CD86 (B70/B7-2) on endothelial cells co-stimulates allogeneic CD4+ T cells.

Abstract:

:In vascularized organ transplantation, vascular endothelial cells (EC) confronting recipient T cells are potentially significant APC initiating cellular immune responses that lead to rejection. In the present study, we studied the ability of human EC to stimulate allogeneic T cells and the co-stimulatory molecules involved in this response. On both human umbilical vein endothelial cells (HUVEC) and microvascular endothelial cells (MVEC), MHC class I, intercellular adhesion molecule (ICAM)-1 and CD86 were constitutively expressed as assessed by flow cytometry. After IFN-gamma treatment, MHC class II expression was induced, and MHC class I and ICAM-1 were up-regulated. In contrast, the expression of CD86 was unchanged and CD80 was undetectable even after IFN-gamma treatment. Highly purified CD4+ T cells proliferated in response to IFN-gamma-treated allogeneic HUVEC and MVEC, and this response was efficiently blocked by mAb to MHC class II, ICAM-1 and CD86. Furthermore, the addition of anti-CD86 mAb to the primary culture with allogeneic EC resulted in the induction of alloantigen-specific anergy. These results suggest that CD86 expressed on EC plays a critical role in initiating cellular immune responses to vascularized allografts and would be an important target for immune intervention.

journal_name

Int Immunol

journal_title

International immunology

authors

Seino K,Azuma M,Bashuda H,Fukao K,Yagita H,Okumura K

doi

10.1093/intimm/7.8.1331

subject

Has Abstract

pub_date

1995-08-01 00:00:00

pages

1331-7

issue

8

eissn

0953-8178

issn

1460-2377

journal_volume

7

pub_type

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