Research output: Contribution to journal › Review article › peer-review
Intravenouse immunoglobuline in dysautonomia. / Gavrilova, N.; Kamaeva, E.; Ignatova, M.; Ryabkova, V.; Lukashenko, M.; Soprun, L.; Churilov, L.P.; Shoenfeld, Y.
In: Clinical Immunology, Vol. 240, 109039, 07.2022.Research output: Contribution to journal › Review article › peer-review
}
TY - JOUR
T1 - Intravenouse immunoglobuline in dysautonomia
AU - Gavrilova, N.
AU - Kamaeva, E.
AU - Ignatova, M.
AU - Ryabkova, V.
AU - Lukashenko, M.
AU - Soprun, L.
AU - Churilov, L.P.
AU - Shoenfeld, Y.
N1 - Publisher Copyright: © 2022 Elsevier Inc.
PY - 2022/7
Y1 - 2022/7
N2 - Nowadays intravenous immunoglobulin (IVIg) treatment is considered to play a promising role in the autoimmune disease therapy. Despite its significant beneficial effects, the precise mechanism of action needs further studies, as well as recommended dosage in the treatment of autoimmune dysautonomia. In some diseases, like Guillain-Barre syndrome (GBS) and chronic inflammatory demyelinating neuropathy (CIDP), IVIg has a strong evidence that allows to recommend and prescribe the medication, while in other diseases only single case studies are available that requires further research. The review summarizes the currently available information on the effectiveness of IVIg in primary autoimmune neuropathies and neurological complications of systemic diseases, as well as side effects, features of clinical use with an emphasis on doses and treatment protocols in dysautonomia. Being safe and effective therapy, immunologic treatment is one of the most promising tools to achieve clinical remission of dysautonomia and good quality of life in autoimmune patients.
AB - Nowadays intravenous immunoglobulin (IVIg) treatment is considered to play a promising role in the autoimmune disease therapy. Despite its significant beneficial effects, the precise mechanism of action needs further studies, as well as recommended dosage in the treatment of autoimmune dysautonomia. In some diseases, like Guillain-Barre syndrome (GBS) and chronic inflammatory demyelinating neuropathy (CIDP), IVIg has a strong evidence that allows to recommend and prescribe the medication, while in other diseases only single case studies are available that requires further research. The review summarizes the currently available information on the effectiveness of IVIg in primary autoimmune neuropathies and neurological complications of systemic diseases, as well as side effects, features of clinical use with an emphasis on doses and treatment protocols in dysautonomia. Being safe and effective therapy, immunologic treatment is one of the most promising tools to achieve clinical remission of dysautonomia and good quality of life in autoimmune patients.
KW - Autoimmune autonomic gangliopathy (AAG)
KW - Neuropathy
KW - Chronic inflammatory demyelinating neuropathy (CIDP)
KW - Guillain-Barre syndrome (GBS)
KW - Small fiber neuropathy (SFN)
KW - Intravenous immunoglobulins
UR - https://www.mendeley.com/catalogue/92b482f3-d50d-3946-8d39-49390e1875ac/
UR - http://www.scopus.com/inward/record.url?scp=85131558429&partnerID=8YFLogxK
U2 - 10.1016/j.clim.2022.109039
DO - 10.1016/j.clim.2022.109039
M3 - Review article
C2 - 35569781
VL - 240
JO - Clinical Immunology
JF - Clinical Immunology
SN - 1521-6616
M1 - 109039
ER -
ID: 95104994