Skin score decrease in systemic sclerosis patients treated with intravenous immunoglobulin--a preliminary report. 2000

Y Levy, and Y Sherer, and P Langevitz, and M Lorber, and P Rotman, and F Fabrizzi, and Y Shoenfeld
Department of Medicine B, Sheba Medical Center, Tel-Aviv University, Israel.

The aim of the study was to determine for the first time the response of systemic sclerosis (SSc) patients to treatment with intravenous immunoglobulin (IVIg). Three patients with progressive and rapidly deteriorating disease (mainly affecting the skin) were planned to receive six monthly courses of high-dose IVIg (2 g/kg). All had a thorough physical examination, clinical evaluation by the modified Rodnan total skin thickness score, and measurement of the titres of PM-Scl antibodies before and after the treatment, and before and after each treatment course. Two of the three patients received six IVIg courses as planned and no adverse effects or disease progression occurred during the therapy. The third patient received three courses, after which he developed renal failure and later died of sepsis. All three patients had a large decrease in their skin score after the treatment compared to that before the treatment. No modification of PM-Scl antibody titres was noted in any patient. Intravenous immunoglobulin (IVIg) may have a role in the treatment of SSc patients with rapidly deteriorating skin disease. The specific indications, as well as the safety of this treatment, should be further researched.

UI MeSH Term Description Entries
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults
D012595 Scleroderma, Systemic A chronic multi-system disorder of CONNECTIVE TISSUE. It is characterized by SCLEROSIS in the SKIN, the LUNGS, the HEART, the GASTROINTESTINAL TRACT, the KIDNEYS, and the MUSCULOSKELETAL SYSTEM. Other important features include diseased small BLOOD VESSELS and AUTOANTIBODIES. The disorder is named for its most prominent feature (hard skin), and classified into subsets by the extent of skin thickening: LIMITED SCLERODERMA and DIFFUSE SCLERODERMA. Sclerosis, Systemic,Systemic Scleroderma,Systemic Sclerosis
D012867 Skin The outer covering of the body that protects it from the environment. It is composed of the DERMIS and the EPIDERMIS.
D016756 Immunoglobulins, Intravenous Immunoglobulin preparations used in intravenous infusion, containing primarily IMMUNOGLOBULIN G. They are used to treat a variety of diseases associated with decreased or abnormal immunoglobulin levels including pediatric AIDS; primary HYPERGAMMAGLOBULINEMIA; SCID; CYTOMEGALOVIRUS infections in transplant recipients, LYMPHOCYTIC LEUKEMIA, CHRONIC; Kawasaki syndrome, infection in neonates, and IDIOPATHIC THROMBOCYTOPENIC PURPURA. Antibodies, Intravenous,Human Intravenous Immunoglobulin,IV Immunoglobulin,IVIG,Intravenous Antibodies,Intravenous Immunoglobulin,Intravenous Immunoglobulins,Alphaglobin,Endobulin,Flebogamma DIF,Gamimmune,Gamimmune N,Gamimune,Gamimune N,Gammagard,Gammonativ,Gamunex,Globulin-N,IV Immunoglobulins,Immune Globulin Intravenous (Human),Immune Globulin, Intravenous,Immunoglobulins, Intravenous, Human,Intraglobin,Intraglobin F,Intravenous IG,Intravenous Immunoglobulins, Human,Iveegam,Modified Immune Globulin (Anti-Echovirus Antibody),Privigen,Sandoglobulin,Venimmune,Venoglobulin,Venoglobulin-I,Globulin N,Human Intravenous Immunoglobulins,Immunoglobulin, Human Intravenous,Immunoglobulin, IV,Immunoglobulin, Intravenous,Immunoglobulins, Human Intravenous,Immunoglobulins, IV,Intravenous Immune Globulin,Intravenous Immunoglobulin, Human,Venoglobulin I
D016896 Treatment Outcome Evaluation undertaken to assess the results or consequences of management and procedures used in combating disease in order to determine the efficacy, effectiveness, safety, and practicability of these interventions in individual cases or series. Rehabilitation Outcome,Treatment Effectiveness,Clinical Effectiveness,Clinical Efficacy,Patient-Relevant Outcome,Treatment Efficacy,Effectiveness, Clinical,Effectiveness, Treatment,Efficacy, Clinical,Efficacy, Treatment,Outcome, Patient-Relevant,Outcome, Rehabilitation,Outcome, Treatment,Outcomes, Patient-Relevant,Patient Relevant Outcome,Patient-Relevant Outcomes

Related Publications

Y Levy, and Y Sherer, and P Langevitz, and M Lorber, and P Rotman, and F Fabrizzi, and Y Shoenfeld
May 2004, Clinical and experimental dermatology,
Y Levy, and Y Sherer, and P Langevitz, and M Lorber, and P Rotman, and F Fabrizzi, and Y Shoenfeld
December 2012, Arthritis and rheumatism,
Y Levy, and Y Sherer, and P Langevitz, and M Lorber, and P Rotman, and F Fabrizzi, and Y Shoenfeld
August 1951, Journal of the American Medical Association,
Y Levy, and Y Sherer, and P Langevitz, and M Lorber, and P Rotman, and F Fabrizzi, and Y Shoenfeld
January 2014, Scandinavian journal of rheumatology,
Y Levy, and Y Sherer, and P Langevitz, and M Lorber, and P Rotman, and F Fabrizzi, and Y Shoenfeld
July 1967, Vox sanguinis,
Y Levy, and Y Sherer, and P Langevitz, and M Lorber, and P Rotman, and F Fabrizzi, and Y Shoenfeld
February 2001, The Journal of rheumatology,
Y Levy, and Y Sherer, and P Langevitz, and M Lorber, and P Rotman, and F Fabrizzi, and Y Shoenfeld
January 2013, Clinical and experimental rheumatology,
Y Levy, and Y Sherer, and P Langevitz, and M Lorber, and P Rotman, and F Fabrizzi, and Y Shoenfeld
February 2019, Clinical immunology (Orlando, Fla.),
Y Levy, and Y Sherer, and P Langevitz, and M Lorber, and P Rotman, and F Fabrizzi, and Y Shoenfeld
March 2004, Arthritis and rheumatism,
Y Levy, and Y Sherer, and P Langevitz, and M Lorber, and P Rotman, and F Fabrizzi, and Y Shoenfeld
January 2015, Acta reumatologica portuguesa,
Copied contents to your clipboard!