Early initiation of prophylactic immune tolerance induction and enzyme replacement therapy in prenatally diagnosed infantile onset Pompe disease with a CRIM-negative mutation

2017 ◽  
Vol 120 (1-2) ◽  
pp. S60
Author(s):  
Punita Gupta ◽  
Brian Shayota ◽  
Alejandra Gomez ◽  
Lorien Tambini-King ◽  
Zoheb Kazi ◽  
...  
2012 ◽  
Vol 14 (1) ◽  
pp. 135-142 ◽  
Author(s):  
Yoav H. Messinger ◽  
Nancy J. Mendelsohn ◽  
William Rhead ◽  
David Dimmock ◽  
Eli Hershkovitz ◽  
...  

2007 ◽  
Vol 92 (4) ◽  
pp. 27
Author(s):  
Dwight D. Koeberl ◽  
Baodong Sun ◽  
Andrew Bird ◽  
Sarah P. Young ◽  
Y.-T. Chen ◽  
...  

2007 ◽  
Vol 81 (5) ◽  
pp. 1042-1049 ◽  
Author(s):  
Baodong Sun ◽  
Andrew Bird ◽  
Sarah P. Young ◽  
Priya S. Kishnani ◽  
Y.-T. Chen ◽  
...  

Author(s):  
Merve Emecen Sanli ◽  
Hacer Ilbilge Ertoy Karagol ◽  
Ayse Kilic ◽  
Ekin Aktasoglu ◽  
Asli Inci ◽  
...  

Abstract Objectives Enzyme replacement therapy (ERT) with alglucosidase alfa (rhGAA) has changed the fatal course of infantile Pompe disease, however, development of anti rhGAA antibodies and infusion-associated reactions (IAR) restrict the tolerability and effectiveness of the treatment. Case presentation We describe a successful concomitant immune tolerance induction (ITI) and desensitization protocols in a cross-reactive immunologic material (CRIM) negative 7-month-old male patient. At the age of 5 months and eighth dose of the ERT, the patient developed IAR and his rhGAA specific IgE was negative however, his rhGAA specific IgG titer was as high as 12,800. ITI therapy to suppress antibody formation and a desensitization protocol was devised to be given concomitantly. At the end of 5-week therapy, his fatigue and weakness improved profoundly and a control antidrug antibody level decreased at 800. At the time of the patient’s follow up, he was still on ERT with desensitization at the age of 15 months without any reactions. Conclusions This is the first report in the literature applying concomitant ITI and desensitization protocols in a CRIM negative infantile-onset Pompe disease patient successfully, hence the importance of the case.


2020 ◽  
Vol 30 (2) ◽  
pp. 275-277
Author(s):  
Drishti Tolani ◽  
Neha Bansal ◽  
Swati Sehgal

AbstractPompe disease is a type-II glycogen storage disease, and clinical manifestations include hypertrophic cardiomyopathy and generalised muscular hypotonia. Enzyme replacement therapy has proven to be effective in reversing the ventricular hypertrophy. The outcomes are variable depending on time to diagnosis and severity of the cardiac disease. We describe two contrasting cases of patients with infantile-onset Pompe disease. The first child was diagnosed late and had severe cardiac hypertrophy with respiratory decompensation and ventilator dependence and eventual death. The second case was diagnosed at birth with early initiation of therapy resulting in a good outcome. Our cases highlight the importance of early initiation of enzyme replacement therapy to improve clinical outcomes.


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