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The host protecting the tumor from the host — targeting PD‑L1 expressed by host cells

*Corresponding author for this work
Scholary Output:
Contribution to journal
Review article
Peer-review

Open access

Abstract

Tumors frequently escape from immune surveillance by hijacking the natural control mechanisms that regulate normal immune responses. The programmed death‑1 receptor (PD‑1) on T cells normally helps limit excessive immune activation, but it can also suppress beneficial antitumor immunity. In the clinic, blocking either PD‑1 or one of its principal counterligands, programmed death–ligand 1 (PD‑L1), can lead to dramatic responses in certain patients. Because PD‑L1 can be expressed by both the tumor cells themselves and also the host cells, including host immune cells, the actual mechanistic target of therapy has remained unclear. In the current issue of the JCI, two papers, one by Tang and colleagues and the other by Lin and colleagues, used a variety of mouse tumor models to demonstrate that the relevant target for therapy in each case was the PD‑L1 molecules expressed by host cells and not by tumor cells. If this finding is generalized to humans, then it would suggest that the tumor persuades the host to actively suppress its own attempted immune response against the tumor cells.

Publication Information

Output type

Scholary Output:
Contribution to journal
Review article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 570-572 (3 pages)

Journal (Volume, Issue Number)

Journal of Clinical Investigation (Volume 128, Issue 2)

Publication milestones

  • Published - 02/01/2018

Publication status

Published - 02/01/2018

ISSN

0021-9738

Publication IDs

  • Scopus: 85041465178
  • PubMed: 29337304

Publication metrics

Metrics

SciVal
FWCI
0.95
SciVal
Author count
1
SciVal
citations
10
SciVal
Paper percentile
81
Fractional count
1
Fractional count
1
Fractional count
1
Fractional count
1
Scopus
citations

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Captures
39
Social media
1
Citation count
16

Funding Details

DHM is supported by NIH R01 CA103320 and CA21229.
FundersFunding numbers
NIH
CA21229, R01 CA103320
NCI
R01CA211229