The OX40 receptor and gp34 ligand system is a recently characterized receptor/ligand pair. First identified on activated rat CD4+ cells, OX40 has been demonstrated to be a 50kD cell surface glycoprotein whose expression in human blood seems to be limited to activated T-cells. Human OX40 is a member of the nerve growth factor receptor/tumor necrosis factor family whose members also include fas/APO-1, CD40, CD27, CD30, and 4-1BB/ILA antigens. These molecules are involved with regulation of cell growth, differentiation and apoptosis. Gp34 was recently discovered to be the ligand for human OX40. It is a type II membrane glycoprotein expressed on HTLV-1 infected T-cell lines. Gp34 is also expressed on EBV-infected B-cells, activated peripheral circulating B-cells, and it appears to mediate binding of activated T- cells to human dermal microvascular endothelial cells. The exact function of this receptor/ligand pair is unclear. However, recent studies have shown that in addition to cell adhesion, OX40/gp34 crosslinking results in propagation of T-cell proliferation, B-cell proliferation and differentiation into antibody producing plasma cells, and an alteration in cytokine secretion. The goal of this proposed investigation is to characterize the distribution of this receptor/ligand pair in murine and human skin and to determine its role in the pathogenesis of cutaneous graft versus host disease (GvHD).

Project Start
1997-03-01
Project End
1998-02-28
Budget Start
1996-10-01
Budget End
1997-09-30
Support Year
4
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Emory University
Department
Type
DUNS #
042250712
City
Atlanta
State
GA
Country
United States
Zip Code
30322
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Costa, Adilson; Bonner, Michael Yi; Arbiser, Jack L (2016) Use of Polyphenolic Compounds in Dermatologic Oncology. Am J Clin Dermatol 17:369-85
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Arbiser, Jack L; Bonner, Michael Y (2016) Seborrheic Keratoses: The Rodney Dangerfield of Skin lesions, and Why They Should Get Our Respect. J Invest Dermatol 136:564-566
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Bhandarkar, Sulochana S; Lanka, Padmavathy; Lanka, Lakshmana Rao et al. (2016) Tuberculosis verrucosa cutis lesions exhibit a greater microvessel count than lupus vulgaris lesions. Exp Dermatol 25:479-80
Arbiser, Jack L (2014) PHIPing out: a genetic basis for tumor ulceration. J Invest Dermatol 134:600-602
Spence-Shishido, Allyson; Carr, Christopher; Bonner, Michael Y et al. (2013) In vivo Gram staining of tinea versicolor. JAMA Dermatol 149:991-2

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