Combination of monoclonal antibodies with DST inhibits accelerated rejection mediated by memory T cells to induce long-lived heart allograft acceptance in mice.

Abstract:

:Donor-reactive memory T cells mediated accelerated rejection is known as a barrier to the survival of transplanted organs. We investigated the combination of different monoclonal antibodies (mAbs) and donor-specific transfusion (DST) in memory T cells-based adoptive mice model. In the presence of donor-reactive memory T cells, the mean survival time (MST) of grafts in the anti-CD40L/LFA-1/DST group was 49.8d. Adding anti-CD44/CD70 mAbs to anti-CD40L/LFA-1/DST treatment. The MST was more than 100 d (MST>100 d). Compared with anti-CD40L/LFA-1/DST group, anti-CD40L/LFA-1/CD44/CD70/DST group notably reduced the expansion of memory T cells, enhanced the proportion of CD4+Foxp3+ regulatory T cells (Tregs) and suppressed donor-specific responses. Our data suggest that anti-CD40L/LFA-1/CD44/CD70mAbs and DST can synergistically inhibit accelerated rejection mediated by memory T cells to induce long-lived heart allograft acceptance in mice.

journal_name

Immunol Lett

journal_title

Immunology letters

authors

Shao W,Chen J,Dai H,Peng Y,Wang F,Xia J,Thorlacius H,Zhu Q,Qi Z

doi

10.1016/j.imlet.2011.03.009

subject

Has Abstract

pub_date

2011-08-30 00:00:00

pages

122-8

issue

2

eissn

0165-2478

issn

1879-0542

pii

S0165-2478(11)00096-4

journal_volume

138

pub_type

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