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Repeat doses of antibody to serum amyloid P component clear amyloid deposits in patients with systemic amyloidosis
Open accessAbstract
Repeat cycles of miridesap, to deplete circulating serum amyloid P component (SAP), followed by the anti-SAP antibody, dezamizumab, cleared visceral amyloid deposits in patients with systemic amyloidosis.
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“Our data demonstrated that CPHPC (miridesap), developed by Pepys’ team at University College London90–92, efficiently reduces SAP concentration in serum (58.5% reduction) and bone marrow (95% reduction) in aged mice.”
From Serum amyloid P secreted by bone marrow adipocytes drives skeletal amyloidosis (2025) · cites this paper as [91]
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Citations
Cites
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Self-citationComplement Is Activated by IgG Hexamers Assembled at the Cell Surface
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Self-citationTargeted pharmacological depletion of serum amyloid P component for treatment of human amyloidosis
Pepys, M. B., Herbert, J., Hutchinson, W. L., Tennent, G. A., Lachmann, H. J., Gallimore, J. R., Lovat, L. B., Bartfai, T., Alanine, A., Hertel, C., et al. (2002) · Nature · doi:10.1038/417254a · Cited by 540
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Richards, D. B., Cookson, L., Berges, A., Barton, S. V., Lane, T., Ritter, J., Fontana, M., Moon, J., Pinzani, M., Gillmore, J., et al. (2015) · New England Journal of Medicine · doi:10.1056/nejmoa1504942 · Cited by 342
Self-citationQuantification of Myocardial Extracellular Volume Fraction in Systemic AL Amyloidosis
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Antibodies to human serum amyloid P component eliminate visceral amyloid deposits
Bodin, K., Ellmerich, S., Kahan, M., Tennent, G. A., Loesch, A., Gilbertson, J. A., Hutchinson, W. L., Mangione, P. P., Gallimore, J. R., Millar, D. J., et al. (2010) · Nature · doi:10.1038/nature09494 · Cited by 336
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“Human serum amyloid P component (SAP) from the plasma is present in all human amyloid deposits due to its avid but reversible bind ing to amyloid fibrils of all types (4).”
BackgroundSelf-citationMilde, R., Ritter, J. M., Tennent, G. A., Loesch, A., Martínez, F. O., Gordon, S., Pepys, M. B., Verschoor, A., & Helming, L. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.10.065 · Cited by 162
Self-citation
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Items 101–121 of 121
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Correia-Rodrigues, Â., Ribeiro-Rodrigues, T. M., Gonçalves, L., Almeida, J., Ferreira, M. J., & Girão, H. (2025) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2025.07.002 · Cited by 1
Nonspecific Interaction of Immunoglobulins (IgG) with Human Beta-2 Microglobulin Fibrils
Polyakov, D., Grudinina, N. A., Antimonova, O., Klysbaeva, L. I., Sakhabeev, R., & Shavlovsky, M. (2025) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093025010120 · Cited by 1
“The works have come out recently [15, 16], including those of the clinical profile, indicative of the prospect of immunological approach based on amyloid degradation under the action of specific antibodies to its components [17–20].”
Antibodies to Congo Red Dye as a Promising Tool for Detection and Destruction of Amyloid
Antimonova, O., Polyakov, D., Grudinina, N. A., Masterova, K. V., & Shavlovsky, M. (2024) · Cell and Tissue Biology · doi:10.1134/s1990519x24700639 · Cited by 1
“…approach has been described in the literature and involves administration of antibodies to serum amyloid P (SAP), which is known to be an obligatory component of all types of amyloid, regardless of the nosological entity (Richards et al., 2015, 2018), to patients suffering from amyloidosis.”
Ma, J.-H., Liu, Q., & White, J. R. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.101136 · Cited by 1
“(2021) 297(4) 101136 10 mM MES buffer, pH 6.”
BackgroundMethodInfluentialMystery in the mediastinum: Rare case of indolent primary thoracic amyloids
Munagala, R., Mishra, P., Lodh, A., Shukla, D., Bhatt, A. N., Taskar, V., & Keshavamurthy, J. (2021) · Lung India · doi:10.4103/lungindia.lungindia_916_20 · Cited by 1
“Some SAP is left in amyloid deposits, which serves as a target for Dezamizumab, an anti-SAP antibody that specifically allows for amyloid clearance.[9] Despite the advancements, no curative treatment for amyloidosis exists.”
BackgroundWITHDRAWN: [Treatment of AL amyloidosis].
