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Published in: Journal of Neurology 11/2006

01-11-2006 | LETTER TO THE EDITORS

Subcutaneous self-infusions of immunoglobulins as a potential therapeutic regimen in immune-mediated neuropathies

Authors: Hubertus Köller, Michael Schroeter, Heinrich Feischen, Hans-Peter Hartung, Bernd C. Kieseier

Published in: Journal of Neurology | Issue 11/2006

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Excerpt

Sirs: Intravenous immunoglobulins (IVIg) represent one of the mainstays in the treatment of chronic immune mediated neuropathies [14]. Although numerous studies demonstrated clinical efficacy of IVIg over the short-term, the appropriate dose and route of administration for long-term maintenance therapy are not fully established [5]. Based on a small number of unblinded clinical trials and case reports clinical improvement is maintained with periodic application of IVIg. In clinical practice a regime of 0.4 g/kg BW every 4 weeks is usually chosen, which most of the patients receive by health care providers. Rapid subcutaneous infusions of immunoglobulins (SCIg), currently labelled and used for patients with primary immune deficiencies (PIDD), result in high and consistent serum IgG levels, are safe with very few systemic adverse reactions, whereas local tissue reactions are common, but usually mild and transitional. SCIg are comparable in the composition of their antibody spectrum to IVIg. The subcutaneous application can be easily learned by patients [6, 7]. In a recent study a preference for the subcutaneous route and for home therapy could be established in chronically treated patients with PIDD, when comparing IVIg with SCIg [8]. …
Literature
1.
go back to reference Kieseier BC, Kiefer R, Gold R, Hemmer B, Willison HJ, Hartung HP (2004) Advances in understanding and treatment of immune-mediated disorders of the peripheral nervous system. Muscle Nerve 30:131–156CrossRefPubMed Kieseier BC, Kiefer R, Gold R, Hemmer B, Willison HJ, Hartung HP (2004) Advances in understanding and treatment of immune-mediated disorders of the peripheral nervous system. Muscle Nerve 30:131–156CrossRefPubMed
2.
go back to reference Köller H, Kieseier BC, Jander S, Hartung HP (2005) Chronic inflammatory demyelinating polyneuropathy. N Engl J Med 352:1343–1356CrossRefPubMed Köller H, Kieseier BC, Jander S, Hartung HP (2005) Chronic inflammatory demyelinating polyneuropathy. N Engl J Med 352:1343–1356CrossRefPubMed
3.
go back to reference Stangel M, Hartung HP, Marx P, Gold R (1998) Intravenous immunoglobulin treatment of neurological autoimmune diseases. J Neurol Sci 153:203–214CrossRefPubMed Stangel M, Hartung HP, Marx P, Gold R (1998) Intravenous immunoglobulin treatment of neurological autoimmune diseases. J Neurol Sci 153:203–214CrossRefPubMed
4.
go back to reference Toyka KV, Gold R (2003) The pathogenesis of CIDP: rationale for treatment with immunomodulatory agents. Neurology 60:S2–7CrossRefPubMed Toyka KV, Gold R (2003) The pathogenesis of CIDP: rationale for treatment with immunomodulatory agents. Neurology 60:S2–7CrossRefPubMed
5.
go back to reference Dalakas MC (2004) Intravenous immunoglobulin in autoimmune neuromuscular diseases. JAMA 291:2367–2375CrossRefPubMed Dalakas MC (2004) Intravenous immunoglobulin in autoimmune neuromuscular diseases. JAMA 291:2367–2375CrossRefPubMed
6.
go back to reference Chapel HM, Spickett GP, Ericson D, Engl W, Eibl MM, Bjorkander J (2000) The comparison of the efficacy and safety of intravenous versus subcutaneous immunoglobulin replacement therapy. J Clin Immunol 20:94–100CrossRefPubMed Chapel HM, Spickett GP, Ericson D, Engl W, Eibl MM, Bjorkander J (2000) The comparison of the efficacy and safety of intravenous versus subcutaneous immunoglobulin replacement therapy. J Clin Immunol 20:94–100CrossRefPubMed
7.
go back to reference Gardulf A, Hammarstrom L, Smith CI (1991) Home treatment of hypogammaglobulinaemia with subcutaneous gammaglobulin by rapid infusion. Lancet 338:162–166CrossRefPubMed Gardulf A, Hammarstrom L, Smith CI (1991) Home treatment of hypogammaglobulinaemia with subcutaneous gammaglobulin by rapid infusion. Lancet 338:162–166CrossRefPubMed
8.
go back to reference Nicolay U, Kiessling P, Berger M, Gupta S, Yel L, Roifman CM, Gardulf A, Eichmann F, Haag S, Massion C, Ochs HD (2006) Health-related quality of life and treatment satisfaction in north american patients with primary immunedeficiency diseases receiving subcutaneous IgG self-infusions at home. J Clin Immunol 26:65–72CrossRefPubMed Nicolay U, Kiessling P, Berger M, Gupta S, Yel L, Roifman CM, Gardulf A, Eichmann F, Haag S, Massion C, Ochs HD (2006) Health-related quality of life and treatment satisfaction in north american patients with primary immunedeficiency diseases receiving subcutaneous IgG self-infusions at home. J Clin Immunol 26:65–72CrossRefPubMed
9.
go back to reference Ad Hoc Subcommittee of the American Academy of Neurology AIDS Task Force (1991) Research criteria for diagnosis of chronic inflammatory demyelinating polyneuropathy (CIDP). Neurology 41:617–618 Ad Hoc Subcommittee of the American Academy of Neurology AIDS Task Force (1991) Research criteria for diagnosis of chronic inflammatory demyelinating polyneuropathy (CIDP). Neurology 41:617–618
10.
go back to reference Merkies IS, Schmitz PI, van der Meche FG, Samijn JP, van Doorn PA (2002) Clinimetric evaluation of a new overall disability scale in immune mediated polyneuropathies. J Neurol Neurosurg Psychiatry 72:596–601CrossRefPubMed Merkies IS, Schmitz PI, van der Meche FG, Samijn JP, van Doorn PA (2002) Clinimetric evaluation of a new overall disability scale in immune mediated polyneuropathies. J Neurol Neurosurg Psychiatry 72:596–601CrossRefPubMed
Metadata
Title
Subcutaneous self-infusions of immunoglobulins as a potential therapeutic regimen in immune-mediated neuropathies
Authors
Hubertus Köller
Michael Schroeter
Heinrich Feischen
Hans-Peter Hartung
Bernd C. Kieseier
Publication date
01-11-2006
Publisher
Steinkopff-Verlag
Published in
Journal of Neurology / Issue 11/2006
Print ISSN: 0340-5354
Electronic ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-006-0258-0

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