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November 11, 2003Physiological Genomics

Tolerance induction by anti-CD80 and anti-CD86 mAbs in murine cardiac allografts was associated with marked expression of pro-inflammatory and apoptosis-related genes maintained >70 days posttransplant.

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Why the study?

Does daily intraperitoneal injection of anti-CD80 and anti-CD86 mAbs alter gene expression profiles in a murine cardiac allograft model?

Population

Murine cardiac allograft model (BALB/c to C57BL/6 mice)

Comparison

Daily intraperitoneal injection of anti-CD80 and… vs Syngeneic isografts and rejecting allografts

Design

Preclinical

Follow-up

more than 70 days posttransplant

Key result

Tolerance induction by anti-CD80 and anti-CD86 mAbs in murine cardiac allografts was associated with marked expression of pro-inflammatory and apoptosis-related genes maintained >70 days posttransplant.

Authors

YMYuichi MatsuiASAkio SaiuraYSYasuhiko Sugawara

Discussion

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Overview

Hypothesis-generating for tolerance despite inflammation in allografts; should not yet influence clinical immunosuppression protocols.

Structured PICO

Does daily intraperitoneal injection of anti-CD80 and anti-CD86 mAbs alter gene expression profiles in a murine cardiac allograft model?

P
Population
Murine model of cardiac allografts from BALB/c to C57BL/6 mice to study gene expression in immunologic tolerance.
I
Intervention
Daily intraperitoneal injection of anti-CD80 and anti-CD86 monoclonal antibodies (mAbs)
C
Comparator
Syngeneic isografts and rejecting allografts
O
Outcome
Global gene expression profile via oligonucleotide microarrayssurrogate

Immunologic tolerance in murine cardiac allografts can be induced and maintained despite prominent pro-inflammatory gene expression.

Cite This Study

Matsui et al. (2003) studied Cardiac allograft tolerance. anti-CD80 and anti-CD86 monoclonal antibodies vs. syngeneic isografts and rejecting allografts was evaluated on Global gene expression analysis. Tolerance induction by anti-CD80 and anti-CD86 mAbs in murine cardiac allografts was associated with marked expression of pro-inflammatory and apoptosis-related genes maintained >70 days posttransplant.

synapsesocial.com/papers/6a8b234ec12eaf65c8b1fc03https://doi.org/10.1152/physiolgenomics.00086.2003
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