Jaccard, A., & Bridoux, F. (2019) · Néphrologie & Thérapeutique · doi:10.1016/j.nephro.2019.03.002 · Cited by 1
Prognose und Therapie der AL-Amyloidose
Hansen, T. (2019) · InFo Hämatologie + Onkologie · doi:10.1007/s15004-019-6380-9 · Cited by 1
Ghosh, S., Khanra, D., Kala, C., Krishna, V., & Thakur, A. (2025) · Journal of Association of Physicians of India · doi:10.59556/japi.73.1050
Transthyretin amyloidosis. Fundamentals of pathogenesis, diagnosis, treatment, prognosis
Shavlovsky, M., Gudkova, A., Krutikov, A. N., & Antimonova, O. (2024) · Medical academic journal · doi:10.17816/maj625774
Karam, S., Kaushal, A., Amer, N. A., Royal, V., & Kitchlu, A. (2024) · Advances in kidney disease and health · doi:10.1053/j.akdh.2024.02.001
Advances in understanding, diagnosis and targeting ATTR cardiomyopathy: a review
Kulak, M., Lang, M., Waśniewski, M., & Lange, N. (2024) · European Journal of Translational and Clinical Medicine · doi:10.31373/ejtcm/189121
“A subsequent phase 2 clinical trial failed to show a positive effect on cardiac amyloid deposits with ATTR-CA, and further studies of Miridesap were aban - doned [99].”
BackgroundKappa chain amyloidosis: a deadly entity not to forget in patients with nondiabetic proteinuria
Abrantes, A., Luz, I., Santos, P. A., Barreto, P., Ferrer, F., & Lobos, A. (2022) · Gazzetta Medica Italiana Archivio per le Scienze Mediche · doi:10.23736/s0393-3660.20.04539-8
Losa, M., Schürch, P., Carta, M. C., Morales, I. C., Frontzek, K., Lysenko, V., Lakkaraju, A. K. K., Delic, M., Schwarz, P., Westermark, G., et al. (2021) · bioRxiv · doi:10.1101/2021.05.01.442282
Nanoparticles targeting amyloid deposits: a potential contrast agent for diagnosis and treatment
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“Only two drugs for amyloid removal are currently in clinical trials.(8,9) However, these drugs are based on immunotherapy, which is very expensive, and have not advanced yet to phase 3 clinical trials.”
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“patients with cardiac involvement [36].”
DUAL expectations in light chain amyloidosis
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“Despite a favorable phase Ia/Ib trial [8], a phase II study was terminated early due to changes in risks/benefits profile [9].”
BackgroundRech, J.-S., Brillet, P., Jeny, F., Kambouchner, M., Nunes, H., Arnulf, B., Valeyre, D., & Uzunhan, Y. (2019) · Pulmonary Manifestations of Systemic Diseases · doi:10.1183/2312508x.10021719
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“A recent phase Ib trial of SAP inhibitor, Miridesap followed by humanized monoclonal antibody Dezamizumab against SAP showed clearance of amyloid fibrils in liver and spleen, confirmed by I-SAP scintigraphy [19].”
Systemic light chain amyloidosis
Sinnakirouchenan, R. (2020) · Onco-Nephrology · doi:10.1016/b978-0-323-54945-5.00017-5
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Metadata
- Authors
- Richards, D. B., Cookson, L. M., Barton, S. V., Liefaard, L., Lane, T., Hutt, D. F., Ritter, J. M., Fontana, M., Moon, J. C., Gillmore, J. D., Wechalekar, A., Hawkins, P. N., & Pepys, M. B.
- Affiliations
- GlaxoSmithKline (United Kingdom) (GB)
- National Health Service (GB)
- Guy's Hospital (GB)
- St Bartholomew's Hospital (GB)
- Corresponding author
- Pepys, Mark B.
- ORCID
- Venue
- Science Translational Medicine
- Published
- 2018-01-03
- Volume
- 10
- Issue
- 422
- ISSN
- 1946-6234 (ISSN-L)
- 1946-6242
- OpenAlex
- W2782423765
- Cited by
- 136
- References
- 0
- Citations by year
- 2026: 4 · 2025: 12 · 2024: 18 · 2023: 8 · 2022: 21 · 2021: 20 · 2020: 20 · 2019: 20 · 2018: 13
- FWCI
- 6.49
- Type
- journal article
- Language
- en
- Open access
- green
- discovery.ucl.ac.uk
- Locations
- Science Translational Medicine (publishedVersion)
- PubMed (publishedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Funders
- GlaxoSmithKline (award308029, N/A)
- Topics
- Health Sciences › Medicine › Internal Medicine › Amyloidosis: Diagnosis, Treatment, Outcomes
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Prion Diseases and Protein Misfolding
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Keywords
- systemic amyloidosis, cardiac amyloidosis, serum amyloid P component, anti-amyloid antibodies, amyloid deposition, spleen, kidney, antibody therapy
- MeSH terms
- Serum Amyloid P-Component, Amyloidosis, Antibodies, Humans, Magnetic Resonance Imaging, Radionuclide Imaging, Plaque, Amyloid
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