Cytokine production during hemodialysis

Effects of dialytic membrane and complement activation

Yuh Feng Lin, Deh Ming Chang, Men Fang Shaio, Kuo Cheng Lu, Shoou Hwa Chyr, Bi Lian Li, Shang Der Sheih

Research output: Contribution to journalArticle

30 Citations (Scopus)

Abstract

Interleukin-1β (IL-1β) and tumor necrosis factor-a (TNF-α) are closely associated with acute and chronic inflammatory processes in hemodialytic patients. However, the mechanisms concerning cytokine production by monocytes during hemodialysis are still conflicting. With the use of the more specific monoclonal antibody ELISA method, contamination detection and crossover protocol of complement-activating and noncomplement-activating hollow fibers, we were able to confirm augmented IL-1β production by zymosan-stimulated monocytes with complement-activating hollow fiber as compared to noncomplement-activating hollow fiber before (1,411.9 ± 143.6 vs. 865.7 ± 149.9 pg/m1/2 x 106 monocytes, p <0.01), at the 15th minute (530.6 ± 89.1 vs. 247.3 ± 45.2 pg/ml/2 x 106 monocytes, p <0.01) and at the end of dialysis (1,201.8 ± 135.1 vs. 707.4 ± 109.3 pg/ml/2 x 106 monocytes, p <0.01). Similar results were observed with TNF-α production. IL-1β as well as TNF-α production decreased significantly at the 15th min of dialysis, thereafter they increased and approached the baseline levels towards the end of hemodialysis with both hollow fibers. Plasma C3a at the 15th minute correlated positively with postdialysis IL-1β and TNF-α production, while plasma C3a did not change in patients dialyzed with noncomplement-activating hollow fiber. Complement activation with complement-activating hollow fiber as well as monocyte-membrane interaction with complement-activating and noncomplement-activating hollow fiber might be involved in the pathogenesis of cytokine production during hemodialysis. Uremic toxin removal as well as stimulation of cytokine production inhibitor might contribute to the decreased cytokine production at the 15th minute of hemodialysis and monocyte-membrane interaction with or without complement activation resulted in augmented cytokine production toward the end of hemodialysis with both hollow fibers. We thus concluded that hollow fiber of bioincompatibility triggered much more cytokine production throughout the dialysis procedure.

Original languageEnglish
Pages (from-to)293-299
Number of pages7
JournalAmerican Journal of Nephrology
Volume16
Issue number4
Publication statusPublished - 1996
Externally publishedYes

Fingerprint

Complement Activation
Renal Dialysis
Monocytes
Cytokines
Membranes
Interleukin-1
Tumor Necrosis Factor-alpha
Dialysis
Zymosan
Enzyme-Linked Immunosorbent Assay
Monoclonal Antibodies

Keywords

  • Complement activation
  • Hemodialysis
  • Interleukin-1β
  • Tumor necrosis factor-α

ASJC Scopus subject areas

  • Nephrology

Cite this

Lin, Y. F., Chang, D. M., Shaio, M. F., Lu, K. C., Chyr, S. H., Li, B. L., & Sheih, S. D. (1996). Cytokine production during hemodialysis: Effects of dialytic membrane and complement activation. American Journal of Nephrology, 16(4), 293-299.

Cytokine production during hemodialysis : Effects of dialytic membrane and complement activation. / Lin, Yuh Feng; Chang, Deh Ming; Shaio, Men Fang; Lu, Kuo Cheng; Chyr, Shoou Hwa; Li, Bi Lian; Sheih, Shang Der.

In: American Journal of Nephrology, Vol. 16, No. 4, 1996, p. 293-299.

Research output: Contribution to journalArticle

Lin, YF, Chang, DM, Shaio, MF, Lu, KC, Chyr, SH, Li, BL & Sheih, SD 1996, 'Cytokine production during hemodialysis: Effects of dialytic membrane and complement activation', American Journal of Nephrology, vol. 16, no. 4, pp. 293-299.
Lin, Yuh Feng ; Chang, Deh Ming ; Shaio, Men Fang ; Lu, Kuo Cheng ; Chyr, Shoou Hwa ; Li, Bi Lian ; Sheih, Shang Der. / Cytokine production during hemodialysis : Effects of dialytic membrane and complement activation. In: American Journal of Nephrology. 1996 ; Vol. 16, No. 4. pp. 293-299.
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abstract = "Interleukin-1β (IL-1β) and tumor necrosis factor-a (TNF-α) are closely associated with acute and chronic inflammatory processes in hemodialytic patients. However, the mechanisms concerning cytokine production by monocytes during hemodialysis are still conflicting. With the use of the more specific monoclonal antibody ELISA method, contamination detection and crossover protocol of complement-activating and noncomplement-activating hollow fibers, we were able to confirm augmented IL-1β production by zymosan-stimulated monocytes with complement-activating hollow fiber as compared to noncomplement-activating hollow fiber before (1,411.9 ± 143.6 vs. 865.7 ± 149.9 pg/m1/2 x 106 monocytes, p <0.01), at the 15th minute (530.6 ± 89.1 vs. 247.3 ± 45.2 pg/ml/2 x 106 monocytes, p <0.01) and at the end of dialysis (1,201.8 ± 135.1 vs. 707.4 ± 109.3 pg/ml/2 x 106 monocytes, p <0.01). Similar results were observed with TNF-α production. IL-1β as well as TNF-α production decreased significantly at the 15th min of dialysis, thereafter they increased and approached the baseline levels towards the end of hemodialysis with both hollow fibers. Plasma C3a at the 15th minute correlated positively with postdialysis IL-1β and TNF-α production, while plasma C3a did not change in patients dialyzed with noncomplement-activating hollow fiber. Complement activation with complement-activating hollow fiber as well as monocyte-membrane interaction with complement-activating and noncomplement-activating hollow fiber might be involved in the pathogenesis of cytokine production during hemodialysis. Uremic toxin removal as well as stimulation of cytokine production inhibitor might contribute to the decreased cytokine production at the 15th minute of hemodialysis and monocyte-membrane interaction with or without complement activation resulted in augmented cytokine production toward the end of hemodialysis with both hollow fibers. We thus concluded that hollow fiber of bioincompatibility triggered much more cytokine production throughout the dialysis procedure.",
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