[HTML][HTML] Intravenous enzyme replacement therapy in mucopolysaccharidoses: clinical effectiveness and limitations

R Parini, F Deodato - International Journal of Molecular Sciences, 2020 - mdpi.com
R Parini, F Deodato
International Journal of Molecular Sciences, 2020mdpi.com
The aim of this review is to summarize the evidence on efficacy, effectiveness and safety of
intravenous enzyme replacement therapy (ERT) available for mucopolysaccharidoses
(MPSs) I, II, IVA, VI and VII, gained in phase III clinical trials and in observational post-
approval studies. Post-marketing data are sometimes conflicting or controversial, possibly
depending on disease severity, differently involved organs, age at starting treatment, and
development of anti-drug antibodies (ADAs). There is general agreement that ERT is …
The aim of this review is to summarize the evidence on efficacy, effectiveness and safety of intravenous enzyme replacement therapy (ERT) available for mucopolysaccharidoses (MPSs) I, II, IVA, VI and VII, gained in phase III clinical trials and in observational post-approval studies. Post-marketing data are sometimes conflicting or controversial, possibly depending on disease severity, differently involved organs, age at starting treatment, and development of anti-drug antibodies (ADAs). There is general agreement that ERT is effective in reducing urinary glycosaminoglycans and liver and spleen volume, while heart and joints outcomes are variable in different studies. Effectiveness on cardiac valves, trachea and bronchi, hearing and eyes is definitely poor, probably due to limited penetration in the specific tissues. ERT does not cross the blood–brain barrier, with the consequence that the central nervous system is not cured by intravenously injected ERT. All patients develop ADAs but their role in ERT tolerance and effectiveness has not been well defined yet. Lack of reliable biomarkers contributes to the uncertainties about effectiveness. The data obtained from affected siblings strongly indicates the need of neonatal screening for treatable MPSs. Currently, other treatments are under evaluation and will surely help improve the prognosis of MPS patients.
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