Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2018 Jul 4;9:1356. doi: 10.3389/fimmu.2018.01356

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

Copyright © 2018 Zhao, Liao, Li, Zhang, Zheng, Zhou, Han, Dong and Sun.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

PMC Copyright notice

Acute antibody-mediated rejection (AMR) established by performing kidney transplant at early stage after skin priming was concomitant with a high ratio of graft-infiltrating macrophages. Balb/c recipient mice were primed with C3H donor skin grafts for 4 days prior to receiving the C3H kidney transplant to establish the AMR model. On day 5 after kidney transplantation, the phenotypes of CD45⁺ immune cells infiltrated in the kidney graft were determined by flow cytometry. (A) Representative dot plots of CD11b⁺F4/80⁺ macrophages, CD8⁺ T cells, CD49b⁺ NK cells, CD4⁺ T cells, and CD220⁺ B cells. (B) Macrophages form the most prominent population in the kidney graft, followed by CD8⁺ T cells, NK cells, CD4⁺ T cells, and B cell subsets. The results represent the mean ± SD of at least four independent samples.