Logo image
Blocking IL-10 signalling at the time of immunization renders the tumour more accessible to T cell infiltration in mice
Journal article   Peer reviewed

Blocking IL-10 signalling at the time of immunization renders the tumour more accessible to T cell infiltration in mice

Shu Chen, Guoying Ni, Xiaolian Wu, Bin Zhu, Zaowen Liao, Yuejian Wang and Xiao Song Liu
Cellular Immunology, Vol.300, pp.9-17
2016
url
https://doi.org/10.1016/j.cellimm.2015.11.002View
Published Version

Abstract

IL-10 signalling blockade immunization T cell infiltration
We recently reported that blockade of IL-10 signalling at the time of a human papillomavirus (HPV) long E7 peptide/LPS immunization leads to the regression of established HPV-16 immortalized tumours in mice similar to that induced by long E7 peptide/incomplete Freund's adjuvant (IFA)-based vaccination. In this paper, we demonstrated that blockade of IL-10 signalling at the time of long E7 peptide/LPS could elicit stronger T cells responses and render the tumour more accessible for immune cell infiltration than vaccination with long E7 peptide/IFA. Furthermore, priming with long E7 peptide/LPS and IL10 signalling blockade then boosting with long E7 peptide/IFA elicits stronger CD8+ T cell responses than long E7 peptide/IFA immunization. The results suggest that priming with long E7 peptide/LPS and IL10 signalling inhibitor, then boosting with long E7 peptide/IFA elicits may lead to better HPV infection related tumour regression in clinic.

Details

Metrics

6 File views/ downloads
966 Record Views

InCites Highlights

These are selected metrics from InCites Benchmarking & Analytics tool, related to this output

Collaboration types
Domestic collaboration
International collaboration
Web Of Science research areas
Cell Biology
Immunology

UN Sustainable Development Goals (SDGs)

This output has contributed to the advancement of the following goals:

#3 Good Health and Well-Being
#5 Gender Equality

Source: InCites

Logo image