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CD64: An Attractive Immunotherapeutic Target for M1-type Macrophage Mediated Chronic Inflammatory Diseases.

作者信息

Akinrinmade Olusiji A, Chetty Shivan, Daramola Adebukola K, Islam Mukit-Ul, Thepen Theo, Barth Stefan

机构信息

South African Research Chair in Cancer Biotechnology, Institute of Infectious Disease and Molecular Medicine (IDM), Department of Integrative Biomedical Sciences, Faculty of Health Sciences, University of Cape Town, 7925 Cape Town, South Africa.

Institute for Transfusion Medicine and Immunohematology and Blood Bank. University Hospital Magdeburg A.ö.R, 39120 Magdeburg, Germany.

出版信息

Biomedicines. 2017 Sep 12;5(3):56. doi: 10.3390/biomedicines5030056.


DOI:10.3390/biomedicines5030056
PMID:28895912
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5618314/
Abstract

To date, no curative therapy is available for the treatment of most chronic inflammatory diseases such as atopic dermatitis, rheumatoid arthritis, or autoimmune disorders. Current treatments require a lifetime supply for patients to alleviate clinical symptoms and are unable to stop the course of disease. In contrast, a new series of immunotherapeutic agents targeting the Fc γ receptor I (CD64) have emerged and demonstrated significant clinical potential to actually resolving chronic inflammation driven by M1-type dysregulated macrophages. This subpopulation plays a key role in the initiation and maintenance of a series of chronic diseases. The novel recombinant M1-specific immunotherapeutics offer the prospect of highly effective treatment strategies as they have been shown to selectively eliminate the disease-causing macrophage subpopulations. In this review, we provide a detailed summary of the data generated, together with the advantages and the clinical potential of CD64-based targeted therapies for the treatment of chronic inflammatory diseases.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b9d/5618314/cf35d5e4feda/biomedicines-05-00056-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b9d/5618314/4ef16fa5d4a5/biomedicines-05-00056-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b9d/5618314/5d2527b66a32/biomedicines-05-00056-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b9d/5618314/cf35d5e4feda/biomedicines-05-00056-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b9d/5618314/4ef16fa5d4a5/biomedicines-05-00056-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b9d/5618314/5d2527b66a32/biomedicines-05-00056-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b9d/5618314/cf35d5e4feda/biomedicines-05-00056-g003.jpg

相似文献

[1]
CD64: An Attractive Immunotherapeutic Target for M1-type Macrophage Mediated Chronic Inflammatory Diseases.

Biomedicines. 2017-9-12

[2]
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Toxins (Basel). 2012-9-14

[3]
Targeting CD64 mediates elimination of M1 but not M2 macrophages in vitro and in cutaneous inflammation in mice and patient biopsies.

MAbs. 2015

[4]
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MAbs. 2014

[5]
Recombinant, ETA'-based CD64 immunotoxins: improved efficacy by increased valency, both in vitro and in vivo in a chronic cutaneous inflammation model in human CD64 transgenic mice.

Br J Dermatol. 2010-4-26

[6]
Fully human MAP-fusion protein selectively targets and eliminates proliferating CD64(+) M1 macrophages.

Immunol Cell Biol. 2016-5

[7]
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Curr Pharm Des. 2009

[8]
CD64-directed microtubule associated protein tau kills leukemic blasts ex vivo.

Oncotarget. 2016-10-11

[9]
CD64-directed immunotoxin inhibits arthritis in a novel CD64 transgenic rat model.

J Immunol. 2006-5-15

[10]
Selective elimination of synovial inflammatory macrophages in rheumatoid arthritis by an Fcgamma receptor I-directed immunotoxin.

Arthritis Rheum. 2003-5

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本文引用的文献

[1]
Human MAP Tau Based Targeted Cytolytic Fusion Proteins.

Biomedicines. 2017-6-27

[2]
CD64-directed microtubule associated protein tau kills leukemic blasts ex vivo.

Oncotarget. 2016-10-11

[3]
Fully human MAP-fusion protein selectively targets and eliminates proliferating CD64(+) M1 macrophages.

Immunol Cell Biol. 2016-5

[4]
Structural mechanism of high affinity FcγRI recognition of immunoglobulin G.

Immunol Rev. 2015-11

[5]
Mouse and human FcR effector functions.

Immunol Rev. 2015-11

[6]
Novel angiogenin mutants with increased cytotoxicity enhance the depletion of pro-inflammatory macrophages and leukemia cells ex vivo.

Cancer Immunol Immunother. 2015-12

[7]
Targeting CD64 mediates elimination of M1 but not M2 macrophages in vitro and in cutaneous inflammation in mice and patient biopsies.

MAbs. 2015

[8]
Much More than M1 and M2 Macrophages, There are also CD169(+) and TCR(+) Macrophages.

Front Immunol. 2015-5-26

[9]
Structural basis for binding of human IgG1 to its high-affinity human receptor FcγRI.

Nat Commun. 2015-4-30

[10]
Angiogenin mutants as novel effector molecules for the generation of fusion proteins with increased cytotoxic potential.

J Immunother. 2015-4

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