Vaccination for Mycobacterium tuberculosis infection: reprogramming CD4 T-cell homing into the lung.

Abstract:

:Development of effective tuberculosis vaccines is hampered by insufficient understanding of protective immunity. Here, Woodworth et al.1 show secondary effector CD4 T cells generated after Mtb challenge of H56/CAF01 vaccinated mice display superior lung homing compared with primary effectors. Vaccination generates large populations of parenchymal lung effector cells by inducing CXCR3+KLRG1- cells that continuously migrate from lymph nodes to lung, and limiting the generation of non-protective CX3CR1+KLRG1+ intravascular effectors, providing insight vaccine-mediated protection against tuberculosis.

journal_name

Mucosal Immunol

journal_title

Mucosal immunology

authors

Barber DL

doi

10.1038/mi.2016.110

subject

Has Abstract

pub_date

2017-03-01 00:00:00

pages

318-321

issue

2

eissn

1933-0219

issn

1935-3456

pii

mi2016110

journal_volume

10

pub_type

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