; John S Yi; Matt Ardito; William D Martin; Priya S Kishnani
Journal:  Front Immunol       Date:  2021-06-16       Impact factor: 7.561

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