Desensitisation of the youngest patient with Pompe disease in response to
نویسندگان
چکیده
sometimes GI diseases are not controlled well with IVIG replacement, because these preparations contain IgG which cannot reach the lumen of the intact gut and also contain very little amount of IgA which is a vital component of mucosal defence. Recent experimental evidence suggests that IVIG could exert an effect more than passive substitution of antibodies could do against pathogenic microbes; it rectifies the defective signalling and induces an optimal functioning of cellular compartment, thus re-establishing immune homeostasis. Theoretically, treatment with oral immunoglobulin has not been successful, because IgG is rapidly destroyed before reaching the small intestine. There is an animal study, which showed an induction of oral tolerance by oral administration of IVIG against anti-phospholipid syndrome in naïve mice. The presented case is a unique one, since the patient experienced improvement of chronic diarrhoea following oral administration of IVIG. Our results point to a possible role of oral IVIG in the improvement of chronic diarrhoea in CVID patients, especially in those infested by organisms such as Giardia. However, further original multi-centre studies are needed to test the efficacy of oral administration of immunoglobulin in improvement of diarrhoea severity in those with CVID.
منابع مشابه
A New Mutation Causing Severe Infantile-Onset Pompe Disease Responsive to Enzyme Replacement Therapy
Pompe disease (PD), also known as “glycogen storage disease type II (OMIM # 232300)” is a rare autosomal recessive disorder characterized by progressive glycogen accumulation in cellular lysosomes. It ultimately leads to cellular damage. Infantile-onset Pompe disease (IOPD) is the most severe type of this disease and is characterized by severe hypertrophic cardiomyopathy and generalized hypoton...
متن کاملHeadache: A Presentation of Pompe Disease; A Case Report
Pompe disease, also termed glycogen storage disease type II or acid maltase deficiency, caused by deficient activity of acid alpha-glucosidase (GAA), the glycogen degrading lysosomal enzyme. As a result, massive lysosomal glycogen deposits in the numerous organs including the muscles. In Pompe disease weakness of truncal muscles is a prominent presentation which results in respiratory failure a...
متن کاملLate-onset Pompe Disease with Elevated Liver Transaminases: A Case Report
Pompe disease or type II glycogen storage disease is a rare autosomal hereditary disease. The prevalence of the disease is about 1 in 40,000 to 1 in 300,000 population. It usually occurs as a result of glycogen accretion following acid maltase deficiency. The current treatment is enzyme replacement therapy, which may slow down the disease progression. Sometimes, the clinical presentation can be...
متن کاملIgE-Mediated Hypersensitivity and Desensitisation with Recombinant Enzymes in Pompe Disease and Type I and Type VI Mucopolysaccharidosis.
Enzyme replacement therapy (ERT) is important for the treatment of lysosomal storage disorders. Hypersensitivity reactions with ERT have been reported, and in these cases, desensitisation with the enzyme is necessary. Here we report the cases of 3 patients with lysosomal storage disorders, including Pompe disease and mucopolysaccharidosis type I and VI, who had IgE-mediated hypersensitivity rea...
متن کاملDesensitisation of the youngest patient with Pompe disease in response to alglucosidase alfa
sometimes GI diseases are not controlled well with IVIG replacement, because these preparations contain IgG which cannot reach the lumen of the intact gut and also contain very little amount of IgA which is a vital component of mucosal defence. Recent experimental evidence suggests that IVIG could exert an effect more than passive substitution of antibodies could do against pathogenic microbes;...
متن کامل