Evaluation of selective IGA deficiency in patients with systemic lupus erythematosus
Keywords:
immunoglobulin A deficiency, juvenile systemic lupus erythematosus, immunodeficiency, rheumatologic diseaseAbstract
Introduction: immunoglobulin A is responsible for protecting the infections of the respiratory and gastrointestinal tracts, and selective immunoglobulin A deficiency is the most common primary humoral immunodeficiency. It is speculated that their occurrence may predispose to the development of systemic lupus erythematous.
Objectives: to study the prevalence of selective immunoglobulin A deficiency in patients with juvenile systemic lupus erythematosus and compared between groups of patients with and without selective immunoglobulin A deficiency, age and clinical manifestations at diagnosis of juvenile systemic lupus erythematosus and the index of disease activity at the time of analysis IgA levels, family history of rheumatic diseases, autoimmune and / or congenital immunodeficiency’s.
Patients and methods: we reviewed the medical records of 63 patients diagnosed with lupus according to the criteria of the American College of Rheumatology. Immunoglobulin A plasma levels of these patients were measured by nephelometry and were considered low when less than 70 mg/dL. Demographic data and clinical and laboratory profile, and family history were obtained by review of medical records.
Results: selective immunoglobulin A deficiency was detected in 3 of 63 patients (4.8 %). The clinical and laboratory profile of selective immunoglobulin A deficiency group was not significantly different from the group without selective immunoglobulin A deficiency and it was not observed higher incidence of infections in this group of patients.
Conclusion: we observed a higher prevalence of selective immunoglobulin A deficiency in patients with juvenile-onset systemic lupus erythematosus compared with the general population, with no significant differences between the clinical and laboratory profile of patients with and without selective immunoglobulin A deficiency.
Downloads
References
Binek A, Jarosz-Chobot P. Selective immunoglobulin A deficiency. Pediatr Endocrinol Diabetes Metab. 2012;18(2):76-8.
Wang N, Shen N, Vyse TJ, Anand V, Gunnarson I, Sturfelt G, et al. Selective IgA deficiency in autoimmune diseases. Mol Med. 2011;17(11-12):1383-96.
Cassidy JT, Kitson RK, Selby CL. Selective IgA deficiency in children and adults with systemic lupus erythematosus. Lupus. 2007;16(8):647-50.
Patiroglu T, Gungor HE, Unal E. Autoimmune diseases detected in children with primary immunodeficiency diseases: results from a reference centre at middle anatolia. Acta Microbiol Immunol Hung. 2012;59(3):343-53.
Phankingthongkum S, Visitsunthorn N, Vichyanond P. IgA deficiency: a report of three cases from Thailand. Asian Pac J Allergy Immunol. 2002;20(3):203-7.
Woof JM, Kerr MA. The function of immunoglobulin A in immunity. J Pathol 2006; 208:270-82.
Mantovani APF, Monclaro MP, Skare TL. Prevalência de deficiência de IgA em pacientes adultos com lúpus eritematoso sistêmico e estudo de sua associação com perfil clínico e de autoanticorpos Rev. Bras. Reumatol. 2010;50(3):273-82.
Tutuncu ZN, Kalunian KC. The definition and Classification of systemic lupus erythematosus. In: Wallace D, Hahn BH (eds.). Dubois' Lupus Erythematosus. Philadelphia: Ed. Lippincot , Willians & Wilkins; 2007. P. 16-20.
Uribe AG, Vilá LM, McGwin G Jr, Sanchez ML, Reveille JD, Alarcón GS. The Systemic Lupus Activity Measure-revised, the Mexican Systemic Lupus Erythematosus Disease Activity Index (SLEDAI), and a modified SLEDAI-2K are adequate instruments to measure disease activity in systemic lupus erythematosus. J Rheumatol. 2004;31(10):1934-40.
Jorgensen GH, Thorsteinsdottir I, Gudmundsson S, Hammarstrom L, Ludviksson BR. Familial aggregation of IgAD and autoimmunity. Clin Immunol. 2009;131:233-9.
Macpherson AJ, McCoy KD, Johansen FE, Brandtzaeg P. The immune geography of IgA induction and function. Mucosal Immunol. 2008;1(1):8-10.
West CD, Hong R. Holan NH. Immunoglobulin levels from the newborn period to adulthood and immunoglobulin deficiency states. J Clin Invest. 1962;41:2054-64.
Bachmman R, Laurekk CB, Svenonius E. Study’s ion the serum gamma 1
Published
How to Cite
Issue
Section
License
Warning of rights of author
The authors that publish in this journal agree with the following terms:
The authors conserve the rights of author and concede to the journal the right of the first publication, fulfilling with the license Creative Commons Attribution License that allows to others share the work with recognition of the authorship of their articles, and the initial publication in this journal.
The authors can establish separately additional agreements for the no exclusive distribution of the version of the work published in the journal (for example, situate it in an institutional repository, in a personal blog or publish it partial or totally in a book), with a recognition of their initial publication in this journal.
To be able to send the manuscript or part of him passed three months of published, for his evaluation to other publishers, identifying it or not with the same title; whenever allusion is made to our journale and know it the new publisher.
The publishing committee of the Cuban Journal of Rheumatology authorizes to other publishers, to reproduce the articles published in our magazine, whenever it indicate the origin of the same.
The authors should send a document in Office Word application format through the electronic address of the magazine with a similar format to that we include next:
---------------------------------------------------------------------------------------------------------------------
Statement of authorship and cede of articles for the publication of the scientific work in the Cuban Journal of Rheumatology
Date:
Those who subscribe certify that are the authors of the work:
Of this form communicate the originality of our article clearing that the concepts and knowledges of other authors that have included in the text of the article, have been quoted properly in the bibliography.
We do proof besides that the article in question is original and has not been published, total neither partially, in another journal.
To be approved for his publication in the Cuban Journal of Rheumatology, do secession of the rights of publication to the same one through the method that realizes it usually.
In front of any catchword that exist by the article that send to evaluate, relieve of of the responsibility to the Cuban Journal of Rheumatology holding us responsible with all the difficulties that can berelated by any situation.
We include to continuation the name and the signature of all authors and collaborators of this article.
Name: Signature: