Mechanisms Involved in Hypersensitivity Reactions to Polysulfone Hemodialysis Membranes

• Published in: Artificial organs 2017-11, Vol.41 (11), p.E285-E295
• Main Authors: Rodríguez‐Sanz, Aranzazu, Sánchez‐Villanueva, Rafael, Domínguez‐Ortega, Javier, Fiandor, Ana‐María, Ruiz, María‐Paz, Trocoli, Filomena, Díaz‐Tejeiro, Rafael, Cadenillas, Carlos, González, Elena, Martínez, Virginia, López‐Trascasa, Margarita, Quirce, Santiago, Selgas, Rafael, Bellón, Teresa
• Format: Article
• Language: English
• Subjects: Aged; Aged, 80 and over; Anaphylaxis; Anaphylaxis - blood; Anaphylaxis - chemically induced; Anaphylaxis - diagnosis; Anaphylaxis - immunology; Basophils - drug effects; Basophils - immunology; Basophils - metabolism; Biomarkers - blood; Case-Control Studies; Cell activation; Cellulose; Cellulose triacetate; Complement; Complement activation; Complement Activation - drug effects; Complement C3 - immunology; Complement C3 - metabolism; Complement C4 - immunology; Complement C4 - metabolism; Complement component C3; Complement component C4; Degranulation; Dialysis; Drug Hypersensitivity - blood; Drug Hypersensitivity - diagnosis; Drug Hypersensitivity - immunology; Equipment Design; Female; Hemodialysis; Humans; Hypersensitivity; Immunity, Cellular - drug effects; Immunity, Humoral - drug effects; Immunological tolerance; Leukocytes; Leukocytes (basophilic); Lymphocyte Activation - drug effects; Lymphocytes; Lymphocytes T; Male; Mast cells; Membranes; Membranes, Artificial; Middle Aged; Patients; Polymers - adverse effects; Polysulfone; Polysulfone membranes; Polysulfone resins; Priming; Renal Dialysis - adverse effects; Renal Dialysis - instrumentation; Risk Factors; Saline solutions; Sulfones - adverse effects; Sulfones - immunology; Systemic reactions; T-Lymphocytes - drug effects; T-Lymphocytes - immunology; T-Lymphocytes - metabolism; Tryptase; Tryptases - blood; Tryptases - immunology
• ISSN: 0160-564X; 1525-1594
• DOI: 10.1111/aor.12954

Several cases of patients with anaphylactic or systemic hypersensitivity reactions to polysulfone (PS) hemodialysis (HD) membranes and tolerance to cellulose triacetate (CTA) membranes have recently been reported. To investigate the mechanisms involved in PS hypersensitivity, basophil, T cell, and complement activation were analyzed in acute‐phase samples from two patients with systemic reactions to PS‐based membranes. Basophil and T cell activation, as well as higher serum tryptase levels were detected in acute‐phase samples compared with basal levels. Complement levels (C3 and C4) were decreased in acute‐phase samples from PS‐allergic patients to a higher extent than in samples from control donors taken at the same time points, indicating complement activation during the acute reactions. An experimental external circuit was established on pediatric membranes after rinsing with low or high priming volumes of saline solution, to analyze basophils, T cells, and complement activation in blood samples from 10 PS‐allergic and 8 nonallergic HD patients upon contact with PS‐based or CTA membranes. Predialysis and postdialysis samples were collected. Basophils from PS‐allergic patients exhibited increased degranulation, and T cells showed significantly increased activation after contact with PS‐based membranes primed with low volumes of saline. No activation was detected in leukocytes from nonallergic patients under the same experimental conditions. Membrane priming with high volumes of saline abrogated activation of basophils and T cells. However, basophils from allergic donors showed significantly higher responses to Fcεc stimulation after contact with PS membranes. Basophil degranulation and elevated serum tryptase levels in allergic patients during acute reactions support the systemic activation of mast cells and basophils during hypersensitivity reactions to PS‐based membranes. A leachable component of the membranes might be responsible for cell activation in some patients.