Clonal enrichments of Vδ2– γδ T cells in Mycobacterium tuberculosis–infected human lungs
Corinna A. Kulicke,1 Deborah A. Lewinsohn,1 and David M. Lewinsohn1,2
1Department of Pulmonary and Critical Care Medicine, Oregon Health and Science University, Portland, Oregon, USA.
2VA Portland Health Care System, Research and Development, Portland, Oregon, USA.
Address correspondence to: David Lewinsohn, Department of Pulmonary and Critical Care Medicine, Oregon Health and Science University, 3181 Southwest Sam Jackson Park Road, Portland, Oregon 97239, USA. Phone: 503.721.1020; Email: lewinsod@ohsu.edu.
Find articles by Kulicke, C. in: JCI | PubMed | Google Scholar
1Department of Pulmonary and Critical Care Medicine, Oregon Health and Science University, Portland, Oregon, USA.
2VA Portland Health Care System, Research and Development, Portland, Oregon, USA.
Address correspondence to: David Lewinsohn, Department of Pulmonary and Critical Care Medicine, Oregon Health and Science University, 3181 Southwest Sam Jackson Park Road, Portland, Oregon 97239, USA. Phone: 503.721.1020; Email: lewinsod@ohsu.edu.
Find articles by
Lewinsohn, D.
in:
JCI
|
PubMed
|
Google Scholar
|
1Department of Pulmonary and Critical Care Medicine, Oregon Health and Science University, Portland, Oregon, USA.
2VA Portland Health Care System, Research and Development, Portland, Oregon, USA.
Address correspondence to: David Lewinsohn, Department of Pulmonary and Critical Care Medicine, Oregon Health and Science University, 3181 Southwest Sam Jackson Park Road, Portland, Oregon 97239, USA. Phone: 503.721.1020; Email: lewinsod@ohsu.edu.
Find articles by
Lewinsohn, D.
in:
JCI
|
PubMed
|
Google Scholar
|
First published November 25, 2019 - More info
© 2020 American Society for Clinical Investigation
Unconventional T cell subsets, including donor-unrestricted T cells (DURTs) and γδ T cells, are promising new players in the treatment and prevention of infectious diseases. In this issue of the JCI, Ogongo et al. used T cell receptor (TCR) sequencing to characterize unconventional T cell subsets in surgical lung resections and blood from Mycobacterium tuberculosis–infected (Mtb-infected) individuals with and without HIV coinfection. The study revealed highly localized expansions of γδ T cell clonotypes not previously associated with the immune response to Mtb and demonstrates the power of high-throughput analysis of the TCR repertoire directly from infected tissue. The findings contribute to our understanding of tuberculosis control and have implications for the development of both therapeutic and vaccination strategies.
- Purchase this article
- $10
- Purchasing this article will give you full access for the calendar year.
- Purchase Site Pass
- $25
- This will give you access to every article on the site for 24 hours.
- Online subscription
- $95
- Individual online subscriptions give you full online access for the calendar year.
- Individual online subscriptions ordered from September 1st on will receive access for the remainder of current year as well as for the full following year subscription term.
- Print subscription
- $830
- Individual print subscriptions give you the print journal and full online access for the year.
- JCI This Month subscription
- $125
- JCI This Month is a 16- to 20-page overview of the articles published each month
- Subscribing to JCI This Month also gives subscribers full online access for the calendar year.
- *Price outside U.S. and Canada: $225.
Copyright © 2019 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)