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Serum and Urine Soluble HLA Class I Antigen Concentrations are Increased in Patients with Hemorrhagic Fever with Renal Syndrome

OBJECTIVES: In order to evaluate the association between the Hantaan virus-induced cellular-immune response and clinical severity in patients with hemorrhagic fever with renal syndrome (HFRS). METHODS: We serially measured the serum (n = 16) and urine (n =6) concentrations of soluble HLA class I ant...

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Detalles Bibliográficos
Autores principales: Park, Choel Whee, Yun, Sung No, Yang, Chul Woo, Kim, Tai Gyu, Han, Hoon, Choi, Euy Jin, Chang, Yoon Sik, Bang, Byung Kee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association of Internal Medicine 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4531974/
https://www.ncbi.nlm.nih.gov/pubmed/9159038
http://dx.doi.org/10.3904/kjim.1997.12.1.52
Descripción
Sumario:OBJECTIVES: In order to evaluate the association between the Hantaan virus-induced cellular-immune response and clinical severity in patients with hemorrhagic fever with renal syndrome (HFRS). METHODS: We serially measured the serum (n = 16) and urine (n =6) concentrations of soluble HLA class I antigen (sHLA-I) and clinical powameters in patients with HFRS. RESULTS: Serum sHLA-I concentrations in patients with HFRS were significantly higher than those in controls throughout all clinical phases (p<0.01). The highly elevated Serum sHLA-I concentrations peaked in the oliguric phase and declined gradually through the phases of HFRS. Serum sHLA-I concentrations in patients with hypotensive episode were higher than in those without the episode (5,585±2,184 vs. 2,389±860ng/ml in oliguric phase, 4.111±1,952 vs. 1,502+592 ng/ml in diuretic phase, p<0.05), and serum sHLA-I levels showed a significant correlation with blood WBC count (r=0.75 in the febrile and hypotensive phase, p<0.01 and serum creatinine concentrations (r=0.64 in the oliguric phase, p<0.01), respectively. Urine sHLA-I levels in the oliguric phase were significantly higher than those in the diuretic phase (390±155 vs. 214±45 ng/mg Cr, p<0.05) and urine sHLA- I levels are associated with severe illness in patients with HFRS. The higher serum sHLA-I are associated with severe illness in patients with HFRS. The persistent elevation of serum sHLA-I during all phases of HFRS might be related to increased production due to prolonged cellular immunologic stimulation by the Hantaan virus rather than decreased excretion of sHLA- I through the kidney. CONCLUSION: We suggest that the serum and urine sHLA- I concentrations can be used as a stable and objective parameter for monitoring clinical severity and renal dysfunction in patients with HFRS.