Slowing blood flow to fight viral infection
T cells produce acetylcholine to dilate blood vessels and migrate into infected tissues Cytotoxic T lymphocytes are the assassins of the immune system, delivering cell death through direct interactions with virally infected or cancerous cells. To successfully execute their mission, these CD8 + T cel...
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Published in: | Science (American Association for the Advancement of Science) Vol. 363; no. 6427; pp. 585 - 586 |
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Main Author: | |
Format: | Journal Article |
Language: | English |
Published: |
United States
The American Association for the Advancement of Science
08-02-2019
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Subjects: | |
Online Access: | Get full text |
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Summary: | T cells produce acetylcholine to dilate blood vessels and migrate into infected tissues
Cytotoxic T lymphocytes are the assassins of the immune system, delivering cell death through direct interactions with virally infected or cancerous cells. To successfully execute their mission, these CD8
+
T cells must navigate a number of key steps, including sensing and entering infected tissues, locating infected cells in the vast tissue space, and supplying the precise mediators or interactions needed to elicit target cell death. Failure, or viral interference, at any of these steps can have devastating consequences for the host, including the establishment of viral persistence. Although some of the pathways and mechanisms involved in T cell purging of viral infection are well understood, the rate of local blood flow in the infected tissue has not been carefully explored as a factor mediating viral clearance. On page 639 of this issue, Cox
et al.
(
1
) demonstrate that T cells express the prototypical neurotransmitter acetylcholine (ACh), which dilates blood vessels, slowing blood flow enough to enhance T cell entry into infected tissues and ultimately allowing clearance of chronic viral infection. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Commentary-3 content type line 23 |
ISSN: | 0036-8075 1095-9203 |
DOI: | 10.1126/science.aaw3618 |