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Application of the diagnostic criteria for Common Variable Immunodeficiency in resource-limited settings
A. Álvarez-Álvarez, J; Gallon Duque, A; Vásquez-Echeverri, E; P. Sánchez, I; D. Gómez-Arias, R; C. Orrego Arango, J; L. Franco, J; M. Trujillo-Vargas, C.
Afiliação
  • A. Álvarez-Álvarez, J; Universidad de Antioquia UdeA. Facultad de Medicina. Grupo de Inmunodeficiencias Primarias. Medellín – Antioquia. Colombia
  • Gallon Duque, A; Universidad de Antioquia UdeA. Facultad de Medicina. Grupo de Inmunodeficiencias Primarias. Medellín – Antioquia. Colombia
  • Vásquez-Echeverri, E; Universidad de Antioquia UdeA. Facultad de Medicina. Grupo de Inmunodeficiencias Primarias. Medellín – Antioquia. Colombia
  • P. Sánchez, I; Universidad de Antioquia UdeA. Facultad de Medicina. Grupo de Inmunodeficiencias Primarias. Medellín – Antioquia. Colombia
  • D. Gómez-Arias, R; UdeA. Facultad Nacional de Salud Pública. Grupo de Epidemiología. Medellín – Antioquia. Colombia
  • C. Orrego Arango, J; Universidad de Antioquia UdeA. Facultad de Medicina. Grupo de Inmunodeficiencias Primarias. Medellín – Antioquia. Colombia
  • L. Franco, J; Universidad de Antioquia UdeA. Facultad de Medicina. Grupo de Inmunodeficiencias Primarias. Medellín – Antioquia. Colombia
  • M. Trujillo-Vargas, C; Universidad de Antioquia UdeA. Facultad de Medicina. Grupo de Inmunodeficiencias Primarias. Medellín – Antioquia. Colombia
Allergol. immunopatol ; 50(4): 129-136, jul. 2022. ilus, tab
Article em En | IBECS | ID: ibc-208903
Biblioteca responsável: ES1.1
Localização: ES15.1 - BNCS
ABSTRACT
Introduction: Common variable immunodeficiency (CVID) is the most prevalent symptom-atic humoral deficiency; however, its heterogeneous presentation makes the diagnosis diffi-cult. The present study is aimed to verify the CVID diagnostic criteria as established by the European Society for Immunodeficiencies in 42 CVID patients from our outpatient clinic. Methods: Information was collected from their medical records and when needed, lymphocyte subpopulations in peripheral blood (PB) were performed by flow cytometry. Results: All the patients fulfilled the clinical working definition for CVID and showed decreased serum IgG and IgA at diagnosis. Over two-thirds of the patients had decreased memory B cell percentages. However, the remaining patients exhibited other quantitative B cell defects in PB. Evaluation of vaccination responses was only found in 13 records and 69% were not respon-sive. None of the patients were subjected to vaccination studies to both, T-cell dependent and independent antigens. The two required tests to evaluate T cell responses were performed in 84.2% of the patients and reported normal. Without the support of third-party payers, only 34.2% of our patients would have completed the required evaluations. Conclusions: Further efforts are needed to speed up CVID diagnosis in low-resourced settings, increasing the availability of the required resources and optimizing the healthcare supply chain (AU)
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Texto completo: 1 Coleções: 06-national / ES Base de dados: IBECS Assunto principal: Imunodeficiência de Variável Comum Limite: Humans Idioma: En Revista: Allergol. immunopatol Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 06-national / ES Base de dados: IBECS Assunto principal: Imunodeficiência de Variável Comum Limite: Humans Idioma: En Revista: Allergol. immunopatol Ano de publicação: 2022 Tipo de documento: Article