Results 31 to 40 of about 70,538 (300)

Serum thyroid hormone antibodies are frequent in patients with polyglandular autoimmune syndrome type 3, particularly in those who require thyroxine treatment [PDF]

open access: yes, 2017
Polyglandular autoimmune syndrome (PAS) type 3 consists of autoimmune thyroid disease (AITD) coexisting with ≥1 non-thyroidal autoimmune disease (NTAID) other than Addison’s disease and hypoparathyroidism. We evaluated the prevalence and repertoire of
Benvenga, Salvatore   +8 more
core   +1 more source

Subcutaneous immunoglobulin replacement therapy

open access: yesCurrent Opinion in Allergy & Clinical Immunology, 2013
Rapid subcutaneous immunoglobulin (SCIg) infusions have been used as an important method of delivering replacement immunoglobulin (Ig) to patients with primary immune deficiencies (PIDs) in Europe over the last 25 years. This review provides a comprehensive interpretation of the literature relating to the administration of SCIg and the services that ...
Chapel, H, Gardulf, A
openaire   +2 more sources

Acute reduction in secretory immunoglobulin A following smoking cessation [PDF]

open access: yes, 2004
Smokers report an increase in upper respiratory infections in the early phase of stopping smoking. One possible cause is a depletion in secretory immunoglobulin A (S-IgA) which has been observed in one study.
Clow, A   +6 more
core   +1 more source

Immunoglobulin Replacement Therapy for Primary Immunodeficiencies

open access: yesImmunotherapy, 2014
Exogenous antibody therapy to protect patients against infections and toxins is over 100 years old, yet progress continues to be made in the manufacture, administration and application of this type of immunotherapy, known as therapeutic human immunoglobulin. For the majority of patients with primary immunodeficiencies, immunoglobulin replacement is the
Peter, J, Chapel, H
openaire   +2 more sources

Intravenous immunoglobulins in immunodeficiencies: more than mere replacement therapy [PDF]

open access: yesClinical and Experimental Immunology, 2011
Summary Intravenous immunoglobulin (IVIG) is a therapeutic compound prepared from pools of plasma obtained from several thousand healthy blood donors. For more than 20 years, IVIG has been used in the treatment of a wide range of primary and secondary immunodeficiencies. IVIG now represents a standard therapeutic option for most antibody
S V, Kaveri   +4 more
openaire   +2 more sources

Mechanisms of action of Ig preparations: immunomodulatory and anti-inflammatory effects

open access: yesFrontiers in Immunology, 2015
Primary immunodeficiency (PIDs) disorders that predispose patients to recurrent infections require immunoglobulin (Ig) replacement therapy. Ig replacement therapy has been defined as beneficial, although the optimal IgG trough level to be maintained over
Andrea eMatucci   +2 more
doaj   +1 more source

Gene expression profiling in peripheral blood mononuclear cells of patients with common variable immunodeficiency: modulation of adaptive immune response following intravenous immunoglobulin therapy.

open access: yesPLoS ONE, 2014
BackgroundRegular intravenous immunoglobulin treatment is used to replace antibody deficiency in primary immunodeficiency diseases; however the therapeutic effect seems to be related not only to antibody replacement but also to an active role in the ...
Marzia Dolcino   +9 more
doaj   +1 more source

Pulmonary Manifestations of Primary Humoral Deficiencies

open access: yesCanadian Respiratory Journal, 2022
Primary immunodeficiencies are a group of conditions characterized by developmental or functional alterations in the immune system caused by hereditary genetic defects.
Ana Casal   +7 more
doaj   +1 more source

Immunodeficiency in DiGeorge Syndrome and Options for Treating Cases with Complete Athymia. [PDF]

open access: yes, 2013
The commonest association of thymic stromal deficiency resulting in T-cell immunodeficiency is the DiGeorge syndrome (DGS). This results from abnormal development of the third and fourth pharyngeal arches and is most commonly associated with a ...
Davies, EG
core   +2 more sources

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