Introducing a new method to detect bound C3d on erythrocytes during complement activation

Author(s):
A AfshariA Afshari, E HolmeE Holme,*
*Corresponding Author: Email: [email protected]

Journal of Inflammatory Diseases:Vol. 5, issue 1; 55-60
Published online:Jun 30, 2001
Article type:Research Article
How to Cite:Afshari A, Holme E. Introducing a new method to detect bound C3d on erythrocytes during complement activation. J Inflamm Dis. 2024;5(1):e154810. doi:

Abstract

Background: Measurement of complement activation products has recently been the popular means of assessing the complement activation. Objective: To introduce a new method to detect bound C3d on erythrocytes during complement activation and to compare it with free C3d levels. Methods: An indirect ELISA used in routine measurement of free C3d levels was developed together with the modified ELISA. To capture bound C3d on erythrocytes, ELISA plate were coated with anti-C3d and after incubation, blood samples were added for two hours. Bound erythrocytes were lysed with 100µl water perwell and the OD were read at 405nm. Findings: The levels of free C3d and bound C3d on the erythrocytes during complement activation was significantly increased compared to the control (800% and 500% respectively). Conclusion: Both free C3d and bound C3d as final dogradation product of C3d reflect the ongoing complement activation.

Copyright

© 2024, Journal of Inflammatory Diseases. This open-access article is available under the Creative Commons Attribution-NonCommercial 4.0 (CC BY-NC 4.0) International License (https://creativecommons.org/licenses/by-nc/4.0/), which allows for the copying and redistribution of the material only for noncommercial purposes, provided that the original work is properly cited.

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