Complement in clinical medicine: Clinical trials, case reports and therapy monitoring
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https://hdl.handle.net/10037/12520Date
2017-05-31Type
Journal articleTidsskriftartikkel
Peer reviewed
Abstract
Research during past decades made it evident that complement is involved in more tasks than fighting infections,
but has important roles in other immune surveillance and housekeeping functions. If the balance between
complement activation and regulation is out of tune, however, complement can quickly turn against the host and
contribute to adverse processes that result in various clinical conditions. Whereas clinical awareness was initially
focused on complement deficiencies, excessive activation and insufficient regulation are frequently the dominant
factors in complement-related disorders. The individual complement profile of a patient often determines the
course and severity of the disease, and the pathophysiological involvement of complement may be highly
diverse. As a consequence, complement assays have evolved as essential tools not only in initial diagnosis but
also for following disease progression and for monitoring complement-targeted therapies, which become
increasingly available in routine clinical use. We herein review the current state of complement-directed drug
candidates in clinical evaluation and provide an overview of extended indications considered for the FDAapproved
inhibitor eculizumab. Furthermore we review the literature describing cases reports and case series
where eculizumab has been used “off-label”. Finally, we give a summary of the currently available tests to
measure complement profiles and discuss their suitability in diagnostics and treatment monitoring. With
complement finally entering the clinical arena, there are intriguing opportunities for treating complementmediated
diseases. However, this progress also requires a new awareness about complement pathophysiology,
adequate diagnostic tools and suitable treatment options among clinicians treating patients with such disorders.
Description
Accepted manuscript version, licensed CC BY-NC-ND 4.0. " Published version available in Molecular Immunology (2017), 89, 10-21.