The Inhibitory Co-Receptor, PECAM-1 Provides a Protective Effect in Suppression of Collagen-Induced Arthritis (Q56797384)

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9 January 2020

title

The inhibitory co-receptor, PECAM-1 provides a protective effect in suppression of collagen-induced arthritis (English)

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9 January 2020

2

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9 January 2020

author name string

Mae-Xhum Wong

series ordinal

1

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9 January 2020

P Mark Hogarth

series ordinal

3

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9 January 2020

Denise E Jackson

series ordinal

4

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9 January 2020

publication date

1 January 2005

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Journal of Clinical Immunology

9 January 2020

published in

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9 January 2020

volume

25

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9 January 2020

issue

1

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9 January 2020

page(s)

19-28

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https://scigraph.springernature.com/pub.10.1007/s10875-005-0354-7

9 January 2020

exact match

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cites work

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Monoclonal antibody to murine PECAM-1 (CD31) blocks acute inflammation in vivo

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Platelet endothelial cell adhesion molecule-1 is a negative regulator of platelet-collagen interactions

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Deletion of fcgamma receptor IIB renders H-2(b) mice susceptible to collagen-induced arthritis

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Soluble domain 1 of platelet-endothelial cell adhesion molecule (PECAM) is sufficient to block transendothelial migration in vitro and in vivo

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PECAM-1 and leukosialin (CD43) expression correlate with heightened inflammation in rat adjuvant-induced arthritis

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Acceleration of the onset of collagen‐induced arthritis by a deficiency of platelet endothelial cell adhesion molecule 1

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A novel leukocyte differentiation antigen: two monoclonal antibodies TM2 and TM3 define a 120-kd molecule present on neutrophils, monocytes, platelets, and activated lymphoblasts

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Type II collagen-induced murine arthritis. I. Induction and perpetuation of arthritis require synergy between humoral and cell-mediated immunity

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Development of inflammation in proteoglycan-induced arthritis is dependent on Fc gamma R regulation of the cytokine/chemokine environment

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Antibodies against the first Ig-like domain of human platelet endothelial cell adhesion molecule-1 (PECAM-1) that inhibit PECAM-1-dependent homophilic adhesion block in vivo neutrophil recruitment

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Type II collagen-induced arthritis in mice. I. Major histocompatibility complex (I region) linkage and antibody correlates

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PECAM-1 is required for transendothelial migration of leukocytes

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Arthritis critically dependent on innate immune system players

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The unfolding tale of PECAM-1

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Physical proximity and functional interplay of PECAM-1 with the Fc receptor Fc gamma RIIa on the platelet plasma membrane

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Induction and suppression of collagen-induced arthritis is dependent on distinct fcgamma receptors

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Antibodies to PECAM-1 and glucocorticoids reduce leukocyte adhesion in adjuvant arthritis of the rat knee synovium in vivo

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Immunisation against heterologous type II collagen induces arthritis in mice

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Antibodies to type II collagen in early rheumatoid arthritis. Correlation with disease progression

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Expression of FcgammaRIII is required for development of collagen-induced arthritis.

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Transgenic mice expressing different levels of soluble platelet/endothelial cell adhesion molecule-IgG display distinct inflammatory phenotypes

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Platelet endothelial cell adhesion molecule-1 (PECAM-1/CD31) acts as a regulator of B-cell development, B-cell antigen receptor (BCR)-mediated activation, and autoimmune disease

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Platelet endothelial cell adhesion molecule-1 serves as an inhibitory receptor that modulates platelet responses to collagen

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Altered vascular permeability and early onset of experimental autoimmune encephalomyelitis in PECAM-1-deficient mice

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Genetic evidence for functional redundancy of Platelet/Endothelial cell adhesion molecule-1 (PECAM-1): CD31-deficient mice reveal PECAM-1-dependent and PECAM-1-independent functions.

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Use of anti-platelet-endothelial cell adhesion molecule-1 antibody in the control of disease progression in established collagen-induced arthritis in DBA/1J mice

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Increased synovial expression of the adhesion molecules CD66a, CD66b, and CD31 in rheumatoid and osteoarthritis

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Type II collagen-induced arthritis in mice. IV. Variations in immunogenetic regulation provide evidence for multiple arthritogenic epitopes on the collagen molecule

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10.1007/S10875-005-0354-7

Identifiers

DOI

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9 January 2020

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